The metabolic syndrome, an epidemic among HIV-infected patients on HAART
Summary Background HAART has dramatically changed the prognosis of AIDS, but has led to long-term toxicities of antiretroviral drugs. A major chronic complication is the metabolic syndrome (MS), including hyperlipidemia, lipodystrophy (LD), and impaired glucose metabolism. Methods A cross-sectional...
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Published in: | Biomedicine & pharmacotherapy Vol. 63; no. 5; pp. 337 - 342 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Paris
Elsevier SAS
01-06-2009
Elsevier |
Subjects: | |
Online Access: | Get full text |
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Summary: | Summary Background HAART has dramatically changed the prognosis of AIDS, but has led to long-term toxicities of antiretroviral drugs. A major chronic complication is the metabolic syndrome (MS), including hyperlipidemia, lipodystrophy (LD), and impaired glucose metabolism. Methods A cross-sectional study of a series of 582 patients from the Serbian HIV/AIDS cohort, treated with HAART for a mean period of 3.3 ± 2.1 years (range 1–10), was performed to evaluate the prevalence and risk factors for MS during HAART. Results The prevalence of LD was 29.1%, with a 100% probability of development after 10 years of treatment. Risk factors for LD included female gender (OR 1.7, 95% CI 1.0–2.7, P = 0.02), age > 40 (OR 1.7, 95% CI 1.1–2.7, P = 0.01) and AIDS at HAART initiation (OR 1.9, 95% CI 1.2–2.2, P < 0.01), as well as prolonged usage of NRTIs (OR 2.7, 95% CI 1.6–4.5, P < 0.01). The NNRTI-based regimens were less likely to induce LD than those PI-based (OR 1.87, 95% CI 1.2–2.9 vs. OR 3.7, 95% CI 2.3–6.1, respectively). Hyperlipidemia occurred in 47% of the patients, and was associated with male gender (OR 2.2, 95% CI 1.4–3.5, P < 0.01) and prolonged usage of PI + NNRTI HAART (OR 3.0, 95% CI 1.8–4.9, P < 0.01). In contrast, regimens composed of 2 NRTI + NNRTI were less likely to induce hyperlipidemia (OR 0.4, 95% CI 0.3–0.7, P = 0.03). Glucose intolerance and/or diabetes mellitus was recorded in 9.6%, if with AIDS at HAART initiation (OR 3.7, 95% CI 1.2–11.4, P < 0.01), male gender (OR 5.2, 95% CI 1.8–15.1, P < 0.01) and age > 40 (OR 2.6, 95% CI 1.1–6.3, P = 0.02). Conclusion MS seems an inevitable consequence of long-term successful HAART. |
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ISSN: | 0753-3322 1950-6007 |
DOI: | 10.1016/j.biopha.2008.09.011 |