Is Afamin a novel biomarker for gestational diabetes mellitus? A pilot study.

Reprod Biol Endocrinol

Division of Genetic Epidemiology, Department of Medical Genetics, Molecular and Clinical Pharmacology, Medical University of Innsbruck, Schöpfstrasse 41, 6020, Innsbruck, Austria.

Published: March 2018

AI Article Synopsis

  • The study investigates afamin, a vitamin E-binding protein, as a potential early biomarker for predicting gestational diabetes mellitus (GDM), focusing on its role in insulin resistance and its increasing levels during pregnancy.
  • Researchers analyzed afamin concentrations in 59 GDM patients and 51 controls in the first trimester, and 105 women in mid-trimester, comparing the results with oral glucose tolerance test outcomes.
  • Findings revealed significantly higher afamin levels in women with GDM in both cohorts, with specific distinctions noted between those treated with insulin and dietary interventions, suggesting afamin's potential as an early predictor for GDM.

Article Abstract

Background: In search of potential early biomarkers for timely prediction of gestational diabetes mellitus (GDM), we focused on afamin, a vitamin E-binding protein in human plasma.. Afamin plays a role in anti-apoptotic cellular processes related to oxidative stress and is associated with insulin resistance and other features of metabolic syndrome. During uncomplicated pregnancy its serum concentrations increase linearly. The aim of this study was to investigate the suitability of afamin as early marker for predicting GDM.

Methods: In a first-trimester cohort from a prospective observational study of adverse pregnancy outcomes we secondarily analyzed afamin concentrations in 59 patients diagnosed with GDM and 51 controls. Additionally, afamin concentrations were cross-sectionally examined in a mid-trimester cohort of 105 women and compared with results from a simultaneously performed oral glucose tolerance test (OGTT). Subgroup analysis comparing patients treated with either insulin (iGDM) or dietary intervention (dGDM) was performed in both cohorts. Patients were recruited at the University Hospital Essen, Germany, between 2003 and 2016.

Results: Results were adjusted for body-mass-index (BMI) and gestational age. First and mid-trimester cohorts yielded significantly elevated afamin concentrations in patients with pathological OGTT compared to patients without GDM (first trimester cohort: mean, 113.4 mg/l; 95% CI, 106.4-120.5 mg/l and 87.2 mg/l; 95% CI, 79.7-94.7 mg/l; mid-trimester cohort: mean, 182.9 mg/l; 95% CI, 169.6-196.2 mg/l and 157.3 mg/l; 95% CI, 149.1-165.4 mg/l, respectively). In the first-trimester cohort, patients developing iGDM later in pregnancy presented with significantly higher afamin concentrations compared to patients developing dGDM and compared to patients without GDM. In the mid-trimester cohort, mean concentrations of afamin differed significantly between patients with dGDM compared to controls and between patients with iGDM and controls. Patients with iGDM showed only slightly higher afamin levels compared to patients with dGDM.

Conclusion: Afamin may serve as a new early biomarker for pathological glucose metabolism during pregnancy. Further research is needed to determine afamin's concentrations during pregnancy, its predictive value for early detection of pregnancies at high risk to develop GDM and its diagnostic role during the second trimester.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870691PMC
http://dx.doi.org/10.1186/s12958-018-0338-xDOI Listing

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