Placenta and appetite genes GDF15 and IGFBP7 are associated with hyperemesis gravidarum

Marlena S. Fejzo(University of Southern California), Olga V. Sazonova(23andMe (United States)), J. Fah Sathirapongsasuti(23andMe (United States)), Ingileif B. Hallgrímsdóttir(Amgen (United States)), Vladimir Vacic(23andMe (United States)), Kimber MacGibbon(Education & Research Foundation), Frederic Paik Schoenberg(University of California, Los Angeles), Nicholas Mancuso(University of California, Los Angeles), Dennis J. Slamon(University of California, Los Angeles), Patrick Mullin(University of Southern California), Michelle Agee(23andMe (United States)), Babak Alipanahi(23andMe (United States)), Adam Auton(23andMe (United States)), Robert K. Bell(23andMe (United States)), Katarzyna Bryc(23andMe (United States)), Sarah L. Elson(23andMe (United States)), Pierre Fontanillas(23andMe (United States)), Nicholas A. Furlotte(23andMe (United States)), David A. Hinds(23andMe (United States)), Bethann S. Hromatka(23andMe (United States)), Karen E. Huber(23andMe (United States)), Aaron Kleinman(23andMe (United States)), Nadia K. Litterman(23andMe (United States)), Matthew H. McIntyre(23andMe (United States)), Joanna L. Mountain(23andMe (United States)), Elizabeth S. Noblin(23andMe (United States)), Carrie A. M. Northover(23andMe (United States)), Steven J. Pitts(23andMe (United States)), Janie F. Shelton(23andMe (United States)), Suyash Shringarpure(23andMe (United States)), Chao Tian(23andMe (United States)), Joyce Y. Tung(23andMe (United States)), Catherine H. Wilson(23andMe (United States))
Nature Communications
March 21, 2018
Cited by 185Open Access
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Abstract

Abstract Hyperemesis gravidarum (HG), severe nausea and vomiting of pregnancy, occurs in 0.3–2% of pregnancies and is associated with maternal and fetal morbidity. The cause of HG remains unknown, but familial aggregation and results of twin studies suggest that understanding the genetic contribution is essential for comprehending the disease etiology. Here, we conduct a genome-wide association study (GWAS) for binary (HG) and ordinal (severity of nausea and vomiting) phenotypes of pregnancy complications. Two loci, chr19p13.11 and chr4q12, are genome-wide significant ( p < 5 × 10 −8 ) in both association scans and are replicated in an independent cohort. The genes implicated at these two loci are GDF15 and IGFBP7 respectively, both known to be involved in placentation, appetite, and cachexia. While proving the casual roles of GDF15 and IGFBP7 in nausea and vomiting of pregnancy requires further study, this GWAS provides insights into the genetic risk factors contributing to the disease.


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