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Shortness at birth is associated with insulin resistance in pre-pubertal Jamaican children
F Bennett1, C Watson-Brown, M Thame
1Tropical Metabolism Research Unit, University of the West Indies, Kingston, Jamaica, West Indies.
Insights
Shortness at birth is linked to insulin resistance in children. Heavier children born shorter show greater insulin insensitivity, impacting glucose metabolism.
Area of Science:
- Pediatrics
- Metabolic Health
- Human Growth and Development
Background:
- Birth anthropometry is a potential predictor of childhood metabolic health.
- Understanding early life factors influencing glucose and insulin metabolism is crucial for public health.
Purpose of the Study:
- To examine the association between birth measurements and childhood glucose/insulin metabolism.
- To assess how birth anthropometry relates to insulin resistance in children aged 7.5-10.5 years.
Main Methods:
- Studied 400 mother/child pairs with available birth and gestational data.
- Conducted oral glucose tolerance tests and measured plasma insulin, pro-insulin, and split pro-insulin.
- Utilized skinfold thicknesses to calculate body fat percentage and fat mass.
Main Results:
- Insulin resistance (120-min post-glucose insulin) was inversely correlated with birth length (P<0.005).
- Children in the shortest birth length quartile who were heaviest at age 8 exhibited the highest insulin concentrations.
- Six children (1.5%) presented with impaired glucose tolerance based on WHO criteria.
Conclusions:
- Shorter birth length is a significant predictor of insulin resistance in childhood.
- The degree of insulin insensitivity is exacerbated in heavier children born shorter.
- Early life anthropometry provides insights into later metabolic health trajectories.
Aim:
To investigate the relationship between anthropometry at birth and glucose/insulin metabolism in childhood using the response to an oral glucose challenge.
Method:
Four hundred mother/child pairs on whom gestational and birth data were available were studied. After an overnight fast, anthropometric measurements were made on the children and an oral glucose tolerance test performed. The plasma concentrations of insulin, pro-insulin and 32-33 split pro-insulin were also measured. Skinfold thicknesses were used to calculate percentage body fat and fat mass was derived from the percentage fat and absolute weight.
Results:
The mean age of the children was 8 y (range 7.5-10.5), and six exhibited impaired glucose tolerance based on WHO criteria. Insulin concentration 120 min after the oral glucose load (a measure of insulin resistance) was inversely related to length at birth (P<0.005). The children who were in the shortest quartile at birth and were heaviest at 8 y old had the highest insulin concentration.
Conclusion:
Shortness at birth is related to insulin resistance. Such insensitivity to the action of insulin is greater in heavier children.
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