1. In order to obtain further insight as to how NVP affects HDL metabolism, the in vivo kinetics of the HDL apolipoprotein, Apo A-1, before and 6 weeks after initiation of NVP containing treatment were evaluated. In addition, the activity of the key enzymes related to HDL metabolism were assessed. \[ Designated as safety issue: No \] 2. In order to determine the relevance of the HDL increase in decreasing cardiovascular risk in HIV-positive subjects we evaluated endothelial function (FMD) as a surrogate marker for cardiovascular disease in patients. \[ Designated as safety issue: No \]
Study Type
INTERVENTIONAL
Purpose
PREVENTION
Enrollment
15
1100.1426.01 Academic Medical Centre
Amsterdam, Netherlands
1100.1426.02 Onze Lieve Vrouwe Gasthuis
Amsterdam, Netherlands
1100.1426.44001 Boehringer Ingelheim Investigational Site
London, United Kingdom
Percentage change of fractional synthetic rate (FSR) of Apo A-1
Time frame: after 6 weeks of treatment
Percentage change of flow mediated dilatation (FMD)
Time frame: after 6 and 24 weeks of treatment
Percentage change in the proteins involved in HDL metabolism
Time frame: after 6 and 24 weeks of treatment
The percentage change in plasma levels of lipoproteins in the fasting lipid panel (TC, LDL, HDL, TG) from Week 0 (baseline) to 6 and 24 weeks of treatment with NVP-based antiretroviral therapy
Time frame: from week 0 to 6, and 24 weeks of treatment
The percentage change in activity (and/or mass) of the constituents of the lipid enzymes panel from Week 0 to 24 weeks of NVP-based antiretroviral therapy
Time frame: from week 0 to 24 weeks of treatment
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