Literature DB >> 33719227

Reduced glycodeoxycholic acid levels are associated with negative clinical outcomes of gestational diabetes mellitus.

Bo Zhu1,2, Zhixin Ma1,2, Yuning Zhu1,2, Lei Fang1,2, Hong Zhang1,2, Hongwei Kong3,4, Dajing Xia5,6.   

Abstract

Gestational diabetes mellitus (GDM) is characterized by glycemia and insulin disorders. Bile acids (BAs) have emerged as vital signaling molecules in glucose metabolic regulation. BA change in GDM is still unclear, which exerts great significance to illustrate the change of BAs in GDM. GDM patients and normal pregnant women were enrolled during the oral glucose tolerance test (OGTT) screening period. Fasting serums were sampled for the measurement of BAs. BA metabolism profiles were analyzed in both pregnant women with GDM and those with normal glucose tolerance (NGT). Delivery characteristics, delivery gestational age, and infant birthweight were extracted from medical records. GDM patients presented distinctive features compared with NGT patients, including higher body mass index (BMI), elevated serum glucose concentration, raised insulin (both fasting and OGTT), and increased hemoglobin A1c (HbA1c) levels. Higher homeostasis model assessment of insulin resistance (HOMA-IR) and decreased β-cell compensation (i.e., oral disposition index (DIo)) were also prevalent in this group. Total BAs (TBAs) remained stable, but glycodeoxycholic acid (GDCA) and taurodeoxycholic acid (TDCA) levels declined significantly in GDM. GDCA was inversely correlated with HOMA-IR and positively correlated with DIo. No obvious differences in clinical outcome between the GDM and NGT groups were observed. However, GDM patients with high HOMA-IR and low DIo tended to have a higher cesarean delivery rate and younger delivery gestational age. In conclusion, GDCA provides a valuable biomarker to evaluate HOMA-IR and DIo, and decreased GDCA levels predict poorer clinical outcomes for GDM.

Entities:  

Keywords:  Bile acid; Gestational diabetes mellitus (GDM); Insulin resistance; β-Cell compensation

Year:  2021        PMID: 33719227      PMCID: PMC7982326          DOI: 10.1631/jzus.B2000483

Source DB:  PubMed          Journal:  J Zhejiang Univ Sci B        ISSN: 1673-1581            Impact factor:   3.066


  39 in total

1.  Development of Multimarker Diagnostic Models from Metabolomics Analysis for Gestational Diabetes Mellitus (GDM).

Authors:  Wolin Hou; Xiyan Meng; Aihua Zhao; Weijing Zhao; Jiemin Pan; Junling Tang; Yajuan Huang; Huaping Li; Wei Jia; Fang Liu; Weiping Jia
Journal:  Mol Cell Proteomics       Date:  2017-12-27       Impact factor: 5.911

2.  Insulin sensitivity indices obtained from oral glucose tolerance testing: comparison with the euglycemic insulin clamp.

Authors:  M Matsuda; R A DeFronzo
Journal:  Diabetes Care       Date:  1999-09       Impact factor: 19.112

Review 3.  Intermediate metabolism in normal pregnancy and in gestational diabetes.

Authors:  G Di Cianni; R Miccoli; L Volpe; C Lencioni; S Del Prato
Journal:  Diabetes Metab Res Rev       Date:  2003 Jul-Aug       Impact factor: 4.876

Review 4.  Gestational Diabetes Mellitus: Mechanisms, Treatment, and Complications.

Authors:  Emma C Johns; Fiona C Denison; Jane E Norman; Rebecca M Reynolds
Journal:  Trends Endocrinol Metab       Date:  2018-10-05       Impact factor: 12.015

5.  Pregnancy outcome in women with gestational diabetes - A longitudinal study of changes in demography and treatment modalities.

Authors:  Ulrika Moll; Mona Landin-Olsson; Charlotta Nilsson; Dag Ursing; Helena Strevens
Journal:  Acta Obstet Gynecol Scand       Date:  2019-12-22       Impact factor: 3.636

6.  Maternal glucose homeostasis is impaired in mouse models of gestational cholestasis.

Authors:  Elena Bellafante; Saraid McIlvride; Vanya Nikolova; Hei Man Fan; Luiza Borges Manna; Jenny Chambers; Mavis Machirori; Anita Banerjee; Kevin Murphy; Marcus Martineau; Kristina Schoonjans; Hanns-Ulrich Marschall; Peter Jones; Catherine Williamson
Journal:  Sci Rep       Date:  2020-07-13       Impact factor: 4.379

7.  Changes in Metabolites During an Oral Glucose Tolerance Test in Early and Mid-Pregnancy: Findings from the PEARLS Randomized, Controlled Lifestyle Trial.

Authors:  Danielle E Haslam; Jun Li; Liming Liang; Marijulie Martinez; Cristina Palacios; Maria A Trak-Fellermeier; Paul W Franks; Kaumudi Joshipura; Shilpa N Bhupathiraju
Journal:  Metabolites       Date:  2020-07-10

Review 8.  Crosstalk between FXR and TGR5 controls glucagon-like peptide 1 secretion to maintain glycemic homeostasis.

Authors:  Hyeonhui Kim; Sungsoon Fang
Journal:  Lab Anim Res       Date:  2018-12-31

9.  Elevated First-Trimester Total Bile Acid is Associated with the Risk of Subsequent Gestational Diabetes.

Authors:  Wolin Hou; Xiyan Meng; Weijing Zhao; Jiemin Pan; Junling Tang; Yajuan Huang; Minfang Tao; Fang Liu; Weiping Jia
Journal:  Sci Rep       Date:  2016-09-26       Impact factor: 4.379

Review 10.  Bile acids in glucose metabolism in health and disease.

Authors:  Hagit Shapiro; Aleksandra A Kolodziejczyk; Daniel Halstuch; Eran Elinav
Journal:  J Exp Med       Date:  2018-01-16       Impact factor: 14.307

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