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Untreated HIV infection may increase risk for cardiovascular disease, and arterial elasticity is a marker of cardiovascular risk and early disease.
HIV-infected participants not taking antiretroviral therapy (n = 32) were compared with HIV-negative controls (n = 30). Large and small artery elasticity (LAE and SAE) were estimated via analysis of radial pulse waveforms. Differences in LAE and SAE by HIV status were compared using analysis of covariance, with and without adjustment for Framingham risk (model 1); covariates that differed between groups [smoking, injection drug use, hepatitis C, and high-density lipoprotein cholesterol (HDLc); model 2]; or age, sex, race/ethnicity, smoking, injection drug use, hepatitis C, HDLc, and non-HDLc (model 3).
HIV infection was associated with impaired LAE (−2.55 mL/mm Hg × 10; P = 0.02) and SAE (−1.50 mL/mm Hg × 100; P = 0.02). Associations with traditional risk factors were often stronger for SAE than LAE, including with Framingham score (per 1% higher; SAE −0.18, P = 0.01; LAE −0.19, P = 0.13). Fasting lipid levels were not significantly associated with LAE and SAE. After adjustment, differences between HIV-infected and HIV-uninfected participants were similar in model 1 (−2.36 for LAE, P = 0.04; −1.31 for SAE, P = 0.04), model 2 (−2.67 for LAE, P = 0.02; −1.13 for SAE, P = 0.07) and model 3 (−2.91 for LAE, P = 0.02; −1.34 for SAE, P = 0.03). CD4 count and HIV RNA level were not associated with LAE and SAE among HIV-infected participants.
Untreated HIV infection is associated with impaired arterial elasticity, of both the large and small vasculature, after controlling for additional risk factors. Pulse waveform analysis is a noninvasive technique to assess cardiovascular disease risk that should be evaluated in larger studies of HIV-infected persons.
Premature atherosclerotic cardiovascular disease (CVD) is an important cause of morbidity and mortality in patients with HIV infection.1,2 CVD risk is influenced by traditional risk factors [ie, blood pressure (BP), blood lipids, and smoking] and antiretroviral therapy (ART)-related mechanisms including metabolic changes (lipid levels and insulin resistance).3,4 In addition, HIV infection itself may promote atherogenesis, in part, via a decrease in high-density lipoprotein cholesterol (HDLc) and increase in triglyceride (TG) levels, immune activation and inflammation, increase in thrombosis and fibrinolysis, and endothelial dysfunction.5–8 Characterizing CVD risk attributed specifically to untreated HIV infection is important and has implications when assessing the risks and benefits of ART use.
Noninvasive markers of early CVD are important tools in understanding the pathogenesis and progression of premature CVD and the impact of therapy. To date, research among HIV-infected patients using carotid intima-media thickness and brachial artery flow-mediated dilation (FMD) has been inconsistent and has primarily focused on the influences of ART use and traditional CVD risk factors.7,9–22 However, a recent report of 82 treatment-naive patients showed improved FMD measures within 4 weeks of initial ART use, and FMD improvement at 24 weeks was associated with declines in HIV RNA.19 Thus, studies are needed using reproducible markers of CVD that distinguish the influence of traditional risk factors, HIV infection, and ART on disease risk.23
In the general population, arterial stiffness is a CVD marker associated with atherosclerotic disease and traditional CVD risk factors in cross-sectional studies, as well as risk for CVD events in longitudinal studies.24–26 There are several techniques to estimate arterial stiffness or elasticity (conceptually the inverse of stiffness). Analysis of the diastolic radial pulse waveform provides an assessment of artery elasticity at the level of the aorta and conduit arteries [large artery elasticity (LAE)] and the peripheral branches and microvascular components [small artery elasticity (SAE)] that contains information about structural and functional vascular changes, including endothelial dysfunction.27–29 This is the first study to examine SAE specifically, in addition to a large artery assessment, within healthy HIV-negative and HIV-infected participants not receiving ART.
