摘要
目的研究Ｎ５，Ｎ１０亚甲四氢叶酸还原酶（ＭＴＨＦＲ）基因多态性及血浆同型半胱氨酸（Ｈｃｙ）水平与脑卒中的关系。方法运用多聚酶链反应限制性内切酶片段长度多态性技术（ＰＣＲＲＦＬＰ）检测８０例脑卒中及１１０例正常人ＭＴＨＦＲ基因多态性，用高效液相色谱仪和荧光检测仪测定８０例脑卒中及１１０例正常人血浆总Ｈｃｙ水平。结果发现ＭＴＨＦＲ基因型有３种，即纯合子突变（＋／＋）型，杂合子突变（＋／－）型，正常（－／－）型。患者组中＋／＋型频率为３１．２５％，＋／－型频率为５６．２５％，－／－型频率为１２．５％，Ｔ等位基因频率为５９．３７％，Ｃ等位基因频率为４０．６２％。正常组中＋／＋型频率为１８．１８％，＋／－型频率为２０．０９％，－／－型频率为５２．７２％，Ｔ等位基因频率为３２．７２％，Ｃ等位基因频率为６２．２７％，两组差异有显著性，且患者组中＋／＋和＋／－型均高于正常组。脑卒中患者血浆总Ｈｃｙ水平显著高于正常组。结论脑卒中患者ＭＴＨＦＲ基因纯合子突变和杂合子突变发生率均显著高于正常组，而Ｔ等位基因频率也明显高于正常组，说明ＭＴＨＦＲ基因突变及高同型半胱氨酸血症与脑卒中发生有一定关系，ＭＴＨＦＲ基因可能是脑卒中的易?
Objective To study the relationship of polymorphisms of MTHFR gene and plasma homocysteine (Hcy) levels with stroke.Methods 80 stroke patients and 110 normal subjects were recruited in the study. Their polymorphisms of MTHFR gene were analyzed using PCR RFLP and their plasma total Hcy levels were measured using high performance liquid chromatography with fluorescence detection. Results There were three kinds of genotype: +/+ (homozygous mutation), +/- (heterozygous mutation) and -/- (wild type). The frequencies of the three genotypes were as follows: +/+, 31.25%; +/-, 56.25%; -/-, 12.5% in stroke patients and +/+, 18.18%; +/- 29.09%; -/-, 52.72% in normal subjects, respectively. The frequency of T alleles was significantly higher in stroke patients than that in normal controls (59.37% and 32.72% , respectively). Mean total plasma homocysteine concentrations were significantly higher in stroke patients than in the normal subjects. Conclusions The frequency of homozygous and heterozygous MTHFR mutation in stroke patients were higher than that in controls and the T alleles in stroke patients was significantly more frequent than that in control subjects. Plasma Hcy levels in stroke patients is higher than that in normal subjects. These results suggest that polymorphisms of MTHFR gene and hyperhomocysteinemia may be an independent risk factor for stroke.
出处
《中华心血管病杂志》
CAS
CSCD
北大核心
1999年第2期121-123,共3页
Chinese Journal of Cardiology
基金
中国博士后科学基金
