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全基因组关联研究日本妊娠期间恶心和呕吐:TMM BirThree 队列研究。

Genome-wide association study of nausea and vomiting during pregnancy in Japan: the TMM BirThree Cohort Study.

机构信息

Division of Molecular Epidemiology, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi, 980-8575, Japan.

Innovation Division, KAGOME CO., LTD, 17 Nishitomiyama, Nasushiobara, Tochigi, 329- 2762, Japan.

出版信息

BMC Pregnancy Childbirth. 2024 Mar 20;24(1):209. doi: 10.1186/s12884-024-06376-4.

Abstract

BACKGROUND

Nausea and vomiting during pregnancy (NVP) and hyperemesis gravidarum (HG), common conditions affecting most pregnant women, are highly heritable and associated with maternal and fetal morbidity. However, the pathologies underlying NVP and HG and their associated loci are scarce.

METHODS

We performed genome-wide association studies (GWAS) of NVP in pregnant women (n = 23,040) who participated in the Tohoku Medical Megabank Project Birth and Three-Generation Cohort Study in Japan from July 2013 to March 2017. Participants were divided into discovery (n = 9,464) and replication (n = 10,051) stages based on the platform used for their genotyping. Loci that achieved the genome-wide significance level (p < 5.0 × 10) in the discovery stage were selected for genotyping in the replication stage. A meta-analysis integrating the discovery and replication stage results (n = 19,515) was conducted. NVP-related variables were identified as categorical or continuous.

RESULTS

GWAS analysis in the discovery phase revealed loci linked to NVP in two gene regions, 11q22.1 (rs77775955) and 19p13.11 (rs749451 and rs28568614). Loci in these two gene regions have also been shown to be associated with HG in a White European population, indicating the generalizability of the GWAS analyses conducted in this study. Of these, only rs749451 and rs28568614 at 19p13.11 reached the genome-wide suggestive level (p < 1.0 × 10) in the replication stage; however, both loci were significant in the meta-analysis.

CONCLUSIONS

NVP-related loci were identified in the Japanese population at 11q22.1 and 19p13.11, as reported in previous GWAS. This study contributes new evidence on the generalizability of previous GWAS on the association between genetic background and NVP.

摘要

背景

妊娠恶心和呕吐(NVP)和妊娠剧吐(HG)是影响大多数孕妇的常见疾病,具有高度遗传性,并与母婴发病率有关。然而,NVP 和 HG 的潜在病理学及其相关基因座却很少。

方法

我们对 2013 年 7 月至 2017 年 3 月期间参加日本东北医科大学百万生物银行项目生育和三代队列研究的孕妇(n=23040)进行了 NVP 的全基因组关联研究(GWAS)。参与者根据其基因分型所使用的平台分为发现(n=9464)和复制(n=10051)阶段。在发现阶段达到全基因组显著水平(p<5.0×10)的基因座被选择用于复制阶段的基因分型。对发现和复制阶段结果(n=19515)进行了荟萃分析。将 NVP 相关变量定义为分类或连续变量。

结果

在发现阶段的 GWAS 分析中,在两个基因区域 11q22.1(rs77775955)和 19p13.11(rs749451 和 rs28568614)中发现了与 NVP 相关的基因座。这两个基因区域的基因座也已被证明与白人欧洲人群中的 HG 相关,表明本研究进行的 GWAS 分析具有普遍性。其中,只有 19p13.11 上的 rs749451 和 rs28568614 达到了复制阶段的全基因组提示水平(p<1.0×10);然而,这两个基因座在荟萃分析中都是显著的。

结论

在日本人群中,在之前的 GWAS 报道的 11q22.1 和 19p13.11 上确定了与 NVP 相关的基因座。本研究为先前关于遗传背景与 NVP 之间关联的 GWAS 具有普遍性提供了新的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a544/10953086/b588878c0444/12884_2024_6376_Fig1_HTML.jpg

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