Abstract
朱江辉,任爱国,郝玲,裴丽君,张伯兰,周敏霞,孙霞美,姜梅芳,陈海兰,李竹.转化生长因子α基因多态性与唇腭裂关联的研究[J].Chinese journal of Epidemiology,2006,27(3):245-248
转化生长因子α基因多态性与唇腭裂关联的研究
Study on the association between transforming growth factor α gene Taqiv variant and cleft lip with orwithout cleft palate
Received:May 30, 2005  
DOI:
KeyWord: 唇腭裂  转化生长因子α  病例父母亲对照研究
English Key Word: Cleft lips with or without cleft palate  Transforming grow th factorα  Case- parent
FundProject:国家重点基础研究专项基金资助项目(G1999055905)
Author NameAffiliation
ZHU Jiang-hui 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 
PEI Li-jun Institute of Reproductive and Child Health, National Reference Laboratory on Reproductive Health Research Ministry of Health, Peking University, Beijing 100083, China 
ZHANG Bo-lan 河北省香河县妇幼保健所 
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所 
JIANG Mei-fang 江苏省苏州市妇幼保健所 
CHEN Hai-lan 浙江省舟山市妇幼保健所 
LI Zhu Institute of Reproductive and Child Health, National Reference Laboratory on Reproductive Health Research Ministry of Health, Peking University, Beijing 100083, China 
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Abstract:
      目的 探讨中国部分地区人群非综合征型唇裂伴或不伴腭裂(nsCL/P)与转化生长因子α基因(TGFα)TaqⅠ位点多态性之间的关系。方法 采用聚合酶链反应-限制片段长度多态性分析方法,对149个nsCL/P核心家庭成员DNA标本进行TGFαTaqⅠ突变位点的基因型检测。利用传递失衡检验和以家庭为基础的关联研究(FBAT)方法,分析TGFαTaqⅠ突变与nsCL/P发生之间的关系。结果 未发现TGFαTaqⅠ突变的致病C2等位基因在nsCL/P核心家庭成员中存在传递不平衡(P>0.05);采用FBAT分析,未发现C2等位基因及C2C1基因型与nsCL/P发病危险之间关联有统计学意义(P>0.05)。结论 TGFαTaqⅠ突变可能不是中国部分地区人群nsCL/P发生的易感基因。
English Abstract:
      Objective To study the association between transforming growth factor A gene( TGFα) Taqiv variant and nonsyndromic cleft lip with or without cleft palate ( nsCL/ P) in Chinese population. Methods TGFα Taqiv variant was detected using polymerase chain reaction- restriction fragment length polymorphism for DNA samples of the 149 triads with nsCL/ P affected child. We performed the Transmission/ disequilibrium test and the family- based association study( FBAT ) to identify the associations between this variant and risk of nsCL/ P. Results Significant distortion of C2 allele at TGFATaqiv locus in nsCL/ P groups ( P > 0.05) was not found. In the family- based association test, C2 allele and offspring C2C1 genotype was not found to be significantly associated with an increase risk of nsCL/ P ( P>0.05). Conclusion Our findings did not suggest an association between offspring TGFα Taqiv variant and the increased risk of nsCL/ P in Chinese population.
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