The protocol was preapproved by the Hennepin County Medical Center (HCMC) Human Subjects Research Committee, and informed consent was signed before participant enrollment. HIV-infected participants had not taken ART in the previous year. Exclusion criteria included pregnancy, current/active bacterial infection, recent hospitalization, systemic vasculitis, valvular disease (including heart valve replacement), atrial fibrillation, and presence of an upper extremity arterial-venous fistula. Participants with clinical atherosclerotic disease (previous myocardial infarction or chronic angina or claudication by history) were also excluded as the focus of this study was to examine early subclinical CVD risk. Participants were recruited through informational flyers and referrals from patients and providers, at an urban HIV clinic (HCMC, Minneapolis, MN). The HIV-negative group was recruited in the same way, and efforts were made to enroll participants so that the control group did not differ from the HIV-infected group with regard to age, sex, race/ethnicity, smoking status, and the presence of diabetes mellitus (DM).
Study participants presented for a single visit at HCMC, where a medical history, peripheral blood draw, and arterial elasticity measurements were performed. A medical history was taken (including a review of the medical record) that included duration of HIV infection, prior AIDS-defining event, prior ART use, history of injection drug use (IDU), smoking status (defined as current), a diagnosis of DM, a list of current medications, and a blood CD4 count within the past 3 months (when available). Study participants were instructed to fast and avoid antihistamines and nonsteroidal anti-inflammatory drugs during the 8-hour period before the visit and avoid alcohol and illicit drugs for at least 24 hours prior, as these substances may affect arterial elasticity estimates. Blood samples were tested for the following: HIV antibody (for HIV-negative participants), HIV RNA level (for HIV-infected participants), serologies for hepatitis B (infection defined as HBsAb negative and hepatitis B surface antigen positive) and hepatitis C (infection defined as hepatitis C virus antibody positive), serum creatinine, total serum cholesterol (TC), low-density lipoprotein cholesterol (LDLc), HDLc, and TG. Non-HDLc levels were calculated as TC minus HDLc and provided a single estimate of all potentially proatherogenic lipid particles, including LDLc particles, TGs, and very low density lipoprotein remnants.30,31 Framingham 10-year CVD risk was estimated from a National Heart, Lung, and Blood Institute calculator (http://hp2010.nhlbihin.net/atpiii/calculator.asp), after entering age, sex, smoking status, TC, HDLc, systolic blood pressure (SBP), and use of BP-lowering medication.
Arterial elasticity was assessed via pulse waveform analysis of the diastolic decay curve, and values of LAE and SAE were calculated using a modified Windkessel model of the circulation (model HDI/PulseWave CR-2000, Eagan, MN).27,29 A tonometer was placed at the dominant wrist overlying the radial artery of resting participants. A stable 30-second measure of the radial pulse waveform was achieved, excluding the dicrotic notch, and was digitized at 200 samples per second. Before and during the waveform assessment, an automated oscillatory BP measurement is taken on the contralateral arm. A typical waveform will have 2 maxima present within the diastolic decay curve. The first occurs at the beginning of diastole and represents the capacitance of the proximal aorta and major branches after cardiac ejection. The second maximum results from a reflective, or oscillatory, wave, corresponding to elasticity in the smaller arteries. Representative pulse waveforms are shown for an HIV-negative and HIV-infected participant in Figure 1. These methods have been previously described in detail and are consistent with established protocols using this technique in large cohort studies.27,29,32,33
A single investigator performed the pulse waveform assessments in triplicate, and the mean (average of 3 values for each participant) LAE and SAE indices were used in statistical analyses. The average SD among the 3 readings for each participant was 1.6 mL/mm Hg × 10 for LAE and 0.5 mL/mm Hg × 100 for SAE. A group of 12 participants (6 were not part of the cross-sectional comparison) were studied at 2 visits approximately 1–4 months apart to assess repeatability of measurements over time. The mean (±SD) difference between the 2 time points was 1.0 (±2.9) mL/mm Hg × 10 for LAE and −0.2 (±1.2) mL/mm Hg × 100 for SAE. The within-person variability between visits was 8.2 for LAE and 1.4 for SAE, and the values exhibited a very high correlation between visits (LAE R = 0.84; SAE R = 0.94).
