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Simvastatin and oxidative stress in humans: A randomized, double-blinded, placebo-controlled clinical trial
Simvastatin reduces the blood concentration of cholesterol by inhibiting hydroxymethylglutaryl-coenzyme A reductase, the rate-limiting enzyme in cholesterol synthesis, and thereby reduces the risk of cardiovascular disease. In addition, simvastatin treatment leads to a reduction in fluxes in mitocho...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906137/ https://www.ncbi.nlm.nih.gov/pubmed/27281490 http://dx.doi.org/10.1016/j.redox.2016.05.007 |
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author | Rasmussen, Sanne Tofte Andersen, Jon Trærup Nielsen, Torben Kjær Cejvanovic, Vanja Petersen, Kasper Meidahl Henriksen, Trine Weimann, Allan Lykkesfeldt, Jens Poulsen, Henrik Enghusen |
author_facet | Rasmussen, Sanne Tofte Andersen, Jon Trærup Nielsen, Torben Kjær Cejvanovic, Vanja Petersen, Kasper Meidahl Henriksen, Trine Weimann, Allan Lykkesfeldt, Jens Poulsen, Henrik Enghusen |
author_sort | Rasmussen, Sanne Tofte |
collection | PubMed |
description | Simvastatin reduces the blood concentration of cholesterol by inhibiting hydroxymethylglutaryl-coenzyme A reductase, the rate-limiting enzyme in cholesterol synthesis, and thereby reduces the risk of cardiovascular disease. In addition, simvastatin treatment leads to a reduction in fluxes in mitochondrial respiratory complexes I and II and might thereby reduce the formation of reactive oxygen species, which have been implicated in the pathogenesis of arteriosclerosis. Therefore, we hypothesized that simvastatin may reduce oxidative stress in humans in vivo. We conducted a randomized, double-blinded, placebo-controlled study in which subjects were treated with either 40 mg of simvastatin or placebo for 14 days. The endpoints were six biomarkers for oxidative stress, which represent intracellular oxidative stress to nucleic acids, lipid peroxidation and plasma antioxidants, that were measured in urine and plasma samples. A total of 40 participants were included, of which 39 completed the trial. The observed differences between simvastatin and placebo groups in the primary outcomes, DNA and RNA oxidation, were small and nonsignificant (p=0.68), specifically, 3% in the simvastatin group compared to 7.1% in the placebo group for DNA oxidation and 7.3% in the simvastatin group compared to 3.4% in the placebo group. The differences in biomarkers related to plasma were not statistically significant between the treatments groups, with the exception of total vitamin E levels, which, as expected, were reduced in parallel with the reduction in plasma cholesterol. In healthy young male volunteers, short-term simvastatin treatment, which considerably reduces cholesterol, does not lead to a clinically relevant reduction in a panel of measures of oxidative stress. Whether simvastatin has effects on oxidative stress in diseased populations, such as diabetes or hemochromatosis, where oxidative stress is prominent, is unknown but seems unlikely. |
format | Online Article Text |
id | pubmed-4906137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-49061372016-06-21 Simvastatin and oxidative stress in humans: A randomized, double-blinded, placebo-controlled clinical trial Rasmussen, Sanne Tofte Andersen, Jon Trærup Nielsen, Torben Kjær Cejvanovic, Vanja Petersen, Kasper Meidahl Henriksen, Trine Weimann, Allan Lykkesfeldt, Jens Poulsen, Henrik Enghusen Redox Biol Research Paper Simvastatin reduces the blood concentration of cholesterol by inhibiting hydroxymethylglutaryl-coenzyme A reductase, the rate-limiting enzyme in cholesterol synthesis, and thereby reduces the risk of cardiovascular disease. In addition, simvastatin treatment leads to a reduction in fluxes in mitochondrial respiratory complexes I and II and might thereby reduce the formation of reactive oxygen species, which have been implicated in the pathogenesis of arteriosclerosis. Therefore, we hypothesized that simvastatin may reduce oxidative stress in humans in vivo. We conducted a randomized, double-blinded, placebo-controlled study in which subjects were treated with either 40 mg of simvastatin or placebo for 14 days. The endpoints were six biomarkers for oxidative stress, which represent intracellular oxidative stress to nucleic acids, lipid peroxidation and plasma antioxidants, that were measured in urine and plasma samples. A total of 40 participants were included, of which 39 completed the trial. The observed differences between simvastatin and placebo groups in the primary outcomes, DNA and RNA oxidation, were small and nonsignificant (p=0.68), specifically, 3% in the simvastatin group compared to 7.1% in the placebo group for DNA oxidation and 7.3% in the simvastatin group compared to 3.4% in the placebo group. The differences in biomarkers related to plasma were not statistically significant between the treatments groups, with the exception of total vitamin E levels, which, as expected, were reduced in parallel with the reduction in plasma cholesterol. In healthy young male volunteers, short-term simvastatin treatment, which considerably reduces cholesterol, does not lead to a clinically relevant reduction in a panel of measures of oxidative stress. Whether simvastatin has effects on oxidative stress in diseased populations, such as diabetes or hemochromatosis, where oxidative stress is prominent, is unknown but seems unlikely. Elsevier 2016-05-30 /pmc/articles/PMC4906137/ /pubmed/27281490 http://dx.doi.org/10.1016/j.redox.2016.05.007 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Rasmussen, Sanne Tofte Andersen, Jon Trærup Nielsen, Torben Kjær Cejvanovic, Vanja Petersen, Kasper Meidahl Henriksen, Trine Weimann, Allan Lykkesfeldt, Jens Poulsen, Henrik Enghusen Simvastatin and oxidative stress in humans: A randomized, double-blinded, placebo-controlled clinical trial |
title | Simvastatin and oxidative stress in humans: A randomized, double-blinded, placebo-controlled clinical trial |
title_full | Simvastatin and oxidative stress in humans: A randomized, double-blinded, placebo-controlled clinical trial |
title_fullStr | Simvastatin and oxidative stress in humans: A randomized, double-blinded, placebo-controlled clinical trial |
title_full_unstemmed | Simvastatin and oxidative stress in humans: A randomized, double-blinded, placebo-controlled clinical trial |
title_short | Simvastatin and oxidative stress in humans: A randomized, double-blinded, placebo-controlled clinical trial |
title_sort | simvastatin and oxidative stress in humans: a randomized, double-blinded, placebo-controlled clinical trial |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906137/ https://www.ncbi.nlm.nih.gov/pubmed/27281490 http://dx.doi.org/10.1016/j.redox.2016.05.007 |
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