HIV is an independent predictor of aortic stiffness
© Rider et al.; licensee BioMed Central 2014
Received: 28 March 2014
Accepted: 16 July 2014
Published: 16 August 2014
Patients with treated Human Immunodeficiency Virus-1 (HIV) infection are at increased risk of cardiovascular events. Traditionally much of this risk has been attributed to metabolic and anthropometric abnormalities associated with HIV, which are similar to the metabolic syndrome (MS), an established risk factor for cardiovascular mortality. It remains unclear whether treated HIV infection is itself associated with increased risk, via increase vascular stiffness.
226 subjects (90 with HIV) were divided into 4 groups based on HIV and MS status: 1) HIV-ve/MS-ve, 2) HIV-ve/MS + ve, 3) HIV + ve/MS-ve and 4)HIV + ve/MS + ve. CMR was used to determine aortic pulse wave velocity (PWV) and regional aortic distensibility (AD).
PWV was 11% higher and regional AD up to 14% lower in the HIV + ve/MS-ve group when compared to HIV-ve/MS-ve (p < 0.01 all analyses). PWV and AD in the HIV + ve/MS-ve group was similar to that observed in the HIV-ve/MS + ve group (p > 0.99 all analyses). The HIV + ve/MS + ve group had 32% higher PWV and 30-34% lower AD than the HIV-ve/MS-ve group (all p < 0.001), and 19% higher PWV and up to 31% lower AD than HIV + ve/MS-ve subjects (all p < 0.05). On multivariable regression, age, systolic blood pressure and treated HIV infection were all independent predictors of both PWV and regional AD.
Across multiple measures, treated HIV infection is associated with increased aortic stiffness and is also an independent predictor of both PWV and regional AD. The magnitude of the effect of treated HIV and MS are similar, with additive detrimental effects on central vascular elasticity.
Effective antiretroviral therapy has markedly improved life expectancy in the HIV-infected population. However, despite immunological modulation, aging with HIV is accompanied by an increased prevalence of metabolic abnormalities, atherosclerotic cardiovascular disease and higher all-cause mortality –. The pathogenesis of this accelerated atherosclerosis in HIV has not been fully elucidated. Even after adjusting for traditional risk factors, which tend to have a higher prevalence in the treated HIV population, elevated rates of coronary disease remain . Recent studies have suggested that viral factors, in addition to traditional vascular risk factors, have independent negative effects, possibly by promoting atherogenic lipid abnormalities , monocyte attraction and migration into the vascular intima  and a chronic inflammatory state ,, all of which produce an environment for accelerated atherogenesis.
In addition, treated HIV is associated with an increase in the prevalence of the cluster of metabolic risk factors that make up the metabolic syndrome . Metabolic complications appear to result from treatments for HIV and, to some degree, from the effect of viral infection itself –. Whether viral factors amplify the atherogenic effect of traditional metabolic risk factors in HIV-infected individuals remains unclear.
Both aortic pulse wave velocity (PWV) and regional aortic distensibility (AD) are sensitive markers of aortic elastic function. Aortic pulse wave velocity is a clinical measure of arterial stiffness that has not only been shown to be predictive of both cardiovascular events and mortality in multiple population studies, , but is also a well-validated surrogate marker of atherosclerosis, corresponding closely to the degree of atherosclerosis as assessed by both computed tomography and post-mortem studies . The aim of this study was to use PWV and AD to investigate 1) if HIV is independently associated with increased arterial stiffness, 2) the magnitude of the detrimental effect of HIV on aortic elastic function when compared to the metabolic syndrome and 3) whether or not the metabolic syndrome and HIV are additive in their detrimental effects.
90 patients with documented HIV infection (13 naive to antiretroviral therapy) and 136 subjects with no history of HIV infection were recruited to this study. Eligibility criteria were age over 18 years, no history or symptoms of cardiovascular disease and no contraindications to cardiovascular magnetic resonance (CMR). All patients with HIV were treated in accordance with national guidelines. Patients with HIV and non-infected subjects were subdivided into those with and without the metabolic syndrome according to the National Cholesterol Education Program-Adult Treatment Panel III (NCEP-ATP III) guidelines . Subjects were diagnosed with the MS when at least 3 of 5 risk determinants increased waist circumference, increased systolic blood pressure (SBP) or diastolic blood pressure (DBP), elevated serum triglycerides, low high-density lipoprotein cholesterol (HDL-C), and impaired fasting glucose (IFG) were present. Subjects were then separated into 4 groups: 1) healthy controls without the MS (HIV-ve/MS-ve), 2) controls with the MS (HIV-ve/MS + ve), 3) patients with HIV without the MS (HIV + ve/MS-ve) and 4) patients with HIV and the MS (HIV + ve/MS + ve). This study was approved by the local ethics committee (ref. 10/H0604/95) and all subjects gave informed written consent prior to participation. Ethics was approved by the Oxford Research Ethics Committee.
