SERUM CONCENTRATIONS OF INSULIN, INSULIN-LIKE-GROWTH-FACTOR (IGF)-I, IGF BINDING-PROTEIN (IGFBP)-1 AND -3 AND GROWTH-HORMONE BINDING-PROTEIN IN OBESE CHILDREN - FASTING IGFBP-1 IS SUPPRESSED IN NORMOINSULINEMIC OBESE CHILDREN
H. Saitoh et al., SERUM CONCENTRATIONS OF INSULIN, INSULIN-LIKE-GROWTH-FACTOR (IGF)-I, IGF BINDING-PROTEIN (IGFBP)-1 AND -3 AND GROWTH-HORMONE BINDING-PROTEIN IN OBESE CHILDREN - FASTING IGFBP-1 IS SUPPRESSED IN NORMOINSULINEMIC OBESE CHILDREN, Clinical endocrinology, 48(4), 1998, pp. 487-492
OBJECTIVE Simple obesity is characterized by normal or accelerated gro
wth in the presence of reduced serum levels of GH, whereas its detaile
d mechanism remains unknown. We, therefore, evaluated interrelationshi
ps among serum levers of insulin, IFG-I, IGF binding protein (IGFBP)-1
and -3 and growth hormone binding protein (GHBP) in prepubertal obese
children. SUBJECTS Prepubertal 20 obese children and 20 age-matched c
ontrol children were included in the study, RESULTS Serum levels of in
sulin, IGF-I and IGFBP-3 in obese children did not differ from those i
n controls. The serum revel of IGFBP-1 was significantly lower in obes
e children (22.1 +/- 18.4 mu g/l, P<0.001) than in control children (7
6.0 +/- 62.9 mu g/l). No relationship was found between the serum leve
ls of insulin and IGF-I, IGFBP-1, or IGFBP-3 in obese subjects, The se
rum revel of GHBP in obese children was significantly elevated as comp
ared with that in controls and was positively correlated with body mas
s index (BMI). No relationship was found between the serum levels of G
HBP and IGF-I in obese subjects. CONCLUSIONS The present study showed
for the first time that the fasting IGFBP-1 level was suppressed in pr
epubertal obese children with fasting normoinsulinaemia, We speculate
that the hyperinsulinaemia which cannot be detected in the fasting sta
te may have suppressed hepatic production of IGFBP-1, Alternatively, t
he reduced IGFBP-1 is likely to be a compensatory response to impaired
insulin sensitivity, Thus, the IGFBP-1 level may be a useful predicto
r for the early identification in the development of insulin resistanc
e in prepubertal obese children.