The Scientific World Journal

Volume 2013 (2013), Article ID 193252, 16 pages

http://dx.doi.org/10.1155/2013/193252

Review Article

Sickle Cell Disease: New Opportunities and Challenges in Africa

J. Makani,1,2 S. F. Ofori-Acquah,3,4 O. Nnodu,⁵ A. Wonkam,6,7 and K. Ohene-Frempong⁸

¹Department of Haematology and Blood Transfusion, Muhimbili University of Health and Allied Sciences, P.O. Box 65001, Dar es Salaam, Tanzania

²Nuffield Department of Medicine, University of Oxford, Oxford, UK

³Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA

⁴School of Allied Health Sciences, College of Health Sciences, University of Ghana, Ghana

⁵Department of Haematology and Blood Transfusion, College of Health Sciences, University of Abuja, Abuja, Nigeria

⁶Division of Human Genetics, Faculty of Heath Sciences, University of Cape Town, South Africa

⁷Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Cameroon

⁸Children’s Hospital of Philadelphia, Philadelphia, PA, USA

Received 23 April 2013; Accepted 9 June 2013

Academic Editors: Y. Al-Tonbary, M. A. Badr, A. El-Beshlawy, A. Mansour, and F. Tricta

Copyright © 2013 J. Makani et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Sickle cell disease (SCD) is one of the most common genetic causes of illness and death in the world. This is a review of SCD in Africa, which bears the highest burden of disease. The first section provides an introduction to the molecular basis of SCD and the pathophysiological mechanism of selected clinical events. The second section discusses the epidemiology of the disease (prevalence, morbidity, and mortality), at global level and within Africa. The third section discusses the laboratory diagnosis and management of SCD, emphasizing strategies that been have proven to be effective in areas with limited resources. Throughout the review, specific activities that require evidence to guide healthcare in Africa, as well as strategic areas for further research, will be highlighted.

1. Introduction

Sickle cell disease (SCD) consists of a group of disorders characterised by the presence of sickle haemoglobin. Although over 700 structural hemoglobin (Hb) variants have been identified, only two (Hb S, Hb C) reach high frequencies in Africa. The common SCD syndromes in this region include homozygous HbSS disease (HbSS) commonly known as sickle cell anaemia (SCA) and Hb SC disease. SCD was known in some parts of Africa before the twentieth century: inhabitants of western Africa gave the disease-specific names that evoke acute, painful episodes or death or refer to children destined to die and to be reborn as their own siblings [1, 2]. Africa is the major origin of the sickle () mutations [3]. There are four chromosomal haplotypes that are associated with the mutation. They are named after the regions where they have the highest frequency: Benin, Senegal, Bantu (Central African Region (CAR)), and Arab-Indian. The haplotypes are defined by restriction fragment length polymorphisms (RFLPs) in the -globin locus. Due to the population specificity of the haplotypes, it is believed that the sickle cell mutation arose independently in these populations and remained to this day [4].

1.1. Normal Human Hemoglobin

Human Hb is encoded by a cluster of genes located on chromosomes 11 and 16 that are expressed in a developmentally regulated manner. They are tetramers of two pairs of -like and -like globin chains. Adult and fetal hemoglobin have (Hb A,,(Hb A2,, or chains (Hb F,, whereas in the embryo, -like chains—termed (Hb Portland, ) or —and and chains form Hb Gower 2 () (Figure 1) [5].

Figure 1: Developmental control of human haemoglobin (Hb) expression [6].

Embryonic hemoglobin production is confined to the yolk sac. Thereafter the major site of synthesis is the fetal liver. HbF is the predominant type of hemoglobin in fetal life, but around birth there is a switch from fetal to adult globin gene expression, when HbF is gradually replaced by adult hemoglobin, such that by 6 months of age the major Hb is HbA (). Residual amounts of HbF, however, continue to be synthesized throughout adult life, and the amounts vary considerably, with the majority of adults having less than 1% HbF.

1.2. Pathophysiology of Clinical Events

Sickle haemoglobin (HbS) results from a substitution of one amino acid (Valine) for another amino acid (Glutamic acid) at position six of the -globin polypeptide chain. This substitution is caused by a single-base mutation in codon 6 within the -globin gene on chromosome 11, where the sequence GAG occurs instead of GTG.

Due to the abnormal amino acid in the -globin chain, HbS forms long, insoluble polymers when deoxygenated, and the red blood cells (RBCs) containing HbS become less deformable and form a “sickle” shape. It was previously thought that the clinical consequences were simply due to this abnormal, rigid sickle red blood cell occluding small blood vessels. However, there is increasing evidence that the pathogenesis of the various clinical events, both acute and chronic, results from a series of complex mechanisms which are not limited to the RBC [7]. These relate to concentration of HbS and other haemoglobin variants such as HbF within the cell which reduces its ability to polymerise [8], disturbances in the red cell membrane making the cell less responsive to oxidant stress, and altered membrane lipids resulting in increased rigidity [9–11]. Additionally, adhesion molecules such as integrins ( ), ( ), their receptors (VCAM-1, ICAM-4), selectins interact with endothelial cells, RBC, and a variety of soluble proteins within the plasma, such as thrombospondin (from platelets) and von Willebrand factor from endothelial cells to mediate vasoocclusion within the macro- and microvasculature [12–16]. Finally there is compelling evidence of the role of nitric oxide (NO) in SCD [17]. NO is a potent regulator of basal vasodilator tone. It also inhibits the expression of cellular adhesion molecules [18]. The increase in haemolysis in SCD results in an excess of haemoglobin in the plasma, which exceeds the scavenging capacity of haptoglobin. The result is that there is abnormal “cell-free” haemoglobin, which circulates in plasma, binding to and consuming NO, so causing a reduction in the concentration of NO [19]. This results in vasoconstriction, increased adhesiveness of erythrocytes, leukocytes and endothelial cells, and platelet aggregation.

1.3. Clinical Events in SCD

Although SCD stems from an abnormality of the RBC, it is essentially a multisystem disorder, affecting almost every organ system of the body, as shown in Figure 2. The clinical consequences can be divided into 4 groups: haemolysis and haematological complications, vasoocclusion, infection, and organ dysfunction.

Figure 2: Selected clinical consequences of SCD.

2. Haemolysis and Haematological Complications

At birth, individuals with SCD do not have anaemia, but with the synthesis of adult Hb, they develop chronic haemolytic anaemia that is present throughout life. This may be interspersed with acute episodes of reduction in haemoglobin “anaemic crises”. Hyperhemolysis crises are defined by a sudden fall in steady state haemoglobin accompanied by increased reticulocytosis and exaggerated hyperbilirubinemia. The chronic haemolysis in SCD may result in gall bladder disease due to high levels of bilirubin. Although the main cause of anaemia in SCD is chronic haemolysis, there are other types of anaemia that may occur. Acute splenic sequestration, when there is rapid onset of trapping of red blood cells in the spleen, is characterised clinically by a sudden increase in splenic size, at least 2 cm below the left coastal margin, accompanied by a reduction in haemoglobin or haematocrit by 20% of baseline level. This has been described in SCD and is a significant cause of mortality [20]. Anaemia may be secondary to infections such as malaria, bacterial and viral diseases. Of the latter, RBC aplasia in the bone marrow has been notably described and has been associated with infection with parvovirus serotype B19 [21].

3. Vasoocclusion

Vasoocclusion (VOC) is thought to be the underlying cause of painful crises, acute splenic sequestration, and priapism (painful and prolonged penile erection). Painful crises, considered the hallmark of SCD, are defined as severe pain lasting for 2 or more hours that is attributable to SCD. The sites that are normally affected include the arms, legs, back, abdomen, chest, and head. Painful crises do not include other causes/types of pain in SCD such as dactylitis, acute chest syndrome, right upper quadrant syndrome, osteomyelitis, and appendicitis. It is the most common cause of hospitalisation and frequent pain (defined as 2 or more painful events a year for three years) is associated with poor quality of life and increased risk of death [22].

4. Infection

Individuals with SCD are reported to be susceptible to infections with encapsulated organisms such as Streptococcus pneumoniae [23–25]. The use of oral penicillin in the USA had a significant impact on reduction in mortality [26], and it is now policy in many high-income countries to give penicillin prophylaxis and antipneumococcal vaccination to SCD patients [27]. It was previously thought that the situation in Africa may be different. Aside from the fact that the data regarding the clinical spectrum of SCD are limited, there was controversy regarding the role and significance of pneumococcal disease in causing morbidity and mortality in SCD in this setting [28]. However, there is emerging evidence to confirm that pneumococcal disease is a significant cause of bacteraemia in SCD [29], with calls to introduce interventions for preventing infections as a critical factor in improving survival [30, 31]. The various factors that are associated with increased infections in SCD may be directly related or unrelated to the immune system. Some infections may be the result of a complication or treatment of SCD itself. SCD patients are at high risk of transfusion-transmissible infections particularly with human immunodeficiency virus and viral hepatitis since they receive frequent, often unplanned emergency blood transfusion (BT) [32–35]. This is particularly important in Africa, given the high prevalence of HIV infection and the operational problems in providing adequate blood-transfusion services. Long-term BT may result in iron overload, which in itself is associated with infections due to Yersinia Enterocolitica [36]. SCD causes end-organ damage to the lung, liver, kidney, and skin, making these sites susceptible to infection by unusual organisms. In addition, skeletal complications, poor perfusion, and blood supply to bone tissue are also thought to contribute to increased susceptibility to infections of the bone, osteomyelitis, which is often due to salmonella infections [37]. Other factors include high bone marrow turnover due to chronic haemolysis which results in increased susceptibility to viral infection. Parvovirus B19 infections are one of the viral infections that predispose to poor outcome with erythrocytic aplasia that may lead to life-threatening anaemia [21, 38, 39]. However, the epidemiology of this virus in Africa is poorly defined [40–42]. Individuals with SCD may have impairment of the immune system, involving both cellular immunity and humoral immunity. The most well-described immune defect is caused by reduced function of the spleen. Patients with SCD have repeated splenic infarction due to vasoocclusion which causes loss of the splenic vasculature leading to hyposplenism [43]. Reports have suggested that 14% patients with SS-SCD are functionally asplenic at 6 months of age, with this number gradually increasing: 28% at 1 year, 58% at 2 years, 78% at 3 years, and by 5 years, 94% are affected [44]. This is from an area without malaria. One of the roles of the spleen is filtration of unopsonised bacteria and remnants of red blood cells from intravascular space as well as opsonised bacteria [45]. Furthermore, the spleen is involved in the synthesis of soluble mediators of immunity. Therefore patients with SCD, with a functional asplenia, have been reported to have impaired antibody responses as well as lacking specific antibodies, particularly against Salmonella species and Streptococcus pneumonia [46]. This is thought to be due to deficiency of a complement factor involved in the activation of the immune system. The classic pathway is activated by antigen-antibody interaction which causes fixation of complement components , , and which then activate , whereas in the alternate pathway the antigen directly activates . Activation of , which is an opsonin, results in fixing of antigens on the microorganism [47] making them susceptible to enhanced phagocytosis by neutrophils and monocytes/macrophage. Johnston et al. illustrated that patients with SCD have an abnormality in the activation of this pathway with failure of full activation and fixing of to encapsulated bacteria [48]. This results in failure of SCD patients to phagocytose invading organisms, particularly Streptococcus pneumoniae. The distinction between factors directly related to the immune system or not is somewhat arbitrary as there is a lot of overlap between the various factors. Although there have been reports of different patterns of infections in patients with SCD, summarised in Table 1, this review focuses on invasive bacterial infections as detected by blood culture. In the absence of prophylaxis, infections are thought to be the leading cause precipitating clinical events and associated with increased mortality [23, 49].

