- Research Article
7
- 10.1097/coh.0000000000000953
Understanding Residual Risk of Cardiovascular Disease in People Living with HIV
- May 16, 2025
- Current opinion in HIV and AIDS
- Laventa M Obare + 2 more +2
Purpose of ReviewTraditional cardiovascular risk factors, combined with persistent systemic inflammation, contribute to the increased prevalence of atherosclerotic cardiovascular disease (ASCVD) in people living with HIV (PLWH). This review highlights key findings from the REPRIEVE trial on statin-based primary prevention of major adverse cardiovascular events in PLWH. It explores HIV-specific immune mechanisms contributing to residual cardiovascular risk.Recent FindingsIn REPRIEVE, statin therapy used for primary prevention of major adverse cardiovascular events in PLWH decreased the plasma lipoprotein-associated phospholipase A2, oxidized low-density lipoprotein, and high-sensitivity C-reactive protein (hs-CRP). However, several inflammatory markers including soluble CD14 (sCD14), sCD163, interleukin (IL)-1β, IL-6, IL-10, and caspase 1 did not change. The HIV reservoir, dysfunctional CD4+ T cells, immunoglobulin G N-glycans, anti-apolipoprotein A1 autoantibodies, trained immunity, and clonal hematopoiesis of indeterminate potential may contribute to residual inflammation.SummaryDespite antiretroviral and statin therapy, residual ASCVD risk in PLWH underscores the need for targeted interventions. Anti-inflammatory therapies, including IL-6 and IL-1β inhibitors, CCR5 antagonists (e.g., maraviroc, cenicriviroc mesylate), and immunomodulatory agents like methotrexate and colchicine, are being explored. Understanding HIV-driven immune dysregulation may lead to novel strategies to mitigate cardiovascular risk in this population.
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