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Accepted Preprint first posted online on 21 April 2008

European Journal of Endocrinology 2008;159:49.

DOI: 10.1530/EJE-07-0682
Copyright © 2008 by European Society of Endocrinology
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RESEARCH

RBP4 is not strongly associated with insulin sensitivity in normal pregnancies

Thor Ueland, Tonje Dalsoren, Nanna Voldner, Kristin Godang, Tore Henriksen and Jens Bollerslev

T Ueland, oslo, 0027, Norway
T Dalsoren, Oslo, Norway
N Voldner, Oslo, Norway
K Godang, Oslo, Norway
T Henriksen, Oslo, Norway
J Bollerslev, Oslo, Norway

Correspondence: Thor Ueland, Email: thor.ueland{at}medisin.uio.no

Abstract

Objective: Recently, experimental and clinical studies suggest that retinol-binding protein-4 (RBP4) may provide a link between obesity and insulin resistance. However, no previous studies have investigated the impact of circulating RBP4 on measures of insulin resistance in normal pregnant women and the objective of this study is to measure serum RBP4 in early and late pregnancy and relate these to measures of insulin resistance and secretion controlling for changes in fat mass.

Design and Methods samples were obtained during OGTT from 44 normal pregnancies at week 14-16 and 30-32. Measures of fat mass were BMI and leptin while insulin sensitivity and secretion were predicted from OGTT. Leptin and RPB4 were measured by immunoassay.

Results: Insulin sensitivity decreased during the course of pregnancy. Insulin sensitivity and secretion were best explained by BMI and circulating leptin, but not RBP4, both in early and late pregnancy. However, a marked increase in fasting RBP4 from early to late pregnancy was observed, and this change was associated with a decline in insulin sensitivity. A marked increase in RBP4 was found during OGTT at week 14-16 with an opposite temporal course at week 30-32.

Conclusion: The increased fat-mass and insulin resistance during normal pregnancy was best explained by measures of fat mass. However, the increase in RBP4 from early to late pregnancy, associated with a decline in insulin sensitivity, potentially indicates interactions with glucose metabolism.




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[Abstract] [Full Text] [PDF]




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