Case Reports in MedicineVolume 2011 (2011), Article ID 385894, 4 pagesdoi:10.1155/2011/385894

Case Report

Huntington's Disease: Two-Year Observational Follow-Up of Executive Function Evaluation with CNS Vital Signs Test in an Adult Patient

Anna Lucia Spear King,1,2,3 Alexandre Martins Valença,1,2,3,4,5 Adriana Cardoso de Oliveira e Silva,1,2,3,6 Ana Claudia Cerqueira,1,2,3 Lígia Maria Chaves Ferraz,3,7 and Antonio Egidio Nardi1,2,3,8

¹Laboratory of Panic and Respiration (LABPR), Instituto de Psiquiatria (IPUB), Universidade Federal do Rio de Janeiro (UFRJ), RJ, Brazil²National Institute of Science Technology Translational Medicine (INCT-TM), Brazil³Instituto de Psiquiatria (IPUB), Centro de Ciências da Saúde (CCS), Universidade Federal do Rio de Janeiro (UFRJ), Av. Venceslau Brás, 71 Praia Vermelha, Cep 22290-140, Rio de Janeiro, RJ, Brazil⁴Department of Psychiatry and Mental Health, Universidade Federal Fluminense (UFF), Niterói, RJ, Brazil⁵Severino Sombra University (USS), Vassouras, RJ, Brazil⁶Laboratory of Thanatology and Psychometrics, Universidade Federal Fluminense (UFF), Niterói, RJ, Brazil⁷Rio de Janeiro Brazil Association of Huntington, Brazil⁸Medical School and Institute of Psychiatry, Universidade Federal do Rio de Janeiro (UFRJ), Brazil

Received 29 July 2011; Revised 4 October 2011; Accepted 19 October 2011

Academic Editor: Walter Schulz-Schaeffer

Copyright © 2011 Anna Lucia Spear King 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.

Huntington's disease (HD) is a genetic, degenerative, and progressive central nervous system disease. It is characterized by motor abnormalities and cognitive and psychiatric symptoms. Objective. To describe the precise degree of clinical severity of patients with HD through a new neurocognitive assessment. Methods. Unprecedented battery of computerized tests, CNSVS (Central Nervous System Vital Signs), was applied at three different moments in 2008, 2009, and 2010. The accurate and reliable CNSVS objectively provided the cognitive state of patients and allowed for the evaluation of disease progression. Case Report. P., 26, female, without any medication, with normal psychomotor development is a parent carrier of HD. In 2008, she was diagnosed with HD in accordance with the Medical Genetics Laboratories. Conclusion. The tests may be useful to reveal the exact measure of the current evolutionary stage of HD patients, allowing for more efficient planning of treatment and future procedures, such as the medication, therapy, and physical activity to be administered.

1. Introduction

Huntington’s disease [1] (HD) is a genetic progressive heredodegenerative disease of the central nervous system (CNS). It is characterized by motor abnormalities and cognitive and psychiatric symptoms. The motor abnormalities may include muscle contractions, involuntary movements, loss of balance, poor coordination, speech difficulties, and excessive movements in stressful situations [1]. There is cognitive difficulty in organizing thoughts to handle new situations, tasks, loss of memory, and concentration. Psychiatric disorders include depression, irritability, anxiety, and behavioral changes [1].

The first studies analyzed the inheritance and identified families from New England [2]. HD is related to the IT 15 gene mutation [3], which encodes the protein Huntingtin (HTT).

The mean age of onset of HD varies between 35 and 45. If the age of the patient is 50 years or older (25% of cases), HD is considered to be “late-onset HD”, and before age 20 (approximately 10% of cases), it is defined as “juvenile HD”, which is the form that the case study patient has.

George Huntington [4] published his paper “On Chorea” that described the familial form of the disorder referred to as “hereditary chorea”, which is a type of involuntary movement. HD occurs in all races, both sexes, and in the western population, with 30 to 70 individuals per million being affected. Using the differential diagnosis, it is not difficult to differentiate the conditions of many other HD choreas. They must observe the mode of inheritance [4], clinical course, prognosis, or findings in laboratory tests.

Diseases of the brain often affect an individual’s behavior, including the impairment of cognitive skills and the production of neuropsychiatry symptoms. This report presents a neurocognitive assessment through a case study of HD. It uses a computerized neurocognitive test battery known as Central Nervous System Vital Signs (CNSVS) [5] that was applied in 2008, 2009, and 2010, with an interval of one year between each assessment, in a patient with HD who was not under any treatment (according to the patient’s own decision).

