The increased life expectancy of the HIV-1-infected population means that physicians are increasingly being faced with previously unrecognized comorbid conditions and antiretroviral-related complications. Atherosclerosis and cardiovascular events, loss of renal function, osteopenia/osteoporosis, and non-AIDS-defining cancers are some of the emerging conditions observed in large observational cohorts, and their incidence seems to be higher than in the general population [
Several studies, including the data collection on adverse events of anti-HIV drugs (D.A.D.) study, have demonstrated an increased rate of premature cardiovascular events, including myocardial infarction, in HIV-1-infected individuals exposed to specific individual antiretroviral drugs [
Encouraging data suggest that the incidence of ischemic heart disease in HIV-1-infected patients could be decreasing in recent years, probably due to the use of new antiretroviral regimens associated with higher suppression rates of HIV-1 replication and more favorable lipid profiles [
We assessed the management of CVRF in the routine clinical practice in HIV-infected subjects already diagnosed for a coronary event.
We performed a retrospective descriptive study to identify all HIV-1-infected patients with a previous coronary event recorded in the database of the HIV unit, internal medicine and cardiology departments of two tertiary hospitals in Barcelona, Spain, from April 1983 through June 2011. The database contained information on 3,760 HIV-1-infected patients in routine follow-up. In addition, the causes of mortality in both cohorts during the period of study (from April 1983 to June 2011) have been checked to identify those related to a cardiovascular event.
A coronary event was defined as a definite or probable acute myocardial infarction or reinfarction, angina, percutaneous coronary angioplasty/stenting, coronary bypass surgery, target vessel revascularization for restenosis, stent thrombosis, and death from ischemic coronary disease according to the criteria of the World Health Organization Multinational Monitoring of Trends and Determinants in Cardiovascular Disease Project (MONICA) [
Cases of myocardial infarction were categorized as fatal or nonfatal.
We determined the prevalence of coronary events by assessing the numbers of subjects per 1000 HIV-infected patients in a Mediterranean cohort to identify all HIV-1-infected patients with a previous coronary event recorded in the database from April 1983 until June 2011.
To evaluate changes in modifiable CVRF before and after the coronary event, we compared the prevalence of the modifiable CVRF in the clinic at three time points: before initiating antiretroviral therapy, at the time of the coronary event, and after the event (the last available visit until June 2011).
Finally, we compared the Framingham risk score at the time of the coronary event and at last follow-up visit.
We recorded the following information: sociodemographic features (age, gender, and race); HIV-related data (time since HIV diagnosis, risk behavior, previous AIDS diagnosis defined according to the Centers for Disease Control and Prevention category C [
In addition, at each of the three time points mentioned above, we recorded laboratory data performed after at least 8 hours of fasting (plasma HIV-1 RNA levels, lymphocyte CD4 T-cell count, total cholesterol, low-density lipoprotein [LDL] cholesterol, high-density lipoprotein [HDL] cholesterol, triglycerides, glomerular filtration rate, and glucose level) and the Framingham risk score. Glycosylated hemoglobin was not considered because it was not a routine laboratory parameter.
Cardiovascular risk was classified according to the Framingham score as low (<10%), moderate (10%–20%), or high (≥20%).
Hypertension was defined as systolic blood pressure ≥140 mm Hg, diastolic blood pressure ≥90 mm Hg, or the need for antihypertensive drugs. Patients were considered to have dyslipidemia if they were taking lipid-lowering drugs or when the total cholesterol level was >200 mg/dL, LDL-cholesterol level was >100 mg/dL (criteria for HIV-infected patients according to the “European Guidelines on cardiovascular disease prevention in clinical practice” [
Antiretroviral drugs were classified according to their impact on lipid metabolism in two groups: those with a negative impact on triglyceride and cholesterol levels (lopinavir, indinavir, and fosamprenavir) and those with a neutral effect (atazanavir, saquinavir, darunavir, and NNRTIs).
