HIV infection is a risk factor for cardiovascular disease (CVD). This risk is accentuated by certain combination antiretroviral therapies (cARTs), independent of their effects on lipid metabolism and insulin sensitivity. We sought to define potential mechanisms for this association through systematic review of clinical and preclinical studies of CVD in the setting of HIV/cART from the English language literature from 1989 to March 2018. We used PubMed, Web of Knowledge and Google Scholar, and conference abstracts for the years 2015–March 2018. We uncovered three themes: (1) a critical role for the HIV protease inhibitor (PI) ritonavir and certain other PI-based regimens. (2) The importance of platelet activation. Virtually all PIs, and one nucleoside reverse transcriptase inhibitor, abacavir, activate platelets, but a role for this phenomenon in clinical CVD risk may require additional postactivation processes, including: release of platelet transforming growth factor-β1; induction of oxidative stress with production of reactive oxygen species from vascular cells; suppression of extracellular matrix autophagy; and/or sustained proinflammatory signalling, leading to cardiac fibrosis and dysfunction. Cardiac fibrosis may underlie an apparent shift in the character of HIV-linked CVD over the past decade from primarily left ventricular systolic to diastolic dysfunction, possibly driven by cART. (3) Recognition of the need for novel interventions. Switching from cART regimens based on PIs to contemporary antiretroviral agents such as the integrase strand transfer inhibitors, which have not been linked to clinical CVD, may not mitigate CVD risk assumed under prior cART. In conclusion, attention to the effects of specific antiretroviral drugs on platelet activation and related profibrotic signalling pathways should help: guide selection of appropriate anti-HIV therapy; assist in evaluation of CVD risk related to novel antiretrovirals; and direct appropriate interventions.
- platelet activation
- oxidative stress
- myocardial fibrosis
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Cardiovascular disease (CVD) is the third most frequent non-AIDS cause of death in HIV+ individuals, and in those on combination antiretroviral therapy (cART), it is the leading cause.1 CVD is predicted to increase markedly with ageing among the HIV infected, presenting obstacles to a normal life span and contributing substantially to healthcare utilisation costs in resource-rich and resource-poor settings.2–5 These disorders affect all demographics, with an equivalent impact on paediatric and adult populations.1 5 In terms of gender, the US Veterans Aging Cohort Study established that, after adjusting for age, race, ethnicity, lipids, tobacco use, blood pressure, diabetes, renal disease, obesity, hepatitis and substance abuse, the HR for substantial cardiovascular (CV) events was 1.48 for all HIV-infected veterans (p<0.05)6 and 2.8 among female veterans (p<0.001).7
In defining the pathophysiology of the association between HIV and CVD, it is important to recognise that the magnitude of CVD risk in the HIV+/ART-naive is low. The large Data Collection on Adverse Events of Anti-HIV Drugs (D:A:D) study found no increase in acute myocardial infarction (AMI) in the absence of antiretroviral therapy (ART).8 In contrast, this risk increased by 26% per year of ART exposure, despite the fact that blood pressure, high density lipoprotein (HDL) cholesterol levels and smoking did not change or declined.8 A very recent report from the Multicenter AIDS Cohort Study (MACS) refined this risk, emphasising the importance of viral control in the setting of cART.9 There was a higher incidence and greater progression of low-attenuation, non-calcified high-risk plaque among HIV-infected men than age-matched controls over a median of 4.5 years. Failure of viraemic control for those on cART was an important correlate of plaque progression.9 These data have been incorporated into new models for assessment of the global risk of CVD in the setting of HIV, which have higher accuracy than classic Framingham equations. One model includes cumulative exposure to HIV protease inhibitors (PIs) as a class, or current use of the nucleoside reverse transcriptase inhibitor abacavir.10 Large observational cohorts document that cART based on other nucleoside or non-nucleoside reverse transcriptase inhibitors does not influence AMI incidence, and although integrase strand transfer inhibitor-based ART has not been in widespread use for periods sufficient to permit long-term follow-up, those agents also do not appear to influence CVD risk.1 11 12
We sought to define potential mechanisms for the impact of specific antiretroviral drugs on CVD risk in the setting of HIV through a systematic review of clinical and preclinical studies from the English language literature from January 1989 to March 2018. We used PubMed, Web of Knowledge and Google Scholar, and reviewed conference abstracts from major national and international HIV/AIDS conferences for years 2015–March 2018. We paid particular attention to recent PI-boosted regimens that substitute cobicistat for ritonavir (RTV),13 as well as two antiretroviral drugs, abacavir and the PI atazanavir, for which links to changes in clinical CVD risk remain controversial. We recognised that cART-mediated effects on lipid metabolism, insulin sensitivity, endothelial function, activation of monocytes and T cells, and the role of oxidative stress in initiation and maintenance of these metabolic and proinflammatory processes, all of which can affect vascular homeostasis and CVD risk, have been extensively reviewed1 14–18 and were not the main focus of our study. What has not received sufficient attention is the concept that these systems are differently impacted by individual antiretroviral agents, and the critical role of specific types of antiretroviral-mediated platelet activation with induction and maintenance of profibrotic pathways.
