Department of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.
Academic Rheumatology, Clinical Sciences Building, Nottingham City Hospital, Hucknall Road, Nottingham, NG5 1PB, United Kingdom.
BMC Pregnancy Childbirth. 2024 Jan 15;24(1):65. doi: 10.1186/s12884-024-06250-3.
Observational studies and randomized controlled trials have found evidence that higher maternal circulating cortisol levels in pregnancy are associated with lower offspring birth weight. However, it is possible that the observational associations are due to residual confounding.
We performed two-sample Mendelian Randomisation (MR) using a single genetic variant (rs9989237) associated with morning plasma cortisol (GWAS; sample 1; N = 25,314). The association between this maternal genetic variant and offspring birth weight, adjusted for fetal genotype, was obtained from the published EGG Consortium and UK Biobank meta-analysis (GWAS; sample 2; N = up to 406,063) and a Wald ratio was used to estimate the causal effect. We also performed an alternative analysis using all GWAS reported cortisol variants that takes account of linkage disequilibrium. We also tested the genetic variant's effect on pregnancy cortisol and performed PheWas to search for potential pleiotropic effects.
The estimated effect of maternal circulating cortisol on birth weight was a 50 gram (95% CI, -109 to 10) lower birth weight per 1 SD higher log-transformed maternal circulating cortisol levels, using a single variant. The alternative analysis gave similar results (-33 grams (95% CI, -77 to 11)). The effect of the cortisol variant on pregnancy cortisol was 2-fold weaker than in the original GWAS, and evidence was found of pleiotropy.
Our findings provide some evidence that higher maternal morning plasma cortisol causes lower birth weight. Identification of more independent genetic instruments for morning plasma cortisol are necessary to explore the potential bias identified.
观察性研究和随机对照试验都发现了证据,表明孕期母体循环皮质醇水平升高与后代出生体重降低有关。然而,观察到的相关性可能是由于残余混杂因素造成的。
我们使用与早晨血浆皮质醇相关的单个遗传变异(rs9989237)(GWAS;样本 1;N=25314)进行两样本 Mendelian Randomisation(MR)。从已发表的 EGG 联盟和英国生物库荟萃分析(GWAS;样本 2;N=最多 406063)中获得该母体遗传变异与后代出生体重之间的关联,该关联是在调整胎儿基因型后获得的,并使用 Wald 比值来估计因果效应。我们还使用所有报告的皮质醇变异的替代分析来考虑连锁不平衡,进行了另一种分析。我们还测试了遗传变异对妊娠皮质醇的影响,并进行了 PheWas 搜索,以寻找潜在的多效性影响。
使用单个变异,母体循环皮质醇对出生体重的估计影响是母体循环皮质醇水平每增加 1 个 SD,log 转换后出生体重降低 50 克(95%CI,-109 至 10)。替代分析得出了类似的结果(-33 克(95%CI,-77 至 11))。皮质醇变异对妊娠皮质醇的影响比原始 GWAS 弱两倍,并且发现了多效性的证据。
我们的研究结果提供了一些证据,表明母体早晨血浆皮质醇升高会导致出生体重降低。有必要确定更多独立的早晨血浆皮质醇遗传工具,以探索已确定的潜在偏差。