Evaluation of growth hormone release and human growth hormone treatment in children with cranial irradiation-associated short stature

1984 ◽  
Vol 104 (2) ◽  
pp. 177-181 ◽  
Author(s):  
Carolyn A. Romshe ◽  
William B. Zipf ◽  
Angela Miser ◽  
James Miser ◽  
Juan F. Sotos ◽  
...  
1990 ◽  
Vol 122 (1) ◽  
pp. 89-95 ◽  
Author(s):  
I. Gil-Ad ◽  
N. Leibowitch ◽  
Z. Josefsberg ◽  
M. Wasserman ◽  
Z. Laron

Abstract Human growth hormone release is affected by a variety of pharmacological and physiological stimuli. We have studied the effect of oral clonidine, insulin hypoglycemia, and exercise on plasma hGH and GHRH levels in 31 healthy short-stature children. Thirteen underwent an oral clonidine test (0.15 mg/m2), 12 an iv. insulin test (0.1 U/kg), and 6 performed exercise (running for 10 min in a defined route). GHRH-1-44 was extracted from plasma on silica columns and determined by RIA. Although all three stimuli induced a marked increase in plasma hGH levels, only clonidine induced a significant increase in plasma GHRH levels. Maximal increment in GHRH during clonidine was 6.82 ± 1.05 pmol/l (mean ± SEM) as compared with 0.51 ± 0.28 and 0.53 ± 0.62 during hypoglycemia and exercise (p<0.0005 and p<0.005), respectively. An additional 24 subjects received TRH 0.2 mg/kg iv: 8 TRH alone, 8 TRH and insulin, and 8 TRH and clonidine. Only insulin potentiated the TRH-induced TSH response with a peak of 22.0 ± 3.2 vs 16.0 ± 0.8 and 15.3 ± 1.5 mU/l (p<0.025) for TRH alone and TRH and clonidine, respectively. It is suggested that clonidine stimulates hGH secretion mainly through an enhancement of GHRH release, whereas stress stimuli such as hypoglycemia and exercise achieve hGH release by a different mechanism, possibly inhibition of somatostatin.


1999 ◽  
Vol 41 (6) ◽  
pp. 655-661 ◽  
Author(s):  
AYTEN Arcasoy ◽  
GÖNÜL Öcal ◽  
SABRI Kemahli ◽  
MERIH Berberoİlu ◽  
YILDIZ Yildirmak ◽  
...  

2020 ◽  
Vol 2020 ◽  
pp. 1-8
Author(s):  
Jing Wu ◽  
Fei Zhao ◽  
Yuan Zhang ◽  
Jiang Xue ◽  
Jiangying Kuang ◽  
...  

It has been recognized that people with obesity are more likely to have low growth hormone secretion. Recent studies have also confirmed that the abnormalities of the growth hormone/insulin-like growth factor 1 axis were associated with cardiovascular complications in people with obesity. However, little is known about whether recombinant human growth hormone therapy could improve cardiovascular and metabolic risks in obese children. This study aims to evaluate the effect of one-year growth hormone therapy on obesity-related comorbidities and to assess the safety in Chinese boys with obesity. Eighteen boys with obesity were treated with recombinant human growth hormone for one year. Anthropometric measurements, endocrine testing, and cardiovascular risk markers were performed in all obese boys in baseline, and follow-up visits were performed at 3 months, 6 months, 9 months, and one year, respectively. After one year of recombinant human growth hormone treatment, the body mass index standard deviation scores decreased (P<0.001) and insulin-like growth factor 1 levels increased (P<0.001). GH treatment also reduced low density lipoprotein cholesterol (P<0.001), total cholesterol (P<0.001), triglycerides (P=0.042), and alanine aminotransferase (P=0.027) when compared with the baseline. One-year of recombinant human growth hormone treatment could improve cardiometabolic risk markers, without adverse effects on glucose homeostasis in boys with obesity.


1975 ◽  
Vol 41 (2) ◽  
pp. 408-411 ◽  
Author(s):  
Kiyoshi Maeda ◽  
Yuzuru Kato ◽  
Kazuo Chihara ◽  
Shozo Ohgo ◽  
Yoshiko Iwasaki ◽  
...  

Author(s):  
Giovanna Weber ◽  
Chiara Prinster ◽  
Marta Meneghel ◽  
Fiorella Russo ◽  
Stefano Mora ◽  
...  

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