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Published on: January 7, 2018
Insulin resistance in pre-school very-low-birth weight pre-term children
1Department of Internal Medicine, University of Turin, Italy. sbo@molinette.piemonte.it
Insights
Rapid weight gain in early childhood in preterm very-low-birthweight (VLBW) children is linked to metabolic issues, regardless of gestational age. This growth pattern predicts higher insulin and insulin resistance in pre-schoolers.
Area of Science:
- Pediatric Endocrinology
- Neonatology
- Metabolic Health
Background:
- Preterm very-low-birthweight (VLBW) infants face long-term health challenges.
- Understanding metabolic patterns in VLBW survivors is crucial for preventative care.
Purpose of the Study:
- To assess metabolic profiles of pre-school small-for-gestational age (SGA) and appropriate-for-gestational age (AGA) VLBW children.
- To determine if early-life growth rate influences later metabolic and anthropometric characteristics.
Main Methods:
- Evaluated 58 VLBW Italian children (16 SGA, 42 AGA) at pre-school age (>2 to <6 years corrected).
- Assessed anthropometric, clinical, and laboratory (34 children) parameters.
- Analyzed weight centile crossing (CC) and its association with metabolic markers.
Main Results:
- SGA and AGA children showed similar pre-school characteristics.
- A significant weight centile crossing (CC) was observed in 69% of SGA and 51% of AGA children by 24 months.
- Higher fasting glucose, insulin, and HOMA-IR were noted in children with CC.
- Weight gain from birth to 24 months strongly predicted pre-school BMI, waist circumference, insulin, and HOMA-IR.
Conclusions:
- Adverse metabolic patterns in pre-school VLBW children are associated with postnatal rapid weight gain.
- This association is independent of whether the child was small- or appropriate-for-gestational age at birth.
Aims:
To evaluate the metabolic pattern of a group of pre-school small- (SGA) and appropriate-for-gestational age (AGA) pre-term very-low-birthweight (VLBW) (<1500 gr) Italian children and retrospectively verify if the growth rate in the first years of life is associated to the laboratory and anthropometric characteristics of these children.
Methods:
58 (16 SGA, 42 AGA) VLBW children, without major congenital malformations/conditions were enrolled; their anthropometric, clinical and (in 34 of them) laboratory characteristics were evaluated at pre-school age (> 2<6 years of corrected age).
Results:
Clinical, anthropometric and laboratory characteristics at pre-school age were similar in SGA and AGA. Sixty-nine percent of SGA and 51% of AGA children showed a significant weight centile crossing (CC) at 24 months. Fasting serum glucose, insulin and insulin resistance (evaluated by the Homeostasis Model Assessment -HOMA-IR-) were higher in AGA and SGA with CC. The increment in weight standard deviation scores from birth-to-24 months was significantly associated with pre-school BMI SDS, waist, fasting insulin, and HOMA-IR values, both in unadjusted and adjusted models. In a multiple regression model, after multiple adjustments, this increment is the only significant predictor of pre-school insulin (B = 0.19; 95%CI 0.07-0.31; P = 0.006) and HOMA-IR levels (B = 0.20; 95%CI 0.08-0.32; P = 0.004) both in SGA and AGA children.
Conclusions:
The adverse metabolic pattern of pre-school VLBW children seems related to post-natal events (rapid weight growth) independently by their being small- or appropriate-for gestational age.
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