Liang Mingbin, Wang Xun, Li Jin, Yang Fan, Fang Zhian, Wang Lihua, Hu Yonghua, Chen Dafang
Department of Epidemiology and Biostatistics, School of Public Health, Peking University Health Science Center, Beijing 100191, China.
J Biomed Biotechnol. 2010;2010:396184. doi: 10.1155/2010/396184. Epub 2010 Mar 9.
Preterm delivery (PTD) is a complicated perinatal adverse event. We were interested in association of G308A polymorphism in tumor necrosis factor-alpha (TNF-alpha) gene with PTD; so we conducted a genetic epidemiology study in Anqing City, Anhui Province, China. Case families and control families were all collected between July 1999 and June 2002. To control potential population stratification as we could, all eligible subjects were ethnic Han Chinese. 250 case families and 247 control families were included in data analysis. A hybrid design which combines case-parent triads and control parents was employed, to test maternal-fetal genotype (MFG) incompatibility. The method is based on a log-linear modeling approach. In summary, we found that when the mother's or child's genotype was G/A, there was a reduced risk of PTD; however when the mother's or child's genotype was genotype A/A, there was a relatively higher risk of PTD. Combined maternal-fetal genotype GA/GA showed the most reduced risk of PTD. Comparison of the LRTs showed that the model with maternal-fetal genotype effects fits significantly better than the model with only maternal and fetal genotype main effects (log-likelihood = -719.4, P = .023, significant at 0.05 level). That means that the combined maternal-fetal genotype incompatibility was significantly associated with PTD. The model with maternal-fetal genotype effects can be considered a gene-gene interaction model. We claim that both maternal effects and fetal effects should be considered together while investigating genetic factors of certain perinatal diseases.
早产(PTD)是一种复杂的围产期不良事件。我们对肿瘤坏死因子-α(TNF-α)基因中的G308A多态性与早产的关联感兴趣;因此我们在中国安徽省安庆市开展了一项遗传流行病学研究。病例家庭和对照家庭均于1999年7月至2002年6月期间收集。为尽可能控制潜在的人群分层,所有符合条件的受试者均为汉族中国人。250个病例家庭和247个对照家庭纳入数据分析。采用了一种结合病例-父母三联体和对照父母的混合设计,以检验母胎基因型(MFG)不相容性。该方法基于对数线性建模方法。总之,我们发现当母亲或孩子的基因型为G/A时,早产风险降低;然而当母亲或孩子的基因型为A/A时,早产风险相对较高。母胎基因型组合为GA/GA时早产风险降低最为明显。似然比检验(LRTs)比较显示,包含母胎基因型效应的模型拟合度显著优于仅包含母亲和胎儿基因型主效应的模型(对数似然值 = -719.4,P = .023,在0.05水平显著)。这意味着母胎基因型组合不相容性与早产显著相关。包含母胎基因型效应的模型可被视为基因-基因相互作用模型。我们认为在研究某些围产期疾病的遗传因素时,应同时考虑母亲效应和胎儿效应。