Table 1: Clinical syndromes and common causative organisms reported in SCD.

Syndrome
Organisms
Reference

Septicaemia
S. pneumoniae, H. influenza, Salmonella spp, E. Coli, S. Aureus, and M. Pneumoniae
[28, 29, 50]

Pneumonia
S. pneumoniae, M. Pneumoniae, Chlamydiae  pneumonia

Meningitis
S. pneumoniae

Osteomyelitis
Salmonella spp., E. Coli, Gram negative organisms, and S. Aureus
[37, 51, 52]

Aplastic anaemia
Parvovirus
[21, 38, 39]

AIDS and Hepatitis
HIV Viral hepatitis B,C
[32, 33, 53]

Abdominal pain
Helicobacter pylori, Yersinia enterocolitica
[36]

5. End-Organ Dysfunction

With increase in survival, major organs in individuals with SCD are eventually damaged. The brain and lungs are particularly affected, with stroke, defined as an acute neurological syndrome due to vascular occlusion or haemorrhage in which symptoms and signs last for more than 24 hours, being a well-described event. Acute chest syndrome (ACS) is an acute respiratory illness characterised by new pulmonary infiltrates on chest X-ray and falling arterial oxygen saturation [54, 55]. Both these events have been reported to occur with high prevalence in SCD and are also risk factors for death [23, 55, 56].

6. Heterogeneity of Clinical Events in SCD

The clinical expression of SCD is heterogeneous (Table 2). There is interindividual variability ranging from near complete asymptomatic to severe debilitating illness. There is also variability within an individual, with changes in the type and frequency of clinical events with age. Finally, there is variability in clinical events depending on the geographical location. This is due to the differences in environmental factors such as nutrition, socioeconomic status, and climate that will influence the natural history of disease. The general pattern of clinical disease is characterised by quiescent periods interspersed with acute events, which are referred to as crises.

Table 2: The prevalence of selected clinical consequences of SCD.

Clinical event
Prevalence
References

Haemolysis

    Anaemia
Chronic
[57–59]

    Cholelithiasis
Prevalence is 40% by adolescence
[60, 61]

    Aplastic anaemia
Associated with parvovirus B19 infection
[61–63]

    Hyperhemolysis
Limited reports from Africa
[64–67]

Vasoocclusion

    Pain
More than 60% patients

Most common cause of admission

Frequent pain is a risk factor for mortality
[22, 23, 68, 69]

    Acute splenic sequestration (ASS)
Frequently occurs before the age of 3 yrs
[23, 70, 71]

    Leg ulcers
Prevalence is 10–25% adults
[72, 73]

    Priapism
Prevalence is 10–40% males

Occurs frequently in 5–14 years age group
[74]

Organ dysfunction

    Neurological events

        Stroke
Prevalence is 10% in children risk factor for mortality

High rate of recurrence

Leads to poor quality of life
[75]

        Cognitive/silent
Prevalence is 20%

Risk factor for overt stroke

Leads to impairment of executive function
[76–79]

        Retinopathy
Prevalence is >30% in HbSC
[80]

    Chest

        Acute chest syndrome (ACS)
Prevalence is 40%

Occurs frequently in children

Has severe consequences in adults 12.8 per 100-patient years 59
[54–56]

        Pulmonary hypertension
Prevalence is 30%

Risk factor for mortality
[79, 81–84]

        Avascular necrosis of femoral head
Prevalence is 10–50% in adults
[85–87]

        Renal disease
Prevalence of chronic renal failure is 5%–20%
[88]

Infections

    Malaria
There is low prevalence of malaria in SCD. However, when malaria occurs in SCD it is associated with increased risk of morbidity due to severe anaemia and mortality
[89, 90]

    Bacterial infections
10% children under 5 years
[91]

Modified from [92, 93].

The reasons for this heterogeneity are not fully understood [94]. Interindividual variation in fetal hemoglobin (HbF) levels is one of the main modifiers that contribute to the clinical heterogeneity observed in SCD patients. Higher expression of HbF in adulthood ameliorates morbidity and mortality in SCD [56, 95].

It is now clear that common HbF variation is a quantitative genetic trait shaped by common polymorphisms. Multiple genes, together with an environmental component, determine the measured value of HbF in any given individual. Genetic variation at three major loci accounts for a relatively large proportion (20%–50%) of the phenotypic variation in HbF levels: (1) a single-base substitution (T/C) at position −158 of the globin gene, termed XmnI site [96]; (2) the HMIP locus (HBS1L-MYB intergenic polymorphism) on chromosome 6q [97]; and (3) the oncogene BCL11A on chromosome 2 [98]. These variants have been well reported in nonanemic Northern Europeans and Sardinians, a -thalassemia cohort, in SCD patients from Brazil, and in the African-American Cooperative Study of Sickle Cell Disease (CSSCD) [99–101]. There is very little description of the three main genetic polymorphisms explaining phenotypic variation in HbF levels and clinical phenotype in native African SCD patients [97, 102].

7. Epidemiology of Sickle Cell Disease

7.1. Prevalence

The prevalence of SCD can be objectively determined by calculating the birth prevalence of affected children, which requires accurate diagnosis and registration at birth. Since this is not done in most African countries, an alternative method is to use the prevalence of the carrier or heterozygous states (HbAS) to calculate the expected birth rate of SCA based on the gene frequency and Hardy-Weinberg equation. Approximately 300,000 children are born every year with SCD in the world, and countries such as the United States of America, United Kingdom, and Jamaica have well-documented SCD population. However, this SCD population constitutes only 1% of the global population of SCD, as over 75% are in Sub-Saharan Africa [103, 104]. It has been estimated that SCD results in the annual loss of several millions of disability-adjusted life years, particularly in the developing world [105]. Hemoglobinopathies alone represent a health burden comparable to that of communicable and other major diseases [106].

7.2. Population Genetics and Dynamics: SCD, Malaria, and Migration

Compared to noncarriers, healthy carriers of recessive genes for SCD have a well-documented survival advantage against the lethal effects of malaria. As a result, carriers are more likely to reach reproductive age. Consequently, the birth prevalence of SCD is high in Africa [107–109]. The resurgence of malaria in many parts of the world will serve to maintain these polymorphisms, but even if this selective force were removed it would take many generations for the gene frequencies of these conditions to fall significantly [110]. Any changes resulting from variation in selection or population dynamics will, however, be very small compared with the effect of the demographic transition that many countries have undergone over recent years [110]. Specifically, there is a high prevalence of hemoglobin S (HbS) in Africa and hemoglobin C (HbC) in parts of West Africa [111]. Since subjects that are homozygous for HbC do not present with severe disease like HbSS, it is anticipated that the frequency of HbC will progressively increase even if malaria is not controlled [112]. Internal migration in Africa has led to SCD, which was previously rare, being introduced in South Africa through an influx of migrants from West and Central Africa [113]. The high birth prevalence of SCD has highlighted the burden of SCD, such that in 2006, the World Health Organization (WHO) recognized SCD as a public health priority [114]. There is limited information about the burden of SCD to the health system and the impact that it has on individuals.

7.3. Mortality

There is a higher rate of mortality among individuals with SCD, with reports suggesting that if untreated most children with SCD die in early childhood. Studies done in Nigeria, reported mortality of up to 90% [115] but recent estimates suggest that mortality rate has decreased and is more likely to be up to 50% by 20 years. This mortality rate in Africa is similar to those reported in the early 1960s in the United States of America and United Kingdom. However, with early diagnosis and comprehensive treatment, significant reductions in mortality have been achieved, with recent reports of improved survival; 85.6% survive to 18 years in the USA [116], 84% in Jamaica, and 99.0% to 16 years in the UK [117]. The common causes of death in the USA, UK, and Jamaica are infections, acute splenic sequestration, and acute chest syndrome [23, 49, 118, 119] with the highest incidence between 1 and 3 years of age.

8. Laboratory Diagnosis of Sickle Cell Disease

The laboratory diagnosis of SCD is based on the demonstration of HbS and the absence or significant reductions in HbA, with variation in the percentage of two other hemoglobins—HbF, HbA₂—in RBCs. Commonly available screening tests in Africa include sodium metabisulphite sickling test and sickle solubility tests and confirmatory tests using electrophoresis and chromatography to confirm the sickle phenotype (SS/AS/SC/Sβ ⁻thalassaemia). The three tests widely used are haemoglobin electrophoresis, isoelectric focusing (IEF), and high performance liquid chromatography (HPLC). DNA-based assays precisely describe the genotype; however, for clinical purposes, diagnosis usually involves screening (sickling or solubility test) followed by confirmation of the sickle phenotype using gel electrophoresis, IEF or HPLC.

