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Fetal growth and glucose and insulin metabolism in four-year-old Indian children

C S Yajnik1, C H Fall, U Vaidya

  • 1King Edward Memorial Hospital Research Centre, Pune, India.

Insights

Low birthweight in Indian children is linked to impaired glucose tolerance, increasing their risk for Type 2 diabetes. This suggests fetal programming may influence diabetes development in India.

Area of Science:

  • Pediatrics
  • Endocrinology
  • Public Health

Background:

  • Low birthweight is associated with impaired glucose tolerance and Type 2 diabetes in British adults.
  • Type 2 diabetes and low birthweight are prevalent in India.

Purpose of the Study:

  • To investigate the association between low birthweight and reduced glucose tolerance in Indian children.
  • To explore if intra-uterine growth restriction impacts glucose homeostasis in early childhood.

Main Methods:

  • Oral glucose tolerance tests were conducted on 379 4-year-old children in Pune, India.
  • Birthweights were recorded, and plasma glucose and insulin concentrations were measured 30 and 120 minutes post-glucose load.
  • Data analysis considered children from routine postnatal wards and a Special Care Baby Unit.

Main Results:

  • Lower birthweight was associated with higher plasma glucose and insulin concentrations 30 minutes after an oral glucose load in children from routine postnatal wards (p=0.01 and p=0.04).
  • Children with birthweights ≤2.4 kg had higher mean glucose (8.1 mmol/l) and insulin (321 pmol/l) levels compared to those >3.0 kg.
  • A similar trend of higher insulin levels was observed in lower birthweight children from the Special Care Baby Unit, though glucose trends were not significant.

Conclusions:

  • Reduced intra-uterine growth, indicated by low birthweight, is associated with impaired glucose homeostasis in Indian children.
  • Findings support the hypothesis that Type 2 diabetes mellitus in India may be programmed during fetal development.
  • Early life factors like birthweight are critical determinants of metabolic health and diabetes risk later in life.

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