Predictors of transitions in frailty severity and mortality among people aging with HIV

PLoS One. 2017 Oct 5;12(10):e0185352. doi: 10.1371/journal.pone.0185352. eCollection 2017.

Abstract

Background: People aging with HIV show variable health trajectories. Our objective was to identify longitudinal predictors of frailty severity and mortality among a group aging with HIV.

Methods: Exploratory analyses employing a multistate transition model, with data from the prospective Modena HIV Metabolic Clinic Cohort Study, based in Northern Italy, begun in 2004. Participants were followed over four years from their first available visit. We included all 963 participants (mean age 46.8±7.1; 29% female; 89% undetectable HIV viral load; median current CD4 count 549, IQR 405-720; nadir CD4 count 180, 81-280) with four-year data. Frailty was quantified using a 31-item frailty index. Outcomes were frailty index score or mortality at four-year follow-up. Candidate predictor variables were baseline frailty index score, demographic (age, sex), HIV-disease related (undetectable HIV viral load, current CD4+ T-cell count, nadir CD4 count, duration of HIV infection, and duration of antiretroviral therapy [ARV] exposure), and behavioral factors (smoking, injection drug use (IDU), and hepatitis C virus co-infection).

Results: Four-year mortality was 3.0% (n = 29). In multivariable analyses, independent predictors of frailty index at follow-up were baseline frailty index (RR 1.06, 95% CI 1.05-1.07), female sex (RR 0.93, 95% CI 0.87-0.98), nadir CD4 cell count (RR 0.96, 95% CI 0.93-0.99), duration of HIV infection (RR 1.06, 95% CI 1.01-1.12), duration of ARV exposure (RR 1.08, 95% CI 1.02-1.14), and smoking pack-years (1.03, 1.01-1.05). Independent predictors of mortality were baseline frailty index (OR 1.19, 1.02-1.38), current CD4 count (0.34, 0.20-0.60), and IDU (2.89, 1.30-6.42).

Conclusions: Demographic, HIV-disease related, and social and behavioral factors appear to confer risk for changes in frailty severity and mortality among people aging with HIV.

MeSH terms

  • Adult
  • Aging*
  • Female
  • HIV Infections / complications
  • HIV Infections / mortality*
  • HIV Infections / physiopathology*
  • Humans
  • Male
  • Middle Aged
  • Models, Theoretical
  • Multivariate Analysis

Grants and funding

TDB was supported by a Canadian Institutes of Health Research Summer Research Studentship and an award from the Dalhousie University Internal Medicine Research Foundation. GG was partially supported by 'Co-morbidity in relation to AIDS' grant agreement (305522), European Union Seventh Framework. KR is supported by the Dalhousie Medical Research Foundation through the Kathryn Allen Weldon Chain in Alzheimer Research. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.