Maternal Glucose Tolerance in Pregnancy Affects Fetal Insulin Sensitivity

Author:

Luo Zhong-Cheng1,Delvin Edgard2,Fraser William D.1,Audibert Francois1,Deal Cheri I.3,Julien Pierre4,Girard Isabelle5,Shear Roberta6,Levy Emile7,Nuyt Anne-Monique3

Affiliation:

1. Department of Obstetrics and Gynecology, CHU Sainte-Justine, University of Montreal, Montreal, Quebec, Canada;

2. Department of Biochemistry, CHU Sainte-Justine, University of Montreal, Montreal, Quebec, Canada;

3. Department of Pediatrics, CHU Sainte-Justine, University of Montreal, Montreal, Quebec, Canada;

4. Lipid Research Centre, Laval University, Quebec City, Quebec, Canada;

5. Department of Obstetrics and Gynecology, St. Mary's Hospital, McGill University, Montreal, Quebec, Canada;

6. Department of Obstetrics and Gynecology, Jewish General Hospital, McGill University, Montreal, Quebec, Canada;

7. Department of Nutrition, CHU Sainte-Justine, University of Montreal, Montreal, Quebec, Canada.

Abstract

OBJECTIVE Offspring of mothers with impaired glucose tolerance are far more likely to develop type 2 diabetes. We tested the hypothesis that maternal glucose tolerance in pregnancy affects fetal insulin sensitivity or β-cell function. RESEARCH DESIGN AND METHODS In a prospective singleton pregnancy cohort study, we analyzed glucose, insulin, and proinsulin concentrations in maternal blood at the 50-g oral glucose tolerance test (OGTT) at 24–28 weeks of gestation and in venous cord blood (n = 248). The cord blood glucose-to-insulin ratio and proinsulin concentration were used as indicators of fetal insulin sensitivity and the proinsulin-to-insulin ratio was used as an indicator of fetal β-cell function. RESULTS Higher OGTT blood glucose levels were associated with significantly lower cord plasma glucose-to-insulin ratios (r = −0.31, P < 0.001) and higher proinsulin concentrations (r = 0.31, P < 0.001) but not with proinsulin-to-insulin ratios. In a comparison of gestational diabetic (n = 26) versus euglycemic pregnancy, cord blood glucose-to-insulin ratios were substantially lower (geometric mean 10.1 vs. 20.0 mg/dl/μU/ml; P < 0.001), whereas proinsulin concentrations were much higher (24.4 vs. 13.8 pmol/l; P < 0.001), despite similar cord blood glucose concentrations indicating adequate management of diabetes. The differences remained significant after controlling for prepregnancy and fetal adiposity, family history of diabetes, gestational age, and other potential confounders. Significant changes in the glucose-to-insulin ratio and proinsulin concentration were also observed in obese (n = 31) mothers, but the differences became not statistically significant after adjustment for maternal glucose tolerance and fetal adiposity. CONCLUSIONS Maternal glucose intolerance may impair fetal insulin sensitivity (but not β-cell function) and consequently “program” the susceptibility to type 2 diabetes.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference24 articles.

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2. The metabolic syndrome: common origins of a multifactorial disorder;Bruce;Postgrad Med J,2009

3. The developmental origins of the metabolic syndrome;Gluckman;Trends Endocrinol Metab,2004

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