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GDF15 linked to maternal risk of nausea and vomiting during pregnancy

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posted on 2024-07-22, 10:48 authored by M Fejzo, N Rocha, I Cimino, SM Lockhart, CJ Petry, RG Kay, K Burling, P Barker, AL George, N Yasara, A Premawardhena, S Gong, E Cook, D Rimmington, K Rainbow, DJ Withers, V Cortessis, PM Mullin, KW MacGibbon, E Jin, A Kam, A Campbell, O Polasek, G Tzoneva, FM Gribble, GSH Yeo, BYH Lam, V Saudek, IA Hughes, KK Ong, JRB Perry, A Sutton Cole, M Baumgarten, P Welsh, N Sattar, GCS Smith, DS Charnock-Jones, AP Coll, CL Meek, S Mettananda, C Hayward, N Mancuso, S O’Rahilly

GDF15, a hormone acting on the brainstem, has been implicated in the nausea and vomiting of pregnancy, including its most severe form, hyperemesis gravidarum (HG), but a full mechanistic understanding is lacking1–4. Here we report that fetal production of GDF15 and maternal sensitivity to it both contribute substantially to the risk of HG. We confirmed that higher GDF15 levels in maternal blood are associated with vomiting in pregnancy and HG. Using mass spectrometry to detect a naturally labelled GDF15 variant, we demonstrate that the vast majority of GDF15 in the maternal plasma is derived from the feto-placental unit. By studying carriers of rare and common genetic variants, we found that low levels of GDF15 in the non-pregnant state increase the risk of developing HG. Conversely, women with β-thalassaemia, a condition in which GDF15 levels are chronically high5, report very low levels of nausea and vomiting of pregnancy. In mice, the acute food intake response to a bolus of GDF15 is influenced bi-directionally by prior levels of circulating GDF15 in a manner suggesting that this system is susceptible to desensitization. Our findings support a putative causal role for fetally derived GDF15 in the nausea and vomiting of human pregnancy, with maternal sensitivity, at least partly determined by prepregnancy exposure to the hormone, being a major influence on its severity. They also suggest mechanism-based approaches to the treatment and prevention of HG.

History

Citation

Nature 625, 760–767 (2024)

Author affiliation

College of Life Sciences Population Health Sciences

Version

  • VoR (Version of Record)

Published in

Nature

Volume

625

Issue

7996

Pagination

760 - 767

Publisher

Springer Science and Business Media LLC

issn

0028-0836

eissn

1476-4687

Acceptance date

2023-11-30

Copyright date

2023

Available date

2024-07-22

Spatial coverage

England

Language

en

Deposited by

Professor Claire Meek

Deposit date

2024-07-19

Data Access Statement

Summary statistics of the GDF15 GWAS in Generation Scotland will be shared in the Generation Scotland DataShare collection (https://datashare.ed.ac.uk/handle/10283/844). For the hyperemesis gravidarum GWAS, qualified researchers can contact apply.research@23andMe.com to gain access to full GWAS summary statistics following an agreement with 23andMe that protects 23andMe participant privacy. The source data files are provided and accompany each figure, except where doing so would result in unauthorized release of summary statistics from the 23andMe HG GWAS. Source data are provided with this paper.

Rights Retention Statement

  • Yes

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