已发表论文

性激素结合球蛋白与产科疾病之间的因果关系:一项双向孟德尔随机化两样本研究

 

Authors Gan Y, Tan X, Tang Y, Shi Q, Qi H

Received 18 February 2025

Accepted for publication 18 June 2025

Published 11 July 2025 Volume 2025:17 Pages 1985—1999

DOI https://doi.org/10.2147/IJWH.S522635

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 4

Editor who approved publication: Dr Everett Magann

Yanqiong Gan,1,2,* Xinlin Tan,2,* Yu Tang,2 Qi Shi,2 Hongbo Qi1 

1Department of Obstetrics, The First Affiliated Hospital of Chongqing Medical University, Chongqing, People’s Republic of China; 2Department of Obstetrics, The Affiliated Hospital of North Sichuan Medical College, Nanchong, People’s Republic of China

*These authors contributed equally to this work

Correspondence: Hongbo Qi, Department of Obstetrics, The First Affiliated Hospital of Chongqing Medical University, Chongqing, People’s Republic of China, Email qihongbo728@163.com

Introduction: Obstetrical disorders critically impact maternal and fetal health. Sex hormone-binding globulin (SHBG) regulates pregnancy maintenance and maternal-infant outcomes through hormonal, metabolic, and inflammatory pathways, yet causal relationships with obstetrical disorders remain unclear. This Mendelian randomization (MR) study examined SHBG’s causal effects on 12 obstetrical conditions.
Methods: Using cis-protein quantitative trait loci (cis-pQTLs) of SHBG as instrumental variables, we conducted MR analyses in FinnGen and UK Biobank (UKBB), followed by meta-analyses. Inverse variance weighting (IVW) was primary method, with sensitivity analyses ensuring robustness.
Results: IVW-MR demonstrated reduced risks with elevated SHBG: gestational diabetes (OR[95%]=0.835[0.785– 0.889], PFDR=2.03× 10− 7), hyperemesis gravidarum (OR[95%]=0.823[0.728– 0.931], PFDR=5.94× 10− 3), gestational hypertension (OR[95%]=0.917[0.852– 0.987], PFDR=0.041), and early-pregnancy hemorrhage (OR[95%]=0.853[0.794– 0.916], PFDR=6.90× 10− 5). Meta-analysis confirmed SHBG’s causal role in gestational diabetes (P_combined< 0.05). COLOC revealed shared loci between SHBG and five disorders: gestational diabetes, hyperemesis, early hemorrhage, preterm delivery, and postpartum hemorrhage.
Conclusion: SHBG causally lowers risks of gestational diabetes, hypertension, hyperemesis, miscarriage, and preterm delivery, highlighting its clinical relevance in obstetrical pathophysiology.

Keywords: sex hormone binding globulin, obstetrical disorders, Mendelian randomization