8.1. Screening Tests

In most African hospitals, screening is done, using the “sickling test”, which involves making a thin blood film which is then put under hypoxic conditions by the addition of sodium metabisulphite. This will result in RBCs containing HbS becoming deformed (i.e., forming sickle cells) as detected by light microscopy. A “positive” sickling test identifies the presence of sickled RBCs, which occurs in both homo- (SS) and heterozygous (AS) states. The sickle solubility test is another method used for screening which is based on the principle that HbS becomes insoluble when it is deoxygenated. Additional confirmatory tests are required to confirm SS-SCD or SCD involving other Hb types, when these screening assays are used.

8.2. Confirmatory Tests

These tests are based on the principle that different haemoglobin isoforms have different overall ionic charge, which makes them migrate with different velocities in an electric field. HBE can be done under alkaline or acidic conditions. HbA, HA₂, HbF, and HbS migrate towards the anode under an electric field with different rate of mobility. During alkaline Hb electrophoresis the resolution between HbS and HbF can be poor, particularly in individuals with high HbF levels, for example, neonates. Under acidic conditions, HbF migrates relatively more rapidly and is therefore distinguishable from both HbA and HbS. Isoelectric focusing uses the same principles but is slightly more expensive than HBE. However, it is able to identify more Hb variants that would not be detected by HBE. It also has the advantage that it does not require commercial reagents. HPLC uses cation exchange chromatography to identify the various hemoglobins in an individual. It has the advantage in that it can also accurately quantify the Hb levels. In resource-rich countries, screening has largely been replaced by HPLC and confirmation is then done by IEF or HBE. This is mainly because HBE and IEF are labour intensive, time consuming and would not identify abnormal bands or quantify Hb. Furthermore, the quantification of Hb fractions by HPLC is used to monitor patients who are on Hydroxyurea therapy or exchange blood transfusion.

8.3. Molecular Diagnosis of SCA

The most popular molecular diagnosis of mutation, based on restriction enzyme digestion, is performed on HBB PCR products. The point mutation, which results in SCD, abolishes the restriction site for the restriction enzyme DdeI. Digestion of DNA of individuals homozygous for HbAA would result in two fragments 188 bp and 192 bp. Analysis of heterozygous HbAS samples would result in three fragments one of 380 bp and the two digested fragments of 180 bp and 192 bp. Homozygous HbSS samples would result in 380 bp fragments being produced (Figure 3). This method is simple and cost effective and could be used for prenatal genetic diagnosis in African settings [120].

Figure 3: RFLP of HBB fragment with DdeI. Lane 1: undigested control, Lane 2: HbAA control, Lane 3: HbAS control, and Lane 4: HbSS MW: molecular weight marker.

9. Management of Sickle Cell Disease

As a chronic disease, the natural history of SCD is characterised by quiescent periods interspersed by acute events, known as crises, leading to patients seeking health care and frequent hospitalisation. The “crises” range from defined syndromes such as acute chest syndrome (ACS), acute splenic sequestration (ASS), to less well-defined symptoms that include pain, fever, anaemia, worsening of jaundice, and leg ulcers. Other circumstances include pregnancy, dehydration, and extreme cold weather. With the increased life span of individuals with SCD, there has been an increasing awareness of the importance of improving the quality of life as well as preventing damage to major organs. SCD is associated with increased mortality. The causes of mortality in the USA, UK, and Jamaica included infections, ACS, ASS, and aplastic crises [23, 49, 118, 119]. The management of patients with SCD involves interventions that improve survival, prevent complications, treat acute events, and reduce end-organ damage. Specific conditions or circumstances when SCD patients require extra care include surgery requiring general anaesthesia, due to increased risk of developing acute sickling complications and sudden death. Over the past 3 decades there has been an improvement in the understanding of the different pathogenic mechanisms responsible for sickle cell events and organ dysfunction. Through a series of clinical trials, effective interventional strategies have been established.

9.1. Newborn Screening (NBS)

The highest incidence of death occurs in the first 3 years of life [23, 49, 118, 121]. Identification of children at birth by newborn screening (NBS), and institution of preventative care has improved survival [116, 122, 123]. Patients who are identified at birth can be given counselling and advice about the course of illness. They can then be enrolled in comprehensive care programmes that provide prompt and effective care of acute events and prophylaxis against complications, resulting in overall positive impact on survival and quality of life. Countries with large SCD populations and adequate resources have started NBS programmes.

9.2. Comprehensive Care Including Dedicated Day Care Facilities

The identification of SCD at birth has to be accompanied by enrolment into programmes that provide comprehensive care by multidisciplinary teams comprising nurses, genetic counsellors, social workers, paediatricians, haematologists, orthopaedic surgeons, ophthalmologists, and internists. These programmes provide appropriate advice, counseling, and support to parents and affected individuals. This includes advice such as drinking adequate quantities of fluid to avoid dehydration and wearing warm clothing in cold weather. Specific health education that will enable them to recognise acute events and seek medical care is also essential. Teaching mothers to recognise enlargement of the spleen and anaemia was effective in diagnosing and treating anaemia due to ASS [71, 124]. Patients are also seen on a regular basis and provided with folic acid supplements. The evidence for the burden of folate deficiency in SCD is limited. Prompt treatment of crises (fever and pain), particularly at outpatient or in day-care facilities, has been found to be effective and reduces the burden of hospitalization to the individual and the health system [125–128]. Long-term care should be provided by a multidisciplinary team including professionals who have specialized in haematology and blood transfusion for adults and paediatric haematologists in children. In settings where there is a low prevalence of SCD or limited number of health care professionals, SCD patients can receive care from general health care workers. In such a setting, guidelines for management can be provided to general health care workers with a system of referral to specialised centres.

9.3. Prevention and Treatment of Infections

In the absence of intervention, bacterial infection is the leading cause of mortality in individuals with SCD, and the age group that is most affected is 1 to 3 years [37, 49, 118]. Bacterial infection in SCD is mainly due to Streptococcus pneumoniae, resulting in pneumonia, sepsis, and meningitis. The highest incidence of invasive pneumococcal disease is in children less than 6 years of age [91, 118]. In a landmark study in the USA, Gaston and colleagues demonstrated an 84% reduction in incidence of pneumococcal infection with the use of oral penicillin [26]. Interventions with daily oral penicillin and vaccination against pneumococcal infections have successfully reduced mortality in developed countries [26, 116, 129]. In Africa, these interventions have not been implemented as the evidence to demonstrate a similar role of bacterial infections was lacking. This made it difficult for hospitals and governments in developing countries to implement these interventions. Furthermore, published reports have actually questioned the role of prophylaxis against Streptococcus pneumoniae (SPN), in Africa [28]. However, there has been increasing evidence of the role of bacterial infections, particularly due to SPN in causing high childhood mortality [130, 131]. Since SCD patients are highly susceptible to SPN infections due to impaired immunity, this makes it even more likely that SPN infections will have a more significant role in SCD mortality. Therefore, there has been an increase in the appeal to implement these interventions [30, 132].

Malaria is widely considered to be one of the major causes of illness and death in patients living with SCD in SSA [90, 104]. Although, SCD individuals have an element of protection against malaria; with a lower prevalence of malaria infection [133–135] and a lower parasite density [136], the risk of mortality when SCD patients get malaria is significantly higher [137]. It is recommended that individuals with SCD who live in a malaria endemic area should receive prophylaxis against malaria [138]. There is ongoing debate as to what is the most appropriate agent that can be used for chemoprophylaxis. The increasing resistance by Plasmodium falciparum parasites to chloroquine has meant that most countries have had to stop using chloroquine. Sulphadoxinepyrimethamine has antifolate properties and is not recommended for prophylaxis in patients with SCD who are considered to be folate deficient. Most malaria-endemic countries have therefore been unable to decide which drug to use for prophylaxis in SCD, with options limited to proguanil (paludrine), mefloquine (Lariam), Malarone, or Doxycycline. Current practice in malaria-endemic countries involves use of insecticide-treated nets and prompt diagnosis and treatment of malaria.

9.4. Blood Transfusion (BT)

SCD is contributing to the anaemia in under fives and pregnant women in areas of high prevalence. Patients with SCD have a compensated chronic haemolytic anaemia which allows them to carry on with normal activities at steady-state haemoglobin with narrow reserve capacity to accommodate strenuous physical activities. The steady state haemoglobin varies from person to person and is related to the level of HbF, co-inheritance of alpha thalassaemia, or heterozygosity for another haemoglobin type such as HbC. Although individuals with SCD have chronic anaemia which is tolerated, rapidly worsening anaemia can occur, and this presents as an emergency. It can be caused by ASS, aplastic crises, and hyperhemolysis or associated with other events such as bacterial infections and malaria. Under these circumstances, anaemia is life threatening and requires prompt treatment with blood transfusion. The products that are used (whole blood or packed RBCs) and the method of transfusion (simple or exchange) are determined by the clinical situation, availability of resources, and the capacity to provide the blood product and establish venous access [139]. Blood transfusion is also effective in other situations, such as acute stroke [140], ACS [141], and perioperatively [142]. Blood transfusion works by increasing the level of Hb, thus improving oxygen delivery. It also reduces the proportion of sickle RBCs in the circulation. Exchange or red cell transfusion has also been shown to be effective in reducing the level of HbS to less than 30% [143–146]. This is thought to reduce the deleterious effects of HbS and improve outcome. Long-term blood transfusion therapy (LTBT) has been found to be effective in the prevention of brain injury due to cerebrovascular disease [140]. Blood transfusion is associated with risks which have to be weighed against the benefits when considering implementing this as an intervention. These will be reviewed in the section on stroke.

