Genetic markers of oxidative stress and coronary atherosclerosis
Autor: | Igor Tchivilev, Marschall S. Runge, Nageswara R. Madamanchi |
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Rok vydání: | 2006 |
Předmět: |
Genetic Markers
Glutathione reductase Coronary Artery Disease Oxidative phosphorylation Mitochondrion medicine.disease_cause Models Biological medicine Animals Humans Genetic Predisposition to Disease Coronary atherosclerosis Genetics chemistry.chemical_classification Reactive oxygen species Polymorphism Genetic biology Paraoxonase Mitochondria Heme oxygenase Oxidative Stress chemistry Heme Oxygenase (Decyclizing) biology.protein Nitric Oxide Synthase Reactive Oxygen Species Cardiology and Cardiovascular Medicine Oxidative stress |
Zdroj: | Current Atherosclerosis Reports. 8:177-183 |
ISSN: | 1534-6242 1523-3804 |
DOI: | 10.1007/s11883-006-0071-3 |
Popis: | Atherosclerosis, the primary cause of coronary artery disease (CAD), is a multifactorial disease, the molecular etiology of which involves interaction of many genes and environmental factors. Reactive oxygen species are integral to many cellular and biomolecular processes that are active in the transition of incipient fatty streaks into acute coronary syndromes. Animal models of atherosclerosis and correlative data from human studies support the oxidative stress hypothesis of atherosclerosis. However, the association of genetic polymorphisms that underlie enhanced oxidative stress with CAD is controversial. In this review, we discuss polymorphisms in genes that are main sources of reactive oxygen species generation (NAD[P]H oxidase, endothelial nitric oxide synthase, and myeloperoxidase) in mitochondria and the antioxidant enzymes paraoxonase, glutathione reductase, and heme oxygenase. The contribution of defined genetic variants involved in oxidative homeostasis to human atherosclerosis susceptibility is modest because regulation of oxidative stress is multifactorial. However, the contribution of genetic haplotypes in concert with environmental factors is likely significant. A more rigorous characterization of genetic and oxidative phenotypes together with characterization of novel gene polymorphisms may help in early therapeutic intervention for CAD. |
Databáze: | OpenAIRE |
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