Increased prevalence of subclinical coronary atherosclerosis detected by coronary computed tomography angiography in HIV-infected men.
Lo, Janeta; Abbara, Suhnyb; Shturman, Leonc; Soni, Anandc; Wei, Jeffreya; Rocha-Filho, Jose Ac; Nasir, Khurramc,d; Grinspoon, Steven Ka
aProgram in Nutritional Metabolism, USA
bDepartment of Radiology, Cardiovascular Imaging Section, USA
cCardiac MR PET CT Program, Massachusetts General Hospital and Harvard Medical School, USA
dDepartment of Internal Medicine at Boston Medical Center, Boston, Massachusetts, USA.
Received 4 September, 2009
Revised 5 October, 2009
Accepted 6 October, 2009
Correspondence to Janet Lo, MD, Program in Nutritional Metabolism, Massachusetts General Hospital, 55 Fruit Street, LON207, Boston, MA 02114, USA. Tel: +1 617 724 9109; fax: +1 617 724 8998; e-mail: firstname.lastname@example.org
Objective: The degree of subclinical coronary atherosclerosis in HIV-infected patients is unknown. We investigated the degree of subclinical atherosclerosis and the relationship of traditional and nontraditional risk factors to early atherosclerotic disease using coronary computed tomography angiography.
Design and methods: Seventy-eight HIV-infected men (age 46.5 ± 6.5 years and duration of HIV 13.5 ± 6.1 years, CD4 T lymphocytes 523 ± 282; 81% undetectable viral load), and 32 HIV-negative men (age 45.4 ± 7.2 years) with similar demographic and coronary artery disease (CAD) risk factors, without history or symptoms of CAD, were prospectively recruited. 64-slice multidetector row computed tomography coronary angiography was performed to determine prevalence of coronary atherosclerosis, coronary stenosis, and quantitative plaque burden.
Results: HIV-infected men demonstrated higher prevalence of coronary atherosclerosis than non-HIV-infected men (59 vs. 34%; P = 0.02), higher coronary plaque volume [55.9 (0–207.7); median (IQR) vs. 0 (0–80.5) μl; P = 0.02], greater number of coronary segments with plaque [1 (0–3) vs. 0 (0–1) segments; P = 0.03], and higher prevalence of Agatston calcium score more than 0 (46 vs. 25%, P = 0.04), despite similar Framingham 10-year risk for myocardial infarction, family history of CAD, and smoking status. Among HIV-infected patients, Framingham score, total cholesterol, low-density lipoprotein, CD4/CD8 ratio, and monocyte chemoattractant protein 1 were significantly associated with plaque burden. Duration of HIV infection was significantly associated with plaque volume (P = 0.002) and segments with plaque (P = 0.0009) and these relationships remained significant after adjustment for age, traditional risk factors, or duration of antiretroviral therapy. A total of 6.5% (95% confidence interval 2–15%) of our study population demonstrated angiographic evidence of obstructive CAD (>70% luminal narrowing) as compared with 0% in controls.
Conclusion: Young, asymptomatic, HIV-infected men with long-standing HIV disease demonstrate an increased prevalence and degree of coronary atherosclerosis compared with non-HIV-infected patients. Both traditional and nontraditional risk factors contribute to atherosclerotic disease in HIV-infected patients.
Survival of HIV-infected patients worldwide has remarkably improved with the use of HAART and increasing access to treatment; however, even among treated HIV patients, survival is still decreased compared with the general population due, in large part, to excess mortality from noninfectious illnesses, including cardiovascular disease [1,2]. Traditional cardiovascular risk factors, including dyslipidemia, diabetes mellitus, and smoking are highly prevalent in the HIV population . Furthermore, immune activation, chronic inflammation, and viral factors may predispose this patient population to increased cardiovascular risk above and beyond that conferred by traditional cardiovascular risk factors .
Prior retrospective studies utilizing healthcare system-based databases have shown the rate of cardiovascular events to be higher in young men and women with HIV infection than non-HIV-infected individuals [5,6]; however, prospective studies examining early subclinical coronary artery disease (CAD), assessing detailed measures of plaque burden beyond calcium scoring, using coronary CT angiography (CTA) to quantitatively measure the extent of coronary plaque, including noncalcified, mixed calcified and noncalcified, and calcified plaque and to assess for coronary artery luminal narrowing in HIV-infected patients compared with concurrently enrolled uninfected controls are still lacking. Therefore, we investigated the prevalence and degree of early subclinical coronary atherosclerosis in young asymptomatic HIV-infected individuals without previously known cardiovascular disease using 64-slice cardiac multidetector row computed tomography (MDCT) and coronary CTA in a prospectively recruited cohort of HIV-infected patients compared with concurrently recruited HIV-seronegative controls with similar demographic and traditional cardiovascular risk factors.
In a prospectively recruited cohort, the prevalence of subclinical CAD in asymptomatic HIV-infected men was compared with that in HIV-seronegative control men. The prevalence of coronary plaque was the primary endpoint. Secondary endpoints included plaque volume, number of coronary segments with plaque, coronary stenosis, and Agatston calcium score.