9.5. Pain

Pain, the defining feature of SCD and its commonest symptom, starts early in life and persists throughout life. It is the commonest symptom of SCD and is related to disease severity. Studies in children in developed countries suggest that painful episodes and acute chest syndrome were the most frequent complications of sickle cell disease and that the pain crises are a major predictor of adverse outcome in children along with anaemia and leucocytosis. In adults, large proportion of patients die during an acute episode of pain, making it a risk factor for early death along with acute chest syndrome and stroke. However due to its subjective nature, patients with SCD may not be having appropriate assessment and adequate pain management necessary to prevent complications relating to the pain such as the development of a chronic pain syndrome resulting in worsening of the sickle cell condition. Training is essential for adequate assessment of pain intensity, reporting, documentation by patients, care giver, and health workers. Prompt management of pain requires attention to the precipitating causes (stress, infection, dehydration, acidosis, and allodynia). Adequate oral analgesic should be administered for mild pain and parenteral for moderate to severe pain according to WHO step ladder for analgesia in patients. When the expected relief is not obtained in response to adequate doses of analgesics, this should alert to the condition of opioid-induced hyperaesthesia, allodynia, or the progression of acute pain to chronic pain [147–149]. However, many health facilities in Africa do not have access to opioids.

9.6. Hydroxyurea

Hydroxyurea (HU) (also known as hydroxycarbamide) has been reported to be effective in improving survival and reducing morbidity in some SCD patients (Table 3). The clinical outcomes include reduction in frequency of painful episodes and hospital admissions [150]. Hydroxyurea therapy is also monitored by a number of laboratory parameters which include increased HbF levels, mean corpuscular volume (MCV), and reduction in WBC count. Hydroxyurea has been found to be effective in the prevention of brain injury due to cerebrovascular disease [151].

Table 3: Summary of study outcomes for hydroxyurea use in adults and children.

Outcome
Impact in adults
Impact in adolescents

Clinical outcomes

    Pain crises
↓ ↓↓
↓ ↓

    Hospitalisations
↓ ↓↓
↓ ↓↓

    Blood transfusion therapy
↓ ↓↓
↔ (insufficient data)

    Acute chest syndrome
↓ ↓↓
↔ (insufficient data)

Laboratory markers

    Foetal haemoglobin
↑↑↑
↑↑↑

    Haemoglobin
↑↑↑
↔ (not significantly significant)

    Mean corpuscular haemoglobin
↑↑↑
↑↑↑

    White blood cell count
↓ ↓↓
↓ ↓↓

Prevention of end organ damage

    Brain
↔
↔

    Spleen
↔
↔

    Kidney
↔
↔

Mortality
↓
↔=

↓ ↓↓: high-grade evidence for decrease; ↓: low-grade evidence for a decrease; ↑↑↑: high-grade evidence for increase; ↑: low-grade evidence for an increase; ↔: not evaluated/not significantly different/insufficient data. Source [152].

9.7. Nitric Oxide

Lung dysfunction results from a combination of repeated pulmonary infections and infarctions as well as increased vasoconstriction leading to pulmonary hypertension [54, 55]. The latter has recently been shown to be associated with reduced bioavailability of nitric oxide [19], which has resulted in the development of potential therapies such as L-arginine, citrulline, and inhaled nitric oxide which is aimed at increasing NO levels through different pathways [153–157].

9.8. Stem Cell Transplant

The only cure that is available for SCD is stem cell transplantation (SCT), which replaces the host’s bone marrow with stem cells containing normal -globin genotype. Since the first successful transplant reported in 1984 [158], there has been significant reduction in risks due to SCT and increasing success, with the best results, of up to 85% event free survival, occurring with HLA-matched sibling donors and transplantation early in the course of the disease before end-organ damage occurs [159]. One limitation of SCT is the availability of sibling donors [160], and therefore there have been attempts to improve survival for unrelated stem-cell donors [161, 162]. The second limitation of SCT is that this line of treatment requires tremendous resources, and it becomes increasingly difficult for transplant physicians practicing in the developing world to reconcile the difference between what is possible and what is available. Moreover, it is more difficult to address because the clinical course of SCD is extremely heterogeneous. Despite the knowledge of various genetic and environmental factors known to alter disease severity, it is still difficult to accurately identify children with risk of severe disease before extensive damage has occurred. Until such time that a low-risk, definitive cure is available, the cornerstone of management of SCD is the prevention of early mortality, prevention of end organ damage, and improvement of the quality of life.

9.9. Gene Therapy

Since SCD is caused by a defective gene, definitive treatment would involve replacement of this gene with a normal gene. This has been done successfully in the sickle transgenic mouse [163], but progress in humans has been limited by identification of appropriate vectors and efficacy for gene transfer and low level expression of globin genes.

9.10. Role of Programmes for Control and Management of SCD

From a public health perspective, the policy for approaching the control of SCD in national health programmes needs to work in the context of countries with limited resources in health. Although, there is ongoing debate whether care of SCD should be integrated into existing health care services or whether there should be separate disease-specific programmes for SCD, the WHO recommends [164] that, for countries where the birth rate of affected infants is above 0.5 per 1,000 births, they should develop separate programmes for these conditions. It is recommended that counties with a high prevalence of SCD start planning effective control measures. In this context, control of SCD encompasses two elements: providing best possible care for affected individuals and preventing the birth of affected individuals.

With regard to providing best possible care, the following are options, depending on available resources, that have been recommended by Weatherall et al. in 2006 [105].

 Option one: best possible patient care with the use of prophylactic penicillin following diagnosis, together with retrospective genetic counselling. Option two: best possible patient care, together with a newborn screening program and the use of penicillin for all homozygous babies, together with retrospective screening and counselling. Option three: best possible patient care, together with newborn screening and the use of prophylactic penicillin from birth for homozygotes, together with population screening and prospective genetic counselling. Option four: option three, plus the availability of prenatal diagnosis, bone marrow transplantation, or both.

The management of SCD involves early diagnosis of affected people, the provision of the most appropriate basic, cost-effective treatment, and genetic counselling and psychosocial support. The long-term goal is to ensure appropriate management at different levels of health care with development of referral centres for specialised diagnosis and treatment. This approach ensures a cost-effective way of effectively dealing with a highly prevalent condition in areas where the resources are limited. However, it is important that these centres are not limited to urban areas or centred on academic or research oriented health facilities. In order to avoid this, there must be active strategies to ensure that appropriate management is built into services at all levels of health care with adequate support from these specialised centres. Management of SCD needs to be accompanied by strategies that aimed at two levels of prevention: tertiary prevention which involves early diagnosis of SCD and prevention of complications and more ambitiously secondary prevention which tries to reduce the number of children that are born with SCD. (Note that primary prevention aims to ensure that individuals are born free of SCD). Preventative services involve community education, population screening, and genetic counselling that would encourage people to undergo screening before conception, during the antenatal or postnatal period. There are several issues that need to be addressed with regard to prevention of SCD. The aim of screening is to detect SCD in the foetus, discuss the consequences of a diagnosis of SCD, and provide options for treatment and prognosis. Since SCD is a recessive disorder, during pre-conception screening, the chances of getting an affected child are variable. There is difficulty in advising a couple not to have children as the risk of getting an affected child may be relatively low (1 in 4) and does not increase with each pregnancy. The highest risk would be for two individuals who are SS who wish to have children. This is different from thalassaemia, where children with the most severe form, thalassaemia major, will inevitably have severe disease. Therefore, one could argue that this therefore justifies the use of prenatal diagnosis as this would identify pregnancies with SCD children, and then parents would be given the appropriate information regarding the consequences and prognosis of SCD and allow more reproductive options to families. Prenatal genetic diagnosis represents one type of reproductive option as it provides parents with the option to test at-risk pregnancies and make decisions regarding affected pregnancies. The availability and acceptability of prenatal diagnosis and termination of an affected pregnancy are of particular importance in low-resource countries where neither health services nor families can afford to pay for long-term treatment of SCA [165]. Close to two-thirds of a sample of 130 Cameroonian parents with affected children reported they would accept termination of an affected pregnancy for SCA [120], a considerably higher proportion when compared to the Cameroonian preclinical, clinical medical student, and physicians in a previous study (22.4, 10.8 and 36.1%, resp.) [166]. Trends reported in Nigerian parents were slightly different where 92% of a sample of 53 SCA heterozygous carrier mothers favored prenatal diagnosis and 63% indicated they would opt for termination of an affected pregnancy [167]. However, in a survey of 403 health workers in a tertiary health care centre in Nigeria, only one-third of the respondents accept termination of pregnancy as an option if prenatal screening is positive for SCA, whereas close to half of the respondents (42%) were against the idea. Another study reported that 21.4% of Nigerian doctors would accept termination of an affected pregnancy for SCA [168]. Experience of the effective practice of prenatal genetic diagnosis for SCD (amniocentesis and fetal DNA analysis) was reported in Nigeria and Cameroon [169, 170]. The views of parents towards prenatal diagnosis and in some cases medical termination of pregnancy may be associated with their experience of affected patients and the psychosocial and/or economic impact of SCA on families. Nevertheless the discrepancy between perception of a professional and parents underscores the necessity for more studies to unravel the ethical dilemma around prenatal genetic diagnosis to offer a service that does not conflict with social and cultural values of the affected population. Preimplantation genetic diagnosis is a mechanism for accurate genetic diagnosis, careful selection of unaffected embryo and implantation to allow fertile or infertile couples to have offspring without SCA. It is an expensive procedure using assisted conception by in vitro fertilization or intracytoplasmic sperm injection. It requires close collaboration between fertility specialists, molecular biologists, geneticists, and genetic and fertility counselors and may be an option to individuals who may object to prenatal diagnosis followed by termination.

Although SCA is the most severe form of the disease (compared to SC/S thalassaemia, etc.), there is still wide variability in disease severity. Therefore, even with the correct identification and diagnosis of SS with screening, it would be difficult to predict those who would develop severe disease and have a poor outcome.

10. Conclusion and Future Challenges

Because of their uneven distribution in high-frequency populations, reflecting their complex population genetics, the true magnitude of burden of SCD is still unknown. In many African countries there are few or virtually no facilities for appropriate diagnosis and management of SCD. There is limited data about frequency, clinical course, or mortality. Without this information it will be impossible to persuade African governments about the burden of this disease. The WHO Africa has recommended a set of public health interventions to reduce the burden of SCD in African region, namely, improving awareness, preventing the disease, early detection, improving the provision of health care for affected individuals by providing effective clinical, laboratory, diagnostic, and imaging facilities adapted to different levels of the health system, screening of newborns, training of health care workers, developing protocols for treatment, providing genetic counseling, patient support groups, advocacy, and research [171]. The situation will be improved by commitment by member states to integrate SCD prevention and control in national health plans and provide conducive environment for various stakeholders to contribute to the reduction of SCD prevalence, morbidity, and mortality. It will also require concerted action on the part of the international community of the richer countries, together with input from other major international health organizations and funding agencies [172, 173].

