Additional attention to combination antiretroviral therapy-related lipodystrophy

The occurrence of lipodystrophy in patients taking anti-human immunodeficiency virus (HIV) medications is a serious problem as it is irreversible even after drug withdrawal. Although it was first recognized in patients taking proteinase inhibitors, other types of anti-HIV agents can also cause lipod...

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Bibliographic Details
Published inWorld Journal of Virology Vol. 6; no. 3; pp. 49 - 52
Main Authors Kobayashi, Norihiko, Nakahara, Masako, Oka, Masako, Saeki, Kumiko
Format Journal Article
LanguageEnglish
Japanese
Published United States Baishideng Publishing Group Inc 12.08.2017
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Summary:The occurrence of lipodystrophy in patients taking anti-human immunodeficiency virus (HIV) medications is a serious problem as it is irreversible even after drug withdrawal. Although it was first recognized in patients taking proteinase inhibitors, other types of anti-HIV agents can also cause lipodystrophy. In a recent publication by Jones et al entitled "Highly active antiretroviral therapy dysregulates proliferation and differentiation of human pre-adipocytes" in , it was reported that simultaneous treatment of human subcutaneous adipocytes with anti-HIV drugs with different mechanisms of action synergistically exerted anti-adipogenesis effects , warning us to take utmost care in every case receiving combination antiretroviral therapy (cART). For elucidation of the molecular basis for cART-related lipodystrophy, multi-faceted approaches should be taken, based on a deeper understanding of the development and organization of adipose tissues.
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Telephone: +81-3-32027181 Fax: +81-3-32071038
Correspondence to: Kumiko Saeki, MD, PhD, Department of Disease Control, Research Institute, National Center for Global Health and Medicine, 1-21-1, Toyama, Shinjuku-ku, Tokyo 162-8655, Japan. saeki@ri.ncgm.go.jp
Author contributions: Kobayashi N, Nakahara M and Oka M collected the materials and wrote the manuscript; Saeki K supervised the publication of this commentary.
ISSN:2220-3249
2220-3249
DOI:10.5501/wjv.v6.i3.49