Morning assessments took place after a minimum 10 hour fast. Height and weight were measured using a digital station (Seca, UK) and used to calculate body mass index (BMI, mass (kg)/height (m)2). Waist circumferences were measured in the standing position at the level of the umbilicus with the average of three measurements taken. Data on duration of HIV infection, nadir CD4 count and Highly Active Antiretroviral Therapy (HAART) were obtained from the treating physicians with the consent of the patients.
A fasting blood sample was obtained for measurement of plasma glucose, free fatty acids, hs-CRP, cholesterol and hs-CRP and were analysed by a commercial hospital laboratory. Insulin was measured using ELISA (Mercodia AB, Uppsala, Sweden). To calculate the homeostasis model assessment for insulin resistance (HOMA-IR) the following formula was used: fasting insulin (pmol/l) × fasting glucose (mM/l)/135 and used as a measure of insulin resistance .
CMR protocol for aortic distensibility
All vascular imaging was performed at 1.5-Tesla (Avanto, Siemens Medical Solutions, Erlangen, Germany). Based on sagittal-oblique (candy cane) pilot images aligned with the aortic arch, thoracic aortic cine images were acquired in transverse planes at 3 levels as previously described:  the crossing of the pulmonary arch through 1) the ascending thoracic aorta (Ao), 2) proximal descending thoracic aorta (PDA) and 3) 12 cm below the PDA level piloted perpendicular to the orientation of the aorta (distal descending aorta, DDA). A brachial artery blood pressure was recorded during image acquisition to provide pulse pressure .
CMR protocol for aortic pulse wave velocity
CMR protocols for visceral fat mass
To measure visceral fat mass, a single breath-hold, single-slice, water-suppressed T1-weighted turbo spin echo sequence centred on L5 was acquired as previously described .
Image analysis was performed using Siemens analytical software (Argus ©, Siemens Medical Solutions, Erlangen, Germany). To analyse aortic PWV, flow images were manually contoured  and aortic PWV was determined as Δx/Δt (m/s), where Δx is the aortic distance between two imaging levels and Δt is time delay between the arrival of the foot of the pulse wave between these imaging levels (Figure 1) . The arrival of the foot of the pulse wave was taken as the intersection of the tangent (determined by a least squares method of the four flow points around the half maximal point of flow) of the upslope of the flow curve and the x (time) axis as previously described ,. To assess visceral fat mass, transverse slices were manually countered as previously described .
All statistical analyses were performed using SPSS statistical software (version 19.0; SPSS Inc., Chicago, Ill, USA). Normality of distribution was assessed using the Kolmogorov-Smirnov test. Normally distributed data are presented as mean ± standard deviation, non-normally distributed data as median (interquartile range). Comparisons between normally distributed data in the 4 groups identified above were performed with one-way analysis of variance with post-hoc Bonferroni correction. Bivariate correlations for all subjects were calculated using Pearson correlation coefficients. Significance was assumed at a probability value of p < 0.05. Variables with p < 0.05 and the strongest relationship with aortic pulse wave velocity and AD were then included as independent variables in forced entry stepwise multiple regression analysis with aortic PWV and AD as the dependent variables.
