Abstract | OBJECTIVE: DESIGN AND METHODS: RESULTS: A rapid and significant decrease of 46% (5.81 +/- 4 mmol/L vs. 3.16 +/- 2.6 mmol/L, P = 0.002) in triglyceride levels was shown. Similarly, a sustained improvement of 18% was observed in total cholesterol levels during the first 24 weeks after switching to atazanavir (6.45 +/- 1.9 mmol/L vs. 5.3 +/- 1.3 mmol/L, P = 0.001). After 24 weeks of treatment there was a significant decrease of 22% in non- HDL cholesterol (5.76 +/- 1.9 mmol/L at baseline vs. 4.5 +/- 1.3 mmol/L at 24 weeks; P = 0.003). HDL and LDL cholesterol profiles did not change significantly as did the viral load or CD4 cell count. CONCLUSIONS: Switching to atazanavir results in a significant improvement in HIV therapy-induced hyperlipidemia. A switch to atazanavir is proposed as a valuable option to improve atherogenic lipid profiles while maintaining virologic control.
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Authors | Ulrike Möbius, Margrit Lubach-Ruitman, Brigitte Castro-Frenzel, Matthias Stoll, Stefan Esser, Esther Voigt, Stefan Christensen, Jörg-Andres Rump, Gerd Fätkenheuer, Georg M N Behrens, Reinhold E Schmidt |
Journal | Journal of acquired immune deficiency syndromes (1999)
(J Acquir Immune Defic Syndr)
Vol. 39
Issue 2
Pg. 174-80
(Jun 01 2005)
ISSN: 1525-4135 [Print] United States |
PMID | 15905733
(Publication Type: Clinical Trial, Comparative Study, Controlled Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Oligopeptides
- Pyridines
- Triglycerides
- Atazanavir Sulfate
- Cholesterol
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Topics |
- Adolescent
- Adult
- Antiretroviral Therapy, Highly Active
(adverse effects)
- Atazanavir Sulfate
- Cholesterol
(blood)
- Cohort Studies
- Female
- HIV Infections
(drug therapy)
- Humans
- Hypercholesterolemia
(epidemiology, prevention & control)
- Hyperlipidemias
(epidemiology, prevention & control)
- Hypertriglyceridemia
(epidemiology, prevention & control)
- Male
- Middle Aged
- Oligopeptides
(therapeutic use)
- Pyridines
(therapeutic use)
- Triglycerides
(blood)
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