EBioMedicine (Sep 2018)

Bile acid metabolites in early pregnancy and risk of gestational diabetes in Chinese women: A nested case-control studyResearch in context

  • Jing Li,
  • Xiaoxu Huo,
  • Yun-Feng Cao,
  • Sai-Nan Li,
  • Zuo Du,
  • Ping Shao,
  • Junhong Leng,
  • Cuiping Zhang,
  • Xiao-Yu Sun,
  • Ronald C.W. Ma,
  • Zhong-Ze Fang,
  • Xilin Yang

Journal volume & issue
Vol. 35
pp. 317 – 324

Abstract

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Background: Bile acid metabolism plays an important role in metabolism but it is uncertain whether bile acid metabolites in early pregnancy are associated with risk of gestational diabetes mellitus (GDM). Methods: We organized a 1:1 case-control study nested in a prospective cohort of 22,302 pregnant women recruited from 2010 to 2012 in China: 243 women with GDM were matched with 243 non-GDM controls on age (±1 year). Conditional logistic regression and restricted cubic spline were used to examine full-range associations of bile acid metabolites with GDM. Findings: All the 9 detectable bile acids were inversely associated with the risk of GDM, among them, 8 in nonlinear and one in largely linear manners in multivariable analysis. Glycoursodeoxycholic acid (GUDCA) at ≤0.07 nmol/mL and deoxycholic acid (DCA) at ≤0.28 nmol/mL had threshold effects and their decreasing levels below the cutoff points were associated with rapid rises in the risk of GDM. In traditional risk factor model, the stepwise procedure identified that GUDCA ≤ 0.07 nmol/mL and DCA ≤ 0.280 nmol/mL were still significant (OR: 6.84, 95%CI: 1.10–42.48 & 2.06, 1.26–3.37), while other bile acids were not. Inclusion of the two bile acids in the model increased the area under operating characteristic's curve from 0.69 to 0.76 (95% CI: 0.71–0.80) (P < .05). Interpretation: Serum GUDCA ≤ 0.07 nmol/mL and DCA ≤ 0.28 nmol/mL in early pregnancy were independently associated with increased risk of GDM in Chinese pregnant women. Funding: Talent Recruitment Scheme grant of Tianjin Medical University and National Key Research and Development Program, etc. Keywords: Gestational diabetes mellitus, Bile acids, Metabolomics, Early-onset marker, Metabolism