Growth hormone treatment in children with GH deficiency followed by digital X-ray radiogrametry on BMD changes

Bone ◽  
2007 ◽  
Vol 40 (6) ◽  
pp. S46
Author(s):  
C. Galesanu ◽  
C. Ciubotariu ◽  
M.R. Galesanu
Pituitary ◽  
2012 ◽  
Vol 16 (3) ◽  
pp. 311-318 ◽  
Author(s):  
Beverly M. K. Biller ◽  
Hyi-Jeong Ji ◽  
Hyunji Ahn ◽  
Conrad Savoy ◽  
E. Christine Siepl ◽  
...  

1994 ◽  
Vol 131 (3) ◽  
pp. 246-250 ◽  
Author(s):  
Jan Åman ◽  
Sten Rosberg ◽  
Kerstin Albertsson-Wikland

Aman J. Rosberg S, Albertsson-Wikland K. Effect of growth hormone treatment on insulin secretion and glucose metabolism in prepubertal boys with short stature. Eur Endocrinol 1994;131:246–50. ISSN 0804–4643 The purpose of this study was to evaluate the effect on insulin secretion and glucose metabolism of daily growth hormone (GH) treatment, 0.1 U/kg. for up to 3 years in 42 short prepubertal boys without GH deficiency. Their median height standard deviation (sd) score increased from −2.7 to −1.7, whereas their weight for height sd score was unchanged after 3 years of treatment. Fasting plasma glucose concentrations were unchanged, but median fasting insulin concentrations increased from 6.0 mU/l before treatment to 7.8 mU/l (p < 0.05) after the first year. No further increase was seen during the second or third years. The median insulin area under the curve 10–60 min after an intravenous glucose tolerance test increased from 480 mU·1−1·min−1 before treatment to 799 mU·1−1 · min−1 (p < 0.05) after 1 year. The median glucose disposal rate (K value) before GH treatment, 2.2%/min, was unchanged after 1 year of treatment. A significant positive correlation was found between the change in the height sd score and the change in fasting insulin concentration during the first (r = 0.45; p < 0.01) and second (r = 0.56; p < 0.05) years of GH treatment. It was concluded that GH treatment in prepubertal children without GH deficiency caused a moderate increase in fasting and stimulated insulin concentrations during the first year of treatment. There was no further change during the following years of treatment, and there were no negative effects on fasting plasma glucose concentrations or glucose disposal rates. The increase in insulin concentration was related positively to the growth response. Jan Åman, Department of Pediatrics, Örebro Medical Centre Hospital, S-701 85 Örebro, Sweden


1995 ◽  
Vol 42 (4) ◽  
pp. 359-363 ◽  
Author(s):  
L. C. K. Low ◽  
E. Y. W. Kwan ◽  
Y. J. Lim ◽  
A. C. W. Lee ◽  
C. F. Tarn ◽  
...  

1995 ◽  
pp. 169-175
Author(s):  
Jens S. Christiansen ◽  
Jens O. L. Jørgensen ◽  
Nina Vahl ◽  
Anders Juul ◽  
Jørn Müller ◽  
...  

2020 ◽  
Vol 4 (Supplement_1) ◽  
Author(s):  
Anne Maria Rochtus ◽  
Joseph Vinckx ◽  
Francis Edouard de Zegher

Abstract Introduction: Intracranial lipomas are rare, congenital lesions, most often located at the midline. Most hypothalamic lipomas are asymptomatic, but some cases have been associated with precocious puberty, hypothermia, headache and/or obesity. Case: A 7-year-old boy was referred for short stature, and proved to be partially growth-hormone deficient. Magnetic resonance imaging (MRI) revealed a lipoma in the paramedian hypothalamus. Growth hormone treatment resulted in swift and uncomplicated catch-up growth. Discussion: The present case appears to be the first to link hypothalamic lipoma to GH deficiency. The neuro-endocrine pathophysiology underpinning this link remains to be explored.


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