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The metabolic syndrome, an epidemic among HIV-infected patients on HAART
D J Jevtović1, G Dragović, D Salemović
1Institute for Infectious and Tropical Diseases, Clinical Centre of Serbia, Belgrade University School of Medicine, Belgrade, Serbia. djordjejevtovic@hotmail.com
Insights
Metabolic syndrome (MS) is a common complication of highly active antiretroviral therapy (HAART) for HIV/AIDS. Long-term HAART use increases the risk of lipodystrophy, hyperlipidemia, and glucose intolerance, suggesting MS is an inevitable consequence.
Area of Science:
- Infectious Diseases
- Endocrinology
- Pharmacology
Background:
- Highly active antiretroviral therapy (HAART) has improved HIV/AIDS prognosis but causes long-term drug toxicities.
- Metabolic syndrome (MS), including hyperlipidemia, lipodystrophy (LD), and impaired glucose metabolism, is a significant chronic complication.
Purpose of the Study:
- To evaluate the prevalence and risk factors for MS in patients receiving long-term HAART.
- To identify specific antiretroviral drug classes and patient characteristics associated with MS development.
Main Methods:
- A cross-sectional study of 582 patients from the Serbian HIV/AIDS cohort was conducted.
- Patients had a mean HAART duration of 3.3 years (range 1-10).
- Prevalence and risk factors for LD, hyperlipidemia, and glucose intolerance were analyzed.
Main Results:
- Lipodystrophy (LD) prevalence was 29.1%, with risk factors including female gender, age >40, AIDS at HAART initiation, and NRTI use. PI-based regimens were more likely to induce LD than NNRTI-based ones.
- Hyperlipidemia affected 47% of patients, associated with male gender and prolonged PI+NNRTI use. NRTI+NNRTI regimens were less likely to induce hyperlipidemia.
- Glucose intolerance/diabetes occurred in 9.6%, linked to AIDS at HAART initiation, male gender, and age >40.
Conclusions:
- Metabolic syndrome (MS) appears to be an unavoidable consequence of successful long-term HAART.
- Understanding risk factors and drug-specific toxicities is crucial for managing MS in HIV/AIDS patients on HAART.
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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