This information has practical clinical ramifications. Recent studies have noted the disparity in quality of cardiovascular care for HIV-infected versus uninfected individuals. When indicated, physicians were much less likely to prescribe aspirin or other antiplatelet agents, or hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors (statins) to HIV-infected individuals (5.1% vs 13.8%, p=0.03 and 23.6% vs 35.8%, p<0.01, respectively).19 Findings on the underutilisation of statins were replicated among 3453 HIV-infected women in the Women’s Interagency HIV Study20 and among a diverse population of 3312 HIV+ individuals in the dialated cardiomyopathy (DC) cohort.21 It was speculated that most HIV patient visits focus on control of HIV viraemia to the detriment of preventive CV care19 but, as highlighted here, the two areas are intimately linked.
Impact of cART on CVD risk: classes of ART versus individual antiretroviral agents
There are no prospective, randomised trials to document a causative relationship between cART in general, or a specific antiretroviral agent, and CVD. However, the fact that the association between CVD and use of only certain PIs is reproducible in multiple, large and diverse observational cohorts (table 1)6 11 17 18 22–26 28 29 and is characterised by a slowly increasing risk as cumulative exposure to these antiretrovirals increases,18 ‘reduces—albeit does not remove—the risk that unknown or unmeasured confounders that could not be adjusted for might explain the association’, in the conclusion of one group.18 Data from preclinical models, derived from our lab and others, support this interpretation, as discussed below.
Table 1 summarises the association of cART with CVD risk in adults. With one major exception, based on Veterans Affairs databases,22 23 large observational studies support the association of PIs versus other ART classes with increased CVD risk. All but one study powered to distinguish among specific PIs linked this risk to RTV, used alone or with certain other PIs, including lopinavir, indinavir, amprenavir, fosamprenavir and darunavir, in so-called PI-boosted regimens. Nearly all PIs are combined with low-dose RTV or, more recently, cobicistat, both of which inhibit cytochrome P450 3-mediated metabolism of PIs in the liver, resulting in increased plasma concentrations.13 Cobicistat-boosted regimens are not included in table 1 as they have not been in clinical use for sufficient periods to assess CVD risk, which would have enabled addressing the issue of whether it is the boosting of the principal PI or the boosting agent itself, which is responsible for some of the long-term side effects of such regimens. One phase III trial contrasting RTV-boosted versus cobicistat-boosted PIs found no variation in high/low density lipoprotein profiles or degree of bone mineral density loss over a 144-week follow-up period, but details of CVD assessment were not included.13 In any event, RTV-boosted PIs continue to be used worldwide, and in recent studies of contemporary two drug regimens in the USA, darunavir/RTV is one of the key components.29 In addition, observational studies suggest that switching from RTV-based or other PI-based cART to alternative drug classes may not mitigate CVD risk30 31 nor reduce existing arterial inflammation.32
In evaluating our pathophysiological model for cART-accelerated CVD based on the importance of platelet activation, it is also important to consider apparent contradictions. For example, the PI atazanavir and RTV-boosted atazanavir had no significant link to CVD (table 1), with one group suggesting a reduced risk for AMI with atazanavir exposure.33 However, these regimens are associated with heightened platelet activation.30 In addition, there is continued argument as to whether abacavir increases CVD risk; some treatment guidelines still suggest caution in its use in individuals with high Framingham CVD risk scores.1 12 15 34 Part of the controversy involving atazanavir concerns the role of residual confounders in analysis of a relatively small cohort.33 Indeed, coronary artery calcium scoring and coronary CT angiography documented an increase in any plaque in association with cumulative exposure to atazanavir (adjusted OR 1.66) or abacavir (adjusted OR 1.38),35 and this is reflected in our contrast of antiretroviral agents linked to an increase in clinical CVD risk as opposed to changes in surrogate markers for such disease (table 2). These issues are explored in our review of the impact of an individual antiretroviral agent on lipid profiles and platelet activation and on extracellular matrix (ECM) autophagy, macrophage polarisation and oxidative stress, all of which can contribute to, or protect against, cardiac fibrosis and dysfunction.
