Differential subcutaneous adipose tissue gene expression patterns in a randomized clinical trial of efavirenz or lopinavir-ritonavir in antiretroviral-naive patients

Antimicrob Agents Chemother. 2014 Nov;58(11):6717-23. doi: 10.1128/AAC.03481-14. Epub 2014 Aug 25.

Abstract

Gene expression studies of subcutaneous adipose tissue may help to better understand the mechanisms behind body fat changes in HIV-infected patients who initiate antiretroviral therapy (ART). Here, we evaluated early changes in adipose tissue gene expression and their relationship to fat changes in ART-naive HIV-infected patients randomly assigned to initiate therapy with emtricitabine/tenofovir plus efavirenz (EFV) or ritonavir-boosted lopinavir (LPV/r). Patients had abdominal subcutaneous adipose tissue biopsies at baseline and week 16 and dual-energy-X-ray absorptiometry at baseline and weeks 16 and 48. mRNA changes of 11 genes involved in adipogenesis, lipid and glucose metabolism, mitochondrial energy, and inflammation were assessed through reverse transcription-quantitative PCR (RT-qPCR). Additionally, correlations between gene expression changes and fat changes were evaluated. Fat increased preferentially in the trunk with EFV and in the limbs with LPV/r (P < 0.05). After 16 weeks of exposure to the drug regimen, transcripts of CEBP/A, ADIPOQ, GLUT4, LPL, and COXIV were significantly down-regulated in the EFV arm compared to the LPV/r arm (P < 0.05). Significant correlations were observed between LPL expression change and trunk fat change at week 16 in both arms and between CEBP/A or COXIV change and trunk fat change at the same time point only in the EFV arm and not in the LPV/r arm. When combined with emtricitabine/tenofovir as standard backbone therapy, EFV and LPV/r induced differential early expression of genes involved in adipogenesis and energy metabolism. Moreover, these mRNA expression changes correlated with trunk fat change in the EFV arm. (This was a substudy of a randomized clinical trial [LIPOTAR study] registered at ClinicalTrials.gov under identifier NCT00759070.).

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acquired Immunodeficiency Syndrome / drug therapy
  • Acquired Immunodeficiency Syndrome / virology
  • Adenine / analogs & derivatives
  • Adenine / therapeutic use
  • Adipogenesis / genetics*
  • Adiponectin / biosynthesis
  • Adult
  • Alkynes
  • Anti-HIV Agents / therapeutic use
  • Benzoxazines / therapeutic use*
  • Body Composition / drug effects*
  • CCAAT-Enhancer-Binding Proteins / biosynthesis
  • Cyclopropanes
  • Deoxycytidine / analogs & derivatives
  • Deoxycytidine / therapeutic use
  • Drug Combinations
  • Emtricitabine
  • Energy Metabolism / genetics
  • Female
  • Gene Expression
  • Glucose / metabolism
  • Glucose Transporter Type 4 / biosynthesis
  • HIV-1 / drug effects
  • Humans
  • Inflammation / genetics
  • Lipid Metabolism / genetics
  • Lipoprotein Lipase / genetics
  • Lopinavir / therapeutic use*
  • Male
  • Organophosphonates / therapeutic use
  • Reverse Transcriptase Inhibitors / therapeutic use
  • Ritonavir / therapeutic use*
  • Subcutaneous Fat / cytology*
  • Tenofovir

Substances

  • ADIPOQ protein, human
  • Adiponectin
  • Alkynes
  • Anti-HIV Agents
  • Benzoxazines
  • CCAAT-Enhancer-Binding Proteins
  • CEBPA protein, human
  • Cyclopropanes
  • Drug Combinations
  • Glucose Transporter Type 4
  • Organophosphonates
  • Reverse Transcriptase Inhibitors
  • SLC2A4 protein, human
  • lopinavir-ritonavir drug combination
  • Deoxycytidine
  • Lopinavir
  • Tenofovir
  • LPL protein, human
  • Lipoprotein Lipase
  • Emtricitabine
  • Glucose
  • Adenine
  • efavirenz
  • Ritonavir

Associated data

  • ClinicalTrials.gov/NCT00759070