Longitudinal Changes in Epigenetic Age Acceleration in Aviremic Human Immunodeficiency Virus–Infected Recipients of Long-term Antiretroviral Treatment

• Published in: The Journal of infectious diseases 2022-01, Vol.225 (2), p.287-294
• Main Authors: Esteban-Cantos, Andrés, Montejano, Rocio, Rodríguez-Centeno, Javier, Saiz-Medrano, Gabriel, De Miguel, Rosa, Barruz, Pilar, Bernardino, Jose I, Mena-Garay, Beatriz, Cadiñanos, Julen, Jiménez-González, María, Nevado, Julián, Valencia, Eulalia, Mayoral-Muñoz, Mario, Arribas, Jose R, Rodés, Berta
• Format: Article
• Language: English
• Subjects: Acquired immune deficiency syndrome; Adult; Aging; Aging - genetics; AIDS; Anti-Retroviral Agents - therapeutic use; Antiretroviral drugs; Antiretroviral therapy; Antiretroviral Therapy, Highly Active - adverse effects; Antiretroviral Therapy, Highly Active - methods; CD4 antigen; DNA methylation; Epigenesis, Genetic; Epigenetics; Epigenomics; Female; HIV; HIV Infections - drug therapy; Human immunodeficiency virus; Humans; Immune system; Longitudinal Studies; Male; Middle Aged
• ISSN: 0022-1899; 1537-6613
• DOI: 10.1093/infdis/jiab338

Epigenetic aging, according to 3 different epigenetic clocks, did not accelerate in a cohort of long-term aviremic HIV-infected adults after 4 years of follow-up. Measures of epigenetic age acceleration might be useful tools to predict the occurrence of clinical outcomes. Abstract Background Human immunodeficiency virus (HIV) infection induces epigenetic age acceleration (EAA), but it remains unclear whether epigenetic aging continues to accelerate during successful antiretroviral therapy (ART) and prolonged virological suppression. Methods We longitudinally analyzed 63 long-term aviremic HIV-infected adults. Using blood DNA methylation patterns, we calculated EAA measures based on 3 epigenetic clocks (Horvath’s clock, PhenoAge, and GrimAge). We recorded the emergence of serious AIDS-related and non-AIDS-related events throughout the study to assess its association with EAA. Results All participants were on stable ART and were virologically suppressed. After 4 years of follow-up, PhenoAge-EAA and GrimAge-EAA showed no differences, whereas Horvath-EAA slightly decreased (median difference, –0.53 years; P = .015). Longitudinal changes in EAA measures were independent of changes in CD4 cell counts, the ART regimen, or other HIV-related factors. Nineteen percent of participants experienced a serious clinical event during the study. Horvath-EAA was significantly higher at baseline in participants with clinical events (P = .027). After adjusting for confounders, we found a trend toward an association of higher levels of all EAA measures at baseline with serious clinical events. Conclusions Epigenetic aging did not accelerate in long-term aviremic HIV-infected adults after 4 years of successful ART. EAA measures deserve further study as potential tools for predicting clinical events.