The role of HIV/cART in modulating traditional CVD risk factors
The D:A:D Study Group concluded that the increase in AMI risk in the setting of HIV ‘may at least in part be explained by cART-induced changes in conventional risk factors. These findings [therefore] provide guidance in terms of choosing lifestyle or therapeutic interventions to decrease those risk factors’.11 Indeed, recent reviews have focused on modification of traditional risk factors, including diet and pharmacological treatment of hyperlipidaemia and inflammation with statins.1 15 Lipid abnormalities are important in proinflammatory processes and atherosclerosis, and both hypercholesterolaemia and hypertriglyceridaemia increase platelet activation,36 which could promote a proinflammatory, procoagulant and profibrotic state regardless of HIV infection or cART use. RTV and darunavir impact platelet function in a manner comparable with tobacco smoke and may synergise with smoking in promotion of a hypercoaguable state.37 With reference to fibrosis, a cross-sectional study of HIV-infected adults on cART documented normal ejection fractions but subclinical systolic dysfunction in association with myocardial steatosis and diffuse myocardial fibrosis.38 (There was no association between exposure to specific classes of ART and intramyocardial lipid content or fibrosis, but specific PIs were not examined.) The authors stated that these observations ‘suggest’ that cardiac fibrosis may simply be secondary to the downstream metabolic effects of HIV infection.38
However, review of 4685 participants from 35 countries in the Strategic Timing of Antiretroviral Treatment (START) trial, a randomised study of immediate versus deferred cART initiation among HIV-infected individuals with CD4+ T cell counts in the normal range (>500 cells/mm3), concluded that the net effect of cART on traditional CVD risk ‘may be clinically insignificant’, at least in the short term, with a mean follow-up of 3.0 years.39 In fact, cART had opposing effects on serum lipids in START, increasing total cholesterol and low-density lipoprotein cholesterol and also increasing high-density lipoprotein cholesterol and decreasing the need for blood pressure medication.39 While accelerated CVD risk linked to RTV, used alone or at much lower doses in many RTV-boosted PI regimens, is accompanied by changes in lipid metabolism,14 18 hyperlipidaemia was not a factor in the high CVD risk related to darunavir/RTV in humans,18 and RTV-driven cardiac disease could be dissociated from hyperlipidaemia in two rodent models.40 41 While lipid profiles were minimally altered, to similar levels, with RTV-boosted darunavir and atazanavir,42 the link to heightened risk for clinical CVD is much greater with the former regimen.18 28
Surrogate markers for CVD and biomarkers of inflammation and coagulopathy in HIV/cART
Circulating levels of immune and other cellular activation biomarkers in HIV-infected individuals vary widely with different antiretroviral regimens, complicating attempts to link these changes to CVD in the setting of HIV/cART. Such biomarker data may offer insight into the severity of cardiovascular-related outcomes in the setting of HIV and HIV/cART,43 but presently they are not reliable indicators of the impact of a specific ART regimen or antiretroviral drug on CVD risk.