References

J. K. Onwubalili, “Sickle cell anaemia and reincarnation beliefs in Nigeria,” The Lancet, vol. 2, no. 8364, p. 1423, 1983.

E. Nzewi, “Malevolent ogbanje: recurrent reincarnation or sickle cell disease?” Social Science and Medicine, vol. 52, no. 9, pp. 1403–1416, 2001.

S. E. Antonarakis, C. D. Boehm, G. R. Serjeant, C. E. Theisen, G. J. Dover, and H. H. Kazazian Jr., “Origin of the β(S) globin gene in Blacks: the contribution of recurrent mutation or gene conversion or both,” Proceedings of the National Academy of Sciences of the United States of America, vol. 81, no. 3, pp. 853–856, 1984.

A. E. Kulozik, J. S. Wainscoat, G. R. Serjeant, et al., “Geographical survey of β(S)-globin gene haplotypes: evidence for an independent Asian origin of the sickle-cell mutation,” American Journal of Human Genetics, vol. 39, no. 2, pp. 239–244, 1986.

D. J. Weatherall, “Towards molecular medicine; reminiscences of the haemoglobin field, 1960–2000,” British Journal of Haematology, vol. 115, no. 4, pp. 729–738, 2001.

D. J. Weatherall, “Phenotype-genotype relationships in monogenic disease: lessons from the thalassaemias,” Nature Reviews Genetics, vol. 2, no. 4, pp. 245–255, 2001.

M. J. Stuart and R. L. Nagel, “Sickle-cell disease,” The Lancet, vol. 364, no. 9442, pp. 1343–1360, 2004.

R. L. Nagel, R. M. Bookchin, and J. Johnson, “Structural bases of the inhibitory effects of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S,” Proceedings of the National Academy of Sciences of the United States of America, vol. 76, no. 2, pp. 670–672, 1979.

C. T. Noguchi, D. A. Torchia, and A. N. Schechter, “Intracellular polymerization of sickle hemoglobin. Effects of cell heterogeneity,” The Journal of Clinical Investigation, vol. 72, no. 3, pp. 846–852, 1983.

C. Brugnara, H. F. Bunn, and D. C. Tosteson, “Regulation of erythrocyte cation and water content in sickle cell anemia,” Science, vol. 232, no. 4748, pp. 388–390, 1986.

M. P. Westerman, L. Unger, O. Kucuk, P. Quinn, and L. J. Lis, “Phase changes in membrane lipids in sickle red cell shed-vesicles and sickle red cells,” American Journal of Hematology, vol. 58, no. 3, pp. 177–182, 1998.

R. P. Hebbel, M. A. B. Boogaerts, J. W. Eaton, and M. H. Steinberg, “Erythrocyte adherence to endothelium in sickle-cell anemia. A possible determinant of disease severity,” The New England Journal of Medicine, vol. 302, no. 18, pp. 992–995, 1980.

P. S. Frenette, “Sickle cell vasoocclusion: heterotypic, multicellular aggregations driven by leukocyte adhesion,” Microcirculation, vol. 11, no. 2, pp. 167–177, 2004.

I. Okpala, “Leukocyte adhesion and the pathophysiology of sickle cell disease,” Current Opinion in Hematology, vol. 13, no. 1, pp. 40–44, 2006.

K. I. Ataga and E. P. Orringer, “Hypercoagulability in sickle cell disease: a curious paradox,” American Journal of Medicine, vol. 115, no. 9, pp. 721–728, 2003.

J.-L. Wautier and M.-P. Wautier, “Erythrocytes and platelet adhesion to endothelium are mediated by specialized molecules,” Clinical Hemorheology and Microcirculation, vol. 30, no. 3-4, pp. 181–184, 2004.

J. Villagra, S. Shiva, L. A. Hunter, R. F. Machado, M. T. Gladwin, and G. J. Kato, “Platelet activation in patients with sickle disease, hemolysis-associated pulmonary hypertension, and nitric oxide scavenging by cell-free hemoglobin,” Blood, vol. 110, no. 6, pp. 2166–2172, 2007.

M. T. Gladwin and G. J. Kato, “Hemolysis-associated hypercoagulability in sickle cell disease: the plot (and blood) thickens!,” Haematologica, vol. 93, no. 1, pp. 1–3, 2008.

C. D. Reiter, X. Wang, J. E. Tanus-Santos et al., “Cell-free hemoglobin limits nitric oxide bioavailability in sickle-cell disease,” Nature Medicine, vol. 8, no. 12, pp. 1383–1389, 2002.

M. de Montalembert, M. Guilloud-Bataille, J. Feingold, and R. Girot, “Epidemiological and clinical study of sickle cell disease in France, French Guiana and Algeria,” European Journal of Haematology, vol. 51, no. 3, pp. 136–140, 1993.

J. R. Pattison, S. E. Jones, J. Hodgson et al., “Parvovirus infections and hypoplastic crisis in sickle-cell anaemia,” The Lancet, vol. 1, no. 8221, pp. 664–665, 1981.

O. S. Platt, B. D. Thorington, D. J. Brambilla et al., “Pain in sickle cell disease—rates and risk factors,” The New England Journal of Medicine, vol. 325, no. 1, pp. 11–16, 1991.

F. M. Gill, L. A. Sleeper, S. J. Weiner et al., “Clinical events in the first decade in a cohort of infants with sickle cell disease,” Blood, vol. 86, no. 2, pp. 776–783, 1995.

T. B. West, D. W. West, and K. Ohene-Frempong, “The presentation, frequency, and outcome of bacteremia among children with sickle cell disease and fever,” Pediatric Emergency Care, vol. 10, no. 3, pp. 141–143, 1994.

K. J. J. Wierenga, I. R. Hambleton, R. M. Wilson, H. Alexander, B. E. Serjeant, and G. R. Serjeant, “Significance of fever in Jamaican patients with homozygous sickle cell disease,” Archives of Disease in Childhood, vol. 84, no. 2, pp. 156–159, 2001.

M. H. Gaston, J. I. Verter, and G. Woods, “Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial,” The New England Journal of Medicine, vol. 314, no. 25, pp. 1593–1599, 1986.

“American Academy of Pediatrics. Committee on Infectious Diseases. Policy statement: recommendations for the prevention of pneumococcal infections, including the use of pneumococcal conjugate vaccine (Prevnar), pneumococcal polysaccharide vaccine, and antibiotic prophylaxis,” Pediatrics, vol. 106, no. 2, part 1, pp. 362–366, 2000.

M. E. Kizito, E. Mworozi, C. Ndugwa, and G. R. Serjeant, “Bacteraemia in homozygous sickle cell disease in Africa: is pneumococcal prophylaxis justified?” Archives of Disease in Childhood, vol. 92, no. 1, pp. 21–23, 2007.

T. N. Williams, S. Uyoga, A. Macharia et al., “Bacteraemia in Kenyan children with sickle-cell anaemia: a retrospective cohort and case-control study,” The Lancet, vol. 374, no. 9698, pp. 1364–1370, 2009.

S. Obaro, “Pneumococcal infections and sickle cell disease in Africa: does absence of evidence imply evidence of absence?” Archives of Disease in Childhood, vol. 94, no. 9, pp. 713–716, 2009.

L. Tshilolo, E. Kafando, M. Sawadogo et al., “Neonatal screening and clinical care programmes for sickle cell disorders in sub-Saharan Africa: lessons from pilot studies,” Public Health, vol. 122, no. 9, pp. 933–941, 2008.

O. Bagasra, R. M. Steiner, and S. K. Ballas, “Viral burden and disease progression in HIV-1-infected patients with sickle cell anemia,” American Journal of Hematology, vol. 59, no. 3, pp. 199–207, 1998.

I. Diagne, G. M. Soares, A. Gueye, et al., “Infections in Senegalese children and adolescents with sickle cell anemia: epidemiological aspects,” Dakar Médical, vol. 45, no. 1, pp. 55–58, 2000.

M. Hassan, S. Hasan, S. Giday et al., “Hepatitis C virus in sickle cell disease,” Journal of the National Medical Association, vol. 95, no. 10, pp. 939–942, 2003.

L. M. Tshilolo, R. K. Mukendi, and S. O. Wembonyama, “Blood transfusion rate in congolese patients with sickle cell anemia,” Indian Journal of Pediatrics, vol. 74, no. 8, pp. 735–738, 2007.

F. Blei and D. R. Puder, “Yersinia enterocolitica bacteremia in a chronically transfused patient with sickle cell anemia: case report and review of the literature,” American Journal of Pediatric Hematology/Oncology, vol. 15, no. 4, pp. 430–434, 1993.

E. Barrett-Connor, “Bacterial infection and sickle cell anemia. An analysis of 250 infections in 166 patients and a review of the literature,” Medicine, vol. 50, no. 2, pp. 97–112, 1971.

G. R. Serjeant, B. E. Serjeant, P. W. Thomas, M. J. Anderson, G. Patou, and J. R. Pattison, “Human parvovirus infection in homozygous sickle cell disease,” The Lancet, vol. 341, no. 8855, pp. 1237–1240, 1993.

K. Smith-Whitley, H. Zhao, R. L. Hodinka et al., “Epidemiology of human parvovirus B19 in children with sickle cell disease,” Blood, vol. 103, no. 2, pp. 422–427, 2004.

P. H. Jones, L. C. Pickett, M. J. Anderson, and G. Pasvol, “Human parvovirus infection in children and severe anaemia seen in an area endemic for malaria,” Journal of Tropical Medicine and Hygiene, vol. 93, no. 1, pp. 67–70, 1990.

T. Teuscher, B. Baillod, and B. R. Holzer, “Prevalence of human parvovirus B19 in sickle cell disease and healthy controls,” Tropical and Geographical Medicine, vol. 43, no. 1-2, pp. 108–110, 1991.

