Mary Ann and J. Milburn Smith Child Health Research Program, Children's Memorial Hospital, Children's Memorial Research Center, Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Hum Genet. 2012 Mar;131(3):341-51. doi: 10.1007/s00439-011-1079-5. Epub 2011 Aug 17.
There is increasing evidence suggesting that higher intakes of fish or n-3 polyunsaturated fatty acids supplements may decrease the risk of preterm delivery (PTD). We hypothesized that genetic variants of the enzymes critical to fatty acids biosynthesis and metabolism may be associated with PTD. We genotyped 231 potentially functional single nucleotide polymorphisms (SNPs) and tagSNPs in 9 genes (FADS1, FADS2, PTGS1, PTGS2, ALOX5, ALOX5AP, PTGES, PTGES2, and PTGES3) among 1,110 black mothers, including 542 mothers who delivered preterm (<37 weeks gestation) and 568 mothers who delivered full-term babies (≥37 weeks gestation) at Boston Medical Center. After excluding SNPs that are in complete linkage disequilibrium or have lower minor allele frequency (<1%) or call rate (<90%), we examined the association of 206 SNPs with PTD using multiple logistic regression models. We also imputed 190 HapMap SNPs via program MACH and examined their associations with PTD. Finally, we explored gene-level and pathway-level associations with PTD using the adaptive rank truncated product (ARTP) methods. A total of 21 SNPs were associated with PTD (p value ranging from 0.003 to 0.05), including 3 imputed SNPs. Gene-level ARTP statistics indicated that the gene PTGES2 was significantly associated with PTD with a gene-based p value equal to 0.01. No pathway-based association was found. In this large and comprehensive candidate gene study, we found a modest association of genes in fatty acid metabolism pathway with PTD. Further investigation of these gene polymorphisms jointly with fatty acid measures and other genetic factors would help better understand the pathogenesis of PTD.
越来越多的证据表明,增加鱼类或 n-3 多不饱和脂肪酸的摄入量可能会降低早产 (PTD) 的风险。我们假设,对脂肪酸生物合成和代谢至关重要的酶的遗传变异可能与 PTD 有关。我们在包括 542 名早产 (<37 周妊娠) 和 568 名足月产 (>37 周妊娠) 母亲在内的 1110 名黑人母亲中,对 9 个基因(FADS1、FADS2、PTGS1、PTGS2、ALOX5、ALOX5AP、PTGES、PTGES2 和 PTGES3)中的 231 个潜在功能单核苷酸多态性 (SNP) 和标签 SNP 进行了基因分型。在排除了那些处于完全连锁不平衡或具有较低次要等位基因频率 (<1%)或调用率 (<90%)的 SNP 后,我们使用多元逻辑回归模型检查了 206 个 SNP 与 PTD 的关联。我们还通过程序 MACH 对 190 个 HapMap SNP 进行了推断,并研究了它们与 PTD 的关联。最后,我们使用自适应秩截断乘积 (ARTP) 方法探索了与 PTD 相关的基因水平和途径水平的关联。共有 21 个 SNP 与 PTD 相关(p 值从 0.003 到 0.05),包括 3 个推断 SNP。基因水平 ARTP 统计数据表明,基因 PTGES2 与 PTD 显著相关,基因水平 p 值等于 0.01。没有发现基于途径的关联。在这项大型综合候选基因研究中,我们发现脂肪酸代谢途径中的基因与 PTD 有一定的关联。进一步研究这些基因多态性与脂肪酸测量值和其他遗传因素的关系,将有助于更好地了解 PTD 的发病机制。