The Relationship between Hyperhomocysteinemia and C677T MTHFR Gene Polymorphism in Patients with Ischemic Stroke.
- Author:
Sang Beom KIM
1
;
Gue Yong LEE
;
Jung Ho SEO
;
Hyun Jo KIM
;
Ok Joon KIM
;
Bo Woo JUNG
;
Do Yeun OH
;
Nam Keun KIM
;
Sun Hee KIM
;
Kyung Cheon CHUNG
;
Byung Ok CHOI
Author Information
1. Department of Neurology, Pochon CHA University College of Medicine, Korea. bochoi@cha.ac.kr
- Publication Type:Original Article
- Keywords:
MTHFR;
Homocysteine;
Small-artery disease;
Large-artery disease;
Risk factor
- MeSH:
Fasting;
Genotype;
Hand;
Homocysteine;
Homozygote;
Humans;
Hyperhomocysteinemia*;
Logistic Models;
Odds Ratio;
Plasma;
Prevalence;
Risk Factors;
Stroke*
- From:Journal of the Korean Neurological Association
2002;20(4):346-352
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: Hyperhomocysteinemia is an independent risk factor for cerebrovascular disease. MTHFR 677TT genotype can induce hyperhomocysteinemia. However, the association between this 677TT genotype and ischemic stroke still remains controversial. This study was undertaken to determine whether MTHFR 677TT genotype was associated with certain subtype of ischemic stroke. METHODS: The case group consisted of 129 patients with ischemic stroke and the control group consisted of 157 healthy individuals. We checked their fasting plasma homocysteine levels and analyzed the C677T mutation in the MTHFR gene. The relative risk of MTHFR 677TT genotype was assessed by odds ratios using multivariate logistic regression. RESULTS: Homocysteine levels in plasma were significantly higher in ischemic stroke patients (10.386.44 mol/L) than in controls (8.002.40) (P<0.05). In small-artery disease (11.366.01), the same result was found (P<0.05). On the other hand, the prevalence of the homozygote mutation was not significantly higher in ischemic stroke patients (20.2%) than in controls (13.4%) (adjusted OR 1.39, 95% CI 0.65 to 2.96). The adjusted OR and 95% CI was 2.59 (1.08 to 6.25) for the TT genotype in patients with small-artery disease compared to controls. The 677TT genotype was increased in small-artery disease compared to large-artery disease (adjusted OR 7.60, 95% CI 1.66 to 34.77). CONCLUSIONS: Our findings suggest that the homozygous C677T mutation in the MTHFR gene is a risk predictor in the subtype of ischemic stroke, such as small-artery disease.
