Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/89967
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Type: Journal article
Title: Altered glucose metabolism in mouse and humans conceived by IVF
Author: Chen, M.
Wu, L.
Zhao, J.
Wu, F.
Davies, M.
Wittert, G.
Norman, R.
Robker, R.
Heilbronn, L.
Citation: Diabetes, 2014; 63(10):3189-3198
Publisher: American Diabetes Association
Issue Date: 2014
ISSN: 0012-1797
1939-327X
Statement of
Responsibility: 
Miaoxin Chen, Linda Wu, Junli Zhao, Fang Wu, Michael J. Davies, Gary A. Wittert, Robert J. Norman, Rebecca L. Robker, and Leonie K. Heilbronn
Abstract: In vitro fertilization (IVF) may influence the metabolic health of children. However, in humans, it is difficult to separate out the relative contributions of genetics, environment, or the process of IVF, which includes ovarian stimulation (OS) and embryo culture. Therefore, we examined glucose metabolism in young adult humans and in adult male C57BL/6J mice conceived by IVF versus natural birth under energy-balanced and high-fat-overfeeding conditions. In humans, peripheral insulin sensitivity, as assessed by hyperinsulinemic-euglycemic clamp (80 mU/m²/min), was lower in IVF patients (n = 14) versus control subjects (n = 20) after 3 days of an energy-balanced diet (30% fat). In response to 3 days of overfeeding (+1,250 kcal/day, 45% fat), there was a greater increase in systolic blood pressure in IVF versus controls (P = 0.02). Mice conceived after either OS alone or IVF weighed significantly less at birth versus controls (P < 0.01). However, only mice conceived by IVF displayed increased fasting glucose levels, impaired glucose tolerance, and reduced insulin-stimulated Akt phosphorylation in the liver after 8 weeks of consuming either a chow or high-fat diet (60% fat). Thus, OS impaired fetal growth in the mouse, but only embryo culture resulted in changes in glucose metabolism that may increase the risk of the development of metabolic diseases later in life, in both mice and humans.
Keywords: Animals; Blood Glucose; Female; Fertilization in Vitro; Glucose; Glucose Clamp Technique; Humans; Insulin; Insulin Resistance; Male; Mice, Inbred C57BL; Proto-Oncogene Proteins c-akt; Risk Factors; Young Adult
Rights: © 2014 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered
RMID: 0030009855
DOI: 10.2337/db14-0103
Appears in Collections:Medicine publications

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