Relation between weight gain and beta-cell secretory activity and non-esterified fatty acid production in 7-year-old African children: results from the Birth to Ten study
Nj. Crowther et al., Relation between weight gain and beta-cell secretory activity and non-esterified fatty acid production in 7-year-old African children: results from the Birth to Ten study, DIABETOLOG, 43(8), 2000, pp. 978-985
Aims/hypothesis. This study aimed to assess the effects of fetal and childh
ood growth on beta-cell activity and insulin sensitivity in 7-year-old chil
dren.
Methods. Insulin, des-31,32 proinsulin, proinsulin, non-esterified fatty ac
ids and glucose concentrations were measured in oral glucose tolerance test
s in 152 South African children for whom longitudinal weight data was avail
able.
Results. Children with low weights at birth and 7 years (low-low) had relat
ively low beta-cell activity whereas children with low birth weight and hig
h weight at 7 years (low-high) had relatively high beta-cell activity. The
low-low group had higher 30-min glucose concentrations than children with h
igh birth weights. When each insulin-related peptide was expressed as a per
centage of all these peptides the low-low children had the highest percenta
ge of insulin but the lowest of the prohormones. The low-high children had
the lowest percentage of insulin but the highest of the prohormones. Non-es
terified fatty acid concentrations were lowest and their suppression post-g
lucose load highest in the low-high group.
Conculsion/interpretation. Poor fetal and neonatal growth give rise to low
beta-cell numbers compensated for by increased efficiency of proinsulin pro
cessing to insulin, Poor fetal followed by higher postnatal growth results
in low beta-cell numbers and reduced whole-body glucose uptake which leads
to reduced efficiency in the processing of proinsulin. Growth in utero and
postnatally therefore have profound effects on beta-cell activity and insul
in sensitivity with poor fetal coupled with high postnatal growth being det
rimental to these processes but not detrimental to the suppression of lipol
ysis.