One hundred and ten men participated in this study. Seventy-eight men with HIV infection were recruited from HIV clinics and community health centers in the Boston area as well as by newspaper advertisements. HIV-negative control men were identically recruited from the same communities using the same advertisements, seeking asymptomatic young men without known cardiac disease. Family members, partners, and friends of the HIV-infected patients were also encouraged to enroll in attempt to ensure the two groups would be similar with respect to demographic characteristics and cardiovascular risk factors. Other than HIV disease, inclusion and exclusion criteria were identical for both groups. Participants aged 18–55 years, without known cardiac disease or symptoms suggestive of cardiac disease (any current or prior heart disease, including angina, arrhythmias, valvular heart disease, pericarditis, congestive heart failure, or any prior treatment for CAD or any heart disease) were recruited. HIV and control participants were not recruited with regard to any changes in body composition, weight, or metabolic criteria. HIV and control participants with known renal disease or creatinine more than 1.5 mg/dl or estimated creatinine clearance less than 70 ml/min were excluded to minimize risk of contrast nephropathy. Participants with contraindications to administration of contrast agent, β-blockade, or nitroglycerin were also excluded. HIV-infected patients receiving HAART at the time of the study were required to be on stable therapy for more than 3 months. HIV-infected patients not receiving antiretroviral therapy (ART) were also recruited. All participants gave informed consent to participate. This study was approved by the institutional review boards of Massachusetts General Hospital and Massachusetts Institute of Technology.
Study procedures and assessment of cardiovascular risk factors
All participants underwent a detailed interview and physical examination by a single investigator. Detailed information on sociodemographic factors, medical history, family history, behavior, including smoking, recreational drug use, and medications was obtained. Duration of known HIV diagnosis and detailed history of prior antiretroviral use were determined. All participants fasted at least 12 h before blood draws and the 75-g oral glucose tolerance test (OGTT). Assessment of traditional cardiovascular risk factors was determined through comparison of individual risk factors and an aggregate risk score using the Framingham risk equation .
Cardiac multidetector row computed tomography and computed tomography angiography
CT imaging was performed using a 64-slice CT scanner (Sensation 64; Siemens Medical Solutions, Forchheim, Germany). In preparation for the scan, participants with heart rate more than 60 beats/min received intravenous β-blocker (metoprolol 5–20 mg) unless contraindications to β-blockers were present or if systolic blood pressure was less than 100 mmHg. Participants also received 0.6 mg sublingual nitroglycerin. Image acquisitions were performed during breathhold in inspiration. As per standard protocol, a test bolus of 20 ml contrast agent was administered with a flow rate of 5 ml/s to determine the optimal timing of contrast injection. Coronary CTA datasets were acquired with 64 × 0.6 mm slice collimation, a gantry rotation time of 330 ms, tube voltage of 120 kVp, and an effective tube current of 850 mAs using ECG-correlated tube current modulation when appropriate. Contrast agent (80–100 ml, iopamidol, Isovue; Bracco Diagnostics, Inc., Princeton, New Jersey, USA) was injected intravenously at a rate of 5 ml/s to ensure homogeneous enhancement of the entire coronary artery tree. Axial images were reconstructed with a slice thickness of 0.75 mm and increment of 0.4 mm using a half-scan algorithm with a temporal resolution of 165 ms. Images were initially reconstructed at 60, 65, 70, and 35% of the cardiac cycle. Additional reconstructions were performed to minimize motion artifacts, if necessary. All reconstructions were transferred to an offline workstation for analysis (Leonardo; Siemens Medical Solutions). Assessment of coronary atherosclerotic plaque, including number of segments with plaque, and degree of stenosis, was determined by a consensus reading between two investigators, including a cardiologist and a radiologist with significant experience in the interpretation of cardiac CT. Physicians analyzing the scans were blinded to the participants' clinical history or HIV status. Agatston calcium score was calculated using the noncontrast CT images by standardized techniques .
Plaque volume measurements were performed by a single experienced reader blinded to participants' HIV status using an offline Vitrea 2 workstation (Vital Images, Minnetonka, Minnesota, USA) and software for plaque analysis (SUREPlaque) . Plaques were identified in the curved multiplanar reconstruction after readers selected the phase of the cardiac cycle with no motion artifact. The plaque length was established visually with a marker in the proximal and distal plaque limits. The inner and outer borders of the vessel/plaque were established using a semiautomatic tracer and plaque volume was calculated automatically. When the contour was visually out of the vessel/plaque border, manual correction was performed. Lesions with motion artifact in all phases of the cardiac cycle were excluded. Interobserver and intraobserver intraclass correlation coefficients determined in 25 patients were more than 0.99 (P < 0.001).
The presence of any coronary atherosclerotic plaque, whether calcified or noncalcified, was assessed. Quantification of atherosclerotic plaque was measured by counting the number of coronary segments with evidence of plaque present (using a modified 17-segment model of the coronary artery tree) ; and by plaque volume. Presence of severe coronary artery stenosis was defined as luminal obstruction more than 70% diameter in any coronary segment.
Body composition and dietary assessment
Weight and anthropometric measurements were determined in the morning, prior to breakfast. To assess abdominal visceral and abdominal subcutaneous adipose tissue area (VAT and SAT, respectively), a cross-sectional abdominal CT scan at the level of the L4 pedicle was performed . Four-day food records were completed by the participants and analyzed using Minnesota Nutrition Data System software.
Metabolic, biochemical, and immunologic parameters
Total cholesterol, high-density lipoprotein (HDL), low-density lipoprotein (LDL), triglycerides, glucose, and creatinine were determined using standard techniques. Monocyte chemoattractant protein-1 (MCP-1) and C-reactive protein (CRP) were measured using enzyme-linked immunosorbent assay (ELISA). Insulin was measured using either a radioimmunoassay (RIA) or a chemiluminescence immunoassay. Cross validation analysis indicated a strong linear correlation (r = 0.99, P < 0.0001). CD4+ and CD8+ T-cell counts were assessed by flow cytometry. CD4+ nadir was obtained by patient report. HIV viral load was determined by ultrasensitive real-time PCR (lower limit of detection = 50 copies/ml). HIV testing was performed by chemiluminometric immunoassay and confirmed by western blot. Cytomegalovirus IgG (CMV IgG) titers were measured using an enzyme-linked fluorescent immunoassay.