Data were analyzed by use of SAS software (Version 9.1; SAS Institute, Inc, Cary, NC). Descriptive statistics are reported as means ± SDs and medians with interquartile range (IQR). Student t test for independent groups and the χ2 test for categorical variables were used to compare HIV-infected and HIV-negative groups. Adjusted mean differences between HIV-infected and HIV-negative groups were obtained using analysis of covariance. To account for traditional CVD risk factors, Framingham risk score was considered (model 1). Given the small sample size, a parsimonious model was next considered including covariates that differed between groups in Table 1: smoking status, IDU, hepatitis C, and HDLc (model 2). Finally, a fully adjusted model included age, sex, race/ethnicity, smoking status, IDU, hepatitis C infection, HDLc, and non-HDLc (model 3). SBP, diastolic blood pressure (DBP), and heart rate are incorporated into LAE and SAE estimates, so these parameters were omitted from adjusted models. Framingham 10-year CVD risk score includes SBP, but smoking status and lipid levels largely explain differences in Framingham risk between groups in this study (Table 1). To explore potential explanations for impaired arterial elasticity among HIV-infected participants, regression models were performed between LAE and SAE indices and log10 transformed HIV RNA levels, CD4 count before and after square root transformation, hepatitis C infection, IDU, and Framingham risk score. The within-participant variability over time, and the correlation of repeat measures, was estimated using data from the 12 participants presenting for 2 study visits.
From March 2007 to August 2008, we enrolled 32 HIV-infected and 30 HIV-negative participants. The demographic and clinical characteristics of the participants are presented in Table 1. HIV-infected and HIV-negative participants did not differ with respect to age, sex, race/ethnicity, DM, SBP, DBP, and the use of BP-lowering drugs. One HIV-infected and 2 HIV-negative participants were using statin medications. The HIV-infected group had a higher mean heart rate, lower HDLc, and serum creatinine levels; were more likely to be infected with hepatitis C; and reported prior IDU. Although not significant, there were a greater number of smokers in the HIV-infected vs. control group. Only 1 participant had evidence of chronic hepatitis B infection (positive hepatitis B surface antigen) and he also had hepatitis C. Most HIV-infected participants (59%) had CD4 counts above the recommended threshold for initiation of ART (350 cells/mm3).34 The majority of HIV-infected participants were naive to ART (84%), and mean and median CD4 counts and HIV RNA levels are shown. No HIV-infected participants were in the acute/early stage of infection (ie, within 6 months of known seroconversion), and only 4 participants had a CD4 count <200 cells per cubic millimeter. Among the 5 participants with prior ART exposure, all had been off therapy for >2 years, at least 3 had protease inhibitor exposure, and 1 had 10 years of ART exposure (unknown duration for the other 4), and the median and mean duration of HIV infection (by self-report) was 13 and 14 years, respectively.
The distribution of LAE and SAE measurements for the full cohort, stratified by HIV status, is presented with box plots (including median and IQR) in Figure 2. The single outlier for LAE (value was >1.5 × IQR above the third quartile) was an HIV-infected 39-year-old African American male with an LAE estimate of 29.9mL/mm Hg × 10 and an SAE estimate of 7.6mL/mm Hg × 100. He was naive to ART, did not smoke; had no history of IDU; was hepatitis C antibody negative; and had a BP of 136/85, an HDLc of 25 mg/dL, a CD4 count of 184 cells per cubic millimeter, and an HIV RNA level of 21,570 copies per milliliter.
Mean (±SD) LAE and SAE were significantly lower for HIV-infected (LAE 16.4 ± 4.6 mL/mm Hg × 10; SAE 6.7 ± 2.5 mL/mm Hg × 100) compared with HIV-negative participants (LAE 18.9 ± 4.0 mL/mm Hg × 10; SAE 8.2 ± 2.4 mL/mm Hg × 100). Univariate associations between LAE and SAE and other baseline measurements are presented in Table 2. LAE was significantly lower with presence of smoking or hepatitis C infection and trended lower with IDU and a higher Framingham risk score. SAE was significantly lower with increased age, female sex, IDU, hepatitis C infection, or a higher Framingham risk score and trended lower with the presence of smoking. LAE and SAE exhibited inverse associations with SBP and DBP as expected because these are in the denominator of LAE and SAE indices. When comparisons were limited to ART-naive participants (n = 5 with prior ART exposure omitted), HIV infection remained associated with lower SAE (−1.50 mL/mm Hg × 100; P = 0.03) but did not reach significance for LAE (−2.28 mL/mm Hg × 10; P = 0.06).
Covariate adjustment did not have a large effect on the differences between HIV-infected and HIV-negative participants (Table 3). Parsimonious models were fit given the small sample size that considered Framingham score to adjust for traditional CVD risk factors (model 1) and the main covariates that differed in Table 1 (model 2). A fully adjusted model then provided similar estimates (model 3). When HIV-infected participants with prior ART exposure (n = 5) were excluded, HIV infection remained significantly associated with lower SAE (−1.37 mL/mm Hg × 100; P = 0.02) in model 3 but differences in LAE did not reach significance (−2.35 mL/mm Hg × 10; P = 0.07).
