Endoplasmic Reticulum Stress Clinical Trial
Official title:
Tauroursodeoxycholic Acid for Protease-inhibitor Associated Insulin Resistance
Rates of cardiovascular disease and diabetes are more than 2-fold greater in HIV infected people than the general population. Protease inhibitor booster antiretroviral therapy (PI-ART) which is used by ~50% of HIV infected people in the USA is an established risk factor for diabetes. Tauroursodeoxycholic acid (TUDCA), a naturally occurring bile salt, improves insulin sensitivity in HIV uninfected subjects, although the mechanisms for these benefits are unclear. This study will explore the hypothesis that TUDCA will improve insulin action in people with HIV who are receiving PI-ART. Further, this project will clarify the molecular mechanisms responsible for these improvements potentially benefiting society, irrespective of HIV status.
The purpose of this study is to determine if, and through which mechanisms,
tauroursodeoxycholic acid improves insulin sensitivity in subjects with protease-inhibitor
associated insulin resistance.
The investigators will perform body composition analysis by using a DEXA machine, liver fat
measurement by using an MRI, and hyperinsulinemic euglycemic clamp procedures in 48 HIV
infected, insulin-resistant/prediabetic subjects before and after 30 days of treatment with
tauroursodeoxycholic acid or matching placebo. Biopsies of adipose tissue and skeletal muscle
will be taken during fasting conditions and during insulin infusion, before and after
treatment to measure markers of endoplasmic reticulum stress and thyroid hormone deiodinase.
Outcome measures:
The primary outcome measures will be change in glucose clearance during insulin infusion,
change in markers of endoplasmic reticulum stress and change in content of D2 in muscle.
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