还原叶酸载体基因多态性与先天性心脏病和唇腭裂关联的研究

裴丽君; 任爱国; 郝玲; 朱慧萍; 朱江辉; 赵文睿; 周敏霞; 孙霞美; 姜梅芳; 陈海兰; 张伯兰; 李竹

Abstract

裴丽君,任爱国,郝玲,朱慧萍,朱江辉,赵文睿,周敏霞,孙霞美,姜梅芳,陈海兰,张伯兰,李竹.还原叶酸载体基因多态性与先天性心脏病和唇腭裂关联的研究[J].Chinese journal of Epidemiology,2004,25(12):1063-1067

还原叶酸载体基因多态性与先天性心脏病和唇腭裂关联的研究

Study on the association between reduced folate gene polymorphism and congenital heart defects and cleft lip with or without cleft palate

Received:September 09, 2004 Revised:September 09, 2004

DOI：

KeyWord: 心脏病,先天性唇腭裂还原叶酸载体基因以家庭为基础的关联检验

English Key Word: congenital heart defects C1eft lip with or without cleft palate Reduced folate carrier gene Family—based association test

FundProject:国家重点基础研究专项基金资助项目(G1999055905)

Author Name	Affiliation
PEI Li-jun	Institute of Reproductive and Child Health, National Reference Laboratory on Reproductive Health Research Ministry of Health, Peking University, Beijing 100083, China
REN Ai-guo	Institute of Reproductive and Child Health, National Reference Laboratory on Reproductive Health Research Ministry of Health, Peking University, Beijing 100083, China
HAO Ling	Institute of Reproductive and Child Health, National Reference Laboratory on Reproductive Health Research Ministry of Health, Peking University, Beijing 100083, China
ZHU Hui-ping	美国得克萨斯州农工大学环境与遗传医学中心生物科学技术研究所
ZHU Jiang-hui	Institute of Reproductive and Child Health, National Reference Laboratory on Reproductive Health Research Ministry of Health, Peking University, Beijing 100083, China
ZHAO Wen-rui	Institute of Reproductive and Child Health, National Reference Laboratory on Reproductive Health Research Ministry of Health, Peking University, Beijing 100083, China
ZHOU Min-xia	江苏省锡山区妇幼保健所
SUN Xia-mei	浙江省海宁市妇幼保健院
JIANG Mei-fang	江苏省苏州市妇幼保健院
CHEN Hai-lan	浙江省舟山市妇幼保健院
ZHANG Bo-lan	河北省香河县妇幼保健院
LI Zhu	Institute of Reproductive and Child Health, National Reference Laboratory on Reproductive Health Research Ministry of Health, Peking University, Beijing 100083, China

Hits: 3208

Download times: 1288

Abstract:

目的检验还原叶酸载体基因(RFC1)A80G多态性与先天性心脏病(CHD)和唇腭裂之间的关联,为寻找CHD和唇腭裂危险因素的遗传易感标志物提供流行病学依据。方法采用RFLP-PCR方法,对67个CHD患儿家庭、82个唇腭裂患儿家庭和100个正常儿童家庭成员的外周血DNA进行RFC1第80位SNP检测,利用核心家庭标本进行以家庭为基础的关联检验(FBAT),并分析了子代RFC1基因型与母亲孕期前后增补叶酸的相互作用。结果不增补叶酸的母亲生育CHD儿的危险高于增补叶酸的母亲(OR=2 68,95%CI:1 14-6 41),即母亲孕期未增补叶酸与CHD发生危险的关联有统计学意义(x2=6.213,P=0 013) 在FBAT检验中,RFC1 G等位基因与CHD发病危险有统计学关联(Z=2 140,P< 0 05),表明RFC1 G等位基因可能是CHD发病的遗传易感基因,未发现唇腭裂与RFC1之间的统计学关联。结论 RFC1 G等位基因可能是CHD发生的遗传易感基因之一,子代RFC1基因GG或GA基因型、母亲孕期叶酸缺乏可能增加CHD的发病危险。

English Abstract:

Objective To study the association between reduced folate carver gene(RFClpolymorphism and congenital heart defects (CHD) as well as cleft lip with or without cleft palate (CLP)and to provide epidemiological evidence on genetic markers of CHD and CLP. Methods RFCl (ASOG)genotype was detected using RFLP-PCR for blood DNA of the 67 triads with nonsyndromic CHD-affected child, the 82 triads with child-affected cleft lip with or without CLP and the 100 control families without child-affected birth defects. We performed a family-based association test and analyzed the interaction between RFCl A80G genotype and maternal periconceptional supplementation of folic acid. Results Offspring of mothers who did not take folic acid had an elevated risk for CHD when comparing with offspring of mothers who did(OR = 2. 68, 95%CI:1，14-6.41).There was a statistical association between the risk of CHD and maternal periconceptional folic acid supplementation (Xz=6.213，P<0.05).In the family-based association test, G allele was positively associated with an increased risk for children CHD ( Z = 2.140，P<0.05) while G allele of RFC1(A80G) polymorphism might increase the risk for CHD. Elevated risks for either CLP group were not observed between RFCl genotype using or not using folic acid. Conclusions Our findings suggested that the G allele was likely to be a genetically susceptible allele for CHD. There was possible association between offspring with GG, GA genotype and maternal periconceptional folic acid deficiency.

View Fulltext Html FullText View/Add Comment Download reader