Given differences in smoking status and IDU between groups in Table 1, the effect of HIV status on LAE and SAE was examined among nonsmokers and non-injection drug users. IDU was chosen over hepatitis C as most participants with hepatitis C also report IDU (73%). Power for these comparisons was limited, although differences between HIV-infected and HIV-negative groups did not differ significantly by smoking status (test for interaction: P = 0.06 for LAE and P = 0.55 for SAE) or IDU (test for interaction: P = 0.56 for LAE and P = 0.98 for SAE). Among nonsmokers, differences between HIV-infected and HIV-negative participants were −3.59 mL/mm Hg × 10 (P = 0.05) for LAE and −1.38 mL/mm Hg × 100 (P = 0.13) for SAE. The corresponding differences for smokers were −0.41 for LAE (P = 0.73) and −1.31 for SAE (P = 0.17). Among non-IDU participants, these differences were −2.05 mL/mm Hg × 10 (P = 0.15) for LAE and −1.60 mL/mm Hg × 100 (P = 0.03) for SAE. For participants reporting a history of IDU, differences were −2.51 for LAE (P = 0.15) and −2.80 for SAE (P = 0.92).
Finally, factors that may account for lower LAE and SAE measures among HIV-infected participants were examined. No trends were apparent by CD4 count (P = 0.46 for LAE; P = 0.37 for SAE) and log10 transformed HIV RNA levels (P = 0.47 for LAE; P = 0.73 for SAE). After square root transformation of CD4 count, there remained no association (per 1 unit higher) with LAE (P = 0.39) or SAE (P = 0.35). Arterial elasticity did not differ between participants with CD4 counts <350 vs. ≥350 cells per cubic millimeter (P = 0.44 for LAE and P = 0.40 for SAE). Coinfection with hepatitis C was associated with lower SAE (−3.16 mL/mm Hg × 100; P < 0.01) but did not reach significance for LAE (−2.58 mL/mm Hg × 10; P = 0.13). IDU was not associated with LAE (P = 0.29) or SAE (P = 0.57) among HIV-infected participants. Finally, a higher Framingham risk score trended toward association with lower LAE (−0.32 mL/mm Hg × 10 per 1% higher; P = 0.07) and SAE (−0.14 mL/mm Hg × 100 per 1% higher; P = 0.15) among HIV-infected participants.
In this study, individuals with untreated HIV infection had lower levels of SAE and LAE than HIV-negative controls. The differences in LAE and SAE remained significant after adjusting for additional risk factors, including Framingham 10-year CVD risk score. The degree of HIV-related impairment reported in arterial elasticity is clinically relevant.26,33 This is the first study using pulse waveform analysis to assess both small and large artery elasticity among HIV-infected patients. The low within-participant variability in LAE and SAE measures, and associations with traditional CVD risk factors, suggests that this noninvasive technique will be a valuable marker to consider in larger studies assessing CVD risk among HIV-infected patients.
Artery stiffness (the inverse of elasticity) can also be assessed via ultrasound estimates of arterial distensibility and compliance, measures of aortic pulse wave velocity (PWV), and the augmentation index (analysis of systolic wave reflection). A recent study of 77 HIV-infected and 52 HIV-negative participants showed impaired carotid and femoral arterial stiffness (distensibility and compliance) with HIV infection.22 In this study, 53 participants were taking ART and ART use was associated with stiffness of the femoral artery among HIV-infected persons.22 In another cross-sectional comparison of 39 untreated HIV-infected persons and 78 HIV-negative controls demonstrated higher PWV or impaired aortic stiffness, among HIV-infected persons.35 Additional studies using PWV and augmentation index have also reported impaired arterial stiffness to be associated with HIV infection and ART use, with one study specifically demonstrating a correlation between PWV and duration of protease inhibitor use.15,35–37 Our study is consistent with these data and shows that LAE is reduced among persons with untreated HIV infection.
