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Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

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posted on 2021-06-18, 13:30 authored by V Steinthorsdottir, R McGinnis, NO Williams, L Stefansdottir, G Thorleifsson, S Shooter, J Fadista, JK Sigurdsson, KM Auro, G Berezina, MC Borges, S Bumpstead, J Bybjerg-Grauholm, I Colgiu, VA Dolby, F Dudbridge, SM Engel, CS Franklin, ML Frigge, Y Frisbaek, RT Geirsson, F Geller, S Gretarsdottir, DF Gudbjartsson, Q Harmon, DM Hougaard, T Hegay, A Helgadottir, S Hjartardottir, T Jääskeläinen, H Johannsdottir, I Jonsdottir, T Juliusdottir, N Kalsheker, A Kasimov, JP Kemp, K Kivinen, K Klungsøyr, WK Lee, M Melbye, Z Miedzybrodska, A Moffett, D Najmutdinova, F Nishanova, T Olafsdottir, M Perola, FB Pipkin, L Poston, G Prescott, S Saevarsdottir, D Salimbayeva, PJ Scaife, L Skotte, E Staines-Urias, OA Stefansson, KM Sørensen, LCV Thomsen, V Tragante, L Trogstad, NAB Simpson, FINNPEC Consortium, GOPEC Consortium, T Aripova, JP Casas, AF Dominiczak, JJ Walker, U Thorsteinsdottir, AC Iversen, B Feenstra, DA Lawlor, HA Boyd, P Magnus, H Laivuori, N Zakhidova, G Svyatova, K Stefansson, L Morgan
Preeclampsia is a serious complication of pregnancy, affecting both maternal and fetal health. In genome-wide association meta-analysis of European and Central Asian mothers, we identify sequence variants that associate with preeclampsia in the maternal genome at ZNF831/20q13 and FTO/16q12. These are previously established variants for blood pressure (BP) and the FTO variant has also been associated with body mass index (BMI). Further analysis of BP variants establishes that variants at MECOM/3q26, FGF5/4q21 and SH2B3/12q24 also associate with preeclampsia through the maternal genome. We further show that a polygenic risk score for hypertension associates with preeclampsia. However, comparison with gestational hypertension indicates that additional factors modify the risk of preeclampsia.

Funding

Research leading to these results was conducted as part of the InterPregGen study, which received funding from the European Union Seventh Framework Programme under grant agreement no. 282540 and was supported by Wellcome Trust grant 098051.

History

Citation

Nat Commun 11, 5976 (2020)

Author affiliation

Department of Health Sciences

Version

  • VoR (Version of Record)

Published in

Nature Communications

Volume

11

Publisher

Nature Research

issn

2041-1723

eissn

2041-1723

Acceptance date

2020-10-26

Copyright date

2020

Available date

2021-06-18

Spatial coverage

England

Language

eng

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