Demographic and clinical parameters were expressed as mean (SD), median (interquartile range, IQR), or frequency and percentage, as appropriate.
Continuous repeated measurements were compared using the
Univariate
We identified 81 HIV-1-infected patients with a previous coronary event in a cohort of 3760 patients. The prevalence of a coronary event was 2.15%.
The most frequent event was acute myocardial infarction (67 patients, 82.7%), followed by unstable angina (10 patients, 12%), reinfarction, or angor following acute myocardial infarction (4 patients, 5.3%).
Coronary angiography was undertaken in 43 patients (53%) and revealed stenosis with single vessel involvement in 19 of them (41.9%) and 2 or more vessels in 25 (58.1%).
Forty-six patients (57%) received invasive treatment: 24 of them (30%) received a percutaneous angioplasty, 18 (22%) open bypass surgery, and 4 (5%) vessel revascularization for restenosis and stent thrombosis. The remaining 35 patients (43%) only required medical treatment.
The mortality rate registered in our cohort among subjects with previous coronary events at the end of study (June 2011) was 13.6% (11/81). Of these, 9 (11%) patients died due to noncardiovascular causes such as kidney failure, liver failure, opportunistic infections, brain subdural hematomas, respiratory infections, and others, and only two patients (2.5%) died as a result of a coronary event (one of them was related to illicit drug use, cocaine).
Table
Patient characteristics at the time of the coronary event.
Characteristics | HIV-infected patients ( |
---|---|
Age, years (median [IQR]) | 48 (40, 57) |
Patients > 50 years (%) | 38.3 |
Gender (male) (%) | 86.1 |
Body mass index >25 (%) | 9.8 |
Men who have sex with men (%) | 38.6 |
HCV coinfection (%) | 4.9 |
HBV coinfection (%) | 12.3 |
|
|
HIV-related characteristics | |
Time since diagnosis of HIV-infection, years (median [IQR]) | 14.9 (10.4, 19.2) |
Cumulative exposure to antiretrovirals (median [IQR]) | 12.7 (9.3, 16.2) |
Cumulative exposure to PIs (median [IQR]) | 5 (0.7, 8) |
Cumulative exposure to NNRTIs (median [IQR]) | 3 (0.1, 7) |
Cumulative exposure to abacavir (median [IQR]) | 2 (0, 11) |
CD4 cells count/ |
224 (89, 422) |
HIV-RNA ≤ 400 copies/mL (median [IQR]) | 46 (56.8%) |
Lipodystrophy (including lipoatrophy) (%) | 36.1 |
|
|
Cardiovascular risk factors | |
Family history of coronary heart disease (%) | 17 (20.5%) |
Smoking (%) | 36 (44%) |
Cumulative exposure to tobacco smoke, years (mean [SD]) | 23 (9.4) |
Hypertension (%) | 49 (60.5) |
*Use of antihypertensive treatment (%) | 43 (87.8) |
Diabetes mellitus (%) | 13 (16) |
*Use of antidiabetic treatment (%) | 10 (76.9) |
Dyslipidemia (%) | 44 (48.1) |
Serum total cholesterol, mg/dL (median [IQR]) | 182 (152, 230) |
Serum HDL-cholesterol, mg/dL (median [IQR]) | 42 (35, 52) |
Serum LDL-cholesterol, mg/dL (median, [IQR]) | 104 (98, 194) |
Serum triglycerides, mg/dL (median, [IQR]) | 168 (106, 248) |
*Use of lipid-lowering agents (%) | 39 (88.6) |
Data was reported as median and interquartile range [IQR].
*Percentages of patients using antihypertensive drugs, antidiabetic treatment or lipid-lowering agents were calculated considering the number of patients receiving that treatment with respect to those who required treatment (considering target parameters according to the guidelines).
From 81 HIV-1-infected patients with a previous coronary event, overall 86% of them were males, the median age was 48 (40, 57) years, and 38% of patients were >50 years old.