The CNSVS was validated [6] reliable and suitable for use as a screening tool that measures speed and accuracy of basic mental functions. The test battery consisted of seven CNSVS tests: (1) visual memory (memorize 15 words and recognize them at the end); (2) verbal memory (memorize 15 geometric figures and recognize them at the end); (3) symbols (fill in the blank spaces with the symbol corresponding to a particular situation required in the proposed model); (4) warning (the computer proposes issues: color and shape or the individual should use the keyboards on the right or left to find the relevant answers); (5) perception of emotions (the individual must match facial expressions with emotions described below the figure proposed); (6) reasoning (various geometric figures are proposed to find associations and/or coordination among them); (7) recall of the first two tests, verbal memory and visual memory.

The results of the CNSVS objectively provided the cognitive state of patients and allowed the determination of the progression of the disease. It may assist the physician in clarifying the diagnosis and may be used periodically to observe the emergence of deficits in executive functions [7].

Executive function [7] is a neuropsychological concept that applies to the cognitive process responsible for the execution and planning of activities including tasks, working memory, sustained attention, and inhibition of impulses. In addition, the memory’s verbal, visual and composite processing speed, executive function, and sustained attention were assessed. People with HD may show changes in executive functions and possible functional manifestation of the brain and the onset of new symptoms [7].

The aim of this case report was to describe the degree of clinical severity of patients with HD through neurocognitive assessment with an unprecedented battery of computerized tests, CNSVS, to provide the cognitive state of patients and allow for the evaluation of disease progression.

2. Case Report

P. is a 26-year-old female who is single, college graduate, and currently does not work. She lives with her mother and stepfather; her birth carried no complications, was breastfed up to 8 months of age, experienced her menarche at 12 years, began to be sexually active at the age of 16, and has normal psychomotor development.

P. was diagnosed with HD in 2008 according to the Medical Genetics Laboratories [8] detected through a blood sample. The father carrier of HD died of medical complications at 40 years and had three more siblings with HD.

In May 2008, when the patient was 25 years old, a genetic test [8] was conducted with a sample of blood. The result showed a mutation detected. Repeats Allele I: 58 and Allele II: 17.

According to the DNA [8], one expanded allele of 58 repeats was detected and the other allele size was within the normal range for the laboratory. Thus, these results indicate that the individual has the common genetic alteration found in HD. Genetic counseling was recommended for at-risk family members.

Analysis of the DNA from this individual has been used to study the size(s) of the CAG [9] (trinucleotide repeat) repeat region of the Huntington gene. The normal range is considered to be up 28 copies of the repeat. Alleles with 27 repeats up to and including 35 repeats are considered to be normal mutable alleles. To date, symptoms of HD have not been reported in individuals with 35 or less repeats. Allele sizes of 36 up to and including 38 repeats are considered to be Huntington alleles with reduced penetrance. HD alleles (mutations) are 40 repeats and greater. The reported sizes for large expansions are approximations due to the precision of the size measurements using current technology. The genotype-phenotype correlations are not precise enough to be used clinically [9].

From diagnosis until the present time, the patient did not use any medication for HD. The family was advised to seek medical treatment and did so by consulting several specialists. The patient decided not to start treatment with medication despite medical advice.

At 25, P. began to present difficulties in dealing with new situations, such as performing daily tasks. Also, she displayed a lack of concentration, coordination, mood swings, and some involuntary movements.

The patient sought treatment with complaints of depression and difficulty with attention and concentration. Then, P. was invited to participate in the study with CNSVS so that we could assess the degree of impairment in her executive functions. The patient signed the informed consent and was made aware of all procedures, and the study was approved by the Ethics Committee for Research of the Institute of Psychiatry (IPUB), Federal University of Rio de Janeiro (UFRJ).

3. Relevance and Originality

Clinicians and researchers, with the help of neurocognitive tests, accurately assessed the pathology of neurological patients and quantitatively measure the health of the higher functions of the brain and CNS.

4. Results

The absence of medication during the evaluation period allowed us to analyze the evolutionary aspects of their clinical and mental function. All tests were applied using the same psychologist, office environment, and evaluator, with the same level of cooperation from the patient.

Table 1 contains five levels of clinical severity from the CNSVS [5] tests, based on a database with more than 1900 subjects and aged between 8 and 90 years. The levels are classified as follows: Above: >110 (high function and high capacity); Average: 90–110 (normal function and normal capacity; Low Average: 80–90 (sight deficit and sight impairment); Low: 70–79 (moderate deficit and impairment possible); Very Low: <70 (deficit and impairment likely).