Presence of plaque (yes or no) as a dichotomized variable was compared between the HIV group and the control group using the χ2 test. Plaque burden as a continuous variable was quantified using total number of coronary segments with plaque and by plaque volume. Comparisons between two groups were performed using Student's t-test for normally distributed continuous variables and Wilcoxon rank-sum test if the distribution was nonnormal. Spearman correlation coefficient was used to assess correlations with plaque burden as number of segments with plaque, plaque volume, and Agatston calcium score had nonnormal distributions. Logistic regression analysis was used to perform adjusted analyses for binary outcome of presence of plaque. Linear regression analysis was used for adjusted analyses for continuous outcome variables. For the assessment of differences between HIV and non-HIV-infected participants, known cardiovascular disease risk markers were included as covariates in regression modeling. In multivariate modeling, among HIV-infected patients, assessing the relationship of duration of HIV to measures of plaque burden, modeling was performed including HIV-related parameters and traditional risk factors as covariates. Additional analyses were performed comparing cardiovascular risk and HIV-related parameters in HIV-infected patients with (n = 46, 59%) and without (n = 32, 41%) coronary plaque. Sensitivity analyses were performed comparing the presence of plaque in the subset excluding any patient with triglyceride more than 200 mg/dl or fasting insulin more than 75th centile for men of this age group (>11.9 μU/ml), using normative data from the Framingham Offspring study (personal communication with Dr James Meigs). Two-tailed probability values are reported and statistical significance was assumed when P value was less than 0.05. All statistical analyses were performed using JMP (SAS Institute Inc., Cary, North Carolina, USA) and SPSS (SPSS Inc., Chicago, Illinois, USA).
Characteristics of participants
One hundred and ten men participated in this study, including 78 HIV-infected men and 32 HIV-seronegative men. Demographic and clinical characteristics of the study participants are described in Table 1. HIV-infected patients had a long duration of known HIV infection of approximately 13.5 years. The great majority (95%) were receiving ART, with an average duration of treatment of 7 years. The percentages receiving each major class of ART use and the duration of this use are also shown in Table 1. Overall, immunological control was good, with CD4 cell count 523 ± 282 cells/μl and 81% with undetectable viral load. A total of 89% of patients had a viral load under 1000 copies/ml. The four patients who were not on ART had never been on ART and had CD4 cell count 815 ± 190 cells/μl and viral load 1039 (156–7038) copies/ml.
Age, race, sex, BMI, and Framingham risk score were similar between both groups (Table 1). Family history of premature coronary heart disease, prevalence of hypertension, prevalence of diabetes mellitus, % of current smokers, blood pressure, fasting glucose, 2-h glucose, hemoglobin A1c, total cholesterol, HDL, LDL, CRP, and IL-6 were also similar between the HIV and control groups. The HIV and non-HIV-infected group had similar Framingham scores (7.7 ± 5.1 vs. 7.0 ± 4.6, P = 0.50) and predicted median 10-year myocardial infarction (MI) risk scores 4 vs. 4.5% risk. The HIV group had a higher triglyceride concentration and borderline higher fasting insulin and these variables were investigated in sensitivity analyses and regression modeling. Dietary intake of total calories, fat, protein, carbohydrates, saturated fat, fiber, and cholesterol were similar between the HIV and non-HIV-infected groups (data not shown).
Prevalence of coronary artery disease and coronary artery stenosis
Significant difference in the prevalence of coronary atherosclerosis was seen between the two groups with 59% of the HIV group having evidence of plaque present in the coronary arteries visualized by CTA vs. 34% of the control group (P = 0.02; Fig. 1; Table 2). Controlling for known cardiovascular risk factors, including age, race, BMI, smoking pack-years, Framingham risk score, hypertension, diabetes mellitus, cocaine use, total cholesterol, LDL, HDL, and triglycerides, prevalence of CAD remained higher in the HIV group (P = 0.02).
Plaque burden measured by number of segments with plaque [1 (0–3) vs. 0 (0–1) segments, P = 0.03] and plaque volume [55.9 (0–207.7) vs. 0 (0–80.5) μl, P = 0.02] indicate higher plaque burden in the HIV group when compared with the control group (Table 2).
Agatston calcium score
Overall Agatston calcium score tended to be higher in HIV patients (P = 0.08) and percentage with score more than 0 was higher in the HIV group (46.2 vs. 25.0%, P = 0.04; Table 2). Among participants with Agatston calcium score of 0, 10 out of 42 HIV patients [23.8% (95% confidence interval 13.5–38.5%)] had evidence of noncalcified plaque seen on CTA and three out of 24 controls [12.5% (4.3–31.0%)] had evidence of noncalcified plaque.
