Impaired distensibility of ascending aorta in patients with HIV infection

The use of highly active antiretroviral therapy (HAART) resulted in a significant decrease in morbidity and mortality in patients with human immunodeficiency virus (HIV) infection [1], turning this lethal infection to a chronic ambulatory disease. However, the initial optimism has been tempered when it became evident that HAART has metabolic side effects such as fat redistribution, dyslipidemia, insulin resistance, glucose intolerance, metabolic syndrome, and overt diabetes; all of them are established risk factors for atherosclerosis and cardiovascular disease [2‐5]. Indeed, soon after the introduction of HAART into the clinical practice, researchers reported unexpected vascular events among young patients. A large prospective study confirmed that HAART, especially the protease inhibitor (PI)–containing regimens, increases the risk for cardio- and cerebro-vascular events in HIV-infected persons [6]. This finding suggests that HAART causes early atherosclerosis [7, 8]. The observed excess cardiovascular risk cannot be attributed solely to the side effects of antiretroviral drugs since chronic HIV infection itself has a role, as it has been shown for other chronic inflammatory diseases [9]. Moreover, HAART increased life expectancy and as HIV seropositive population ages, chronic diseases like atherosclerotic cardiovascular disease become increasingly important [10, 11].

It is difficult to dissect relative contributions of conventional cardiovascular risk factors, metabolic side effects of antiretroviral drugs, and HIV infection itself on early atherosclerosis and cardiovascular events, as these factors frequently co-exist in the same patient. Moreover, studies using clinical endpoints to investigate cardiovascular outcomes in patients with HIV infection, who typically are young or middle-aged, need large numbers of patients because of the low event rate. Therefore, studies using surrogate markers for early atherosclerosis are required.

Researchers have reported that the reduction of the elastic properties of aorta represents an early stage in the atherosclerotic process [12‐16]. Aortic distensibility (AD) is an elasticity index of the ascending aorta, and along with carotid artery intima-media thickness (c-IMT) are simple and reproducible markers of subclinical arteriosclerotic disease and have been identified as strong predictors of cardiovascular mortality in different clinical settings [17‐24]. There are no studies for early atherosclerosis of ascending aorta among HIV-infected patients. The aim of this study was to investigate the distensibility of the ascending aorta and c-IMT in HIV-infected patients compared with age and sex matched uninfected controls, and to investigate whether HIV infection itself, conventional risk factors for atherosclerosis, and/or HAART are associated with early atherosclerosis.

We enrolled in the study a total of 105 consecutive, HIV-infected patients attending the outpatient clinic of the Athens Laikon Hospital. Controls were 124 healthy volunteers recruited from hospital staff, as well as their relatives or friends. HIV infection was ruled out in controls by serologic testing with their consent. Control subjects were individually matched with patients by age (± 5 years) and sex.

Demographic and clinical data such as age, sex, body weight, arterial blood pressure, and history of smoking were obtained from all patients and control subjects, as well as blood samples for laboratory measurements, including blood count, glucose, total cholesterol, triglyceride, high density lipoprotein (HDL), low-density-lipoprotein (LDL) and creatinine levels. Hypertriglyceridemia and hypercholesterolemia were defined as triglyceride and cholesterol level equal or more than 150 and 200 mg/dl, respectively. Hypertension was defined as systolic and diastolic blood pressure level above 140mmHg and 90mmHg, respectively. Moreover, for each HIV-infected patient the following information corresponding to the sampling time point was recorded: risk group, disease duration, CDC stage, CD4 cell count, viral load, and HAART. The study was approved by the Institutional Review Board of the Laikon General Hospital, Athens, Greece. All participants gave their informed consent.

All HIV-infected patients and seronegative controls were evaluated to determine c-IMT and AD. Visualization of the carotid artery was obtained via high resolution, B-mode carotid artery ultaronography, and c-IMT was measured by the same investigator. Measurement of c-IMT was performed in the common carotid artery, of both left and right side, 1cm proximal to carotid bulb and at least three separate measurements of each side were obtained according to previous recommendations [25]. Abnormal c-IMT was defined as a value of equal or more than 0.9 mm. AD was determined noninvasively based on the relationship between changes in aortic diameter and pressure with each cardiac pulse [26, 27]. The echocardiographic study was carried out using a Hewlett Packard Sonos 1000 ultrasound system (Hewlett Packard), using a 2·5-MHz transducer. Each subject was placed in the mild left recumbent position and the ascending aorta was recorded at a level 3 cm above the aortic valve in the M-mode tracings guided by the two-dimensional echocardiogram in the parasternal long axis view [26]. Internal aortic diameters were measured by means of a caliper in systole and diastole as the distance between the trailing edge of the anterior aortic wall and the leading edge of the posterior aortic wall. Systolic aortic diameter was measured as the maximal anterior motion of the aorta and diastolic diameter at the peak of the QRS complex on the simultaneously recorded electrocardiogram. Ten consecutive cardiac beats were measured routinely and averaged [26, 27]. Blood pressure was measured with a Dinamap TM XL vital signs monitor (Johnson-Johnson, Arlington, VA). AD was calculated according to the formula [26, 28]:

Where ΔD is the change of the aortic diameter between systole and diastole, Dd is the aortic diameter in diastole, Ps is the systolic arterial blood pressure and Pd is the diastolic arterial blood pressure. The cardiologist who performed the measurements (IM) was blind of the results of the autonomic function tests of the examined subjects. The intraobserver and interobserver mean percentage error (absolute difference between two observations divided by the mean and expressed as percentage) was determined for the aortic dimensions in 20 randomly selected subjects and were 4.2% and 4.6% for the systolic and 4.1% and 4.4% for the diastolic dimensions in our centre, respectively.