Table 1: Clinical levels of severity (CNSVS). The CNSVS [5] contains five degrees of clinical severity based on a database with more than 1900 subjects, aged between 8 and 90 years.

Above
>110
High function and high capacity

Average
90–110
Normal function and normal capacity

Low Average
80–90
Sight deficit and sight impairment

Low
70–79
Moderate deficit and impairment possible

Very Low
<70
Deficit and impairment likely

Table 2 contains the instrument panel regarding neurocognitive assessments 2008, 2009, and 2010. The test results of the CNSVS reported in Table 2 are that the patient did not achieve any results categorized as “Above” in the tests from 2008, 2009, and 2010, which indicates that she did not display high function or high capacity in the proposed tasks.

Table 2: Dashboard neurocognitive. Test Results CNSVS the years 2008, 2009, and 2010.

Subject: P.
Percentile range

>74
25−74
9–24
2–8
<2

Ages: 25, 26, 27
Standard score range

>109
90–109
80–89
70–79
<70

Profile

Scores
Subject score
Standard score
Percentile
Above
Average
Low Average
Low
Very Low

08
09
10
08
09
10
08
09
10
08
09
10
08
09
10
08
09
10
08
09
10
08
09
10

Composite memory
102
87
79
103
75
59
58
5
1

X

X

X

Verbal memory
52
45
42
97
71
61
42
3
1

X

X

X

Visual memory
50
42
37
107
85
71
68
16
3

X

X

X

Processing speed
34
45
31
62
75
58
1
5
1

X

X

X

Executive function
47
46
44
94
93
90
34
32
25

X
X
X

Social acuity
7
5
6
92
80
86
30
9
18

X

X
X

Reasoning
1
1
−1
76
76
69
5
5
2

X
X

X

Sustained attention
22
27
22
88
96
88
21
40
21

X

X

X

Working memory
5
9
6
81
95
84
10
37
14

X

X

X

*Additional data
1
1
1
2
2
2
3
3
3
4
4
4
4
4
4
4
4
4
4
4
4
4
4
4

Obs. 2008 (08); 2009 (09); 2010 (10).

Reaction time (milliseconds). In 2008—1171; In 2009—1180; In 2010—1315.

Total test time: 2008 (20 : 44 min/sec); 2009 (22 : 24 min/sec); 2010 (21 : 48 min/sec).

*Additional data:

(1) Subject scores: computed from the raw score calculations using the data values of the individual subtests and are simply the number of correct responses, incorrect responses, and reaction times.

(2) Standard score: In CNSVS the average standard score of the group is 100 and standard deviation is 15.

(3) Scale of 1 to 100.

(4) Normative scores.

As shown in Table 2, the patient’s verbal and visual memory were “Average” in 2008. In 2009, the patient’s composite and verbal memory had declined to “Low”, in 2010, the patient’s composite and verbal memory were “Very Low”, representing injury unlike the results for visual memory, which only showed a moderate deficit.

The patient’s processing speed was “Very Low” in 2008 and improved to “Low” in 2009 but in 2010 was reduced to “Very Low”, showing deficits and probable injury.

The patient’s executive function remained “Average” in 2008, 2009, and 2010, showing normal function and capabilities. Her social acuity in 2008 was “Average”, and in 2009 and 2010, it was “Low Average” showing a slight deficit and slight impairment.

In 2008 and 2009, the patient’s ability to reason was already “Low” and decayed a bit in 2010 to “Very Low”, which indicates probable deficits and impairment. The patient’s ability to sustain attention in 2008 was “Low Average” and in 2009 recovered to “Average” but returned in 2010 to “Low Average”, indicating a slight deficit and impairment. Similarly her working memory was “Low Average” in 2008 and recovered to “Average” in 2009 but returned in 2010 to “Low Average”, indicating a slight deficit and impairment.

5. Discussion

Brain injuries [10] often produce the loss of cognitive skills, neuropsychiatry symptoms, and behavioral changes. The precise knowledge of the presence and characteristics of these manifestations may help in the diagnosis and neurological, psychological, and psychiatric management and care in patients with HD.

In our case study, we observed a significant decrease of cognitive and social function in the patient studied, which contributed to a loss of social, occupational, and impairment in the quality of life. The CNSVS [5] may help clinicians to assess cognitive function of the individual and to accurately identify their symptoms, impairments, and comorbidities.

