TY - JOUR
T1 - Retinol-binding protein 4
T2 - A novel adipokine implicated in the genesis of LGA in the absence of gestational diabetes mellitus
AU - Mazaki-Tovi, Shali
AU - Romero, Roberto
AU - Vaisbuch, Edi
AU - Kusanovic, Juan Pedro
AU - Chaiworapongsa, Tinnakorn
AU - Kim, Sun Kwon
AU - Mittal, Pooja
AU - Dong, Zhong
AU - Pacora, Percy
AU - Yeo, Lami
AU - Hassan, Sonia S.
PY - 2010/3/1
Y1 - 2010/3/1
N2 - Objective: Adipokines (cytokines produced by adipose tissue) play a major role in the control of body weight and energy distribution. Retinol-binding protein 4 (RBP4), only recently recognized as an adipokine, has been proposed to modulate systemic insulin sensitivity. The goal of this study was to determine whether there is an association between maternal plasma RBP4 concentration and the birth of a large-for-gestational-age (LGA) newborn in women with and without gestational diabetes mellitus (GDM). Study design: This cross-sectional study included pregnant women at term in the following groups: 1) normal pregnancy with an appropriate-for-gestational-age (AGA) neonate (n=64); 2) normal pregnancy with an LGA neonate (n=44); 3) GDM with an AGA neonate (n=55); and 4) GDM with an LGA neonate (n=42). Maternal plasma RBP4 concentration was determined by ELISA. Parametric and non-parametric statistics were used for analyses. Results: 1) Patients with GDM, either with AGA or LGA neonates, had a higher median plasma concentration of RBP4 than normal pregnant women who delivered an AGA neonate (P=0.01 and P=0.008, respectively); 2) mothers without GDM but with LGA neonates had a higher median plasma concentration of RBP4 than those with normal pregnancy and AGA newborns (P=0.001); 3) these findings remained significant after adjusting for maternal age, body mass index and gestational age at blood sampling. Conclusion: GDM is characterized by alterations in maternal circulating RBP4 concentrations akin to those of Type 2 diabetes mellitus. RBP4 concentrations in maternal plasma may play a role in accelerated fetal growth in the absence of overt carbohydrate intolerance.
AB - Objective: Adipokines (cytokines produced by adipose tissue) play a major role in the control of body weight and energy distribution. Retinol-binding protein 4 (RBP4), only recently recognized as an adipokine, has been proposed to modulate systemic insulin sensitivity. The goal of this study was to determine whether there is an association between maternal plasma RBP4 concentration and the birth of a large-for-gestational-age (LGA) newborn in women with and without gestational diabetes mellitus (GDM). Study design: This cross-sectional study included pregnant women at term in the following groups: 1) normal pregnancy with an appropriate-for-gestational-age (AGA) neonate (n=64); 2) normal pregnancy with an LGA neonate (n=44); 3) GDM with an AGA neonate (n=55); and 4) GDM with an LGA neonate (n=42). Maternal plasma RBP4 concentration was determined by ELISA. Parametric and non-parametric statistics were used for analyses. Results: 1) Patients with GDM, either with AGA or LGA neonates, had a higher median plasma concentration of RBP4 than normal pregnant women who delivered an AGA neonate (P=0.01 and P=0.008, respectively); 2) mothers without GDM but with LGA neonates had a higher median plasma concentration of RBP4 than those with normal pregnancy and AGA newborns (P=0.001); 3) these findings remained significant after adjusting for maternal age, body mass index and gestational age at blood sampling. Conclusion: GDM is characterized by alterations in maternal circulating RBP4 concentrations akin to those of Type 2 diabetes mellitus. RBP4 concentrations in maternal plasma may play a role in accelerated fetal growth in the absence of overt carbohydrate intolerance.
KW - Adipokine
KW - Adipose tissue
KW - Appropriate-for-gestational-age (AGA)
KW - Body mass index (BMI)
KW - Cytokine
KW - Insulin resistance
KW - Insulin sensitivity
KW - Metabolism
KW - Obesity
KW - Overweight
KW - Pregnancy
UR - http://www.scopus.com/inward/record.url?scp=77749289234&partnerID=8YFLogxK
U2 - 10.1515/JPM.2010.044
DO - 10.1515/JPM.2010.044
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C2 - 20146659
AN - SCOPUS:77749289234
SN - 0300-5577
VL - 38
SP - 147
EP - 155
JO - Journal of Perinatal Medicine
JF - Journal of Perinatal Medicine
IS - 2
ER -