Fl. Culler et Lr. Meacham, EFFECT OF HYPERSOMATOSTATINEMIA ON GROWTH-HORMONE SECRETION IN CYSTIC-FIBROSIS PATIENTS WITH DIABETES, Neuroendocrinology, 58(4), 1993, pp. 473-477
We have recently shown that hypersomatostatinemia is a feature of cyst
ic fibrosis (CF) when these patients have CF-associated pancreatogenic
diabetes mellitus (CFDM). To address the possibility that patients wi
th CFDM might have suppressed pituitary growth hormone (GH) release as
a result of increased plasma somatostatin, GH secretion in 8 CFDM pat
ients and 8 normal male controls was studied using a standard arginine
infusion stimulus. Concentrations of the GH-dependent peptides, insul
in-like growth factor I (IGF-I) and insulin-like growth factor binding
protein 3 (IGFBP-3) were also measured. We found that mean GH concent
rations in the CFDM group were significantly increased P<0.05) rather
than decreased at the 30-min (12.3 +/- 3.6 vs. 3.8 +/- 1.9 ng/ml), 45-
min (15.4 +/- 2.9 vs. 6.1 +/- 2.3 ng/ml) and 60-min (13.2 +/- 2.3 vs.
6.2 +/- 2.2 ng/ml) time points of study. Mean GH area under the curve
(633 +/- 128 vs. 249 +/- 107 ng/ml) was also significantly greater (p<
0.05) in the CFDM group. Despite higher GH levels in the CFDM patients
, their IGF-I and IGFBP-3 concentrations were low. We conclude that pl
asma somatostatin elevations in the CFDM group are not of sufficient m
agnitude to suppress pituitary GH release. Decreased levels of growth
mediating peptides ill the relatively malnourished CF subjects suggest
a pattern of malnutrition-induced GH resistance which may contribute
to poor weight and height gain.