Adiponectin and HIV-Lipodystrophy: Taking HAART
Abstract
Infection with HIV and consequent AIDS is a major public health problem affecting more than 40 million people worldwide. Successful combination therapy based on HIV protease inhibitors, reverse transcriptase inhibitors (both nucleoside analogs and nonnucleoside analogs), and fusion inhibitors, with the goal of complete suppression of viral replication and meaningful immune restoration [highly active antiretroviral therapy (HAART)], has improved the prognosis of patients to the point that long-term complications of treatment have become an important clinical concern. Such major complications that have emerged are metabolic and have been termed the “HIV-lipodystrophy syndrome,” although it is not clear that all of the described metabolic abnormalities are truly part of a single syndrome. These metabolic abnormalities were first associated with protease inhibitors, but both nonnucleoside analogs and at least one of the nucleoside analogs (stavudine) have also been implicated. The picture includes lipodystrophy, hypertriglyceride- and cholesterol-emia, and insulin resistance, with or without hyperglycemia (1, 2). This raises two major concerns. First is the specter of increased risk for cardiovascular disease, which could mitigate the prospect of longevity offered by HAART. Second is that cosmetic aspects as well as heightened concern about cardiovascular disease could impel patients to reject effective therapy. In this issue of Endocrinology, Xu et al. (3) describe a promising therapeutic approach in a mouse model of HIV-lipodystrophy.
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Lipodystrophy is highly prevalent in patients on highly active antiretroviral therapy, occurring in 40% to 80% of patients.
“Lipodystrophy, characterized by morphological (peripheral lipoatrophy, localized fat accumulation) and metabolic changes (hyperlipidemia, insulin resistance and hyperglycemia), is highly prevalent in patients on highly active antiretroviral therapy (HAART), occurring in 40% to 80% of patients [115].”
From Metformin: An Old But Still the Best Treatment for Type 2 Diabetes (2013) · cites this paper as [115]
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- Authors
- Kinlaw, W. B., & Marsh, B.
- Affiliations
- Dartmouth College (US)
- Corresponding author
- Kinlaw, William B.
- ORCID
- Kinlaw, William B.
- Venue
- Endocrinology
- Publisher
- The Endocrine Society
- Published
- 2004-02
- Volume
- 145
- Issue
- 2
- Pages
- 484-486
- ISSN
- 0013-7227 (ISSN-L)
- 1945-7170
- OpenAlex
- W2018963910
- Cited by
- 44
- References
- 32
- Citations by year
- 2026: 1 · 2025: 1 · 2023: 1 · 2022: 2 · 2020: 2 · 2018: 1 · 2017: 2 · 2016: 2 · 2015: 3 · 2014: 1 · 2013: 2 · 2012: 3
- FWCI
- 5.70
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Endocrinology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Emergency Medicine › HIV-related health complications and treatments
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
- Keywords
- adiponectin, highly active antiretroviral therapy, protease inhibitors, non-nucleoside reverse transcriptase inhibitors, stavudine, lipodystrophy, insulin resistance, hypertriglyceridemia, dyslipidemia, hyperglycemia, cardiovascular risk, mouse model
- MeSH terms
- Acquired Immunodeficiency Syndrome, Animals, Cardiovascular Diseases, DNA-Binding Proteins, Humans, Insulin Resistance, Proteins, Transcription Factors, CCAAT-Enhancer-Binding Proteins, Antiretroviral Therapy, Highly Active, Intercellular Signaling Peptides and Proteins, HIV-Associated Lipodystrophy Syndrome, Mice, Sterol Regulatory Element Binding Protein 1, Adiponectin
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