Critical coronary stenosis
A total of 6.5% (95% confidence interval 2–15%) of HIV patients had greater than 70% stenosis in one or more coronary segments compared with 0% in controls (Table 2). The median Framingham 10-year risk among HIV patients with stenosis more than 70% was 12% (IQR 6–19%) vs. 4% (2–6%) (P = 0.006) among HIV-infected patients without stenosis more than 70%. Further clinical follow-up information was obtained in the five asymptomatic HIV-infected patients we identified with severe CAD (>70% coronary luminal narrowing) by CTA. Due to the data obtained by cardiac CTA from our study, these patients were referred to cardiologists by their primary care physicians. One patient underwent cardiac stress testing, which yielded normal results, and continues to do well. Another patient was recommended by his provider to undergo cardiac stress testing, which has not yet been obtained. After formal evaluation by cardiologists, three patients underwent subsequent cardiac catheterization and in all three patients, coronary angiography confirmed their cardiac CTA findings. Of these three patients, one patient underwent coronary artery bypass graft surgery for four-vessel revascularization and is doing well; the second patient was found to have 85% stenosis of the proximal left anterior descending artery (LAD) on cardiac catheterization for which he underwent single vessel stent placement and is doing well; and the third patient was found to have severe stenosis of the proximal left circumflex artery and diffuse mild-moderate coronary disease in other vessels. After failed stent placement, he received medical therapy but was unable to tolerate statins. Two and a half years later, he developed new symptom of angina manifested as left arm pain with exertion. A subsequent repeat cardiac catheterization showed rapid progression of his coronary disease to near-complete stenosis of five coronary branches requiring coronary artery bypass graft surgery and patient is currently doing well.
Characteristics of HIV patients with evidence of coronary atherosclerosis
HIV patients with evidence of plaque seen on CTA were more likely to be older (P = 0.004) and have longer duration of known HIV infection (P = 0.02), higher Framingham risk score (P = 0.002), higher total cholesterol (P = 0.01), higher triglycerides (P = 0.04), higher LDL (P = 0.046), and lower CD4/CD8 ratio (P = 0.001). However, there were no differences in BMI, VAT, SAT, duration of protease inhibitor use, duration of ART, HDL, fasting glucose, 2-h glucose, fasting insulin, 120-min insulin, viral load, CRP, or IL-6 among HIV patients with coronary atherosclerosis vs. HIV patients without coronary atherosclerosis. In addition, HIV patients with coronary atherosclerosis were not more likely to have been on ART or have CMV IgG seropositivity, but tended to have higher CMV IgG titers (P = 0.05; Table 3).
Relationship of cardiovascular risk factors to plaque burden and calcium score in HIV patients
Age, Framingham risk score, duration of known HIV infection, duration of protease inhibitor use, CD4/CD8 ratio, total cholesterol, LDL, CMV IgG antibody titers, and MCP-1 were associated with total number of coronary segments with plaque (Table 4). Plaque volume was associated with age, Framingham risk score, duration of known HIV infection, CD4/CD8 ratio, total cholesterol, and LDL. Agatston coronary calcium score was related to age, Framingham risk score, duration of known HIV infection, total cholesterol, LDL, triglycerides, glucose area under the curve (AUC), VAT, and MCP-1.
In multivariate regression analysis, controlling for age and Framingham risk score, the duration of known HIV infection remained significantly associated with plaque burden measured by number of segments with plaque (P = 0.04) and plaque volume (P = 0.05). The relationship between plaque volume and duration of HIV infection also remained significant in a model controlling for age, duration of protease inhibitor use, triglycerides, LDL, and HDL (P = 0.047). Controlling for parameters associated with HIV disease, including current CD4 cell count, nadir CD4 count, HIV viral load, and duration of ART, duration of HIV disease remained significantly associated with number of segments with plaque (P = 0.007).
Sensitivity analysis (in those with triglyceride <200 mg/dl, with insulin <75th centile of Framingham offspring study)
In participants without hypertriglyceridemia (triglyceride <200 mg/dl, n = 88), prevalence of coronary atherosclerosis was increased in HIV patients (54%) compared with controls (31%; P = 0.04); the number of segments with plaque was higher in HIV patients [1 (0–3)] compared with controls [0 (0–1)] (P = 0.03); and plaque volume was higher in HIV patients [36 (0–166) μl] compared with controls [0 (0–50) μl] (P = 0.02). In participants without hyperinsulinemia (fasting insulin ≤11.9 μU/ml, n = 98), prevalence of coronary atherosclerosis was increased in HIV patients (59%) compared with controls (33%) (P = 0.02); the number of segments with plaque was higher in HIV patients [1 (0–3)] compared with controls [0 (0–1)] (P = 0.03); and plaque volume was higher in HIV patients [42 (0–197) μl] compared with controls [0 (0–64) μl] (P = 0.02).
The current study shows an increased prevalence and greater degree of subclinical CAD in asymptomatic young HIV-infected men without prior history of cardiovascular disease. The prevalence in the HIV-infected patients was significantly greater than that seen in concurrently recruited HIV-seronegative men with similar demographics, Framingham risk scores, and similar traditional risk factors (age, sex, family history, BMI, smoking, total cholesterol, and LDL).
Surprisingly and of important clinical relevance, even among asymptomatic young HIV-infected men, 6.5% had evidence of severe CAD defined as coronary artery stenosis more than 70% as compared with 0% in the control group. The information obtained from the coronary angiography led to further work-up confirming coronary disease and cardiac procedures that may have prevented major adverse cardiac events. The fact that 6.5% of the HIV patients, all without any known cardiac disease or symptoms, were found to have severe obstructive CAD is of potential clinical significance. In contrast, none of the controls had severe obstructive CAD.