In a second step, a univariate and multivariate linear regression (using a stepwise, backward selection technique) were performed in HIV-positive group only to identify influential factors for AD. A two-sided P-value <0.05 was considered as statistically significant.

The main findings of our study were that HIV-infected patients had significantly reduced distensibility of the ascending aorta compared to age and sex matched control subjects. On the contrary, no difference in c-IMT was observed between the two groups. Multiadjusted analysis showed that after adjustment for conventional cardiovascular risk factors HIV infection was independently associated with decreased AD. Among HIV-infected patients, those exposed to HAART had significantly decreased AD compared to HAART-naïve patients. In multivariate analysis, increasing age and duration of HAART exposure were factors independently associated with decreased AD. Moreover, the effect of HAART on the distensibility was more pronounced among patients older than 40 years old (Figure 1).

The reduced distensibility of the ascending aorta that we found among HIV-infected patients compared to uninfected controls is a marker of subclinical arteriosclerotic disease and has been identified as a strong predictor of cardiovascular mortality in different clinical settings [17‐21]. In a large population study, AD was inversely related to conventional cardiovascular disease risk factors, such as older age, hypertension, smoking, and low HDL-cholesterol levels [29]. In accordance, in our study multiadjusted analysis showed that vascular risk factors such as obesity, and increasing diastolic pressure were also important for decreased distensibility of the ascending aorta. It is interesting that we found decreased distensibility among HIV-infected patients despite the fact that obesity and blood pressure were significantly higher among controls. One explanation could be that dislipidemia was statistically more frequent among HIV-infected patients, due to the HAART side effects or to the chronic infection per se.

Multi-adjusted analysis showed that after correction for other vascular risk factors, HIV infection was independently associated with decreased AD. In fact, premature atherosclerosis has been reported in young adults with HIV infection in the pre–HAART era [30]. The cardiovascular disease risk associated with HIV infection appears to be partially attenuated by antiretroviral treatment, since treatment interruption increases short-term risk of cardiovascular disease events [11]. These findings suggest that HIV infection itself may increase the risk for cardiovascular disease, as it has been shown for other chronic inflammatory diseases [9] in the non-HIV setting. Many markers of inflammation are markedly elevated in individuals with untreated HIV infection and are only partially reversed by effective combination antiretroviral therapy [31].

Our data are consistent with previous studies showing that HIV infection per se, as well as HAART is associated with increased stiffness [30, 32‐36] of peripheral arteries (femoral and branchial) and the carotid artery. Interestingly, recent investigations have shown that biological and vascular age in HIV infected patients is increased [37, 38]. Our study did not find increased c-IMT in HIV-infected patients compared to uninfected controls. Conflicting evidence exists in the bibliography on the c-IMT: some studies reported increased c-IMT in HIV- infected patients compared with HIV-negative controls [30, 33, 39‐44] but others did not [45‐48]. It is noteworthy that our HIV-infected population had decreased distensibility of the ascending aorta and a normal c-IMT. This may imply that there are differences in the effect of HIV along the arterial system and reduced AD is an earlier marker of subclinical atherosclerosis compared to c-IMT. An alternative explanation could be that although arterial stiffening is thought to be a generalized phenomenon, different arterial segments are known to respond differently to atherosclerotic risk factors [49‐51].

Our study showed that among HIV-infected patients, increasing age and longer exposure to HAART contribute further to decreased distensibility of the ascending aorta. Moreover, the effect of HAART on the AD was more pronounced among patients older than 40 years old. While increasing age is a well known risk for atherosclerosis, the effect of HAART on accelerating atherosclerosis remains controversial. Chronic HIV infection may lead to vascular endothelial damage and damage the elastic properties of an artery by sustaining a low degree of inflammation [52]. HAART has beneficial effects by reducing the inflammation due to active HIV infection, and detrimental effects such as dyslipidemia. Although it is difficult to determine the net effect in an individual patient and in different arterial segments, a recent study showed that endothelial dysfunction actually improved after start of HAART despite the rapid onset of dyslipidemia [53]. Our study had not enough statistical power to detect if PI containing regimens had different effect on the AD compared to NNRTI-containing regimens.

Our study has some limitations. Aortic diameters were measured echocardiographically and not invasively. A previous study has shown that aortic diameter can be determined with a high degree of accuracy in subjects whose cardiothoracic anatomy permits an echocardiographic signal of satisfactory quality, and the values obtained by echocardiography were not significantly different from those obtained by angiography [26]. In addition, pulse pressure estimated non-invasively from the brachial artery by external sphygmomanometry has been used for the calculation of AD in previous reports [26, 54‐56]. These non-invasive techniques have also been used for calculating AD in previous studies [55‐57]. Thus a reliable estimation of the elastic properties of the ascending aorta using completely non-invasive techniques is feasible. Another limitation was the very high proportion of male subjects included in the cohort, which could limit the generalization of results to female HIV-infected patients. Moreover, the potential impact of past/active drug abuse could not be reliably evaluated, as only 3 patients (3%) had a history of drug abuse.

HIV infection is independently associated with decreased distensibility of the ascending aorta, a marker of premature atherosclerosis. This suggests that patients with HIV infection may be at increased cardiovascular disease risk, independent of the presence of classical cardiovascular risk factors. Study of arterial elasticity as early marker of vascular damage could be promising and more appropriate investigation in HIV people than evaluation of cIMT.