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Published on: January 7, 2018
Insulin Resistance and the cardiometabolic syndrome in HIV infection
Maurizio Bevilacqua1, Ligia J Dominguez, Mario Barbagallo
1Endocrinology and Diabetes Unit, Department of Medicine, Luigi Sacco Hospital (Vialba), University of Milan, Milan, Italy. mauriziobevilacqua@fastwebnet.it
Insights
Highly active antiretroviral therapy (HAART) improves HIV prognosis but can cause metabolic issues like insulin resistance (IR) and lipodystrophy. Lifestyle changes and specific medications may help manage these adverse effects.
Area of Science:
- Internal Medicine
- Infectious Diseases
- Endocrinology
Background:
- Highly active antiretroviral therapy (HAART) significantly improves outcomes for HIV-positive individuals.
- Long-term HAART use is associated with adverse metabolic effects, including dyslipidemia, insulin resistance (IR), lipodystrophy, and cardiometabolic syndrome (CMS).
Purpose of the Study:
- To evaluate the impact of HAART on metabolic complications in HIV patients.
- To explore strategies for managing insulin resistance and associated conditions in this population.
Main Methods:
- Review of literature concerning HAART, metabolic side effects, and management strategies.
- Analysis of the relationship between specific antiretroviral drug classes and metabolic alterations.
Main Results:
- Insulin resistance (IR) in HIV patients may not be an independent cardiovascular risk factor but contributes to increased risk when combined with dyslipidemia, fat redistribution, and CMS.
- Nucleoside analogue reverse transcriptase inhibitors are linked to visceral fat accumulation and IR.
- Lifestyle modifications and judicious HAART regimen selection can mitigate IR progression.
Conclusions:
- Managing IR and associated metabolic complications is crucial for improving the long-term health of HIV-positive patients on HAART.
- Metformin and exercise may benefit patients with significant IR and preserved fat distribution, while rosiglitazone is not recommended.
Abstract:
Highly active antiretroviral therapy (HAART) has dramatically improved the prognosis of HIV-positive patients. However, long-term adverse effects of this therapy include dyslipidemia, insulin resistance (IR), changes in body fat distribution (lipodystrophy), and cardiometabolic syndrome (CMS). IR in HIV-positive patients does not seem to represent a significant independent risk factor for the development of cardiovascular disease; nevertheless, the association with other metabolic complications (dyslipidemia, fat redistribution) and CMS may increase the risk of type 2 diabetes and cardiovascular disease. The use of nucleoside analogue reverse transcriptase inhibitors is associated with the development of upper trunk and visceral fat accumulation and may cause IR. The progression of IR toward diabetes may be impeded with the choice of HAART regimens with less IR effects and encouraging patients to adhere to a healthy lifestyle. For patients with marked IR but relatively preserved fat, the use of metformin may consent the improvement of CMS and lipodystrophy, especially when combined with an appropriate exercise program. Therapy with rosiglitazone is not indicated in these patients.
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