Suboptimal Adherence to Combination Antiretroviral Therapy Is Associated With Higher Levels of Inflammation Despite HIV Suppression

Abstract
Human immunodeficiency virus (HIV)–infected individuals exhibit residual inflammation regardless of virologic suppression. We evaluated whether suboptimal adherence to combination antiretroviral therapy (cART) is associated with greater residual inflammation than optimal adherence, despite virologic suppression. Longitudinal self-reported cART adherence data and serum concentrations of 24 biomarkers of inflammation and immune activation were measured at the same study visit in HIV RNA–suppressed (P < .05) was reported. These same differences were observed in person-visits reporting P < .001) in person-visits at which <100% adherence was reported. Higher concentrations of inflammatory biomarkers were observed among HIV RNA–suppressed men who reported <100% cART adherence than among more adherent men. Residual HIV replication (ie, below the limit of detection), more likely among men with suboptimal adherence, is a plausible mechanism. Whether improving cART adherence could affect residual inflammation and associated morbidity and mortality rates should be investigated.
Funding Information
  • NIAID
  • National Cancer Institute
  • National Institute on Drug Abuse (NIDA)
  • National Institute of Mental Health (NIMH)
  • National Heart, Lung, and Blood Institute
  • National Institute on Deafness and Communication Disorders
  • National Center for Advancing Translational Sciences
  • NIH (UL1-TR001079)
  • Johns Hopkins University Institute for Clinical and Translational Research
  • NIH Roadmap for Medical Research
  • HIV Prevention Trials Network
  • NIAID
  • NIDA
  • NIMH
  • Office of AIDS Research, NIH (UM1-AI068613)
  • NIAID (K23 AI104315, K24 AI120834)