J. Yeats, H. Daley, and D. Hardie, “Parvovirus B19 infection does not contribute significantly to severe anaemia in children with malaria in Malawi,” European Journal of Haematology, vol. 63, no. 4, pp. 276–277, 1999.

H. A. Pearson, R. P. Spencer, and E. A. Cornelius, “Functional asplenia in sickle-cell anemia,” The New England Journal of Medicine, vol. 281, no. 17, pp. 923–926, 1969.

A. K. Brown, L. A. Sleeper, S. T. Miller, C. H. Pegelow, F. M. Gill, and M. A. Waclawiw, “Reference values and hematologic changes from birth to 5 years in patients with sickle cell disease,” Archives of Pediatrics and Adolescent Medicine, vol. 148, no. 8, pp. 796–804, 1994.

G. J. Noel, S. Katz, and P. J. Edelson, “Complement-mediated early clearance of Haemophilus influenzae type b from blood is independent of serum lytic activity,” Journal of Infectious Diseases, vol. 157, no. 1, pp. 85–90, 1988.

J. A. Winkelstein and R. H. Drachman, “Deficiency of pneumococcal serum opsonizing activity in sickle-cell disease,” The New England Journal of Medicine, vol. 279, no. 9, pp. 459–466, 1968.

S. Ruddy, L. G. Hunsicker, and K. F. Austen, “C3b inactivator of man. 3. Further purification and production of antibody to C3b INA,” Journal of Immunology, vol. 108, no. 3, pp. 657–664, 1972.

R. B. Johnston Jr., S. L. Newman, and A. G. Struth, “An abnormality of the alternate pathway of complement activation in sickle-cell disease,” The New England Journal of Medicine, vol. 288, no. 16, pp. 803–808, 1973.

S. L. Leikin, D. Gallagher, T. R. Kinney, D. Sloane, P. Klug, and W. Rida, “Mortality in children and adolescents with sickle cell disease,” Pediatrics, vol. 84, no. 3, pp. 500–508, 1989.

H. O. Okuonghae, M. U. Nwankwo, and E. C. Offor, “Pattern of bacteraemia in febrile children with sickle cell anaemia,” Annals of Tropical Paediatrics, vol. 13, no. 1, pp. 55–64, 1993.

E. W. Hook, C. G. Campbell, H. S. Weens, and B. R. Cooper, “Salmonella osteomyelitis in patients with sickle-cell anemia,” The New England Journal of Medicine, vol. 257, no. 9, pp. 403–407, 1957.

W. W. Ebong, “Acute osteomyelitis in Nigerians with sickle cell disease,” Annals of the Rheumatic Diseases, vol. 45, no. 11, pp. 911–915, 1986.

L. Tshilolo, R. Mukendi, and R. Girot, “Sickle cell disease in south Zaire. Study of two series of 251 and 340 patients during the period 1988–1992,” Archives de Pediatrie, vol. 3, no. 2, pp. 104–111, 1996.

O. Castro, D. J. Brambilla, B. Thorington et al., “The acute chest syndrome in sickle cell disease: incidence and risk factors,” Blood, vol. 84, no. 2, pp. 643–649, 1994.

E. P. Vichinsky, L. D. Neumayr, A. N. Earles et al., “Causes and outcomes of the acute chest syndrome in sickle cell disease,” The New England Journal of Medicine, vol. 342, no. 25, pp. 1855–1865, 2000.

O. S. Platt, D. J. Brambilla, W. F. Rosse et al., “Mortality in sickle cell disease—life expectancy and risk factors for early death,” The New England Journal of Medicine, vol. 330, no. 23, pp. 1639–1644, 1994.

R. J. Hayes, M. Beckford, Y. Grandison, K. Mason, B. E. Serjeant, and G. R. Serjeant, “The haematology of steady state homozygous sickle cell disease: frequency distributions, variation with age and sex, longitudinal observations,” British Journal of Haematology, vol. 59, no. 2, pp. 369–382, 1985.

M. A. F. El-Hazmi, F. A. Jabbar, F. Z. Al-Faleh, A. R. Al-Swailem, and A. S. Warsy, “The haematological, biochemical and clinical—presentation of haemoglobin S in Saudi Arabia (i). Haematological & clinical expression,” Tropical and Geographical Medicine, vol. 39, no. 2, pp. 157–162, 1987.

G. Akenzua, O. Akinyanju, A. Kulozik et al., “Sickle cell anaemia in Nigeria: a comparison between Benin and Lagos,” African Journal of Medicine and Medical Sciences, vol. 23, no. 2, pp. 101–107, 1994.

J. W. Childs, “Sickle cell disease: the clinical manifestations,” Journal of the American Osteopathic Association, vol. 95, no. 10, pp. 593–598, 1995.

M. G. Neonato, M. Guilloud-Bataille, P. Beauvais et al., “Acute clinical events in 299 homozygous sickle cell patients living in france,” European Journal of Haematology, vol. 65, no. 3, pp. 155–164, 2000.

G. R. Serjeant, J. M. Topley, K. Mason, et al., “Outbreak of aplastic crises in sickle cell anaemia associated with parvovirus-like agent,” The Lancet, vol. 2, no. 8247, pp. 595–597, 1981.

A. I. Juwah, E. U. Nlemadim, and W. Kaine, “Types of anaemic crises in paediatric patients with sickle cell anaemia seen in Enugu, Nigeria,” Archives of Disease in Childhood, vol. 89, no. 6, pp. 572–576, 2004.

V. G. Nolan, D. F. Wyszynski, L. A. Farrer, and M. H. Steinberg, “Hemolysis-associated priapism in sickle cell disease,” Blood, vol. 106, no. 9, pp. 3264–3267, 2005.

G. J. Kato, V. McGowan, R. F. Machado et al., “Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease,” Blood, vol. 107, no. 6, pp. 2279–2285, 2006.

S. K. Ballas and M. J. Marcolina, “Hyperhemolysis during the evolution of uncomplicated acute painful episodes in patients with sickle cell anemia,” Transfusion, vol. 46, no. 1, pp. 105–110, 2006.

J. G. Taylor VI, V. G. Nolan, L. Mendelsohn, G. J. Kato, M. T. Gladwin, and M. H. Steinberg, “Chronic hyper-hemolysis in sickle cell anemia: association of vascular complications and mortality with less frequent vasoocclusive pain,” PLoS One, vol. 3, no. 5, Article ID e2095, 2008.

J. O. Olabode and W. A. Shokunbi, “Types of crises in sickle cell disease patients presenting at the haematology day care unit (HDCU), University College Hospital (UCH), Ibadan,” West African Journal of Medicine, vol. 25, no. 4, pp. 284–288, 2006.

C. T. Quinn, E. P. Shull, N. Ahmad, N. J. Lee, Z. R. Rogers, and G. R. Buchanan, “Prognostic significance of early vaso-occlusive complications in children with sickle cell anemia,” Blood, vol. 109, no. 1, pp. 40–45, 2007.

J. M. Topley, D. W. Rogers, M. C. G. Stevens, and G. R. Serjeant, “Acute splenic sequestration and hypersplenism in the first five years in homozygous sickle cell disease,” Archives of Disease in Childhood, vol. 56, no. 10, pp. 765–769, 1981.

A. M. Emond, R. Collis, and D. Darvill, “Acute splenic sequestration in homozygous sickle cell disease: natural history and management,” Journal of Pediatrics, vol. 107, no. 2, pp. 201–206, 1985.

M. Koshy, R. Entsuah, A. Koranda et al., “Leg ulcers in patients with sickle cell disease,” Blood, vol. 74, no. 4, pp. 1403–1408, 1989.

M. A. Durosinmi, S. M. Gevao, and G. J. Esan, “Chronic leg ulcers in sickle cell disease: experience in Ibadan, Nigeria,” African Journal of Medicine and Medical Sciences, vol. 20, no. 1, pp. 11–14, 1991.

A. D. Gbadoé, A. Géraldo, K. Guédénon, S. Koffi, K. Agbétiafa, and P. Akpako, “Stuttering priapism in children with sickle cell anemia in Togo,” Archives de Pediatrie, vol. 14, no. 7, pp. 861–863, 2007.

K. Ohene-Frempong, S. J. Weiner, L. A. Sleeper et al., “Cerebrovascular accidents in sickle cell disease: rates and risk factors,” Blood, vol. 91, no. 1, pp. 288–294, 1998.

M. R. DeBaun, J. Schatz, M. J. Siegel et al., “Cognitive screening examinations for silent cerebral infarcts in sickle cell disease,” Neurology, vol. 50, no. 6, pp. 1678–1682, 1998.

T. R. Kinney, L. A. Sleeper, W. C. Wang et al., “Silent cerebral infarcts in sickle cell anemia: a risk factor analysis,” Pediatrics, vol. 103, no. 3, pp. 640–645, 1999.

S. T. Miller, E. A. Macklin, C. H. Pegelow et al., “Silent infarction as a risk factor for overt stroke in children with sickle cell anemia: a report from the Cooperative Study of Sickle Cell Disease,” Journal of Pediatrics, vol. 139, no. 3, pp. 385–390, 2001.

R. Marouf, R. Gupta, M. Z. Haider, and A. D. Adekile, “Silent brain infarcts in adult Kuwaiti sickle cell disease patients,” American Journal of Hematology, vol. 73, no. 4, pp. 240–243, 2003.

R. J. Hayes, P. I. Condon, and G. R. Serjeant, “Haematological factors associated with proliferative retinopathy in sickle cell-haemoglobin C disease,” British Journal of Ophthalmology, vol. 65, no. 10, pp. 712–717, 1981.

O. Castro, M. Hoque, and B. D. Brown, “Pulmonary hypertension in sickle cell disease: cardiac catheterization results and survival,” Blood, vol. 101, no. 4, pp. 1257–1261, 2003.

M. T. Gladwin, V. Sachdev, M. L. Jison et al., “Pulmonary hypertension as a risk factor for death in patients with sickle cell disease,” The New England Journal of Medicine, vol. 350, no. 9, pp. 886–895, 2004.

K. I. Ataga, C. G. Moore, S. Jones et al., “Pulmonary hypertension in patients with sickle cell disease: a longitudinal study,” British Journal of Haematology, vol. 134, no. 1, pp. 109–115, 2006.