Baseline characteristics of the study populations
Anthropometric characteristics of the study population
HIV-ve/MS-ve (n = 92)
HIV-ve/MS + ve (n = 44)
HIV + ve/MS-ve (n = 73)
HIV + ve/MS + ve (n = 17)
P value from analysis of variance
45 ± 10
49 ± 11
44 ± 10
48 ± 8
BMI (kg/m 2 )
25 ± 4
33 ± 7*
25 ± 4Φ
30 ± 6*ψ
Visceral Fat (cm 2 )
71 ± 39
160 ± 71*
86 ± 49Φ
120 ± 66*
0.9 ± 0.5
1.7 ± 0.8*
1.3 ± 1.0
2.4 ± 1.7*ψ
4.8 ± 0.9
5.1 ± 1.2
4.5 ± 1.4
4.6 ± 1.4
1.6 ± 0.4
1.1 ± 0.3*
1.2 ± 0.4*
1.0 ± 0.4*
4.8 ± 0.5
5.4 ± 0.8*
5.0 ± 0.8
6.0 ± 1.3*Φψ
1.1 ± 1.0
3.5 ± 2.7*
1.4 ± 1.3Φ
4.6 ± 6.1*ψ
0.7 ± 1.6
3.1 ± 4.0*
2.2 ± 2.7*
4.6 ± 4.5*ψ
117 ± 12
130 ± 14*
118 ± 16Φ
138 ± 16*ψ
73 ± 9
80 ± 8*
75 ± 9Φ
85 ± 8*ψ
Waist circumference (cm)
88 ± 14
110 ± 17*
89 ± 11Φ
106 ± 16*ψ
5.6 ± 1.0
6.7 ± 1.7*
6.2 ± 1.9*
7.4 ± 2.4*ψ
HIV specific data for the HIV + ve/MS-ve and HIV + ve/MS + ve groups, data presented as median (Interquartile range)
HIV + ve/MS-ve
HIV + ve/MS + ve
On HAART (n = 61)
No HAAR (n = 12)
On HAART (n = 16)
No HAART (n = 1)
Duration of HIV infection (years)
Time on HAART (years)
Nadir CD4 cell count (10 6 /L)
Current CD4 cell count (10 6 /L)
HIV viral load (copies/mL)
Protease inhibitors (%)
The effect of HIV on aortic elastic function
Comparing the effects of HIV and the metabolic syndrome on aortic elastic function
In order to compare the effect of HIV and the Metabolic syndrome on PWV and AD, subjects with the metabolic syndrome but without a history of HIV infection (HIV-ve/MS + ve, n = 44) were compared to patients with HIV infection without the metabolic syndrome (HIV + ve/MS-ve, n = 73). As expected, the group with metabolic syndrome had higher blood pressures, BMI, visceral fat and waist circumference when compared to the group without metabolic syndrome (Table 1). Interestingly, despite this, both the HIV-ve/MS + ve and the HIV + ve/MS-ve groups had similar PWV (6.7 ± 1.9 vs 6.2 ± 1.9 m/s p = 0.94), which were 16-20% higher than the HIV-ve/MS-ve group (p < 0.05 for both analyses). A similar pattern was seen comparing distensibility in the HIV-ve/MS + ve and the HIV + ve/MS-ve with aortic distensibility measures at all three levels of the aorta being similar across the two groups (Figure 3). This suggests HIV and the metabolic syndrome have a similar magnitude of effect on aortic elastic function.
Investigating an additive effect of treated HIV and the metabolic syndrome
To investigate whether HIV and the metabolic syndrome are additive in their negative effects on PWV, patients with HIV infection without the metabolic syndrome (HIV + ve/MS-ve, n = 73) were compared to subjects with both HIV infection and the metabolic syndrome (HIV + ve/MS + ve, n = 17). As would be expected the HIV + ve/MS + ve group had increased BMI, SBP, DBP, waist circumference, HOMA-IR, glucose and hs-CRP when compared to the HIV+/MS-ve group (Table 1). Again, as expected, both the HIV + ve/MS-ve and the HIV + ve/MS + ve groups had higher PWV than the HIV-ve/MS-ve group (PWV by 15% and 38% respectively p < 0.05 for both analyses) In agreement with this, both the HIV + ve/MS-ve and the HIV + ve/MS + ve groups had lower aortic distensibility than the HIV-ve/MS-ve group (Ao by 16% and 44%, PDA by 20% and 45%, DDA by 18% and 38%, respectively all p < 0.05). Importantly, PWV in the HIV + ve/MS + ve group was 19% higher and aortic distensibility 31%, lower (= 0.011, Figure 3) than that recorded in the HIV + ve/MS-ve group (7.4 ± 2.4 vs 6.2 ± 1.9 m/s, p < 0.05). Put together, this suggests an additive detrimental effect of HIV and the metabolic syndrome on aortic elastic function.