As for CVRF, 60.5% of patients had a history of hypertension, 48% dyslipidaemia, and 16% diabetes mellitus; of them, 12.2%, 23.1%, and 11.4% required treatment for these conditions, respectively, but they did not receive it or this information was not available in the patient’s records. Forty-four percent of patients were current smokers and 9.8% had a body mass index >25. The information in the medical records revealed that only 3 patients (3.7%) were questioned about physical exercise.
At the time of the coronary event, the median follow-up since diagnosis of HIV infection was 14.9 (10.4; 19.2) years, the median time (IQR) from starting antiretroviral treatment until the coronary event and the median time from the coronary event until the last follow-up visit (June 2011) were 8 (5; 12) and 7 (4; 11) years, respectively, and the median time of receiving antiretroviral treatment was 12.7 (9.3, 16.2) years. Regarding antiretroviral treatment, 33 patients (41%) were receiving a PI-based regimen: 22 patients (67%) were receiving PI-based regimen with an unfavorable lipid profile and 11 (33%) a PI-based regimen with favorable lipid profile; 26 (32%) were receiving a NNRTI-based regimen: 11 patients were on efavirenz (42%) and 15 on nevirapine (58%); 6 patients (7%) were receiving other regimens (integrase inhibitors, CCR5 antagonist) and 17 patients (20%) were not taking antiretroviral treatment.
At the time of the coronary event, the calculation of Framingham score was only possible in 12 patients (15%) due to the lack of some necessary parameters (mainly determination of HDL-cholesterol levels, tobacco, and blood pressure). Among those 12 patients, the CVR was classified as high in 1 patient (8%), moderate in 8 (67%) patients, and low in 3 (25%) patients.
Changes among the three time points of the study in smoking habit, exercise, body mass index, use of lipid-lowering drugs, and antihypertensive and oral antidiabetic drugs/insulin were not routinely assessed or correctly registered in the routine follow-up (were not coded). This information was mainly available in the clinical record at the time of the coronary event, but not in other points in many patients. Similarly, in most cases, it was not possible to evaluate variations in Framingham score, due to the lack of necessary information to calculate it.
Metabolic parameters at the three time points are summarized in Table
Changes in modifiable cardiovascular risk factors and Framingham score at the three time points of the study in the 81 included patients.
Laboratory data | Before starting ARV | At the time of the coronary eventa | Last observationb |
c
|
d
|
---|---|---|---|---|---|
CD4, cell/ |
224 (89, 422) | 497 (384, 776) | 559 (375, 767) |
|
0.201 |
HIV-RNA, log (median [IQR]) | 4.6 (3.6, 5.3) | 1.8 (1.4, 2.7) | 1.4 (1.3, 1.7) |
|
|
Serum total cholesterol, mg/dL (median [IQR]) | 185 (154, 213) | 182 (152, 230) | 174 (147, 205) | 0.402 |
|
Serum HDL-cholesterol, mg/dL (median [IQR]) | 41 (30, 43) | 42 (35, 52) | 45 (33, 53) | 0.155 | 0.974 |
Serum LDL-cholesterol, mg/dL (median [IQR]) | 102 (97, 189) | 104 (98, 194) | 95 (86, 124) | 0.305 |
|
CT/HDL-cholesterol ratio mmol/L | 4.3 (3.8, 5.6) | 4.1 (3.1, 5.8) | 4 (3.1, 5.2) | 0.110 | 0.339 |
Serum triglycerides, mg/dL (median [IQR]) | 151 (106, 204) | 168 (106, 248) | 142 (95, 204) | 0.778 | 0.111 |
Glycemia, mg/dL (median [IQR]) | 90 (85, 103) | 97 (88, 108) | 95 (88, 108) | 0.140 | 0.299 |
Glomerular filtration rate, mL/min (median [IQR]) | 60 (60, 60) | 60 (60, 60) | 60 (60, 60) | 0.317 | 0.317 |
Serum total cholesterol >200 mg/dL ( |
18 (49) | 29 (45) | 25 (35.2) | 0.265 | 0.738 |
Serum HDL-cholesterol <40 mg/dL ( |
73 (90) | 21 (44) | 25 (39.7) |
|
1.000 |
Serum LDL-cholesterol >100 mg/dL ( |
7 (46) | 17 (45) | 25 (41%) | — | 0.103 |
Serum triglycerides >200 mg/dL ( |
15 (41) | 30 (37) | 26 (32.1) |
|
|
Serum triglycerides >500 mg/dL ( |
1 (2.7) | 4 (6.3) | 3 (4.1) | 0.118 | 0.193 |
Glycemia >110 mg/dL ( |
5 (15) | 15 (23) | 17 (24.3) |
|
|
Framingham <10% (low) ( |
2 (50) | 3 (25) | 11 (44) | — | — |
Framingham 10%–20% (moderate) ( |
2 (50) | 8 (67) | 8 (32) | — | — |
Framingham >20% (high) ( |
— | 1 (8) | 6 (24) | — | — |
aMedian time (IQR) from starting antiretroviral treatment until the coronary event: 8 (5; 12) years; bmedian time (IQR) from the coronary event until the last follow-up visit (June 2011): 7 (4; 11) years.
