Hyperhomocysteinemia, Endothelial Nitric Oxide Synthase Polymorphism, and Risk of Coronary Artery Disease
Author(s) -
Mohsen Kerkeni,
Faouzi Addad,
Maryline Chauffert,
Anne Myara,
Mohamed Ben Farhat,
Abdelhédi Miled,
Khira Maaroufi,
F Trivin
Publication year - 2005
Publication title -
clinical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.705
H-Index - 218
eISSN - 1530-8561
pISSN - 0009-9147
DOI - 10.1373/clinchem.2005.057950
Subject(s) - hyperhomocysteinemia , enos , coronary artery disease , homocysteine , medicine , genotype , gastroenterology , biology , endocrinology , cardiology , nitric oxide synthase , nitric oxide , genetics , gene
Hyperhomocysteinemia is an independent, graded risk factor for coronary artery disease (CAD). The G894T variant of endothelial nitric oxide synthase (eNOS) was postulated to be associated with hyperhomocysteinemia and could influence individual susceptibility to CAD. The aims of this study were to investigate (a) the relationship of the eNOS G894T polymorphism with the presence and the severity of CAD and (b) the possible relationship between hyperhomocysteinemia and the eNOS G894T variant for the risk of CAD severity in a Tunisian population.
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