For example, changes in plasma markers of inflammation, monocyte activation and coagulation among individuals starting cART within 6 months of HIV infection in AIDS Clinical Trials Group protocol A5217 found d-dimer levels, an indication of a hypercoaguable state, lowered on viral suppression (p=0.031) but high-sensitivity C reactive protein (hsCRP), a marker of inflammation, and monocyte sCD14 levels were unchanged regardless of regimen.44 In another study, only hsCRP correlated directly with advancing carotid intima-media thickness (CIMT).45 Integrase strand transfer inhibitor-based regimens led to greater decreases in sCD14, hsCRP and lipoprotein-associated phospholipase A2, a marker of vascular inflammation, compared with a non-nucleoside reverse transcriptase-based regimen, but interleukin (IL)-6, tumour necrosis factor-alpha (TNF-α)-receptor 1 and another monocyte activation marker, sCD163, were unaltered.46 There was a decline in IL-6 and sCD14 on integrase strand transfer inhibitor but not PI-based ART, but levels of sCD163 and hsCRP did not differ between treatments.47 In the Switching From PI to RALtegravir in HIV Stable Patients (SPIRAL) study of 273 HIV+ individuals switched from RTV-boosted PIs to integrase strand transfer inhibitor-based cART, there were declines in hsCRP, monocyte chemoattractant protein-1, osteoprotegerin, IL-6, TNF-α and d-dimers, with magnitudes ranging from 8% for d-dimers to 40% for hsCRP and 46% for IL-6.31 However, there were no significant changes in related biomarkers, including IL-10, soluble intercellular adhesion molecule-1 (sICAM-1), vascular cell adhesion molecule-1 (sVCAM-1), E-selectin and P-selectin.31 Another procoagulant marker, tissue factor (TF), is also elevated following HIV and simian immunodeficiency virus infection, and levels are not normalised in the setting of cART.48
In terms of biomarker correlations with functional measures of preclinical CVD, elevated levels of sCD163, sCD14 and monocyte chemoattractant protein-1 were associated with subclinical atherosclerosis based on coronary CT angiography in one MACS study.49 However, there was only a very modest level of correlation among these monocyte markers. Baseline sCD14 levels correlated with CIMT progression in the setting of HIV,49 50 though cART, regardless of class, did not influence these levels.31 46 In addition, absolute levels of HIV in cART-treated individuals did not correlate with many biomarkers of inflammation or CVD risk.47
These studies indicate that current biomarker datasets are insufficient for evaluation of HIV-related CVD risk. For example, in the Women’s Interagency HIV Study, elevated hsCRP was positively associated with focal plaque progression in HIV-uninfected women, with a relative risk of 6.0, but this was not the case for their cohort of HIV-infected women.51 The investigators concluded that ‘subclinical CVD pathogenesis may be different in HIV-infected women’.51
Biomarkers more specific for fibrosis may be of clinical value to assessing the importance of cardiac fibrosis in HIV/cART-linked CVD. Although markers of inflammation and immune activation did not correlate with an MRI-based myocardial fibrosis index of HIV-infected individuals on cART,52 elevation of plasma factors linked to pathological cardiac fibrosis in the general population, including soluble ST2, an IL-1 receptor family member and biomarker of cardiomyocyte stretch, galectin-3, and growth differentiation factor 15, a transforming growth factor (TGF)-β superfamily member,53 54 have been linked to CVD among HIV+ populations.18 Plasma TGF-β1 levels are similarly increased twofold in HIV+/ART-naïve asymptomatic individuals, with a further rise in advancing disease, and this is not suppressed by cART.55 56 Levels of a classic marker of oxidative stress, plasma F2-isoprostane, also correlate with CVD and other serious metabolic events in HIV/cART patients, with a sensitivity of 95.3% and a specificity of 49.6%.57 Similarly, RTV-induced cardiac dysfunction in rats correlated with a 50% increase in the plasma F2-isoprostane 8-isoprostane over controls.40 Median F2-isoprostane levels are significantly lower in virally suppressed HIV+ patients on non-nucleoside reverse transcriptase inhibitor-based cART versus other forms of cART, predominantly PI based.58
As noted above, correlations among many of these biomarkers, preclinical indicators of CVD and clinical cardiac dysfunction often do not reach significant levels. In terms of TGF-β1, an important caveat is the failure of many investigators, when collecting mouse or human blood, to use controls for ex vivo platelet activation with TGF-β1 secretion.59 60 The dichotomy in TGF-β1 levels between HIV negative controls and HIV-infected individuals with and without cART exposure may therefore be more prominent than reported in the literature. In addition, measures of the levels of functional TGF-β1, the activation product from its latent form, have not been assessed in the setting of HIV/cART and, as reviewed in the section on platelets, could be influenced by different antiretroviral agents. Finally, as discussed below, those PIs most closely linked clinically to accentuated CVD risk, and shown to promote platelet activation and proinflammatory and profibrotic signalling in vitro and in murine models by our group and others, may not act through alteration of circulating levels of these factors but rather by affecting their signalling pathways.