Studies [11] on cognitive ability (thinking, judging, and memory) are necessary to further our knowledge of diseases such as HD, a degenerative disease with symptoms that hinder emotional growth and development during its progression and evolution due to a loss of cells in the basal ganglia [11].

The possibility of a step-by-step follow-up is necessary because the onset of symptoms allows us [12] to more efficiently assign immediate therapies targeted to specific deficits and, therefore, offers a possible opportunity to slow the development of HD.

Only in recent decades have researchers [13] begun to study cognitive deficits and neurological disorder at the molecular level. What emerged from these studies [12] was how the cells within the CNS communicate with each other during the process of learning.

Recall that our study had a limited time period (2008–2010) taking advantage of the period in which the patient did not use medication to not interfere in the results. We recommend a possible use of this tool (CNSVS) in long-term clinical trials and with larger samples and also compared with other cognitive tests. We know that Huntington’s disease may have a broader course of 10–20 years.

Consider it relevant to the use of computerized tests that allow to accurately assess the patient’s reaction time to disease progression related to executive functions. That is, with this type of test, periodically we see the emergence or absence of deficits in these functions.

6. Conclusion

The study of the degree of clinical severity through CNSVS may be very important for measuring cognitive disturbances [14, 15] in HD patients, helping the clinician to more effectively plan the treatment and procedures, such as pharmacological treatment, psychotherapy, and physical activity to be administered.

Acknowledgments

The authors would like to thank their team at the Panic and Respiration Laboratory at Psychiatry Institute of the Federal University of Rio de Janeiro/Brazil (IPUB/UFRJ), National Institute for Technological Science-Translational Medicine (INCT-TM), and the National Council of Scientific and Technological Development (CNPq). Antonio Egidio Nardi is a Full Professor at the Medical School and Institute of Psychiatry, UFRJ, Brazil.

References

M. S. Haddad, “Huntington's disease guide for families and health professionals,” B. Quagliato and M. G. N. Marques, Eds., pp. 21–28, Brazil Huntington Association, 2009.

J. Bell, “Huntington’s chorea,” in Treasury of Human Inheritance, R. A. Fisher, Ed., pp. 1–67, Cambridge University Press, 1934.

F. G. Gervais, R. Singara, and S. Xanthaudakis, “Recruitment and activation of caspase-8 by Huntington-interacting protein Hip-1 and a novel partner Hippi,” Nature Cell Biology, no. 4, pp. 95–105, 2002.

G. Huntington, “On chorea,” Medical and Surgical Reports of Philadelphia, no. 26, pp. 317–321, 1872.

T. Gualtieric and L. G. Johnson, “Neurocognitives tests. Central Nervous System Vital Signs (CNSVS),” Archives of Clinical Neuropsychology, no. 7, pp. 623–643, 2006.

C. T. Gualtieri and L. G. Johnson, “Reliability and validity of a computerized neurocognitive test battery, CNS Vital Signs,” Archives of Clinical Neuropsychology, vol. 21, no. 7, pp. 623–643, 2006.

S. E. Voss and R. A. Bullock, “Executive function: the core feature of dementia?” Dementia and Geriatric Cognitive Disorders, vol. 18, no. 2, pp. 207–216, 2004.

DNA Diagnostic Laboratory, “[serial online 2008 DNA Number: 430921] 2008 [cited 2008 May 21]. 2450 Holcombe Boulevard-Houston, TX 77021-1 -800-411-4363,” http://www.bcm.edu/geneticlabs/

H. Telenius, B. Kremer, Y. P. Goldberg et al., “Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm,” Nature Genetics, vol. 6, no. 4, pp. 409–414, 1994.

N. Quinn and A. Schrag, “Huntington's disease and other choreas,” Journal of Neurology, vol. 245, no. 11, pp. 709–716, 1998.

A. Rosenblatt and I. Leroi, “Neuropsychiatry of Huntington's disease and other basal ganglia disorders,” Psychosomatics, vol. 41, no. 1, pp. 24–30, 2000.

P. Lombroso, “Learning and memory,” Revista Brasileira de Psiquiatria, vol. 26, no. 3, pp. 207–210, 2004.

L. R. Squire and E. R. Kandel, Memory: From Mind to Molecule, Scientific American Library, New York, NY, USA, 1999.

A. Brodal, Neurological Anatomy with Clinical Correlations, Roca, 3rd edition, 1984.

American Psychiatric Association, Diagnostic and Statistical Manual of Mental Disorders, Artes Médicas, Porto Alegre, Brazil, 5th edition, 2000.