Bmd. Brennan et al., GROWTH-HORMONE STATUS IN ADULTS TREATED FOR ACUTE LYMPHOBLASTIC-LEUKEMIA IN CHILDHOOD, Clinical endocrinology, 48(6), 1998, pp. 777-783
OBJECTIVE Growth hormone status was assessed in a cohort of 32 (16 mal
e) adults who had received cranial irradiation (XRT) in childhood as p
art of their treatment for acute lymphoblastic leukaemia (ALL) and com
pared with 35 age matched young adults (18 mate). DESIGN Height and we
ight were measured in all subjects and the heights of the patients at
XRT were obtained from their case notes. Each patient and control unde
rwent two provocative tests of growth hormone (GH) secretion using ins
ulin (0.2 IU/kg body weight) and arginine (20g/m(2)). Basal serum insu
lin like growth factor-1 (IGF-1) and IGFBP-3 (binding protein-3) conce
ntrations were also measured. RESULTS The patient group had a signific
antly lower peak GH response to both provocative tests (P<0.01), and l
ower IGF-1 and IGFBP-3 levels compared with the normal controls (P<0.0
1). Nine of the patient group were severely GH deficient (peak GH resp
onse <9 mU/l to both provocative agents) and a further 12 patients wer
e GH insufficient (peak GH response <20 mU/l to both tests with at lea
st one peak GH response >9 mU/l), Overall a significant median change
in height from XRT to final height of -0.5 SDS was found which was eve
n greater in the severely GH deficient group (median change in height
of -2.1 SDS), CONCLUSION These data suggest that a significant proport
ion of adults treated with cranial XRT in childhood with irradiation d
oses between 18-25 Gy, as part of their treatment for ALL, are severel
y GH deficient now and should be considered for GH replacement, Change
s in GH secretion evolve with time following irradiation-induced damag
e to the hypothalamic-pituitary axis; therefore long-term surveillance
will be required in those remaining patients, in whom GH status is co
nsidered currently to be insufficient or even normal.