Is HIV a model of accelerated or accentuated aging?

J Gerontol A Biol Sci Med Sci. 2014 Jul;69(7):833-42. doi: 10.1093/gerona/glt168. Epub 2013 Oct 24.

Abstract

Background: Antiretroviral therapy has reduced the incidence of adverse events and early mortality in HIV-infected persons. Despite these benefits, important comorbidities that increase with age (eg, diabetes, cardiovascular disease, cancer, liver disease, and neurocognitive impairment) are more prevalent in HIV-infected persons than in HIV-uninfected persons at every age, and geriatric syndromes such as falls and frailty occur earlier in HIV-infected persons. This raises a critical research question: Does HIV accelerate aging through pathways and mechanisms common to the aging process or is HIV simply an additional risk factor for a wide number of chronic conditions, thus accentuating aging?

Methods: Extensive literature review.

Results: The purpose of this review is to briefly outline the evidence that age-related clinical syndromes are exacerbated by HIV, examine the ways in which HIV is similar, and dissimilar from natural aging, and assess the validity of HIV as a model of premature aging. Specific biomarkers of aging are limited in HIV-infected hosts and impacted by antiretroviral therapy, and a high rate of modifiable life style confounders (eg, smoking, substance abuse, alcohol) and coinfections (eg, hepatitis) in HIV-infected participants.

Conclusions: There is a need for validated biomarkers of aging in the context of HIV. Despite these differences, welldesigned studies of HIV-infected participants are likely to provide new opportunities to better understand the mechanisms that lead to aging and age-related diseases.

Keywords: AIDS; Biomarkers of aging; HIV; Immunosenescence; Multimorbidity.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Aging
  • Aging, Premature / epidemiology
  • Aging, Premature / etiology*
  • Aging, Premature / pathology
  • Biomarkers
  • Comorbidity
  • Cytomegalovirus Infections / complications
  • Digestive System / immunology
  • Digestive System / microbiology
  • Eye / pathology
  • Eye / physiopathology
  • HIV Infections / complications
  • HIV Infections / epidemiology
  • HIV Infections / etiology*
  • Humans
  • Models, Biological*
  • T-Lymphocytes / immunology

Substances

  • Biomarkers