Why the study?
Persistent immune activation and asymptomatic CMV reactivity in HIV contribute to excess cardiovascular risk despite undetectable viral levels, but whether statins reduce subclinical atherosclerosis in this population is uncertain.
Does atorvastatin reduce carotid intima media thickness in statin-naive virally-suppressed HIV-infected patients with CMV seropositivity?
Does atorvastatin reduce carotid intima media thickness in statin-naive virally-suppressed HIV-infected patients with CMV seropositivity?
This study protocol outlines a randomized trial to evaluate whether atorvastatin 20 mg daily reduces subclinical atherosclerosis (measured by CIMT) in virally-suppressed HIV patients with CMV seropositivity.
Answers are grounded in this paper and cite their sources.
Tests atorvastatin on CIMT in CMV-seropositive virally suppressed HIV; leaves open whether statins mitigate inflammation-driven atherosclerosis beyond LDL effects.
<ns4:p> <ns4:bold>Background:</ns4:bold> Persistent immune activation and inflammation in HIV-infection are linked to excess cardiovascular risk and other non-communicable diseases. Periodic asymptomatic CMV-reactivity in HIV infected patients over a lifetime may contribute to non-AIDS defining morbidity. Despite undetectable levels of HIV and CMV, these patients continue to have increased levels of biomarkers and immune activations. Statin administration is thought to reduce subclinical atherosclerosis by decreasing LDL-C levels. It may also add beneficial effects against CMV infection. </ns4:p> <ns4:p> <ns4:bold>Methods:</ns4:bold> We are conducting a double-blind placebo-controlled trial in which patients are randomized to receive either atorvastatin or placebo with a ratio of 1:1. This trial aims to study the effect of atorvastatin in statin-naive virally-suppressed HIV-infected patients with stable ART and CMV seropositivity on carotid intima media thickness (CIMT), tool that evaluates subclinical atherosclerosis. The study recruits 80 patients at HIV integrated care unit of Cipto Mangunkusumo hospital. All eligible subjects have CIMT evaluation as primary outcome, along with flow mediated vasodilatation (FMD), liver fibrosis and steatosis evaluation, fasting lipid, neurocognitive test, community periodontal index (CPI), and residual immune activation as secondary outcomes in 48 weeks. </ns4:p> <ns4:p> <ns4:bold>Ethics and dissemination:</ns4:bold> This study has received an ethical approval from Health Research Ethics Commitee–Universitas Indonesia and Cipto Mangunkusumo Hospital. Before joining the study, all participants fill in an informed consent form. At the end of study analysis, the trial results will be published and disseminated in peer-reviewed journals. </ns4:p> <ns4:p> <ns4:bold>Discussion:</ns4:bold> The main purpose of our study is to evaluate the effect of atorvastatin administration on CIMT changes in statin naïve virally suppressed HIV-infected patients with stable ART and CMV seropositivity </ns4:p> <ns4:p> <ns4:bold>Registration:</ns4:bold> ClinicalTrials.gov ID <ns4:ext-link xmlns:ns5="http://www.w3.org/1999/xlink" ext-link-type="uri" ns5:href="https://www.clinicaltrials.gov/ct2/show/NCT04101136?term=NCT04101136&draw=2&rank=1">NCT04101136</ns4:ext-link> ; registered on 24 September 2019. </ns4:p>
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Yunihastuti et al. (2021) studied this question.
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