Prevalence and predictors of glucose metabolism disorders among People Living with HIV on combination antiretroviral therapy

PLoS One. 2022 Jan 19;17(1):e0262604. doi: 10.1371/journal.pone.0262604. eCollection 2022.

Abstract

Objective: We investigated prevalence and predictors of glucose metabolism disorders (GMDs) among People Living with HIV (PLWH) on efavirenz- and atazanavir/ritonavir-based combination antiretroviral therapy (cART).

Methods: This cross-sectional study involved adult PLWH on efavirenz- (n = 240) and atazanavir/ritonavir-based (n = 111) cART. The prevalence of GMDs was determined by fasting serum glucose, insulin, and homeostasis model assessment. A logistic regression model was used to determine predictors.

Results: The overall prevalence of GMDs for all regimens was 27.6% (97/351) [95% CI 23.0-32.6%] s, with 31.1% (75/240) [95% CI 25.4-37.5%] for efavirenz-based and 19.8% (22/111) [95% CI 12.9-28.5%)] for atazanavir/ritonavir-based cART group. The prevalence of impaired fasting glycemia was significantly higher (p = 0.026) in the efavirenz- [(15.4%) (37/240); 95%CI (11.1-20.6%)] than atazanavir/ritonavir-based [(7.2%) (8/111), (95%CI (3.2-13.7%)] cART. However, no significant difference was observed in the prevalence of diabetes mellitus and insulin resistance between the two regimens. Age ≥46 years old and specific type of ARV contained in cART, such as TDF, were independent predictors of GMD in both groups. Whereas the male gender and BMI category were predictors of GMDs among EFV-based cART group, AZT- and ABC- containing regimens and triglyceride levels were predictors in the ATV/r-based group.

Conclusions: GMDs were highly prevalent among adults on EFV- than ATV/r-based cARTs. Age ≥46 years and TDF-containing cARTs are common predictors in both regimens. Close monitoring for impaired fasting glucose during long-term EFV-based cART is recommended for early diagnosis of type-2 diabetes and management.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alkynes / therapeutic use
  • Anti-HIV Agents / therapeutic use
  • Antiretroviral Therapy, Highly Active / methods
  • Atazanavir Sulfate / therapeutic use
  • Benzoxazines / therapeutic use
  • Blood Glucose / analysis
  • Cross-Sectional Studies
  • Cyclopropanes / therapeutic use
  • Drug Combinations
  • Drug Therapy, Combination / adverse effects*
  • Drug Therapy, Combination / methods
  • Ethiopia / epidemiology
  • Female
  • Glucose / metabolism
  • Glucose Metabolism Disorders / epidemiology*
  • Glucose Metabolism Disorders / virology
  • HIV / pathogenicity
  • HIV Infections / metabolism*
  • Humans
  • Insulin / metabolism
  • Male
  • Prevalence
  • Ritonavir / therapeutic use

Substances

  • Alkynes
  • Anti-HIV Agents
  • Benzoxazines
  • Blood Glucose
  • Cyclopropanes
  • Drug Combinations
  • Insulin
  • atazanavir, ritonavir drug combination
  • Atazanavir Sulfate
  • Glucose
  • efavirenz
  • Ritonavir

Grants and funding

This work is funded by Office of the Graduate program of Addis Ababa University. WT is recipient of the grant (GPO/275/12/20). The URL of the funder is www.aau.edu.et. The funder did not have any role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The Swedish Research Council (Vetenskapsrådet) and the European and Developing countries Clinical Trials Partnership (EDCTP) also granted fellowship and stipend to WT.