4.6 Article

Associations between Human Chorionic Gonadotropin, Maternal Free Thyroxine, and Gestational Diabetes Mellitus

期刊

THYROID
卷 31, 期 8, 页码 1282-1288

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/thy.2020.0920

关键词

free thyroxine; gestational diabetes mellitus; human chorionic gonadotropin; mediation

资金

  1. National Key Research and Development Program of China [2018YFC1004602]
  2. National Natural Science Foundation of China [81974235, 81501274]
  3. Chinese Academy of Medical Sciences Research Unit [2019RU056]
  4. Shanghai Jiao Tong University, CAMS Innovation Fund for Medical Sciences (CIFMS) [2019-I2M-5-064]
  5. Shanghai Municipal Key Clinical Specialty, Shanghai, China

向作者/读者索取更多资源

The study found that higher hCG concentrations in early pregnancy are associated with a lower risk of GDM, and this association may be mediated through maternal thyroid hormones, specifically free thyroxine (fT4).
Background: Human chorionic gonadotropin (hCG) is a marker of placental function, which also stimulates the maternal thyroid gland. Maternal thyroid function can be associated with the pathophysiology of gestational diabetes mellitus (GDM). We aimed to study whether there is an association of hCG concentrations in early pregnancy with GDM and whether it is mediated through maternal thyroid hormones. Methods: This study included 18,683 pregnant women presenting at a tertiary hospital in Shanghai, China, between January 2015 and December 2016. GDM was diagnosed using a 2-hour, 75-g, oral glucose tolerance test (OGTT) according to the American Diabetes Association guidelines. Multivariable logistic or linear regression models were used to identify associations, adjusting for maternal age, education level, family history of diabetes, parity, fetal sex, thyroperoxidase antibody (TPOAb) status, and prepregnancy body-mass index. Results: Higher hCG concentrations were associated with a lower plasma glucose level during the OGTT, but not with fasting plasma glucose or hemoglobin A1c concentrations tested during early pregnancy. hCG in early pregnancy was negatively associated with GDM risk (p = 0.027). Mediation analysis identified that an estimated 21.4% of the association of hCG-associated GDM risk was mediated through changes in free thyroxine (fT4) concentrations (p < 0.05). In the sensitivity analysis restricted to TPOAb-positive women, hCG was not associated with GDM (p = 0.452). Conclusions: Higher hCG levels in early pregnancy are associated with a lower risk of GDM. Maternal fT4 may act as an important mediator in this association.

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