We found increased prevalence of atherosclerosis and increased plaque burden by indices of plaque volume and number of coronary segments affected in the HIV vs. non-HIV participants. Prior studies to assess atherosclerotic vascular disease in the HIV population have used brachial artery flow-mediated vasodilation, carotid intima–media thickness (IMT), and electron beam computed tomography (EBCT) calcium score without CT coronary angiography [11–21]. Despite evidence from data registry studies showing a greater prevalence of MIs in HIV vs. non-HIV-infected patients , studies using surrogate markers show mixed results, though studies of Hsue et al.  found carotid IMT to be higher in HIV patients than in age-matched controls and to progress at a more rapid rate than in noninfected controls. In a recent large study, carotid IMT was found to be higher in HIV patients from the study of Fat Redistribution and Metabolic Change in HIV (FRAM), compared with uninfected controls even after adjustment for traditional risk factors .
Previous studies utilizing CT to assess CAD in HIV patients assessed only coronary calcifications by coronary calcium scoring, but did not investigate noncalcified plaques nor visualized lumen caliber [18,20]. In a study by Kingsley et al. , HIV infection and long-term HAART use increased the likelihood of coronary calcium being present; however, after adjustment for traditional cardiovascular risk factors, HAART had no significant association with presence or extent of coronary calcium.
Although coronary calcification is specific for atherosclerotic lesions and the Agatston calcium score has been associated with cardiac event risk in non-HIV populations , atherosclerotic plaques can be present without detectable coronary calcium at the site. Coronary calcium score alone may not provide a true measure of early atherosclerosis in young HIV patients as plaque calcification usually occurs at a later stage and may not detect more vulnerable plaque lesions, which tend to be noncalcified or mixed calcified and noncalcified. In addition, the atherosclerotic disease process in HIV may be different from conventional atherosclerosis . No published studies to date have used coronary CTA to assess noncalcified plaques in HIV patients. Our data using CTA show that a significant proportion of patients with coronary atherosclerosis would have been missed if calcium score was used as the sole criterion for coronary atherosclerosis as 23.8% (95% confidence interval 13.5–38.5%) of HIV patients had evidence of noncalcified plaque seen on CTA among those with calcium score of zero. Moreover, the differences between the HIV and control groups were more consistent comparing indices of plaque that included noncalcified plaques beyond calcium score alone (e.g. presence of any plaque, segments with plaque, and plaque volume, all P < 0.05). Thus, our data suggest that CTA gives different and potentially more sensitive information than the coronary calcium score alone.
Participants in our study were screened to exclude patients with known ischemic heart disease or any symptoms of CAD, and were, on average, young, with an estimated 10-year Framingham risk of only 4%, similar to that of the controls. Clinicians might not consider such patients at risk for CAD, yet 6.5% of these asymptomatic young patients had critical stenosis in at least one vessel. These patients with critical stenosis did, however, have the highest Framingham score and thus this score still appears to be useful to identify those with the greatest degree of subclinical coronary atherosclerosis, even among a population of young asymptomatic patients. Moreover, those HIV patients with plaque clearly had elevated traditional risk factors, including age, Framingham risk score, total cholesterol, and LDL.
Our data suggest relationships between traditional and nontraditional risk factors to indices of plaque burden. For example, traditional risk factors such as age, total cholesterol, and LDL were strongly related to all indices of plaque burden as is also evidenced in the strong relationship between the Framingham risk score and plaque burden. 2-h glucose and triglycerides were more strongly related to Agatston score than to plaque volume or segments with plaque.
Our data also support the hypothesis that there is a relationship between HIV infection and coronary artery atherosclerosis independent of traditional cardiovascular risk factors, as traditional risk factors were generally similar between the groups, yet significant differences in plaque prevalence and plaque burden were seen between the HIV and non-HIV groups. Age, smoking, family history and overall Framingham score, as well as LDL, HDL, and glucose parameters were similar between the groups. Triglyceride and insulin levels were higher among the HIV-infected group, but we performed sensitivity analyses excluding any patient in either group with hypertriglyceridemia and hyperinsulinemia, and found similar results. We also confirmed our results in regression analyses, controlling for traditional cardiovascular risk factors, as well as triglyceride and insulin levels.
Data from the Strategies for Management of Antiretroviral Therapy (SMART) study [26,27] suggest that inflammatory, immune, or viral factors might contribute to increased CAD in the HIV population. We found that CD4/CD8 cell ratio was negatively associated with plaque volume and the relationship between CD4/CD8 ratio and plaque volume was stronger than that seen with CD4 cell count or viral load with plaque volume. Atherosclerosis is an inflammatory disease in which T lymphocytes can play a role in atheroma development [28,29]. Activated T cells, including CD8 cells, are present in atherosclerotic plaques  and may contribute to atherosclerosis [31,32]. Hsue et al.  have demonstrated increased carotid IMT in HIV-infected individuals who are able to maintain undetectable HIV RNA without ART, a group with heightened T-lymphocyte activation.
MCP-1 was significantly associated with the number of segments with plaque and with calcium score in our study. MCP-1 is a chemokine important for monocyte migration into the vascular intima during the development of atherogenesis . HIV-1 Tat protein promotes MCP-1 secretion, leading to increased transmigration of monocytes across endothelium . Furthermore, HIV patients with the MCP-1 2518G allele were found to have an associated five-fold increased risk for atherosclerosis  and this same polymorphism has also been associated with severity of CAD in non-HIV patients .
In this study, we have also shown that CMV IgG antibody titers are positively associated with degree of coronary atherosclerosis, as measured by number of coronary segments with plaque and Agatston calcium score, suggesting that immune activation as well as CMV-specific immune response may also be contributory to atherosclerosis in HIV patients. CMV infection has been associated with cardiac transplant vasculopathy and also implicated in the pathogenesis of atherosclerosis in HIV [38–40].
