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Associations between gene polymorphisms in fatty acid metabolism pathway and preterm delivery in a US urban black population.

机译:脂肪酸代谢途径中的基因多态性与美国城市黑人人口中的早产之间的关联。

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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.
机译:越来越多的证据表明,较高的鱼或n-3多不饱和脂肪酸补充剂的摄入量可能会降低早产(PTD)的风险。我们假设,对于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相关。我们对1,110名黑人母亲中的9个基因(FADS1,FADS2,PTGS1,PTGS2,ALOX5,ALOX5AP,PTGES,PTGES2和PTGES3)中的231种潜在功能性单核苷酸多态性(SNP)和tagSNPs进行了基因分型,其中包括542名分娩早产的母亲(<37孕周)和568名在波士顿医学中心分娩足月(孕37周以上)的母亲。在排除完全连锁不平衡或具有较低次要等位基因频率(<1%)或召集率(<90%)的SNP之后,我们使用多种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估算了190个HapMap SNP,并检查了它们与PTD的关联。最后,我们使用自适应秩截短乘积(ARTP)方法探索了与PTD的基因水平和途径水平的关联。共有21个SNP与PTD相关(p值在0.003到0.05之间),包括3个估算的SNP。基因水平的ARTP统计表明,基因PTGES2与PTD显着相关,基于基因的p值等于0.01。找不到基于路径的关联。在这项大型而全面的候选基因研究中,我们发现脂肪酸代谢途径中的基因与PTD之间存在适度的关联。对这些基因多态性与脂肪酸测定及其他遗传因素的进一步研究将有助于更好地了解PTD的发病机理。

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