c
CT: total cholesterol; HDL: high-density lipoprotein; LDL: low-density lipoprotein.
Levels of LDL-cholesterol and HDL-cholesterol were only determined in 18.5% of subjects at the baseline visit (previous antiretroviral therapy); 46% of them had an LDL-cholesterol level of >100 mg/dL. At the time of the coronary event, an LDL-cholesterol determination was available for 47% of patients, and it was >100 mg/dL in 45% of them. Finally, at the last available visit (after the coronary event), LDL-cholesterol determination was available for 73% of patients, and in 41% it was >100 mg/dL.
A significant decrease from the time of the coronary event to the last visit available was observed in total cholesterol [from 182 ((152, 230) mg/dL to 174 (147, 205),
No significant differences among the three time points were observed in HDL-cholesterol, total/HDL-cholesterol ratio, triglyceride levels, and glycemia.
The percentage of patients receiving PIs with an unfavorable lipid profile decreased from 67% during the coronary event to 37% at the last follow-up visit (
Current antiretroviral therapy during coronary event and at the last follow-up visit.
Coronary event |
Last follow-up visita |
| |
---|---|---|---|
Without treatment ( |
17 (20) | 11 (14) | 0.3 |
|
33 (41) | 35 (43) | 0.87 |
PI (with an unfavorable lipid profile) | 22 (67) | 13 (37) |
|
Indinavir/r | 7 (21) | 2 (6) | 0.13 |
Lopinavir/r | 15 (45) | 10 (29) | 0.23 |
Fosamprenavir/r | 0 | 1 (3) | 1 |
PI (with a favorable lipid profile) | 11 (33) | 22 (63) |
|
Saquinavir/r | 2 (6) | 0 | 0.45 |
Atazanavir/r | 6 (18) | 11 (31) | 0.33 |
Darunavir/r | 3 (9) | 11 (31) |
|
|
26 (32) | 31 (38) | 0.51 |
Nevirapine | 15 (58) | 14 (45) | 0.5 |
Efavirenz | 11 (42) | 17 (55) | 0.5 |
Other treatments ( |
6 (7) | 4 (5) | 0.74 |
Without treatment | 0 | 5 (33) | 1 |
|
|||
Nucleoside reverse transcriptase inhibitor | |||
Abacavir | 15 (52) | 14 (48) | 1 |
aMedian time (IQR) from the coronary event until the last follow-up visit (June 2011): 7 (4; 11) years.
b
PI: protease inhibitors; NNRTI: nonnucleoside analog reverse-transcriptase inhibitors.
