Risk of hypertension in people with HIV in the USA initiating modern antiretroviral regimens: pooled analysis of blood pressure data from five clinical trials

dc.contributor.authorY Hsue, Priscilla
dc.contributor.authorWaters, Laura
dc.contributor.authorOrkin, Chloe
dc.contributor.authorTiraboschi, Juan Manuel
dc.contributor.authorAvihingsanon, Anchalee
dc.contributor.authorMarongiu, Andrea
dc.contributor.authorS Whiteman, Andrew
dc.contributor.authorTian, Yuan
dc.contributor.authorM Nielson, Carrie
dc.contributor.authorAizen, Keith
dc.contributor.authorCohen, Calvin
dc.contributor.authorT Hindman, Jason
dc.contributor.authorK Rockstroh, Jürgen
dc.date.accessioned2026-05-06T07:36:40Z
dc.date.available2026-05-06T07:36:40Z
dc.date.issued2026-02-02
dc.date.updated2026-04-21T13:22:13Z
dc.description.abstractBackground People with HIV have a greater risk of cardiovascular disease than the general population. Current literature suggests that some ARTs may exacerbate this risk.Objectives To estimate the risk of hypertension in treatment-na & iuml;ve people with HIV receiving integrase strand transfer inhibitor (INSTI)/tenofovir alafenamide (TAF) or INSTI/non-TAF versus NNRTI/non-TAF regimens.Methods Post hoc pooled analysis evaluating data from US participants in five Phase 3 randomized studies. Adjusted prevalence of Stage 1 and 2 hypertension (American College of Cardiology/American Heart Association criteria) and conditional odds of higher blood pressure ratios were estimated using proportional odds mixed-effect regression through 108 weeks after ART initiation. Time to incident hypertension through 96 weeks was modelled using Cox proportional-hazards regression.Results In total, 2411 participants were included (528, 749 and 1134 received NNRTI/non-TAF, INSTI/non-TAF and INSTI/TAF regimens, respectively). Nearly half of participants had hypertension (Stage >= 1) at baseline. The Week 96 adjusted estimates of risk of hypertension (95% CI) were 1.06 (0.99, 1.13) and 1.12 (0.98, 1.27) for Stages >= 1 and >= 2 hypertension, respectively, for NNRTI/non-TAF versus INSTI/non-TAF, and 1.01 (0.95, 1.08) and 1.02 (0.91, 1.17) for Stages >= 1 and >= 2 hypertension, respectively, for NNRTI/non-TAF versus INSTI/TAF. There were no significant differences in conditional odds of high blood pressure between treatment groups. No significant differences were identified in time to incident composite hypertension for INSTI/non-TAF and INSTI/TAF versus NNRTI/non-TAF regimens; estimated hazard ratios (approximate 95% CI) were 0.88 (0.66, 1.17) and 0.98 (0.75, 1.28), respectively.Conclusions Results suggest the risk of hypertension is not significantly different across INSTI/TAF, INSTI/non-TAF and NNRTI/non-TAF regimens.
dc.format.mimetypeapplication/pdf
dc.identifier.urihttps://hdl.handle.net/2445/229334
dc.language.isoeng
dc.publisherOxford University Press (OUP)
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1093/jac/dkag005
dc.relation.ispartofJournal of Antimicrobial Chemotherapy, 2026, vol. 81, issue. 3
dc.relation.urihttps://doi.org/10.1093/jac/dkag005
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.titleRisk of hypertension in people with HIV in the USA initiating modern antiretroviral regimens: pooled analysis of blood pressure data from five clinical trials
dc.typeinfo:eu-repo/semantics/article

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