G. J. Kato, O. C. Onyekwere, and M. T. Gladwin, “Pulmonary hypertension in sickle cell disease: relevance to children,” Pediatric Hematology and Oncology, vol. 24, no. 3, pp. 159–170, 2007.

J. Griffiths, “Avascular necrosis of femoral head in Kenyan africans,” East African Medical Journal, vol. 45, no. 9, pp. 613–618, 1968.

W. W. Ebong, “Avascular necrosis of the femoral head associated with haemoglobinopathy,” Tropical and Geographical Medicine, vol. 29, no. 1, pp. 19–23, 1977.

R. E. J. Lee, J. S. R. Golding, and G. R. Serjeant, “The radiological features of avascular necrosis of the femoral head in homozygous sicke cell disease,” Clinical Radiology, vol. 32, no. 2, pp. 205–214, 1981.

K. C. Abbott, I. O. Hypolite, and L. Y. Agodoa, “Sickle cell nephropathy at end-stage renal disease in the United States: patient characteristics and survival,” Clinical Nephrology, vol. 58, no. 1, pp. 9–15, 2002.

A. F. Fleming, J. Storey, L. Molineaux, E. A. Iroko, and E. D. Attai, “Abnormal haemoglobins in the Sudan savanna of Nigeria. I. Prevalence of haemoglobins and relationships between sickle cell trait, malaria and survival,” Annals of Tropical Medicine and Parasitology, vol. 73, no. 2, pp. 161–172, 1979.

A. F. Fleming, “The presentation, management and prevention of crisis in sickle cell disease in Africa,” Blood Reviews, vol. 3, no. 1, pp. 18–28, 1989.

G. D. Overturf, D. Powars, and L. J. Baraff, “Bacterial meningitis and septicemia in sickle cell disease,” American Journal of Diseases of Children, vol. 131, no. 7, pp. 784–787, 1977.

P. J. Campbell, P. O. Olatunji, K. E. Ryan, and S. C. Davies, “Splenic regrowth in sickle cell anaemia following hypertransfusion,” British Journal of Haematology, vol. 96, no. 1, pp. 77–79, 1997.

A. Yardumian and C. Crawley, “Sickle cell disease,” Clinical Medicine, vol. 1, no. 6, pp. 441–446, 2001.

M. H. Steinberg, “Pathophysiology of sickle cell disease,” Bailliere's Clinical Haematology, vol. 11, no. 1, pp. 163–184, 1998.

H. F. Bunn, “Pathogenesis and treatment of sickle cell disease,” The New England Journal of Medicine, vol. 337, no. 11, pp. 762–769, 1997.

D. Labie, J. Pagnier, C. Lapoumeroulie, et al., “Common haplotype dependency of high (G)γ-globin gene expression and high Hb F levels in β-thalasssemia and sickle cell anemia patients,” Proceedings of the National Academy of Sciences of the United States of America, vol. 82, no. 7, pp. 2111–2114, 1985.

L. E. Creary, P. Ulug, S. Menzel et al., “Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patients,” PLoS One, vol. 4, no. 1, Article ID e4218, 2009.

M. Uda, R. Galanello, S. Sanna et al., “Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of β-thalassemia,” Proceedings of the National Academy of Sciences of the United States of America, vol. 105, no. 5, pp. 1620–1625, 2008.

G. Lettre, V. G. Sankaran, M. A. C. Bezerra et al., “DNA polymorphisms at the BCL11A, HBS1L-MYB, and β-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease,” Proceedings of the National Academy of Sciences of the United States of America, vol. 105, no. 33, pp. 11869–11874, 2008.

A. E. Sedgewick, N. Timofeev, P. Sebastiani et al., “BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies,” Blood Cells, Molecules, and Diseases, vol. 41, no. 3, pp. 255–258, 2008.

S. L. Thein and S. Menzel, “Discovering the genetics underlying foetal haemoglobin production in adults,” British Journal of Haematology, vol. 145, no. 4, pp. 455–467, 2009.

J. Makani, S. Menzel, S. Nkya et al., “Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia,” Blood, vol. 117, no. 4, pp. 1390–1392, 2011.

World Health Organisation, “Sickle cell anaemia. Agenda item 11.4,” in 59th World Health Assembly, 27 May 2006, World Health Organisation, Geneva, Switzerland, 2006.

D. Diallo and G. Tchernia, “Sickle cell disease in Africa,” Current Opinion in Hematology, vol. 9, no. 2, pp. 111–116, 2002.

D. J. Weatherall, O. Akinyanju, S. Fucharoen, N. F. Olivieri, and P. Musgrove, “Inherited disorders of hemoglobin,” in Disease Control Priorities in Developing Countries, D. Jamison, Ed., pp. 663–680, Oxford University Press, New York, NY, USA, 2006.

D. J. Weatherall, “Hemoglobinopathies worldwide: present and future,” Current Molecular Medicine, vol. 8, no. 7, pp. 592–599, 2008.

A. Enevold, J. P. Lusingu, B. Mmbando et al., “Reduced risk of uncomplicated malaria episodes in children with alpha⁺-thalassemia in Northeastern Tanzania,” American Journal of Tropical Medicine and Hygiene, vol. 78, no. 5, pp. 714–720, 2008.

T. N. Williams, S. Wambua, S. Uyoga et al., “Both heterozygous and homozygous α ⁺ thalassemias protect against severe and fatal Plasmodium falciparum malaria on the coast of Kenya,” Blood, vol. 106, no. 1, pp. 368–371, 2005.

M. Aidoo, D. J. Terlouw, M. S. Kolczak et al., “Protective effects of the sickle cell gene against malaria morbidity and mortality,” The Lancet, vol. 359, no. 9314, pp. 1311–1312, 2002.

D. J. Weatherall and J. B. Clegg, “Inherited haemoglobin disorders: an increasing global health problem,” Bulletin of the World Health Organization, vol. 79, no. 8, pp. 704–712, 2001.

D. Modiano, G. Bancone, B. M. Ciminelli et al., “Haemoglobin S and haemoglobin C: ‘quick but costly’ versus ‘slow but gratis’ genetic adaptations to Plasmodium falciparum malaria,” Human Molecular Genetics, vol. 17, no. 6, pp. 789–799, 2008.

J. Simpore, S. Pignatelli, S. Barlati, and S. Musumeci, “Modification in the frequency of Hb C and Hb S in Burkina Faso: an influence of migratory fluxes and improvement of patient health care,” Hemoglobin, vol. 26, no. 2, pp. 113–120, 2002.

P. Beighton and M. C. Botha, “Inherited disorders in the black population of southern Africa—part I: historical and demographic background; genetic haematological conditions,” South African Medical Journal, vol. 69, no. 4, pp. 247–249, 1986.

World Health Organisation, Genomics and World Health, Report of the Advisory Committee on Health Research, World Health Organisation, Geneva, Switzerland, 2002.

L. Molineaux, A. F. Fleming, and R. Cornille-Brogger, “Abnormal haemoglobins in the Sudan savanna of Nigeria. III. Malaria immunoglobulins and antimalarial antibodies in sickle cell disease,” Annals of Tropical Medicine and Parasitology, vol. 73, no. 4, pp. 301–310, 1979.

C. T. Quinn, Z. R. Rogers, and G. R. Buchanan, “Survival of children with sickle cell disease,” Blood, vol. 103, no. 11, pp. 4023–4027, 2004.

P. Telfer, P. Coen, S. Chakravorty et al., “Clinical outcomes in children with sickle cell disease living in England: a neonatal cohort in East London,” Haematologica, vol. 92, no. 7, pp. 905–912, 2007.

A. N. Thomas, C. Pattison, and G. R. Serjeant, “Causes of death in sickle-cell disease in Jamaica,” British Medical Journal, vol. 285, no. 6342, pp. 633–635, 1982.

M. Brozovic and E. Anionwu, “Sickle cell disease in Britain,” Journal of Clinical Pathology, vol. 37, no. 12, pp. 1321–1326, 1984.

V. G. Sankaran and M. V. Sapp, “Persistence of fetal hemoglobin expression in an older child with trisomy 13,” Journal of Pediatrics, vol. 160, no. 2, p. 352, 2012.

A. Lee, P. Thomas, L. Cupidore, B. Serjeant, and G. Serjeant, “Improved survival in homozygous sickle cell disease: lessons from a cohort study,” British Medical Journal, vol. 311, no. 7020, pp. 1600–1602, 1995.

E. Vichinsky, D. Hurst, A. Earles, K. Kleman, and B. Lubin, “Newborn screening for sickle cell disease: effect on mortality,” Pediatrics, vol. 81, no. 6, pp. 749–755, 1988.

T. Frempong and H. A. Pearson, “Newborn screening coupled with comprehensive follow-up reduced early mortality of sickle cell disease in Connecticut,” Connecticut Medicine, vol. 71, no. 1, pp. 9–12, 2007.

Z. M. Al-Hawsawi and G. A. Ismail, “Acute splenic sequestration crisis in children with sickle cell disease,” Saudi Medical Journal, vol. 22, no. 12, pp. 1076–1079, 2001.

J. A. Wilimas, P. M. Flynn, S. Harris et al., “A randomized study of outpatient treatment with ceftriaxone for selected febrile children with sickle cell disease,” The New England Journal of Medicine, vol. 329, no. 7, pp. 472–476, 1993.

M. C. Rahimy, A. Gangbo, G. Ahouignan, S. Anagonou, V. Boco, and E. Alihonou, “Outpatient management of fever in children with sickle cell disease (SCD) in an African setting,” American Journal of Hematology, vol. 62, no. 1, pp. 1–6, 1999.

R. E. Ware, S. A. Zimmerman, and W. H. Schultz, “Hydroxyurea as an alternative to blood transfusions for the prevention of recurrent stroke in children with sickle cell disease,” Blood, vol. 94, no. 9, pp. 3022–3026, 1999.

M. C. Rahimy, A. Gangbo, G. Ahouignan et al., “Effect of a comprehensive clinical care program on disease course in severely ill children with sickle cell anemia in a sub-Saharan African setting,” Blood, vol. 102, no. 3, pp. 834–838, 2003.

