Statin use in HIV: European AIDS Clinical Society guidance for the primary prevention of cardiovascular disease
- PMID: 40316403
- DOI: 10.1016/S2352-3018(25)00047-5
Statin use in HIV: European AIDS Clinical Society guidance for the primary prevention of cardiovascular disease
Abstract
Atherosclerotic cardiovascular disease (ASCVD) is an important comorbidity in people ageing with HIV. Over-representation of classic risk factors such as smoking, and other factors such as HIV infection and its therapy, which are exclusive to people with HIV, are responsible for the increased risk of developing ASCVD. The tools to estimate risk, including Systematic Coronary Risk Evaluation 2 (SCORE2), generally underestimate risk in people with HIV. The Randomized Trial to Prevent Vascular Events in HIV (REPRIEVE) study showed that pitavastatin among people with HIV with low-to-moderate ASCVD risk significantly reduced the incidence of major adverse cardiovascular events. Following these results, the European AIDS Clinical Society recommends the use of moderate-intensity statins for people with HIV with a SCORE2 value between 5% and less than 10%, or ≥2·5% if older than 50 years with no additional listed risk factors. Moderate-intensity statins can be considered in people with HIV aged 40 years and over with a SCORE2 <5%. Although the REPRIEVE study findings are expected to have a major effect on clinical care, implementation could be hampered by the absence of adequate guidance or access to statins, concerns about tolerability and potential drug interactions, and difficulties in maintaining adherence. These key recommendations from the European AIDS Clinical Society aim to provide support in this remit.
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Conflict of interest statement
Declaration of interests JA has received a research grant from Gilead Sciences, paid to her institution, and has received speakers honoraria from Gilead Sciences, MSD, and ViiV Healthcare, unrelated to this work. JA is a coauthor on the British HIV Association (BHIVA) rapid guidance on statins use in people with HIV. KvB has received speakers honoraria and payment for advisory boards from Gilead Sciences, MSD, and ViiV Healthcare, and support for travelling and attending meetings from Gilead Sciences and ViiV Healthcare, all unrelated to this work. GMNB has received payments for research grants, advisory boards, or lectures from Novartis, ViiV Healthcare, Gilead Sciences, Johnson & Johnson, and MSD, unrelated to this work. FB has received consulting fees from Novartis, Novo Nordisk, and Sanofi. He has received payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or educational events from Amgen,Boehringer Ingelheim, Servier, ViiV Healthcare, Gilead Sciences, and MSD, as well as support for travelling and attending meetings from Servier. MG has received research grants from Gilead Sciences and honoraria as a speaker, and was a data safety monitoring board committee member or scientific advisor for Amgen, AstraZeneca, Biogen, Bristol Myers Squibb, Gilead Sciences, GlaxoSmithKline–ViiV Healthcare, Janssen–Cilag, MSD, Novocure, Novo Nordisk, Pfizer, and Sanofi. All mentioned engagements have concluded and are not ongoing. GG has received speakers honoraria from Gilead Sciences, ViiV Healthcare, Merck, and Janssen. PWGM has received honoraria, speaker fees, or conference travel support from Gilead Sciences, MSD, ViiV Healthcare, AstraZeneca, and Janssen–Cilag. CM has received speakers honoraria from Gilead Sciences and ViiV Healthcare and a research grant from Gilead Sciences, paid to her institution, unrelated to this work. JMM has received a personal 80:20 research grant from Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), between 2017 and 2025. JMM has received consulting honoraria, speakers honoraria or research grants from Angelini, Basilea, Contrafect, Cubist, Genentech, Gilead Sciences, Janssen, Lysovant, MSD, Novartis, Pfizer, and ViiV Healthcare, unrelated to this work. EN has received research funding, consultancy fees, and lectures sponsorship from, and has served on the advisory boards for, MSD, Gilead Sciences, ViiV Healthcare, and Janssen–Cilag. PR has received independent scientific grant support from Gilead Sciences, ViiV Healthcare, and MSD; and honoraria for serving on scientific advisory boards from Gilead Sciences and ViiV Healthcare, all paid to his institution; and travel support from Gilead Sciences. MvdV has received research grants and fees for participation in advisory boards from Gilead Sciences, MSD, and ViiV Healthcare, all paid to his institution. AW is a coauthor on the BHIVA rapid guidance on statins use in people with HIV. SDN has received unrestricted research grants from Independent Research Fund Denmark, Novo Nordisk Foundation, Svend Andersen Fonden, and Augustinus Fonden; and speakers honoraria and fees for participation in advisory boards from GSK, Gilead Sciences, and Takeda. EM has received honoraria for lectures or advisory boards from Gilead Sciences, Janssen, MSD, and ViiV Healthcare, and his institution has received research grants from MSD and ViiV Healthcare. EM is an investigator on the REPRIEVE trial and is a coauthor on the Spanish HIV Society (Grupo de Estudio del SIDA) position document on the use of statins for the primary prevention of cardiovascular disease in people with HIV. All other authors declare no competing interests.
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