Defining the pathophysiology of HIV/cART-linked CVD: focus on platelet activation and cardiac fibrosis
Cardiac fibrosis has been documented in HIV-infected individuals with lower peak diastolic as well as systolic longitudinal strain38 and may underlie an apparent shift in character of HIV-associated CVD over the past decade from primarily left ventricular (LV) systolic dysfunction to LV diastolic dysfunction.16 61 In one study, 49% of HIV-infected subjects had evidence of diastolic dysfunction compared with 29% of uninfected controls (p=0.008), a difference that persisted after adjustment for hypertension.61 Only 4% of HIV-infected individuals had evidence of LV systolic dysfunction.61 The increase in LV mass was also highly significant for the HIV group (p=0.001).61 No association with ART class was found, but individual antiretroviral agents were not examined. In addition, the mechanisms underlying these changes were not explored, although subclinical atherosclerosis and infiltration of the myocardium with inflammatory cells were thought to be involved.61 These changes are consistent with our pathophysiologic model, as detailed below. .
Further insight into the pathophysiology of diastolic and other CVD in the setting of HIV/cART should come from the recently announced Characterizing Heart Function on Antiretroviral Therapy study, which will include measures of myocardial fibrosis by cardiac magnetic resonance and biomarkers of fibrosis and oxidative stress.16 However, based on current knowledge, two points for intervention can be highlighted now: platelet activation and related signalling pathways for fibrosis and oxidative stress.
Although persistent platelet activation is well documented in the setting of HIV and HIV/cART,30 55 62 its role in pathological fibrosis-mediating CVD in these settings is rarely emphasised. The relationship of chronic platelet activation, directly or indirectly mediated by certain PIs, to CVD is consistent with the clinical association of only certain PI-based regimens with an accentuated risk of CVD. We focus on pathological cardiac and vascular fibrosis in relationship to platelet activation for the following reasons:
TGF-β1 is critical to initiation and maintenance of pathological fibrosis. We evaluated fibrosis and a canonical TGF-β1 signalling event, Smad2/3 phosphorylation, in autopsy hearts of ART-naïve HIV+ children.55 Deposition of collagen and increased phosphorylated Smad2 was seen, with a strong correlation between fibrosis score and pSmad2 staining.55 Simian immunodeficiency virus-infected macaques show cardiac dysfunction similar to that of HIV infection, in association with interstitial and vascular fibrosis and infiltration of cardiac tissue with proinflammatory macrophages.63 64
The role of TGF-β1 in development of CVD and other non-AIDS defining fibrotic disorders in the setting of HIV/cART is of increasing interest.55 65 66 Aortic arterial fibrosis is prominent in HIV-infected individuals versus controls and is not suppressed by cART.32 Focal and diffuse myocardial interstitial fibrosis is of high prevalence in the setting of HIV/cART16 38 52 67 and linked to LV diastolic dysfunction and heart failure with preserved ejection fraction in these individuals.16 23
RTV induces LV fibrosis at pharmacological concentrations in ApoE−/− mice in conjunction with increased TGF-β1 in plasma and cardiac tissue, independent of RTV-associated alterations in lipid metabolism.41 Our group demonstrated decreased cardiac function and cardiac fibrosis in mice exposed to pharmacological doses of RTV daily for 8 weeks.68 Fibrosis correlated with plasma TGF-β1 levels and activation of both canonical (Smad2/3) and non-canonical (TAK1/MKK3/p38) TGF-β1 signalling pathways in the heart.68
As shown in figure 1, under homeostatic conditions, synthesis of collagen and other ECM components, along with their degradation by macroautophagy, is mediated by TGF-β1 signalling through both canonical and non-canonical pathways.55 69 Autophagy is a prominent negative regulator acting through the latter pathway; the importance of RTV in this process was demonstrated by the fact that our group found that mice null for microtubule-associated protein 1 light chain 3 (LC3−/−), and thus lacking autophagosomes, were particularly susceptible to RTV-induced cardiac fibrosis.68
The critical role of the platelet in this system was defined by the fact that mice with targeted deletion of TGF-β1 only in megakaryocytes/platelets (PF4CreTgfb1flox/flox mice) were protected from RTV-induced cardiac dysfunction and fibrosis.68 Platelets contain 40–100 times the concentration of TGF-β1 as other cells, contributing the major fraction of circulating TGF-β1, and are key to clinical and other murine models of fibrosis with heart failure.60 69 70
In terms of pathological fibrosis, HIV infection itself leads to increases in TGF-β1 levels, along with a variety of proinflammatory factors such as IL-6, IL-8 and TF. Inflammatory cytokines can induce TF in endothelial cells and monocytes/macrophages, mediating thrombin generation, thereby activating platelets via protease-activated receptors. This leads to persistent inflammation and continued platelet activation, with TGF-β1 release.69 71 72 As illustrated in figure 2, other cells involved in this inflammatory milieu, such as injured endothelial cells, monocytes/macrophages, along with activated platelets, also contribute to reactive oxygen species (ROS) generation. This establishes a positive feedback loop with platelet activation for the transition of latent to active TGF-β1, as ROS is a potent activator of latent TGF-β1.69
