Boyles Abee L, Wilcox Allen J, Taylor Jack A, Shi Min, Weinberg Clarice R, Meyer Klaus, Fredriksen Ase, Ueland Per Magne, Johansen Anne Marte W, Drevon Christian A, Jugessur Astanand, Trung Truc Nguyen, Gjessing Håkon K, Vollset Stein Emil, Murray Jeffrey C, Christensen Kaare, Lie Rolv T
Epidemiology Branch, NIEHS/NIH, Durham, North Carolina 27709, USA.
Genet Epidemiol. 2009 Apr;33(3):247-55. doi: 10.1002/gepi.20376.
An increased risk of facial clefts has been observed among mothers with lower intake of folic acid or vitamin A around conception. We hypothesized that the risk of clefts may be further moderated by genes involved in metabolizing folate or vitamin A. We included 425 case-parent triads in which the child had either cleft lip with or without cleft palate (CL/P) or cleft palate only (CPO), and no other major defects. We analyzed 108 SNPs and one insertion in 29 genes involved in folate/one-carbon metabolism and 68 SNPs from 16 genes involved in vitamin A metabolism. Using the Triad Multi-Marker (TRIMM) approach we performed SNP, gene, chromosomal region, and pathway-wide association tests of child or maternal genetic effects for both CL/P and CPO. We stratified these analyses on maternal intake of folic acid or vitamin A during the periconceptional period. As expected with this high number of statistical tests, there were many associations with P-values<0.05; although there were fewer than predicted by chance alone. The strongest association in our data (between fetal FOLH1 and CPO, P=0.0008) is not in agreement with epidemiologic evidence that folic acid reduces the risk of CL/P in these data, not CPO. Despite strong evidence for genetic causes of oral facial clefts and the protective effects of maternal vitamins, we found no convincing indication that polymorphisms in these vitamin metabolism genes play an etiologic role.
在受孕前后叶酸或维生素A摄入量较低的母亲中,观察到面部裂隙的风险增加。我们假设,裂隙风险可能会受到参与叶酸或维生素A代谢的基因的进一步调节。我们纳入了425个病例-父母三联体,其中孩子患有唇裂伴或不伴腭裂(CL/P)或仅患有腭裂(CPO),且无其他主要缺陷。我们分析了参与叶酸/一碳代谢的29个基因中的108个单核苷酸多态性(SNP)和1个插入位点,以及参与维生素A代谢的16个基因中的68个SNP。使用三联体多标记(TRIMM)方法,我们对CL/P和CPO的儿童或母亲遗传效应进行了SNP、基因、染色体区域和通路范围的关联测试。我们根据母亲在受孕前后叶酸或维生素A的摄入量对这些分析进行了分层。正如预期的那样,由于进行了大量的统计测试,有许多P值<0.05的关联;尽管关联数量比仅由偶然因素预测的要少。我们数据中最强的关联(胎儿FOLH1与CPO之间,P = 0.0008)与流行病学证据不一致,该证据表明叶酸可降低这些数据中CL/P的风险,而非CPO的风险。尽管有充分证据表明口腔面部裂隙存在遗传原因以及母亲维生素具有保护作用,但我们没有发现令人信服的迹象表明这些维生素代谢基因中的多态性起病因作用。