A. Albanese et al., REVERSIBILITY OF PHYSIOLOGICAL GROWTH-HORMONE SECRETION IN CHILDREN WITH PSYCHOSOCIAL DWARFISM, Clinical endocrinology, 40(5), 1994, pp. 687-692
OBJECTIVE Reversibility of GH insufficiency with a change of environme
nt is characteristic of psychosocial dwarfism, and excludes an organic
endocrinopathy. However, the change in GH pulsatility has not previou
sly been described. We therefore wished to study spontaneous GH secret
ion before and after change to a more favourable environment in 11 chi
ldren with psychosocial deprivation and short stature in order to eval
uate if separation from the families can modify their patterns of GH s
ecretion. PATIENTS AND DESIGN We describe 11 prepubertal children (6 M
and 5 F; 2.2-13.5 years of age) who had growth failure and psychosoci
al deprivation. They were diagnosed by a multidisciplinary team as hav
ing environmental growth failure after admission to hospital for 3 wee
ks. Six of them were discovered to have been sexually abused. During t
he uninterrupted hospital admission parental access was restricted. Th
ree sets of 18-hour GH profiles were performed on each child, except o
ne child who had only two, during the 3-week admission. MEASUREMENTS P
ulse analysis of GH profiles was by Fourier transformation. RESULTS On
the first day of admission spontaneous GH secretion demonstrated a sp
ectrum of abnormalities in the pattern of basal values, pulse frequenc
y and pulse amplitude. Such GH insufficiency showed reversibility duri
ng the 3 weeks in hospital. Indeed, there was a significant increase i
n GH secretion which was amplitude modulated without any significant m
odification in pulse frequency. CONCLUSION Our data indicate that ther
e is abnormal physiological GH secretion in children with psychosocial
deprivation, which is associated with growth failure. Despite a patho
logical situation, each child retained his own characteristic pattern
of GH pulsatility. The pattern of reversibility of abnormal GH pulsati
lity provides information for the mechanism of the control of GH secre
tion.