In terms of the involvement of cART, RTV, many other PIs and abacavir can directly activate platelets.30 37 55 62 68 73 74 RTV, and certain other PIs, can also elevate mRNA expression for markers of oxidative stress, including IL-8, TNF-α and inducible haem oxygenase-1, when compared with the integrase strand transfer inhibitor raltegravir, which has not been implicated in CVD.75–77 Macrophage polarisation may also be involved through upregulation of M1 inflammatory subsets with production of procoagulant TF,48 55 in concert with loss of M2c regulatory macrophages acting via upregulation of regulatory T cells and TAK1/MKK3/p38 signalling with promotion of autophagy.68
Our group, and others, has also suggested interconnected roles for ubiquitin-proteasome systems with oxidative stress and dysregulation of redox in HIV and cART-linked CVD.68 78 79 Traditional risk factors for atherosclerosis, including tobacco, hyperlipidaemia and insulin resistance are associated with increased production of ROS, which have adverse effects on endothelial cell and platelet function14 69 77 (figure 2). Heightened ROS generation occurs early in HIV infection and persists despite many cART regimens79 (figure 2). ROS is an important aspect of CVD risk as cardiomyocytes are abundant in phospholipids, which are highly sensitive to oxidative stress.68 Such stress is also extremely efficient in converting latent TGF-β1 into its active, profibrotic form.69 As certain PIs could trigger ROS production through platelet activation, altered lipid metabolism and inhibition of ECM autophagy,68 69 80 we proposed a positive feedback loop by which HIV and certain PIs drive increases in ROS, in turn activating TNF receptor-associated factor 6 (TRAF6), a nuclear signalling adapter protein and ubiquitin E3 ligase, promoting TGF-β1 signalling (figure 1).55 68 This pathway has been shown, in other models, to exacerbate pathological cardiac hypertrophy via TAK1/MKK3/p38-dependent signalling.81
Finally, the signalling activity of TGF-β1, but not its plasma concentration, may be enhanced by ART-mediated facilitation of TRAF6 activity through specific inhibition of immunoproteasome function, with resultant suppression of TRAF6 degradation. Certain PIs, including RTV, block immunoproteasome formation at low pharmacological concentrations, while having no effect on the constitutive proteasome unless suprapharmacological, often cytotoxic, concentrations are employed.82 83 As TRAF6 is regulated through the immunoproteasome, such blockade would impede degradation of TRAF6, accelerating cytokine pathways dependent on this molecule. We demonstrated this in dissecting the mechanism of RTV-based acceleration of bone mineral loss in postmenopausal women treated with PI-based versus other cART regimens.82 84 RTV facilitated differentiation of monocytes into bone resorbing osteoclasts induced by RANKL. RANKL is the obligate cytokine for osteoclastogenesis and signals via TRAF6-related pathways. This occurred in association with prolongation of TRAF6 half-life, in the absence of changes in RANKL levels in RTV-treated individuals. As TGF-β1 and IL-6 and IL-8, inducers of TGF-β1, are also regulated by TRAF6, RTV-mediated interference with the immunoproteasome could lead to increased collagen accumulation mediated through the TAK1/MKK3/p38 pathway (figure 1). TRAF6 is known to exacerbate pathological cardiac hypertrophy and a variety of other cardiovascular disorders and appears to be a drugable target in treating CVD incurred by inflammatory processes.81 85
The role of autophagy in this system awaits further investigation. TRAF6-mediated potentiation of TAK1/MKK3/p38-associated autophagy and ROS induction of autophagy could be promoted by ART, but accompanying nitrosative stress with induction of reactive nitrogen species (RNS) can inhibit autophagy via S-nitrosylation and subsequent blockade of transcription factors that regulate Beclin 1, a component, along with LC3, of the autophagasome.69
Distinguishing features of antiretrovirals correlated with accelerated CVD
Based on our pathophysiological scheme, RTV should have a prominent role in clinical CVD and cardiac fibrosis as it can directly activate platelets and promotes pathological cardiac fibrosis and cardiac dysfunction in mice exposed to pharmacological levels of drug, acting through upregulation of TGF-β1 signalling. In contrast, individuals receiving the integrase strand transfer inhibitor raltegravir have platelets exhibiting markedly lower levels of platelet activation, at least as measured by expression of P-selectin on adenosine diphosphate (ADP) stimulation, when compared with other antiretrovirals,86 and raltegravir has not been implicated in accentuating CVD (table 2). However, the correlation between ART-linked platelet activation and clinical CVD risk is more nuanced.
