Opposite effects of chronic HIV infection and antiretroviral medication on organismal and organ-specific biological aging

People with HIV (PWH) on combination antiretroviral therapy have an elevated risk for aging-related non-AIDS comorbidities. We assess whether HIV infection accelerates biological aging in two independent cohorts of PWH using six organ-specific and three organism-wide aging clocks derived from plasma proteomics of healthy individuals. Proteomic age acceleration significantly correlates with DNA methylation age and is linked to comorbidities and mortality. HIV infection accelerates systemic biological aging, with Mendelian randomization demonstrating causality between organ aging and inflammatory or metabolic complications. Accelerated aging in PWH is further related to the total HIV reservoir, and specific antiretroviral drugs reduce age acceleration. These data reveal important causal effects between chronic HIV infection, antiretroviral medication, biological aging and age-associated diseases, highlighting targets for improving health span in PWH.

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Publication Details

Journal
Nature Communications
Published
2026-02-10
DOI
https://doi.org/10.1038/s41467-026-69412-1
Primary Topic
HIV-related health complications and treatments
Type
article
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article

Opposite effects of chronic HIV infection and antiretroviral medication on organismal and organ-specific biological aging

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Nature Communications
HIV-related health complications and treatments
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Opposite effects of chronic HIV infection and antiretroviral medication on organismal and organ-specific biological aging

Cheng-jian Xu, Vasiliki Matzaraki, Twan Otten, Nadira Vadaq, Mareva Delporte, L.A.B. Joosten, Marc J T Blaauw, Yubo Zhang, Albert Groenendijk, Louise van Eekeren, Marvin AH Berrevoets, Mihai G. Netea, Linos Vandekerckhove, Wilhelm Vos, Andre van der Ven, Casper Rokx, Yang Li
article en

Abstract

People with HIV (PWH) on combination antiretroviral therapy have an elevated risk for aging-related non-AIDS comorbidities. We assess whether HIV infection accelerates biological aging in two independent cohorts of PWH using six organ-specific and three organism-wide aging clocks derived from plasma proteomics of healthy individuals. Proteomic age acceleration significantly correlates with DNA methylation age and is linked to comorbidities and mortality. HIV infection accelerates systemic biological aging, with Mendelian randomization demonstrating causality between organ aging and inflammatory or metabolic complications. Accelerated aging in PWH is further related to the total HIV reservoir, and specific antiretroviral drugs reduce age acceleration. These data reveal important causal effects between chronic HIV infection, antiretroviral medication, biological aging and age-associated diseases, highlighting targets for improving health span in PWH.

Nature CommunicationsVol. 17(1)
University of Bonn (DE), Radboud University Nijmegen (NL), Iuliu Hațieganu University of Medicine and Pharmacy (RO), Ghent University Hospital (BE), Erasmus MC (NL), Radboud University Medical Center (NL), Medizinische Hochschule Hannover (DE), OLVG (NL), Radboud Institute for Molecular Life Sciences (NL), Helmholtz Centre for Infection Research (DE), Elisabeth-TweeSteden Ziekenhuis (NL), Centre for Individualised Infection Medicine (DE), Center for Experimental and Clinical Infection Research (DE)
Good health and well-being
Openalex Percentile: Top 63%
HIV-related health complications and treatments
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