Journal
PLOS ONE
Volume 9, Issue 6, Pages -Publisher
PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0100337
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Funding
- Institut National de la Sante et de la Recherche Medicale (INSERM)
- Programme Hospitalier de Recherche Clinique [06-136]
- Pfizer Inc.
- Institut Appert
- INSERM
- SFEDP
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Background: Being born small for gestational age (SGA) is a risk factor for later development of type 2 diabetes. The development of glucose tolerance disorders in adults involves insulin resistance and impaired insulin secretion. Objective: To evaluate insulin secretion and insulin sensitivity in a 4-yr old cohort of SGA. Methods: 85 children were prospectively followed from mid-gestation to 4 years of age. Fetal growth velocity (FGV) was measured using ultrasound measurements. Body composition and hormonal profile were measured at birth, 1 and 4 years. Results: 23 SGA babies had lower birth weight compared to 62 AGA (-1.9 +/- 0.3 vs. 0.6 +/- 0.8 z-score; p<0.0001) and they were thinner at birth (ponderal index 24.8 +/- 1.8 vs. 26.3 +/- 3.1 kg/m3; p=0.01 and fat mass 11 +/- 2.6 vs. 12.9 +/- 3.1%; p =0.01). No significant differences in other measured metabolic and hormonal parameters were observed between two groups at birth. SGA infants experienced an early catch-up growth in weight (mean gain of 1.1 +/- 0.6 SD) during the first year of life. At 4 years, SGA children remain lighter than AGA, but with weight z-score in the normal range (-0.1 +/- 1.3 vs. 0.5 +/- 1.3 z-score; p = 0.05). No excess of fat mass was observed (19 +/- 4.8 vs. 19.7 +/- 4.1%; pz=0.45). 120-min plasma glucose was significantly higher (6.2 +/- 1.1 vs. 5.6 +/- 0.9 mmol/1; p =0.006) and insulinogenic index was significantly lower (0.28 +/- 0.15 vs. 0.40 +/- 2.4; p=0.02) in the SGA group at 4-yrs of life contrasting with a preserved insulin sensitivity (QUICK! 0.47 +/- 0.09 vs. 0.43 +/- 0.05; p = 0.06). Conclusion: SGA children with compensatory catch-up growth in first year of life show mild disturbances of glucose tolerance associated to a lower insulinogenic index at 4-yrs of age suggesting impairment of 13-cell function.
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