Higher Plasma Homocyst(e)ine and Increased Susceptibility to Adverse Effects of Low Folate in Early Familial Coronary Artery Disease
| Autor: | Roger R. Williams, Steven C. Hunt, Barbara James, G M Vincent, James T. Wu, Paul N. Hopkins, Lily L. Wu |
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| Rok vydání: | 1995 |
| Předmět: |
Adult
Male Vitamin medicine.medical_specialty Homocysteine Coronary Disease Folic Acid Deficiency Coronary artery disease chemistry.chemical_compound Folic Acid Risk Factors Internal medicine Blood plasma Humans Medicine Sibling Risk factor Adverse effect Aged business.industry Pyridoxine Middle Aged medicine.disease Homocyst(e)ine Vitamin B 12 Endocrinology chemistry Regression Analysis Female Cardiology and Cardiovascular Medicine business |
| Zdroj: | Arteriosclerosis, Thrombosis, and Vascular Biology. 15:1314-1320 |
| ISSN: | 1524-4636 1079-5642 |
| DOI: | 10.1161/01.atv.15.9.1314 |
| Popis: | Abstract To examine the graded risks for coronary artery disease (CAD) associated with plasma homocyst(e)ine [H(e)] and to evaluate the extent to which this risk is mediated by altered vitamin status, we measured plasma concentrations of H(e), vitamins B 6 and B 12 , and folate as well as other coronary risk factors in subjects with early familial CAD and in control subjects. We studied 120 male and 42 female patients with early CAD who were unrelated to each other but were from families in which at least one other sibling had early CAD. Control subjects were 85 men and 70 women with the same age range (38 to 68) as the subjects with CAD at screening. Increasing H(e) was associated with graded increased risks of CAD that appeared consistent with a multiplicative model. Relative odds for CAD were approximately 12.8 in women when those with H(e) levels of 19 μmol/L and above were compared with those with H(e) levels of 9 μmol/L or less ( P =.007). For men, the same comparison yielded relative odds of 13.8 ( P =.0002). Plasma H(e) remained a strong, independent risk factor after adjustment for standard risk factors and plasma vitamin levels in multiple logistic regression (relative odds, 8.1 for a 10-μmol/L increase in H(e); 95% confidence interval, 3.2 to 20.4; P P =.0035). These data suggest that high plasma H(e) is an important, independent contributor to risk for early familial CAD. Furthermore, subjects with early familial CAD who had low plasma folate levels had exaggerated elevations in plasma H(e), suggesting a possible genetic sensitivity to the detrimental effects of lower folate intake. |
| Databáze: | OpenAIRE |
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