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Insulin sensitivity in prematurely born adults: relation to preterm growth restraint
Joost Rotteveel1, Mirjam M van Weissenbruch, Jos W R Twisk
1Department of Pediatrics, VU University Medical Center, Amsterdam, The Netherlands. J.Rotteveel@Vumc.nl
Insights
Adults born very preterm with normal term weight but restricted growth show lower insulin sensitivity. This difference is linked to current body composition, not birth size alone.
Area of Science:
- Neonatal Medicine
- Metabolic Health
- Endocrinology
Background:
- Preterm infants face increased risk of developing insulin resistance later in life.
- The impact of term-birth weight status on adult insulin sensitivity among very preterm individuals is not well understood.
Purpose of the Study:
- To investigate differences in insulin sensitivity in young adults who were born very preterm.
- To compare insulin sensitivity between those with small-for-gestational-age (SGA) status, appropriate-for-gestational-age with preterm growth restriction (AGA-PGR), and appropriate-for-gestational-age without growth restriction (AGA-non-PGR) at term.
Main Methods:
- Utilized the hyperinsulinemic euglycemic clamp technique to measure insulin sensitivity.
- Studied 21-year-old adults born before 32 weeks of gestation.
- Categorized participants into SGA (n=17), AGA-PGR (n=12), and AGA-non-PGR (n=28) groups.
Main Results:
- Insulin sensitivity (M value) was lower in AGA-non-PGR individuals (8.9 mg/kg/min) compared to SGA (11.0 mg/kg/min) and AGA-PGR (10.4 mg/kg/min) groups.
- These observed differences in insulin sensitivity were no longer significant after adjusting for current body size.
- Significant differences in linear growth trajectories were noted between AGA-non-PGR and SGA groups, and between AGA-non-PGR and the combined AGA-PGR/SGA groups from infancy to young adulthood.
Conclusions:
- In adults born very preterm, variations in insulin sensitivity among SGA, PGR, and non-PGR groups are associated with current body composition.
- Body size and composition, rather than solely birth weight status, appear to be key determinants of insulin sensitivity in this population.
Objective:
Preterm infants are at risk of developing insulin resistance. It is not known whether insulin resistance in adult life is different between those with a low weight at term (preterm growth restraint, PGR) and those with a normal weight at term.
Study Design:
Insulin sensitivity, measured by the hyperinsulinemic euglycemic clamp, was investigated in 21-year-old adults born very preterm (i.e. <32 gestational weeks), of whom 17 were small for gestational age (SGA), 12 were appropriate for gestational age with PGR (AGA-PGR) and 28 were AGA-non-PGR.
Results:
Insulin sensitivity expressed as M value (glucose disposal mg/kg/min) was lower in AGA-non-PGR (8.9) than in SGA (11.0) or AGA-PGR subjects (10.4). These differences disappeared after adjustment for current body size. Linear growth between 3 months and 21 years of age was different between AGA-non-PGR and SGA subjects and between AGA-nonPGR subjects and the combined AGA-PGR and SGA subjects.
Conclusion:
In young adults born very preterm, differences in insulin sensitivity between those born SGA, with PGR and without PGR are related to the current body composition.
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