We found a significant and robust relationship between measures of coronary atherosclerosis and duration of known HIV infection. We controlled for duration of antiretroviral treatment and traditional cardiovascular risk factors in regression modeling. The relationship between duration of HIV and indices of coronary atherosclerosis (number of coronary segments with plaque, plaque volume, and calcium score) remained significant controlling for age, traditional cardiovascular risk factors, duration of ART, and specific HIV-related markers of disease and immune function. Duration of HIV disease may, therefore, reflect a relevant integrated measure of chronic subacute inflammation and altered immune function, processes that may contribute to increased CAD beyond the risk due to traditional risk factors. CRP and IL-6 were not increased in our participants; however, the participants in this study were specifically selected to have no history of CAD and were not acutely ill, in contrast to other studies investigating CRP in relationship to rates of MIs between HIV and non-HIV-infected patients . Taken together, our data suggest that both traditional and nontraditional HIV-specific risk factors contribute to increased CAD in young asymptomatic HIV-infected men.
The current study has limitations, including the cross-sectional design, from which causality cannot be inferred. Second, the study was performed in men only and thus results may not be generalizable to HIV-infected women. Our results also cannot be generalized to a more high-risk population of HIV-infected patients or to symptomatic patients, in whom traditional risk may dominate more and in whom an even greater prevalence of plaque and potentially calcified plaque might be seen. Based on the data in our study, further studies are now needed to investigate the clinical implications and clinical course of CAD in HIV-infected patients with subclinical coronary atherosclerosis.
Our findings suggest a high prevalence and significant degree of coronary atherosclerosis among young HIV-infected men with a long duration of HIV disease, without any symptoms of cardiac disease or a prior diagnosis of cardiac disease and with a generally low Framingham risk score. Participants were recruited with a goal to have a similar traditional cardiac risk profile in HIV and control participants, yet various measures of atherosclerosis, including unique indices of plaque volume and, the number of coronary segments of plaque were different between the groups. These data suggest that both traditional and nontraditional risk factors contribute to increase subclinical atherosclerosis in HIV-infected patients. The findings from the current study support the need for increased efforts and attention to reducing modifiable traditional and nontraditional cardiovascular risk factors in this patient population. Our data highlight the need to address cardiac risk reduction early on in the course of HIV disease, before significant subclinical disease accrues and before cardiac events occur.
We wish to thank the participants of this study and the Nursing and Bionutrition Staff of the Massachusetts General Hospital and Massachusetts Institute of Technology General Clinical Research Centers. Principal contributions of authors are study conception (J.L., S.G.), study design (J.L., S.A., A.S., K.N., S.G.), participant recruitment (J.L., J.W.), history-taking and physical examination (J.L.), data acquisition and database management (J.L., J.W.), cardiac imaging data acquisition and analysis (S.A., L.S., A.S., J.R.), statistical analysis and interpretation (J.L., S.G.), drafting of the manuscript (J.L., S.G.), critical revision of manuscript (J.L., S.A., L.S., J.R., K.N., J.W., S.G.), and supervision of study (S.G.).
The funding was received from Bristol Myers Squibb, Inc., NIH K23 HL092792 (J.L.), K24 DK064545 (S.K.G.), F32 HL088991 (J.L.), T32 HL076136 (L.S., A.S. and K.N.), and M01 RR01066-25S1. Funding sources had no role in the design of the study, data analysis or the writing of the manuscript.
S.K.G. received research funding for this investigator-initiated research project through Bristol Myers Squibb, Inc. Data will be presented at the American Heart Association Scientific Session in November 2009.
1. Lohse N, Hansen A-BE, Pedersen G, Kronborg G, Gerstoft J, Sorensen HT, et al
. Survival of persons with and without HIV infection in Denmark, 1995–2005. Ann Intern Med 2007; 146:87–95.
2. Palella FJ Jr, Baker RK, Moorman AC, Chmiel JS, Wood KC, Brooks JT, Holmberg SD. Mortality in the highly active antiretroviral therapy era: changing causes of death and disease in the HIV outpatient study. J Acquir Immune Defic Syndr 2006; 43:27–34.
3. Hadigan C, Meigs J, Corcoran C, Rietschel P, Piecuch S, Basgoz N, et al
. HIV/AIDSMAJOR ARTICLE: metabolic abnormalities and cardiovascular disease risk factors in adults with human immunodeficiency virus infection and lipodystrophy. Clin Infect Dis 2001; 32:130–139.
4. Wilson PWF, D'Agostino RB, Levy D, Belanger AM, Silbershatz H, Kannel WB. Prediction of coronary heart disease using risk factor categories. Circulation 1998; 97:1837–1847.
5. Currier JS, Taylor A, Boyd F, Dezii CM, Kawabata H, Burtcel B, et al
. Coronary heart disease in HIV-infected individuals. J Acquir Immune Defic Syndr 2003; 33:506–512.
6. Klein D, Hurley LB, Quesenberry CP Jr, Sidney S. Do protease inhibitors increase the risk for coronary heart disease in patients with HIV-1 infection? J Acquir Immune Defic Syndr 2002; 30:471–477.
7. Agatston AS, Janowitz WR, Hildner FJ, Zusmer NR, Viamonte M Jr, Detrano R. Quantification of coronary artery calcium using ultrafast computed tomography. J Am Coll Cardiol 1990; 15:827–832.
