期刊
METABOLISM-CLINICAL AND EXPERIMENTAL
卷 65, 期 6, 页码 874-882出版社
W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.metabol.2016.03.003
关键词
Leptin; Cord blood; Birth cohort; Growth; Childhood
资金
- Special Account for Research of the University of Crete, Greece [321/10-09-2010]
- Greek Ministry of Health (Program ofPrevention of obesity and neurodevelopmental disorders in preschool children, in Heraklion district, Crete, Greece)
Objective. Leptin represents a potential modulator of developmental programming of childhood obesity. We investigated the association of cord blood leptin with growth trajectories from birth to early childhood. Materials/methods. We used data from the prospective mother child cohort Rhea, Crete, Greece. Cord blood samples from 642 neonates were collected. 578 (90%) children had complete follow up data from birth to 4 years. We measured child weight, height, waist circumference, skinfold thicknesses, blood pressure, and serum lipids, leptin, adiponectin and C-reactive protein in early childhood (median 4.2 years). We estimated growth trajectories from 3 months up to 4 years using random-effects linear-spline models. Multivariable logistic and linear regression models were used adjusting for confounders. Results. Mean cord blood leptin levels were 7.3 ng/mL (standard deviation: 6.3). Children with high cord blood leptin (>90th percentile) exhibited lower weight, height and body mass index from 6 months to early childhood. Each SD increase in cord blood leptin was associated with lower weight at the age of 4 by 242 g (95% CI: -416, -69). In a stratified analysis, the reverse association was observed in children born small for gestational age (p for interaction = 0.001), and in those exhibiting rapid infant growth during the first 3 months of life (p for interaction = 0.002). Cord blood leptin levels were not associated with cardiometabolic risk factors at 4 years. Conclusions. Long term programming effects of in utero exposure to leptin extends beyond infancy into early childhood. Further studies are needed to explore potential effect modification by intrauterine and early infancy growth patterns. (C) 2016 Elsevier Inc. All rights reserved.
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