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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Abu-Amero, Khaled K. Al-Boudari, Olyan M. Mousa, Ahmed Gonzalez, Ana M. Larruga, Jose M. Cabrera, Vicente M. Dzimiri, Nduna |
| Spatial Coverage | Saudi Arabia |
| Description | Country affiliation: Saudi Arabia Author Affiliation: Abu-Amero KK ( Molecular Genetics Laboratory, Department of Ophthalmology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.) |
| Abstract | By virtue of the functional role of the mitochondrion in energy and reactive oxygen species production, mutations in mitochondrial DNA (mtDNA) are potential candidates for cardiovascular-related disorders. Further, the mtDNA is extremely polymorphic and several diagnostic single-nucleotide polymorphisms have been used to assort sequences into haplogroups with defined continental and regional ranges. However, the relevance of these haplogroups and mutations with respect to coronary artery disease (CAD) susceptibility remains unclear. In this study, we evaluated the role of the 16189T>C variants and mtDNA haplogroups as predisposing factors for CAD in 669 Saudi patients with angiographically established disease compared with 258 disease-free controls. The 16189T>C was associated with CAD (1.524 [1.076-2.159]; p = 0.017). However, this association was influenced by age as well as the presence of myocardial infarction and hypertension. Among the haplogroups, only the N1c showed a borderline protective relationship (p = 0.074) with CAD as an independent risk factor. This association turned significant in the total sample (0.176 [0.042-0.736]; p = 0.017) and in the <50-year age group (0.075 [0.008-0.743]; p = 0.027), when included as a possible confounding factor. Our results suggested that the impact of mtDNA polymorphism on CAD manifestation is influenced by important confounders, particularly the presence of myocardial infarction, hypertension, and age. |
| File Format | HTM / HTML |
| ISSN | 19450265 |
| Issue Number | 1 |
| Volume Number | 14 |
| e-ISSN | 19450257 |
| Journal | Genetic Testing and Molecular Biomarkers |
| Language | English |
| Publisher | Mary Ann Liebert |
| Publisher Date | 2010-02-01 |
| Publisher Place | United States |
| Access Restriction | Subscribed |
| Subject Keyword | Discipline Genetics Discipline Molecular Biology Coronary Artery Disease Genetics Dna, Mitochondrial Myocardial Infarction Polymorphism, Single Nucleotide Adult Arabs Case-control Studies Etiology Female Genetic Predisposition To Disease Haplotypes Humans Hypertension Complications Male Middle Aged Saudi Arabia Journal Article Research Support, Non-u.s. Gov't |
| Content Type | Text |
| Resource Type | Article |
| Subject | Genetics (clinical) |
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