The rate of patients with suppressed HIV-1 RNA viral load significantly increased after the coronary event (
The prevalence of coronary events in our cohort of HIV-1-infected subjects (2.15%) was lower than that observed by other groups [
Traditional CVRF were highly prevalent in patients with a history of coronary heart disease at the time of the event. The percentage of patients routinely undertaking fasting lipid profiles significantly increased after the coronary event and a decrease in total and LDL-cholesterol levels was observed after the event. Nevertheless, many patients (41%) did not achieve the recommended target in lipid parameters. Additionally, other CVRF such as smoking, lack of exercise, or hypertension were not regularly controlled.
HIV-1-infected individuals receiving HAART have a higher risk for ischemic heart disease than the general population [
A meta-analysis including 19 studies evaluating cardiovascular and cerebrovascular events in Spanish population showed that the prevalence of angina in Spain was about 7%, while it was 2.6% in men and 3.5% in women aged from 25 to 74 years in another cohort [
The pathogenic mechanism of premature atherosclerosis in HIV-1-infected individuals has not been clearly defined, although it is considered a multifactorial process. HIV infection and antiretroviral therapy might accelerate atherogenesis, as do traditional risk factors. First, a chronic systemic inflammatory state, endothelial dysfunction, and prothrombotic state caused by the virus itself contribute to the pathogenesis of coronary disease [
Finally, traditional CVRF and smoking, cocaine use, or coinfection with hepatitis C virus (all of which are proatherogenic factors) are more common in HIV-1-infected individuals than in the general population, [
Fortunately, the incidence of cardiovascular events in the HIV-1-infected population has fallen in recent years. This is possibly as a result of more aggressive management of the risk of CVD, the use of drugs with better cardiovascular profile [
Surprisingly, in our cohort, the number of patients who were receiving treatment for concomitant conditions (lipid-lowering agents, antihypertensive drugs, or antidiabetic drugs) was extremely high. Similarly, LDL- and HDL-cholesterols were more frequently determined during recent years, indicating increased efforts in achieving a better control of lipid metabolism. However, treatment for dyslipidemia was suboptimal or poorly controlled in most cases. Lipid levels improved after the coronary event, although almost half (41%) of the patients maintained an LDL-cholesterol level > 100 mg/dL after the coronary event. Second, other CVRF, such as smoking, hypertension, lack of exercise, and body mass index, are not routinely assessed. These data were not available in the clinical histories of most of our patients, suggesting poor monitoring of these risk factors in our clinical practice.
The mortality rate registered in our cohort among subjects with previous coronary events was 2.5%, slightly lower than that observed by other groups (4.2%) [
The retrospective design of our study did not enable us to determine the real rate of some risk factors and thus evaluate changes. However, the study provides us a clear picture of real clinical practice. In addition, despite performing an exhaustive search, we cannot exclude the possibility of missed coronary events attended at other centers and not reported in our database. However, this rate would be low and is unlikely to drive a significant change in the study results.
In summary, the management of CVRF in our cohort was far from optimal, in subjects already diagnosed for prior CV major events. However, as this group is aging, we expect a progressive increase in the incidence of CVD paralleling the age group. Cardiovascular health plans are a priority if this increase is to be curbed and need to carefully monitor the CVRF to assess the effectiveness of such plans. Optimal selection of antiretroviral treatment, together with aggressive management of other modifiable risk factors, will diminish cardiovascular risk in HIV-1-infected patients.
None of the authors has a financial or beneficial interest in concepts mentioned in the present paper. This is a statement that the paper has been presented as a poster in the 6th IAS Conference on HIV pathogenesis, treatment, and prevention from 17 to 20 July 2011 in Rome, Italy.
This paper was made possible through the collaboration of the staff of the AIDS care unit of Germans Trias i Pujol University Hospital and Santa Creu i Sant Pau University Hospital, Barcelona, Spain. This study was supported by the Spanish AIDS network “Red Temática Cooperativa de Investigación en SIDA” (RD06/0006) and the Gala contra la sida, Barcelona, 2011. P. Echeverría is a researcher from Fundació Lluita contra la SIDA, Universitary Hospital Germans Trias i Pujol, Barcelona, Spain. All authors have contributed to the writing of the paper and approved the final, submitted version of the paper.