|Title||Vitamin intake: a possible determinant of plasma homocyst(e)ine among middle-aged adults.|
|Publication Type||Journal Article|
|Year of Publication||1997|
|Authors||Shimakawa T, Nieto FJ, Malinow MR, Chambless LE, Schreiner PJ, Szklo M|
|Date Published||1997 May|
|Keywords||Analysis of Variance, Arteriosclerosis, Carotid Arteries, Case-Control Studies, Diet, Female, Folic Acid, Homocysteine, Humans, Male, Middle Aged, Nutrition Surveys, Pyridoxine, Regression Analysis, Sampling Studies, United States, Vitamin B 12|
PURPOSE: Many epidemiologic studies have identified elevated plasma homocyst(e)ine as a risk factor for atherosclerosis and thromboembolic disease. To examined the relationship between vitamin intakes and plasma homocyst(e)ine, we analyzed dietary intake data from a case-control study of 322 middle-aged individuals with atherosclerosis in the carotid artery and 318 control subjects without evidence of this disease.
METHODS: All of these individuals were selected from a probability sample of 15,800 men and women who participated in the Atherosclerosis Risk in Communities (ARIC) Study.
RESULTS: Plasma homocyst(e)ine was inversely associated with intakes of folate, vitamin B6, and vitamin B12 (controls only for this vitamin)--the three key vitamins in homocyst(e)ine metabolism. Among nonusers of vitamin supplement products, on average each tertile increase in intake of these vitamins was associated with 0.4 to 0.7 mumol/L decrease in plasma homocyst(e)ine. An inverse association of plasma homocyst(e)ine was also found with thiamin, riboflavin, calcium, phosphorus, and iron. Methionine and protein intake did not show any significant association with plasma homocyst(e)ine.
CONCLUSIONS: In almost all analyses, cases and controls showed similar associations between dietary variables and plasma homocyst(e)ine. Plasma homocyst(e)ine among users of vitamin supplement products was 1.5 mumol/L lower than that among nonusers. Further studies to examine possible causal relationships among vitamin intake, plasma homocyst(e)ine, and cardiovascular disease are needed.
|Alternate Journal||Ann Epidemiol|
|Grant List||N01-HC-55016 / HC / NHLBI NIH HHS / United States |
N01-HC-55018 / HC / NHLBI NIH HHS / United States
N01-HC55015 / HC / NHLBI NIH HHS / United States