8. Brodoefel H, Burgstahler C, Heuschmid M, Reimann A, Khosa F, Kopp A, et al
. Accuracy of dual-source CT in the characterization of noncalcified plaque: use of a colour-coded analysis compared with virtual histology intravascular ultrasound. Br J Radiol 2009; 82:805–812.
9. Austen WG, Edwards JE, Frye RL, Gensini GG, Gott VL, Griffith LS, et al
. A reporting system on patients evaluated for coronary artery disease. Report of the Ad Hoc Committee for Grading of Coronary Artery Disease, Council on Cardiovascular Surgery, American Heart Association. Circulation 1975; 51:5–40.
10. Borkan GA, Gerzof SG, Robbins AH, Hults DE, Silbert CK, Silbert JE. Assessment of abdominal fat content by computed tomography. Am J Clin Nutr 1982; 36:172–177.
11. Stein JH. Endothelial function in patients with HIV infection. Clin Infect Dis 2006; 43:540–541.
12. Stein JH, Klein MA, Bellehumeur JL, McBride PE, Wiebe DA, Otvos JD, Sosman JM. Use of human immunodeficiency virus-1 protease inhibitors is associated with atherogenic lipoprotein changes and endothelial dysfunction. Circulation 2001; 104:257–262.
13. Charakida M, Donald AE, Green H, Storry C, Clapson M, Caslake M, et al
. Early structural and functional changes of the vasculature in HIV-infected children: impact of disease and antiretroviral therapy. Circulation 2005; 112:103–109.
14. Paladugu R, Fu W, Conklin BS, Lin PH, Lumsden AB, Yao Q, Chen C. HIV Tat protein causes endothelial dysfunction in porcine coronary arteries. J Vasc Surg 2003; 38:549–555, discussion 555–546.
15. Currier JS, Kendall MA, Zackin R, Henry WK, Alson-Smith B, Torriani FJ, et al
. Carotid artery intima-media thickness and HIV infection: traditional risk factors overshadow impact of protease inhibitor exposure. AIDS 2005; 19:927–933.
16. Hsue PY, Lo JC, Franklin A, Bolger AF, Marin JN, Deeks SG, Waters DD. Progression of atherosclerosis as assessed by carotid intima-media thickness in patients with HIV infection. Circulation 2004; 109:1603–1608.
17. Johnsen S, Dolan SE, Fitch KV, Kanter JR, Hemphill LC, Connelly JM, et al
. Carotid intimal medial thickness in HIV infected women: effects of protease inhibitor use, cardiac risk factors and the metabolic syndrome. J Clin Endocrinol Metab 2006; 91:4916–4924.
18. Meng Q, Lima JA, Lai H, Vlahov D, Celentano DD, Strathdee SA, et al
. Coronary artery calcification, atherogenic lipid changes, and increased erythrocyte volume in black injection drug users infected with human immunodeficiency virus-1 treated with protease inhibitors. Am Heart J 2002; 144:642–648.
19. Chironi G, Escaut L, Gariepy J, Cogny A, Teicher E, Monsuez JJ, et al
. Brief report: carotid intima-media thickness in heavily pretreated HIV-infected patients. J Acquir Immune Defic Syndr 2003; 32:490–493.
20. Talwani R, Falusi OM, Mendes de Leon CF, Nerad JL, Rich S, Proia LA, et al
. Electron beam computed tomography for assessment of coronary artery disease in HIV-infected men receiving antiretroviral therapy. J Acquir Immune Defic Syndr 2002; 30:191–195.
21. Kingsley LA, Cuervo-Rojas J, Munoz A, Palella FJ, Post W, Witt MD, et al
. Subclinical coronary atherosclerosis, HIV infection and antiretroviral therapy: multicenter AIDS Cohort study. AIDS 2008; 22:1589–1599.
22. Triant VA, Lee H, Hadigan C, Grinspoon SK. Increased acute myocardial infarction rates and cardiovascular risk factors among patients with human immunodeficiency virus disease. J Clin Endocrinol Metab 2007; 92:2506–2512.
23. Grunfeld C, Delaney JA, Wanke C, Currier JS, Scherzer R, Biggs ML, et al
. Preclinical atherosclerosis due to HIV infection: carotid intima-medial thickness measurements from the FRAM study. AIDS 2009; 23:1841–1849.
24. Keelan PC, Bielak LF, Ashai K, Jamjoum LS, Denktas AE, Rumberger JA, et al
. Long-term prognostic value of coronary calcification detected by electron-beam computed tomography in patients undergoing coronary angiography. Circulation 2001; 104:412–417.
25. TaR A, Leroux C, Mornex JF, Loire R. Accelerated coronary atherosclerosis and arteriosclerosis in young human-immunodeficiency-virus-positive patients. Coron Artery Dis 2000; 11:41–46.
26. El-Sadr WM, Lundgren JD, Neaton JD, Gordin F, Abrams D, Arduino RC, et al
. CD4+ count-guided interruption of antiretroviral treatment. N Engl J Med 2006; 355:2283–2296.
27. Stein JH. Cardiovascular risks of antiretroviral therapy. N Engl J Med 2007; 356:1773–1775.
28. Libby P. Inflammation in atherosclerosis. Nature 2002; 420:868–874.
29. Ross R. Atherosclerosis: an inflammatory disease. N Engl J Med 1999; 340:115–126.
30. Jonasson L, Holm J, Skalli O, Bondjers G, Hansson G. Regional accumulations of T cells, macrophages, and smooth muscle cells in the human atherosclerotic plaque. Arterioscler Thromb Vasc Biol 1986; 6:131–138.