J. Knight-Madden and G. R. Serjeant, “Invasive pneumococcal disease in homozygous sickle cell disease: Jamaican experience 1973–1997,” Journal of Pediatrics, vol. 138, no. 1, pp. 65–70, 2001.

J. A. Berkley, B. S. Lowe, I. Mwangi et al., “Bacteremia among children admitted to a rural hospital in Kenya,” The New England Journal of Medicine, vol. 352, no. 1, pp. 39–47, 2005.

A. Roca, B. Sigaúque, L. Quintó et al., “Invasive pneumococcal disease in children >5 years of age in rural Mozambique,” Tropical Medicine and International Health, vol. 11, no. 9, pp. 1422–1431, 2006.

M. de Montalembert, V. Brousse, and J.-R. Zahar, “Pneumococcal prophylaxis for children with sickle cell disease in Africa,” Archives of Disease in Childhood, vol. 93, no. 8, pp. 715–716, 2008.

J. R. Aluoch, “Higher resistance to Plasmodium falciparum infection in patients with homozygous sickle cell disease in Western Kenya,” Tropical Medicine and International Health, vol. 2, no. 6, pp. 568–571, 1997.

H. O. Okuonghae, M. U. Nwankwo, and E. Offor, “Brief reports malarial parasitaemia in febrile children with sickle cell anaemia,” Journal of Tropical Pediatrics, vol. 38, no. 2, pp. 83–85, 1992.

R. Kotila, A. Okesola, and O. Makanjuola, “Asymptomatic malaria parasitaemia in sickle-cell disease patients: how effective is chemoprophylaxis?” Journal of Vector Borne Diseases, vol. 44, no. 1, pp. 52–55, 2007.

O. Awotua-Efebo, E. A. Alikor, and K. E. Nkanginieme, “Malaria parasite density and splenic status by ultrasonography in stable sickle-cell anaemia (HbSS) children,” Nigerian Journal of Medicine, vol. 13, no. 1, pp. 40–43, 2004.

J. Makani, A. N. Komba, S. E. Cox et al., “Malaria in patients with sickle cell anemia: burden, risk factors, and outcome at the outpatient clinic and during hospitalization,” Blood, vol. 115, no. 2, pp. 215–220, 2010.

O. Oniyangi and A. A. Omari, “Malaria chemoprophylaxis in sickle cell disease,” Cochrane Database of Systematic Reviews, no. 4, Article ID CD003489, 2006.

S. Wahl and K. C. Quirolo, “Current issues in blood transfusion for sickle cell disease,” Current Opinion in Pediatrics, vol. 21, no. 1, pp. 15–21, 2009.

R. J. Adams, V. C. McKie, L. Hsu, et al., “Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography,” The New England Journal of Medicine, vol. 339, no. 1, pp. 5–11, 1998.

J. M. Turner, J. B. Kaplan, H. W. Cohen, and H. H. Billett, “Exchange versus simple transfusion for acute chest syndrome in sickle cell anemia adults,” Transfusion, vol. 49, no. 5, pp. 863–868, 2009.

E. P. Vichinsky, C. M. Haberkern, L. Neumayr et al., “A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease,” The New England Journal of Medicine, vol. 333, no. 4, pp. 206–213, 1995.

K. A. Stegenga, P. Ward-Smith, P. S. Hinds, J. A. Routhieaux, and G. M. Woods, “Quality of life among children with sickle cell disease receiving chronic transfusion therapy,” Journal of Pediatric Oncology Nursing, vol. 21, no. 4, pp. 207–213, 2004.

R. Prasad, S. Hasan, O. Castro, E. Perlin, and K. Kim, “Long-term outcomes in patients with sickle cell disease and frequent vaso-occlusive crises,” American Journal of the Medical Sciences, vol. 325, no. 3, pp. 107–109, 2003.

M. J. Telen, “Principles and problems of transfusion in sickle cell disease,” Seminars in Hematology, vol. 38, no. 4, pp. 315–323, 2001.

K. Ohene-Frempong, “Indications for red cell transfusion in sickle cell disease,” Seminars in Hematology, vol. 38, no. 1, supplement 1, pp. 5–13, 2001.

R. J. Dunlop and K. C. Bennett, “Pain management for sickle cell disease,” Cochrane Database of Systematic Reviews, no. 2, Article ID CD003350, 2006.

D. C. Rees, A. D. Olujohungbe, N. E. Parker, A. D. Stephens, P. Telfer, and J. Wright, “Guidelines for the management of the acute painful crisis in sickle cell disease,” British Journal of Haematology, vol. 120, no. 5, pp. 744–752, 2003.

S. K. Ballas, “Pain management of sickle cell disease,” Hematology/Oncology Clinics of North America, vol. 19, no. 5, pp. 785–802, 2005.

S. Charache, M. L. Terrin, R. D. Moore et al., “Effect of hydroxyurea on the frequency of painful crises in Sickle cell anemia,” The New England Journal of Medicine, vol. 332, no. 20, pp. 1317–1322, 1995.

R. E. Ware, M. H. Steinberg, and T. R. Kinney, “Hydroxyurea: an alternative to transfusion therapy for stroke in sickle cell anemia,” American Journal of Hematology, vol. 50, no. 2, pp. 140–143, 1995.

National Institutes of Health, National Institutes of Health: Consensus Development Conference Statement: Hydroxyurea Treatment for Sickle Cell Disease, National Institutes of Health, 2008.

W. H. Waugh, C. W. Daeschner III, B. A. Files, M. E. McConnell, and S. E. Strandjord, “Oral citrulline as arginine precursor may be beneficial in sickle cell disease: early phase two results,” Journal of the National Medical Association, vol. 93, no. 10, pp. 363–371, 2001.

C. R. Morris, E. P. Vichinsky, J. van Warmerdam et al., “Hydroxyurea and arginine therapy: impact on nitric oxide production in sickle cell disease,” Journal of Pediatric Hematology/Oncology, vol. 25, no. 8, pp. 629–634, 2003.

M. Oppert, A. Jörres, D. Barckow, K.-U. Eckardt, U. Frei, and U. Kaisers, “Inhaled nitric oxide for ARDS due to sickle cell disease,” Swiss Medical Weekly, vol. 134, no. 11-12, pp. 165–167, 2004.

D. L. Weiner and C. Brugnara, “Hydroxyurea and sickle cell disease: a chance for every patient,” Journal of the American Medical Association, vol. 289, no. 13, pp. 1692–1694, 2003.

M. T. Gladwin, J. H. Shelhamer, F. P. Ognibene et al., “Nitric oxide donor properties of hydroxyurea in patients with sickle cell disease,” British Journal of Haematology, vol. 116, no. 2, pp. 436–444, 2002.

F. L. Johnson, A. T. Look, and J. Gockerman, “Bone-marrow transplantation in a patient with sickle-cell anemia,” The New England Journal of Medicine, vol. 311, no. 12, pp. 780–783, 1984.

M. C. Walters, R. Storb, M. Patience et al., “Impact of bone marrow transplantation for symptomatic sickle cell disease: an interim report,” Blood, vol. 95, no. 6, pp. 1918–1924, 2000.

L. Krishnamurti, S. Abel, M. Maiers, and S. Flesch, “Availability of unrelated donors for hematopoietic stem cell transplantation for hemoglobinopathies,” Bone Marrow Transplantation, vol. 31, no. 7, pp. 547–550, 2003.

P. Woodard, B. Lubin, and M. C. Walters, “New approaches to hematopoietic cell transplantation for hematological diseases in children,” Pediatric Clinics of North America, vol. 49, no. 5, pp. 989–1007, 2002.

T. V. Adamkiewicz, P. S. Mehta, M. W. Boyer et al., “Transplantation of unrelated placental blood cells in children with high-risk sickle cell disease,” Bone Marrow Transplantation, vol. 34, no. 5, pp. 405–411, 2004.

R. Pawliuk, K. A. Westerman, M. E. Fabry et al., “Correction of sickle cell disease in transgenic mouse models by gene therapy,” Science, vol. 294, no. 5550, pp. 2368–2371, 2001.

World Health Organisation, Guidelines for the Control of Haemoglobin Disorders, World Health Organisation, Geneva, Switzerland, 1994.

A. Alwan and B. Modell, “Recommendations for introducing genetics services in developing countries,” Nature Reviews Genetics, vol. 4, no. 1, pp. 61–68, 2003.

A. Wonkam, A. K. Njamnshi, and F. F. Angwafo III, “Knowledge and attitudes concerning medical genetics amongst physicians and medical students in Cameroon (sub-Saharan Africa),” Genetics in Medicine, vol. 8, no. 6, pp. 331–338, 2006.

M. A. Durosinmi, A. I. Odebiyi, I. A. Adediran, N. O. Akinola, D. E. Adegorioye, and M. A. Okunade, “Acceptability of prenatal diagnosis of sickle cell anaemia (SCA) by female patients and parents of SCA patients in Nigeria,” Social Science and Medicine, vol. 41, no. 3, pp. 433–436, 1995.

A. S. Adeyemi and D. A. Adekanle, “Knowledge and attitude of female health workers towards prenatal diagnosis of sickle cell disease,” Nigerian Journal of Medicine, vol. 16, no. 3, pp. 268–270, 2007.

O. O. Akinyanju, R. F. Disu, J. A. Akinde, T. A. Adewole, A. I. Otaigbe, and E. E. Emuveyan, “Initiation of prenatal diagnosis of sickle-cell disorders in Africa,” Prenatal Diagnosis, vol. 19, no. 4, pp. 299–304, 1999.

J. Xu, C. Peng, V. G. Sankaran et al., “Correction of sickle cell disease in adult mice by interference with fetal hemoglobin silencing,” Science, vol. 334, no. 6058, pp. 993–996, 2011.

World Health Organisation, Sickle Cell Disease: A Strategy for the WHO Africa Region, R.o.t.R. Director, 2010.

D. J. Weatherall, “Genomics and global health: time for a reappraisal,” Science, vol. 302, no. 5645, pp. 597–599, 2003.

D. Weatherall, K. Hofman, G. Rodgers, J. Ruffin, and S. Hrynkow, “A case for developing North-South partnerships for research in sickle cell disease,” Blood, vol. 105, no. 3, pp. 921–923, 2005.