Jasper Elizabeth A, Hellwege Jacklyn N, Greene Catherine A, Edwards Todd L, Velez Edwards Digna R
Division of Quantitative Sciences, Department of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, TN USA.
Center for Precision Medicine, Vanderbilt University Medical Center, Nashville, TN USA.
NPJ Womens Health. 2024;2(1):42. doi: 10.1038/s44294-024-00035-x. Epub 2024 Dec 6.
Gestational weight gain (GWG) is linked to adverse outcomes in pregnant persons and offspring. The Early Growth Genetics Consortium previously identified genetic variants contributing to GWG from fetal and maternal genomes. However, their biologic mechanisms and tissue-specificity are unknown. We evaluated the association between genetically predicted gene expression in relevant maternal (subcutaneous and visceral adipose, breast, uterus, and whole blood) tissues from GTEx (v7) and fetal (placenta) tissue and early, late, and total GWG using S-PrediXcan. We tested for pathway enrichment using the GENE2FUNC module from Functional Mapping and Annotation of Genome-Wide Association Studies. After Bonferroni correction, we found no associations between maternal or fetal gene expression and GWG. Among nominally significant ( < 0.05) maternal genes, there was enrichment of several biological pathways, including metabolic processes, secretion, and intracellular transport, that varied across pregnancy. These results indicate the likely influence of diverse pathways, varying by tissue and weeks of gestation, on GWG.
孕期体重增加(GWG)与孕妇及其后代的不良结局有关。早期生长遗传学联盟此前已从胎儿和母体基因组中鉴定出与GWG相关的基因变异。然而,它们的生物学机制和组织特异性尚不清楚。我们使用S-PrediXcan评估了GTEx(v7)中相关母体组织(皮下和内脏脂肪、乳腺、子宫和全血)以及胎儿组织(胎盘)中基因预测的基因表达与早期、晚期和总GWG之间的关联。我们使用全基因组关联研究的功能图谱和注释中的GENE2FUNC模块测试了通路富集情况。经过Bonferroni校正后,我们发现母体或胎儿基因表达与GWG之间没有关联。在名义上显著(<0.05)的母体基因中,有几个生物学通路存在富集,包括代谢过程、分泌和细胞内运输,这些通路在整个孕期有所不同