We also report impaired elasticity specifically at the distal part of the circulation (SAE) as a result of HIV infection and demonstrate a high degree of reproducibility in SAE measurements within participants over time. In the general population, SAE is associated with traditional CVD risk factors and is a marker of endothelial dysfunction and future CVD event risk.26,28,33,38–40 In a study of 419 individuals (41% with a CVD event), a 2-unit (mL/mm Hg × 100) decrease in SAE was associated with a 50% increased risk (95% confidence interval: 1.19 to 1.88) for CVD event after adjusting for age.26 Recent findings from 6047 participants in Multi-Ethnic Study of Atherosclerosis demonstrated that impaired SAE but not LAE was associated with future risk for CVD events after controlling for other surrogate risk markers including BP, carotid intima-media thickness, and coronary artery calcium score.33 Although the classic lesions of atherosclerotic disease (plaques) are described in large conduit arteries, the early events in this process begin with injury to endothelial surfaces throughout the vasculature, whether mediated through traditional risk factors, inflammation or oxidative stress, or other factors.41,42 Endothelial dysfunction promotes atherogenesis through alterations in vascular tone, inflammation, and thrombosis, and the microcirculation accounts for most of the vascular surface area.41,43 When endothelial dysfunction is induced in normal volunteers via an infusion of a nitric oxide (NO) inhibitor, L-NAME (NG-nitro-L-arginine-methyl ester), systemic vascular resistance increases and SAE measures become impaired, whereas LAE remains unchanged.28 Our findings suggest that HIV-mediated vessel damage and dysfunction are present throughout the arterial vasculature.
Inflammation and immune activation is both a hallmark of HIV infection and an important factor in the pathogenesis of atherosclerotic CVD.44,45 A recent randomized study of 100 healthy individuals reported acute worsening of large artery stiffness (PWV and augmentation index) after administration of Salmonella typhi vaccine, when compared with placebo.46 In addition, LAE and SAE measures were impaired, and C-reactive protein and soluble vascular cell adhesion molecule-1 levels were elevated in a study of 53 patients with rheumatoid arthritis, when compared with non-rheumatoid arthritis controls.47 Lower LAE measures have also been associated with higher C-reactive protein levels among asymptomatic individuals.48 Some of the most convincing evidence that untreated HIV infection increases risk for CVD comes from SMART (Strategies for Management of Antiretroviral Therapy), which reported that intermittent ART use, compared with continuous ART use, led to greater CVD and other end-organ disease events, and this risk then declined when ART was reinitiated.49,50 In SMART, baseline levels of inflammatory (IL-6) and thrombotic (D-dimer) markers were predictive of both CVD and non-CVD mortality, leading authors to suggest that upregulation of tissue factor coagulation pathways on endothelial surfaces was a potential mechanism.8 Additional studies are needed to further examine the relationship between HIV-mediated inflammation, endothelial dysfunction, thrombogenesis, and clinical events among persons with HIV infection.
We show an association between traditional CVD risk factors and lower LAE and SAE measures. This is important and further validates LAE and SAE as a noninvasive CVD risk marker among persons with HIV infection. In the general population, both LAE and SAE showed a greater association with Framingham risk score than with FMD in a study of 122 participants.24 In addition, FMD was not associated with Framingham risk score in a recent study of 100 HIV-infected and HIV-uninfected participants.18
There are several limitations to our study. The cross-sectional nature does not allow temporal relationships to be assessed, although artery elasticity will be assessed in a subset of participants within the Strategic Timing of Antiretroviral Therapy (START) trial. Given the size of this pilot study, there is also limited power to identify modest associations or to study the determinants of LAE and SAE among HIV-infected participants. By design, our study does not allow an assessment of ART use on differences in LAE and SAE. Finally, we were not able to specifically adjust for the presence of metabolic syndrome, but BP did not differ between groups, body mass index trended lower in HIV-infected vs. control group, only 2 participants from each group had DM, and HDLc was accounted for in adjusted models.
In summary, these data support the use of LAE and SAE measures, obtained via arterial pulse waveform analysis, as a marker of CVD risk in HIV-infected patients. Future research should focus on the HIV-related mechanisms of impaired artery elasticity and the influence of ART use and other treatments on these measures in HIV-infected patients.
The authors would like to thank the participants who volunteered for this research and the staff of the HCMC Positive Care Center for their tireless support. We would specifically like to acknowledge the critical contributions of Edie Gunderson, Bette Borndenave, Miki Olson, Sarah Bruemmer, Jack Hall, and Rachel Prosser.
Supported by the National Institutes of Health (5 T32 GM12453-03) and the Minneapolis Medical Research Foundation.