Maternal plasma cortisol's effect on offspring birth weight: a Mendelian Randomisation study

W D Thompson*, R M Reynolds, R N Beaumont, N M Warrington, J Tyrrell, A R Wood, D M Evans, T J McDonald, A H Hattersley, R M Freathy, D A Lawlor, M C Borges

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

8 Citations (Scopus)

Abstract

Background: 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.

Methods: 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.

Results: 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.

Conclusions: 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.
Original languageEnglish
Article number65
Number of pages11
JournalBMC Pregnancy and Childbirth
Volume24
Issue number1
DOIs
Publication statusPublished - 15 Jan 2024

Bibliographical note

© 2024. The Author(s).

Research Groups and Themes

  • Bristol Population Health Science Institute

Keywords

  • Female
  • Humans
  • Pregnancy
  • Birth Weight/genetics
  • Causality
  • Genome-Wide Association Study
  • Genotype
  • Hydrocortisone
  • Mendelian Randomization Analysis/methods
  • Polymorphism, Single Nucleotide
  • Infant, Newborn

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  • 8073 MRC IEU - Programme 6

    Lawlor, D. A. (Principal Investigator)

    1/04/1831/03/23

    Project: Research

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