For example, abacavir also activates platelets,73 yet as noted earlier, data linking abacavir to clinical CVD are conflicting.1 15 33 In terms of the PIs, cumulative exposure to lopinavir/RTV or darunavir/RTV is associated with an increased incidence of AMI, but atazanavir/RTV is not,18 28 87 even though atazanavir has been linked to platelet activation in vivo.30 As suggested above, lipid alterations cannot account for this difference; darunavir/RTV and atazanavir/RTV both cause similar, minimal changes in lipids.39 42Unrecognised confounding factors may be involved. There are many more patients followed for much longer periods on older PIs than atazanavir, and use of atazanavir, alone or with RTV-boosting has been recently linked to subclinical coronary artery disease.33 35 Other mitigating factors may also mitigate the platelet activation response.
One major issue is that the systems in which these platelet studies were performed, and the read-out for ‘activation’, are not uniform. The intensity of these effects among specific antiretrovirals, and their character, particularly with reference to release of latent or active forms of platelet TGF-β1, remain to be characterised. In addition, the mechanism(s) by which they activate platelets is unclear. Several pathways may be involved, including generation of systemic ROS and proinflammatory cytokines such as IL-6 and IL-8, thrombin and other coagulation factors and TF, which are strong platelet activators. We showed that even very low levels of RTV (<1 µM) alone can directly activate platelets and lead to release of latent TGF-β1,55 as well as elevate total TGF-β1 levels in plasma of RTV-exposed mice.68 However, active TGF-β1 levels could not be detected in our system (unpublished data) perhaps due to its very rapid clearance.59 Furthermore, in vitro models for platelet activation may not accurately reflect the situation in vivo, where interactions among divergent cell populations and platelets can contribute to platelet activation and release of active TGF-β188 89 (figure 2). These aspects need to be further studied in the setting of HIV/cART.
In addition, as summarised in figure 3, a single antiretroviral agent may demonstrate positive and negative influences on the pathophysiological pathways outlined in figure 2 and figure 4. Those antiretrovirals linked clinically to heightened CVD incidence appear to enhance the high-risk factors. Using atazanavir as an example, this PI directly activates platelets and so may release platelet TGF-β1 as does RTV. However, atazanavir is also a strong inducer of autophagy,90 elevates antioxidant bilirubin-linked pathways18 and does not induce ROS release from macrophages,76 while RTV and other PIs linked to CVD do not promote autophagy, may block autophagy-based degradation of collagen and other ECM components,68 and generate pro-oxidant ROS.76 Abacavir may directly activate platelets but, unlike many of the PIs, it does not induce oxidative stress in macrophages.76 (Its effects on autophagy have not been studied.) Such differences are catalogued for these are other antiretroviral drugs in table 2.
Novel interventions in HIV/cART-associated cardiac fibrosis
We used our RTV-exposed cardiac fibrosis model in mice to explore novel interventions based on alterations of TGF-β1 signalling, autophagy and macrophage polarisation. We examined inhaled, low dose carbon monoxide (CO), a potent inducer of endogenous antioxidant and anti-inflammatory pathways acting via the leucine zipper transcription factor nuclear factor erythroid 2-related factor 2 (Nrf2).68 Exposure of mice to RTV plus daily CO inhalations (250 ppm for 4 hours, five times/week) for 8 weeks led to suppression of cardiac fibrosis and Smad2 activation in conjunction with a decrease in proinflammatory M1 cells and a dramatic increase in the anti-inflammatory M2c subset in the heart, compared with RTV-exposed mice kept in ambient air.68 The CO-based changes in macrophage subsets in the heart are important to emphasise as, given the increasing attention to cardiac fibrosis in the setting of HIV/cART, TGF-β1 inhibition may seem a logical intervention. However, pan-neutralisation of TGF-β fails to suppress or reverse pathological fibrosis in many murine models and clinical trials.69 This lack of response may relate to divergent TGF-β1-dependent signalling pathways, which can either augment collagen synthesis or promote its degradation (figure 1), as well as production of low levels of TGF-β1 by regulatory M2c macrophage subsets, inducing anti-inflammatory regulatory T cells.
