Folate, Vitamin B 12 , and Risk of Ischemic and Hemorrhagic Stroke

Background and Purpose— Folate metabolism has been implicated in stroke. However, the possibility of a role for folate and vitamin B 12 , independent of their effects on homocysteine status, remains to be explored. The aim of this prospective, nested case-referent study was to relate plasma and diet...

Full description

Bibliographic Details
Published in:Stroke
Main Authors: Van Guelpen, Bethany, Hultdin, Johan, Johansson, Ingegerd, Stegmayr, Birgitta, Hallmans, Göran, K. Nilsson, Torbjörn, Weinehall, Lars, Witthöft, Cornelia, Palmqvist, Richard, Winkvist, Anna
Format: Article in Journal/Newspaper
Language:English
Published: Ovid Technologies (Wolters Kluwer Health) 2005
Subjects:
Online Access:http://dx.doi.org/10.1161/01.str.0000169934.96354.3a
https://www.ahajournals.org/doi/full/10.1161/01.STR.0000169934.96354.3a
Description
Summary:Background and Purpose— Folate metabolism has been implicated in stroke. However, the possibility of a role for folate and vitamin B 12 , independent of their effects on homocysteine status, remains to be explored. The aim of this prospective, nested case-referent study was to relate plasma and dietary intake levels of folate and vitamin B 12 to risk of stroke, taking into consideration plasma homocysteine concentrations and methylenetetrahydrofolate reductase polymorphisms. Methods— Subjects were 334 ischemic and 62 hemorrhagic stroke cases and matched double referents from the population-based Northern Sweden Health and Disease Cohort. Results— Plasma folate was statistically significantly associated with risk of hemorrhagic stroke in an inverse linear manner, both in univariate analysis and after adjustment for conventional risk factors including hypertension (odds ratio [OR] for highest versus lowest quartile 0.21 (95% confidence interval [CI], 0.06 to 0.71; P for trend=0.008)). Risk estimates were attenuated by inclusion of homocysteine in the model (OR, 0.34; 95% CI, 0.08 to 1.40; P for trend=0.088). A similar pattern was observed for increasing folate intake (multivariate OR, 0.07; 95% CI, 0.01 to 0.55; P for trend=0.031 without homocysteine, and OR, 0.16, 95% CI, 0.02 to 1.23; P for trend=0.118 with homocysteine in the analysis). We found little evidence of an association between plasma or dietary folate and risk of ischemic stroke. Neither plasma nor dietary vitamin B 12 was associated with risk of either stroke subtype. Conclusions— The results of this study suggest a protective role for folate, possibly in addition to its effects on homocysteine status, in hemorrhagic but not ischemic stroke.