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Observational Study
Changes in plasma adipokines in prepubertal children with a history of extrauterine growth restriction.
- María Ortiz-Espejo, Juan Luís Pérez-Navero, Josune Olza, María Carmen Muñoz-Villanueva, Concepción María Aguilera, and Mercedes Gil-Campos.
- Unit of Metabolism and Pediatric Investigation, Department of Pediatrics, University Reina Sofia Hospital, Córdoba, Spain.
- Nutrition. 2013 Nov 1;29(11-12):1321-5.
ObjectiveBecause nutritional support in perinatal life has been associated with metabolic programming, children with a history of extrauterine growth restriction (EUGR) might display alterations in the adipocyte and in the secretion of adipokines. The aim of this study was to assess adiponectin, resistin, and leptin concentrations in prepubertal children with a history of EUGR, and to determine the potential correlation between these adipokines and metabolic parameters.MethodsThis case-control study sample included 38 prepubertal children with a history of EUGR and a control group of 123 healthy children of similar age and sex. Anthropometric measures and blood pressure were assessed. Biochemical markers and blood adipokine concentrations (adiponectin, resistin, and leptin) were evaluated.ResultsAdiponectin concentration was significantly lower in the EUGR group compared with controls (EUGR: 11.49 ± 6.07 versus control: 25.72 ± 10.13 μg/mL), and resistin concentration was higher (EUGR: 20332.95 ± 6401.25 versus control: 8056.31 ± 3823.63 pg/mL), even after adjustment for gestational age, weight, and size at birth. Systolic blood pressure was associated with adipokines concentrations in the EUGR group (P < 0.001). In EUGR children adiponectin was associated with high-density lipoprotein cholesterol (P = 0.042), whereas resistin was associated with carbohydrate metabolism parameters (P < 0.001).ConclusionsEarly postnatal malnutrition in EUGR children could program adipose tissue. Plasma adipokines can be measured in childhood to identify precocious changes that may be associated with a higher risk for metabolic syndrome or cardiovascular disease later in life.Copyright © 2013 Elsevier Inc. All rights reserved.
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