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Switch to Raltegravir From Protease Inhibitor or Nonnucleoside Reverse-Transcriptase Inhibitor Does not Reduce Visceral Fat In Human Immunodeficiency Virus-Infected Women With Central Adiposity
Author(s) -
Jordan E. Lake,
Grace A. McComsey,
Todd Hulgan,
Christine Wanke,
Alexandra Mangili,
Sharon Walmsley,
Judith S. Currier
Publication year - 2015
Publication title -
open forum infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.546
H-Index - 35
ISSN - 2328-8957
DOI - 10.1093/ofid/ofv059
Subject(s) - raltegravir , medicine , adipose tissue , integrase inhibitor , virology , protease inhibitor (pharmacology) , human immunodeficiency virus (hiv) , reverse transcriptase inhibitor , lipodystrophy , reverse transcriptase , antiretroviral therapy , viral load , polymerase chain reaction , biology , gene , biochemistry
Human immunodeficiency virus-infected women with central adiposity switched to raltegravir-based antiretroviral therapy immediately or after 24 weeks. No statistically significant changes in computed tomography-quantified visceral adipose tissue (VAT) or subcutaneous fat were observed, although 48 weeks of raltegravir was associated with a 6.4% VAT decline. Raltegravir for 24 weeks was associated with improvements in lipids.

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