We then sought a more practical method to activate Nrf2 than inhaled CO. Nrf2 is a key regulator of the expression of genes coding for the majority of antioxidant and anti-inflammatory proteins affected by endogenous CO and inducible haem oxygenase and activated by exogenous CO.91 In endothelial cells, the Nrf2 pathway serves as a mechanosensitive regulator of redox signalling, suppressing TGF-β1 activation that may be induced by shear flow forces.92 Such forces might come into play in the setting of HIV-linked CVD. The Nrf2 pathway also has a protective role in atherosclerosis, consistent with its suppression of NADP(P)H oxidase (NOX)4, which can injure endothelium.93 The orally bioavailable Nrf2 activator S-adenosyl-L-methionine (SAMe), the main endogenous methyl donor,94 could prevent and treat ethanol-associated and lipid-associated hepatic fibrosis and asthma-associated pulmonary fibrosis in mice.95 96 It is a potent inhibitor of platelet activation induced by a variety of agents in rodent and human blood97 and can block TGF-β1 signalling through the canonical Smad3 pathway.96 Several natural and synthetic compounds apart from SAMe, including sulforaphane, plant phenolics, triterpenoids such as bardoxolone methyl and itaconate are also potent Nrf2 activators.98 99 As depicted in figure 4, such agents could influence multiple pathways involved in HIV/cART-linked CVD.
Our review illuminates the critical role of RTV and certain other PIs as specific antiretrovirals involved in accentuating CVD risk in the setting of HIV. Limitations to definitively establishing those associations, and their mechanisms of action, include the lack of randomised clinical trials with the power to dissect effects of specific antiretroviral drugs on clinical CVD and surrogate markers for such disorders, as well as the failure to use standardised methodology to assess platelet activation, oxidative stress and cytokine production linked to profibrotic pathways in association with those agents.
Probable mechanisms by which a specific antiretroviral could induce CVD include:
Platelet activation, with secretion of latent TGF-β1 and its subsequent activation, perpetuation of a positive feedback loop involving ROS generation, and induction of fibrosis.
Suppression of TRAF6 degradation through effects on immunoproteasome formation, thereby prolonging signalling events related to proinflammatory and profibrotic cytokines and ROS, even if circulating levels of these factors are unperturbed.
Inhibition of ECM autophagy, exacerbating the profibrotic effects of TGF-β1 signalling.
Macrophage polarisation, increasing proinflammatory subsets and decreasing regulatory cells.
In terms of intervention in HIV/cART-linked CVD, our review suggests that:
Use of statins to mitigate the cardiovascular impact of certain antiretroviral drugs may have a limited impact. The Randomized Trial to Prevent Vascular Events in HIV (REPRIEVE) trial will address whether pitavastatin can prevent vascular events in HIV+ individuals without known CVD.100 However, in terms of the lipid-modifying action of statins, lopinavir/RTV is linked to hyperlipidaemia while darunavir/RTV is not, yet both have been implicated in heightened CVD risk. The impact of statins on PI-mediated oxidative stress and attendant endothelial cell injury, documented in vitro, could play a role,77 although a retrospective analysis of cART-treated HIV+ individuals from the Nutrition for Healthy Living cohort found that statins had no effect on incidence of myocardial infarction or stroke.101
A recent commentary advised that ‘Low CVD risk antiretrovirals should be considered and prescribed whenever possible’.12 We advocate creating a summary of the effects of a given antiretroviral drug on the parameters listed in table 2 and figure 3 to help assess the levels of such risk.
Novel interventions in HIV/cART-linked CVD, based on promotion of antioxidant pathways such as those linked to activation of Nrf2, should be pursued.
Contributors All authors drafted the review.
Funding Financial support was provided by National Institutes of Health grants R21 HL125044 (JL and JA) and R01 HL123605 (JA), and the Angelo Donghia Foundation (JL). National Institute of General Medical Sciences (grant GM114731), and National Cancer Institute (grant CA213987).
Competing interests None declared.
Patient consent Not required.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement No additional data are available.
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