31. Hansson GK. Immune mechanisms in atherosclerosis. Arterioscler Thromb Vasc Biol 2001; 21:1876–1890.
32. Ludewig B, Freigang S, Jaggi M, Kurrer MO, Pei YC, Vlk L, et al
. Linking immune-mediated arterial inflammation and cholesterol-induced atherosclerosis in a transgenic mouse model. Proc Natl Acad Sci U S A 2000; 97:12752–12757.
33. Hsue PY, Hunt PW, Schnell A, Kalapus SC, Hoh R, Ganz P, et al
. Role of viral replication, antiretroviral therapy, and immunodeficiency in HIV-associated atherosclerosis. AIDS 2009; 23:1059–1067.
34. Gosling J, Slaymaker S, Gu L, Tseng S, Zlot CH, Young SG, et al
. MCP-1 deficiency reduces susceptibility to atherosclerosis in mice that overexpress human apolipoprotein B. J Clin Invest 1999; 103:773–778.
35. Park IW, Wang JF, Groopman JE. HIV-1 Tat promotes monocyte chemoattractant protein-1 secretion followed by transmigration of monocytes. Blood 2001; 97:352–358.
36. Alonso-Villaverde C, Coll B, Parra S, Montero M, Calvo N, Tous M, et al
. Atherosclerosis in patients infected with HIV is influenced by a mutant monocyte chemoattractant protein-1 allele. Circulation 2004; 110:2204–2209.
37. Szalai C, Duba J, Prohaszka Z, Kalina A, Szabo T, Nagy B, et al
. Involvement of polymorphisms in the chemokine system in the susceptibility for coronary artery disease (CAD). Coincidence of elevated Lp(a) and MCP-1-2518 G/G genotype in CAD patients. Atherosclerosis 2001; 158:233–239.
38. Melnick JL, Adam E, DeBakey ME. Possible role of cytomegalovirus in atherogenesis. JAMA 1990; 263:2204–2207.
39. Hsue PY, Hunt PW, Sinclair E, Bredt B, Franklin A, Killian M, et al
. Increased carotid intima-media thickness in HIV patients is associated with increased cytomegalovirus-specific T-cell responses. AIDS 2006; 20:2275–2283.
40. Epstein SE, Zhu J, Najafi AH, Burnett MS. Insights into the role of infection in atherogenesis and in plaque rupture. Circulation 2009; 119:3133–3141.
41. Triant VA, Meigs JB, Grinspoon SK. Association of C-reactive protein and HIV infection with acute myocardial infarction. J Acquir Immune Defic Syndr 2009; 51:268–273.
This article has been cited 13 time(s).
Plos OneSilent Ischemic Heart Disease and Pericardial Fat Volume in HIV-Infected Patients: A Case-Control Myocardial Perfusion Scintigraphy StudyPlos One
Immunological ReviewsMonocyte/macrophages and their role in HIV neuropathogenesisImmunological Reviews
Janac-Journal of the Association of Nurses in AIDS CareCardiovascular Risk Assessment for Persons Living With HIVJanac-Journal of the Association of Nurses in AIDS Care
Trends in Molecular MedicineHIV-associated lipodystrophy: from fat injury to premature agingTrends in Molecular Medicine
Journal of InfectionThe CD4/CD8 ratio in HIV-infected subjects is independently associated with T-cell activation despite long-term viral suppressionJournal of Infection
Anadolu Kardiyoloji Dergisi-the Anatolian Journal of CardiologyUse of cardiac CT angiography imaging in an epidemiology study - the Methodology of the Multicenter AIDS Cohort Study cardiovascular disease substudyAnadolu Kardiyoloji Dergisi-the Anatolian Journal of Cardiology
European Journal of Nuclear Medicine and Molecular ImagingShould HIV-infected patients be screened for silent myocardial ischaemia using gated myocardial perfusion SPECT?European Journal of Nuclear Medicine and Molecular Imaging
Current Pharmaceutical Design
Infections and Atheromatous Plaque: Current Therapeutic Implications
Current Pharmaceutical Design, 19(9):
American Journal of CardiologyAngiographic Features and Cardiovascular Risk Factors in Human Immunodeficiency Virus-Infected Patients With First-Time Acute Coronary SyndromeAmerican Journal of Cardiology
Endothelial Dysfunction in HIV Infection - The Role of Circulating Endothelial Cells, Microparticles, Endothelial Progenitor Cells and Macrophages
AIDS Reviews, 14(4):
Bmc Infectious DiseasesSoluble CD163 does not predict first-time myocardial infarction in patients infected with human immunodeficiency virus: a nested case-control studyBmc Infectious Diseases
Cardiovascular Journal of AfricaEpidemiology of ischaemic heart disease in sub-Saharan AfricaCardiovascular Journal of Africa
atherosclerosis; cardiovascular risk factors; coronary artery disease; coronary computed tomography angiography; HIV
© 2010 Lippincott Williams & Wilkins, Inc.
What does "Remember me" mean?
By checking this box, you'll stay logged in until you logout. You'll get easier access to your articles, collections,
media, and all your other content, even if you close your browser or shut down your
To protect your most sensitive data and activities (like changing your password),
we'll ask you to re-enter your password when you access these services.
What if I'm on a computer that I share with others?
If you're using a public computer or you share this computer with others, we recommend
that you uncheck the "Remember me" box.
Highlight selected keywords in the article text.
Data is temporarily unavailable. Please try again soon.