Institute for Computational Health Sciences, University of California, San Francisco, 94143, CA, USA.
Department of Pediatrics, University of California, San Francisco, San Francisco, CA, USA.
Sci Rep. 2018 Jan 9;8(1):226. doi: 10.1038/s41598-017-18246-5.
Preterm birth (PTB), or the delivery prior to 37 weeks of gestation, is a significant cause of infant morbidity and mortality. Although twin studies estimate that maternal genetic contributions account for approximately 30% of the incidence of PTB, and other studies reported fetal gene polymorphism association, to date no consistent associations have been identified. In this study, we performed the largest reported genome-wide association study analysis on 1,349 cases of PTB and 12,595 ancestry-matched controls from the focusing on genomic fetal signals. We tested over 2 million single nucleotide polymorphisms (SNPs) for associations with PTB across five subpopulations: African (AFR), the Americas (AMR), European, South Asian, and East Asian. We identified only two intergenic loci associated with PTB at a genome-wide level of significance: rs17591250 (P = 4.55E-09) on chromosome 1 in the AFR population and rs1979081 (P = 3.72E-08) on chromosome 8 in the AMR group. We have queried several existing replication cohorts and found no support of these associations. We conclude that the fetal genetic contribution to PTB is unlikely due to single common genetic variant, but could be explained by interactions of multiple common variants, or of rare variants affected by environmental influences, all not detectable using a GWAS alone.
早产(PTB),即妊娠 37 周前分娩,是婴儿发病率和死亡率的重要原因。尽管双胞胎研究估计,母亲的遗传贡献约占 PTB 发病率的 30%,其他研究也报道了胎儿基因多态性的关联,但迄今为止,尚未确定一致的关联。在这项研究中,我们针对胎儿信号进行了迄今为止规模最大的、针对 1349 例 PTB 病例和 12595 名匹配的对照的全基因组关联研究分析。我们在五个亚群(非洲人(AFR)、美洲人(AMR)、欧洲人、南亚人和东亚人)中测试了超过 200 万个单核苷酸多态性(SNP)与 PTB 的关联。我们仅在全基因组水平上鉴定出两个与 PTB 相关的基因间位点:在 AFR 人群中位于 1 号染色体上的 rs17591250(P=4.55E-09)和在 AMR 人群中位于 8 号染色体上的 rs1979081(P=3.72E-08)。我们已经查询了几个现有的复制队列,没有发现这些关联的支持。我们得出结论,胎儿遗传对 PTB 的贡献不太可能是由于单个常见遗传变异引起的,而是可能是由多个常见变异的相互作用或受环境影响的罕见变异引起的,这些都不能仅通过全基因组关联研究来检测。