Lipid and glucose abnormalities and associated factors among children living with HIV in Asia

Tulathip Suwanlerk1, Dhanushi Rupasinghe2, Watsamon Jantarabenjakul3

  • 1TREAT Asia, amfAR - The Foundation for AIDS Research, Bangkok, Thailand.

Antiviral Therapy
|April 28, 2023
PubMed

Insights

Children on long-term HIV treatment face risks of abnormal cholesterol and glucose levels. Protease inhibitor use is linked to these metabolic issues, highlighting the need for monitoring and alternative treatments.

Area of Science:

  • Pediatric Infectious Diseases
  • Metabolic Disorders
  • HIV/AIDS Research

Background:

  • Children living with HIV (CLHIV) on prolonged antiretroviral therapy (ART) are susceptible to lipid and glucose abnormalities.
  • Assessing the prevalence and contributing factors of these metabolic disturbances is crucial for managing long-term health outcomes in this population.

Purpose of the Study:

  • To determine the prevalence of lipid and glucose abnormalities in a multicentre Asian paediatric HIV cohort.
  • To identify factors associated with these metabolic abnormalities, particularly the role of antiretroviral therapy (ART) and protease inhibitor (PI) use.

Main Methods:

  • A longitudinal study of 951 children living with HIV (CLHIV) across multiple Asian centres.
  • Lipid and glucose levels were assessed using defined clinical thresholds; logistic regression was employed to analyze associated factors, including PI exposure.

Main Results:

  • Over half of CLHIV exhibited dyslipidemia (hypercholesterolemia, low HDL, high LDL, hypertriglyceridemia), and 17% had hyperglycemia.
  • Female sex was associated with hypercholesterolemia.
  • Current or prior protease inhibitor (PI) use was significantly linked to various lipid abnormalities and hyperglycemia.

Conclusions:

  • A substantial proportion of CLHIV experience dyslipidemia and hyperglycemia.
  • Metabolic monitoring should be a routine component of pediatric HIV care.
  • The strong association between PI use and dyslipidemia underscores the importance of transitioning to integrase inhibitor-based regimens.
Abstract

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