valid diagnostic information regarding children exhibiting short stature. T
hus, an IGF-I value should always be evaluated together with auxological in
formation and GH testing results before a decision is taken on whether or n
ot to start GH therapy. Circulating insulin-like growth factor I (IGF-I) le
vels are stable throughout the day and correlate, with pulsatile endogenous
growth hormone (GH) secretion. A single measurement of IGF-I may, therefor
e, provide information on the GH secretory status of an individual. The cli
nical use of IGF-I determination in the evaluation of short stature in chil
dren suspected of GH deficiency will be discussed. Previous methodological
problems have now mostly been overcome, and IGF-I can be determined in seru
m from healthy children, although concentrations exhibit large inter-indivi
dual variations relating to age, gender and pubertal maturation. These vari
ations must be taken into account before IGF-I can be evaluated in a clinic
al situation, and before it can be stated whether a certain value is too lo
w for a given age. The diagnostic sensitivities of IGF-I reported in relati
on to the outcome of GH provocative testing are variable (47-100%). This va
riability probably results from the use of different IGF-I assays, IGF-I re
ference ranges, and different GH testing procedures. When proper IGF-I assa
ys and reference ranges are used, however, IGF-I determination results in C
opyright (C) 2001 S. Karger AG, Basel.