Determinants of aortic PWV in study population
Associations between PWV and study characteristics of HIV and the metabolic syndrome
Aortic distensibility (mmHg-1)
Pulse wave velocity
BMI (kg/m 2 )
Visceral Fat (cm 2 )
Waist circumference (cm)
Past or present smoking
Viral load (copies/mL)
Nadir CD4 count (10 6 /L)
Current CD4 count (10 6 /L)
Duration of HAART (years)
Determinants of regional aortic distensibility
In order to investigate the associations between regional AD and other study parameters of the metabolic syndrome and HIV infection, all 203 subjects were included in this analysis. Associations between anthropometric, metabolic and HIV-related characteristics and aortic AD are presented in Table 3. In agreement with the published literature, aortic distensibility was negatively correlated with age, systolic blood pressure, diastolic blood pressure, visceral fat mass, fasting serum glucose and hs-CRP levels at all levels measured. Importantly, HIV infection was also associated with reduced distensibility at all three levels measured. In addition, as expected, BMI, waist circumference and triglyceride levels were negatively correlated with proximal descending and negatively with distal descending thoracic aortic distensibility (Table 3). In a similar pattern to that seen with PWV, there was no association between duration of HAART, antiretroviral class, viral load or nadir CD4 count and aortic AD. To investigate if there were any independent predictors of pulse wave velocity, multivariable regression was used as described above. The strongest stepwise multivariable models in this study consisted of aortic distensibility (Ao, PDA, DDA) as the dependent variables and age, BMI, SBP, fasting serum glucose, presence of the metabolic syndrome, smoking status and HIV infection as independent variables. This showed that age (Ao β = −0.108, PDA β = −0.05, DDA β = −0.06, all p < 0.001), SBP (Ao β = −0.09, PDA β = −0.03, DDA β = −0.04, all p < 0.01) and HIV infection (Ao β = −0.41, PDA β = −0.08, DDA β = −1.2, all p <0.02) were all independent predictors of aortic AD at all levels measured. In addition, again as expected BMI was an independent predictor of DDA (β = − 0.12, p = 0.001). Overall R2 of the models; Ao = 0.48, PDA 0.43, DDA 0.39, all p < 0.001. This suggests that along with age, blood pressure and BMI, HIV infection is independently associated with increased aortic stiffness.
This study has shown that, after matching for potential confounders, HIV infection is independently associated with increased aortic PWV and decreased aortic distensibility, both sensitive markers of reduced aortic elastic function. In addition HIV infection is an independent predictor of both increased pulse wave velocity and decreased aortic distensibility, clinical measures of aortic stiffness linked to increased cardiovascular mortality. The size of this detrimental effect is similar to that seen with the metabolic syndrome, a powerful cardiovascular risk factor. We have shown that HIV and the metabolic syndrome are additive in their negative effects on PWV and aortic distensibility, suggesting that both are risk factors that act in different ways to impair vascular elasticity. The mechanism of vascular alterations in patients with HIV may be secondary to direct effects of the HIV virus on vascular function, including direct alteration in endothelial function, inflammation, and modification of aortic wall vascular smooth muscle cell behaviour and extra-cellular matrix composition.
There is significant evidence that HIV infection is associated with chronic systemic and vascular inflammation even in patients on stable HAART with preserved CD4 counts and HIV RNA levels < 50 copies/ml, , and these patients also have a greater burden of subclinical atherosclerosis . Elevations in inflammatory markers, such as CRP, are associated with both increased arterial stiffness  and a higher risk of mortality . In support of a chronic inflammatory HIV-related vasculopathy explaining our findings, a recent 18 F-FDG-PET study demonstrated signs of increased arterial inflammation in treated subjects with HIV . Moreover, hsCRP was not only elevated in patients with HIV in this study but was also positively correlated to aortic PWV and negatively correlated to AD at all three levels, and furthermore was strongly correlated with visceral fat, which is thought to play a central role in this inflammatory process, with macrophage release of IL-6 and TNF-α  both which are associated with increased PWV. This may suggest a role for elevated visceral fat in vascular elastic dysfunction in treated HIV .
This study has demonstrated impaired vascular function in HIV subjects, independent of traditional risk factors, and, together with other studies of contemporary cohorts of patients with treated HIV, suggest that chronic inflammation in HIV infection may partially underlie the reduced vascular function and premature atherosclerosis. Prospective studies to reduce chronic inflammation beyond HAART are required to investigate whether or not this improves vascular inflammation and function and ultimately reduces atherosclerotic risk in patients with HIV.
