Yadav Upendra, Kumar Pradeep, Gupta Sanjay, Rai Vandana
Human Molecular Genetics Laboratory, Department of Biotechnology, VBS Purvanchal University, Jaunpur, UP 222 003 India.
Department of Psychiatry, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
Indian J Clin Biochem. 2017 Oct;32(4):399-410. doi: 10.1007/s12291-016-0619-0. Epub 2016 Oct 11.
Methylenetetrahydrofolate reductase (MTHFR) is a key enzyme of folate pathway. Several polymorphisms were reported in gene but C677T polymorphism is most studied and it has been reported to be risk factor for several diseases/disorders. The present study was designed to explore the frequency of C677T polymorphism in North Indian healthy population. In addition to this a meta-analysis of published articles was also performed to estimate the global prevalence of C677T polymorphism. A total of 1000 unrelated healthy subjects were selected for C677T polymorphism analysis. Different databases were searched for eligible articles. Prevalence proportion with 95 % CI was used to determine global prevalence of T allele and TT genotype. Meta-analysis was performed by Open meta-analyst. In 1000 blood samples analyzed, the frequency of T allele and TT genotype was 11 and 1 % respectively. Results of the meta-analysis showed that the global prevalence of T allele and TT genotype were 24.0 % (95 % CI 21.7-26.5) and 7.7 % (95 % CI 6.5-8.9) respectively. In sub-group meta-analysis, the lowest frequency of T allele was found in Africans (10.3 %; 95 % CI 3.8-16.8), and highest in Europeans (34.1 %; 95 % CI 31.9-36.3). The frequency of T allele in the North India is 11 %. The results of the meta-analysis showed that the frequency of the T allele and the TT genotype of C677T is highest in the Caucasian population.
亚甲基四氢叶酸还原酶(MTHFR)是叶酸代谢途径中的关键酶。该基因已报道有多种多态性,但C677T多态性研究最多,据报道它是多种疾病/病症的危险因素。本研究旨在探讨北印度健康人群中C677T多态性的频率。除此之外,还对已发表文章进行了荟萃分析,以估计C677T多态性的全球流行率。总共选择了1000名无亲缘关系的健康受试者进行C677T多态性分析。在不同数据库中搜索符合条件的文章。采用95%置信区间的患病率比例来确定T等位基因和TT基因型的全球流行率。通过开放式荟萃分析软件进行荟萃分析。在分析的1000份血样中,T等位基因和TT基因型的频率分别为11%和1%。荟萃分析结果显示,T等位基因和TT基因型的全球流行率分别为24.0%(95%置信区间21.7 - 26.5)和7.7%(95%置信区间6.5 - 8.9)。在亚组荟萃分析中,T等位基因频率在非洲人中最低(10.3%;95%置信区间3.8 - 16.8),在欧洲人中最高(34.1%;95%置信区间31.9 - 36.3)。北印度T等位基因的频率为11%。荟萃分析结果显示,C677T的T等位基因和TT基因型频率在白种人群中最高。