Endothelial dysfunction in HIV
Endothelial dysfunction is a common feature of atherosclerosis . There is a growing body of evidence suggesting HIV itself may have deleterious effects on endothelial function. Patients with HIV (but without the metabolic syndrome) have been shown to have reduced vascular reactivity in a pattern similar to that seen in type 2 diabetes mellitus . The direct effect of HIV on endothelial biology has been extensively investigated. As a result of increased secretion of monocyte chemo-attractant protein 1  and increased expression of the adhesion molecules, vascular cell adhesion molecule-1 (VCAM-1) intercellular adhesion molecule 1 and E-selectin , vascular endothelium from patients with HIV have increased monocyte adherence and monocyte migration into the vascular intima during atherosclerotic plaque development . In addition, several HIV proteins, notably Tat and gp120 are themselves associated with endothelial cell activation and increased expression cell adhesion molecules . Put together with the evidence that HIV infection affects lipid processing  and is associated with lower HDL cholesterol, lower apolipoprotein B levels (in advanced disease)  and smaller LDL cholesterol particles, this environment provides an atherogenic milieu . Although studies have now shown that HAART may to some extent reduce endothelial activation, it does not appear to completely ameliorate the effects of HIV infection, suggesting that even during complete virological suppression, endothelial dysfunction persists and continues to promote atherosclerosis (and excess cardiovascular risk) in HIV ,.
The additive effect of treated HIV infection and the metabolic syndrome on arterial stiffness
The detrimental effect of the metabolic syndrome on aortic stiffness is well established –. This study has not only shown that treated HIV infection has a similar sized effect on aortic stiffness to the metabolic syndrome, but has also shown that the combination of HIV and the metabolic syndrome are additive in their negative effects. This suggests that patients with both are likely to be at even higher risk of cardiovascular events. As hs-CRP was significantly higher in HIV subjects with the MS compared to HIV subjects without the MS, and CRP has been shown to be a marker of excess risk,  inflammation is a potential unifying mechanism that may underlie the pathogenesis of vascular disease in both groups.
Due to the observational nature of this study, it is not possible to confirm causality or mechanisms which might underlie the increased aortic PWV and decreased aortic distensibility in patients with HIV. The study was not powered to detect differences in HAART-naïve and treated subjects. Nor was it possible to determine the effects of individual anti-retroviral medications on vascular function. Given the beneficial effect of antiretroviral treatments on the vasculature and improved markers of vascular function that are observed after commencement of antiretroviral therapy ,, antiretroviral agents are an unlikely cause of the vascular dysfunction. Nevertheless, longitudinal studies are needed to investigate this further. However, by including both HAART naïve and HAART treated patients this study provides a representative dataset of HIV infected subjects in the UK.
Distensibility was calculated using pulse pressure measurements taken from brachial blood pressure rather than central blood pressure recordings. Although we accept central pressure recording may have changed the absolute aortic distensibility measures, given the magnitude of the changes the DDA segment (i.e. up to 45% change in distensibility), the pattern of change, i.e. the main finding of this paper would not be expected to be affected.
Given the increase in cardiovascular events and cardiovascular related mortality in HIV-infected patients treated with effective antiretroviral therapy, identifying those at higher cardiovascular risk is of great clinical importance. We have shown that patients with treated HIV have reduced vascular function, which is independent of the metabolic syndrome and other traditional cardiovascular risk factors, suggesting a virus-related aetiology, such as chronic inflammation. Importantly we have shown that the magnitude of the effect of treated HIV infection is the same as that of the metabolic syndrome, a well-established and powerful predictor of cardiovascular mortality. Given the additive effect of HIV and the metabolic syndrome on reducing vascular function, aggressive management of both HIV and the metabolic syndrome are likely needed to reduce the high incidence of vascular disease in this population.
Cameron Holloway would like to acknowledge support from the Oxford NIHR Biomedical Research Centre programme and the Australian Heart Foundation. Stefan Neubauer acknowledges support from the BHF Centre of Research. The British Heart Foundation (FS07/030) supported this work. The research was supported by the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre based at The Oxford University Hospitals Trust at the University of Oxford.
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