Literature DB >> 8636336

Monitoring of growth hormone replacement therapy in adults, based on measurement of serum markers.

H de Boer1, G J Blok, C Popp-Snijders, L Stuurman, R C Baxter, E van der Veen.   

Abstract

The optimal dose for GH replacement therapy in GH-deficient (GHD) adults is not known, nor is there a consensus as to which method is the most appropriate for the monitoring of treatment. To establish a general guideline for GH replacement therapy in adults, we evaluated the relationship between the administered GH dose and the achieved serum levels of three GH-dependent serum markers. Serum levels of insulin-like growth factor I (IGF-I), IGF-binding protein-3 (IGFBP-3), and the acid-labile subunit (ALS) were measured in 46 GHD men participating in a 1-yr, double blind, and placebo-controlled dose-response study. The doses of recombinant human GH ranged from 0.33-3.0 IU/m(2)-day. During GH treatment, dose reduction was necessary because of side-effects in 18 of 46 patients, i.e. in 18% of the patients receiving a maintenance dose of 1 IU/M(2)-day, in 35% of the patients receiving a dose of 2 IU/m(2)-day, and in 67% of the patients receiving a dose of 3 IU/M(2)-day. In the untreated state, serum levels of all three markers were below the normal range in 90% of the patients. The rise in serum marker concentrations during the first month of treatment was dose dependent. Significant increases in IGF-I, IGFBP-3, and ALS levels were observed with a dose as low as 0.33 IU/M(2)-day. The minimal GH dose required for normalization of the serum IGF-I concentration was 0.66 IU/M(2)-day, and it was 1.0 IU/M(2)-day for ALS and IGFBP-3. In patients receiving 2.0 IU/M(2)-day, the mean serum IGF-I concentration rose to an abnormally high level, whereas at this dose, the mean IGFBP-3 and ALS levels were not different from normal. The lower sensitivity of IGFBP-3 and ALS to GH doses in the high range was also apparent during long term treatment. The number of patients who developed IGFBP-3 or ALS levels that exceeded the upper normal limit was substantially smaller than the number of patients with elevated IGF-I concentrations (2, 8, and 19 of 46 patients, respectively). In conclusion, serum IGF-I appears to be the preferred biochemical marker for the detection of GH excess in adults receiving GH replacement therapy, because it is more sensitive than IGFBP-3 and ALS to GH doses in the high range. If normalization of the serum IGF-I concentration is taken as the criterion for optimal GH replacement therapy, the predicted optimal GH dose for GHD men 20 - 40 yr old is 1.4 IU/M(2)-day, and the 95% confidence interval is 1.2-1.6 IU/M(2)-day.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8636336     DOI: 10.1210/jcem.81.4.8636336

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  12 in total

1.  Normal IGF-I and enhanced IGFBP-3 response to very low rhGH dose in patients with dilated cardiomyopathy.

Authors:  F Broglio; A Benso; E Arvat; G Aimaretti; C Gottero; R Granata; M F Boghen; M Bobbio; F Camanni; E Ghigo
Journal:  J Endocrinol Invest       Date:  2000-09       Impact factor: 4.256

Review 2.  Long-term growth hormone replacement therapy in hypopituitary adults.

Authors:  Johan Verhelst; Roger Abs
Journal:  Drugs       Date:  2002       Impact factor: 9.546

Review 3.  Current guidelines for adult GH replacement.

Authors:  Mauro Doga; Stefania Bonadonna; Monica Gola; Sebastiano Bruno Solerte; Giovanni Amato; Carlo Carella; Andrea Giustina
Journal:  Rev Endocr Metab Disord       Date:  2005-01       Impact factor: 6.514

4.  DHEA-S levels in hypopituitaric patients with severe GH deficiency are strongly reduced across lifespan. Comparison with IGF-I levels before and during rhGH replacement.

Authors:  G Aimaretti; C Baffoni; M R Ambrosio; M Maccario; G Corneli; S Bellone; M Gasperi; E Degli Uberti; E Ghigo
Journal:  J Endocrinol Invest       Date:  2000-01       Impact factor: 4.256

5.  Effects of growth hormone deficiency and recombinant growth hormone therapy on postprandial gallbladder motility and cholecystokinin release.

Authors:  Antonio Moschetta; Th B Twickler; Jens F Rehfeld; Nancy A M van Ooteghem; Manuel Castro Cabezas; Piero Portincasa; Gerard P van Berge-Henegouwen; Karel J van Erpecum
Journal:  Dig Dis Sci       Date:  2004-03       Impact factor: 3.199

6.  Usefulness of IGF-I assay for the diagnosis of GH deficiency in adults.

Authors:  G Aimaretti; G Corneli; P Razzore; S Bellone; C Baffoni; J Bellone; F Camanni; E Ghigo
Journal:  J Endocrinol Invest       Date:  1998-09       Impact factor: 4.256

Review 7.  Effects of GH and insulin-like growth factor-I on body composition.

Authors:  J Svensson; L Lönn; G Johannsson; B A Bengtsson
Journal:  J Endocrinol Invest       Date:  2003-09       Impact factor: 4.256

Review 8.  Treatment of adult growth hormone deficiency with human recombinant growth hormone: an update on current evidence and critical review of advantages and pitfalls.

Authors:  Ana M Ramos-Leví; Mónica Marazuela
Journal:  Endocrine       Date:  2018-02-07       Impact factor: 3.633

9.  Short children with familial short stature show enhancement of somatotroph secretion but normal IGF-I levels.

Authors:  S Bellone; G Corneli; J Bellone; C Baffoni; S Rovere; C de Sanctis; G Bona; E Ghigo; G Aimaretti
Journal:  J Endocrinol Invest       Date:  2002-05       Impact factor: 5.467

Review 10.  Growth Hormone Research Society perspective on biomarkers of GH action in children and adults.

Authors:  Gudmundur Johannsson; Martin Bidlingmaier; Beverly M K Biller; Margaret Boguszewski; Felipe F Casanueva; Philippe Chanson; Peter E Clayton; Catherine S Choong; David Clemmons; Mehul Dattani; Jan Frystyk; Ken Ho; Andrew R Hoffman; Reiko Horikawa; Anders Juul; John J Kopchick; Xiaoping Luo; Sebastian Neggers; Irene Netchine; Daniel S Olsson; Sally Radovick; Ron Rosenfeld; Richard J Ross; Katharina Schilbach; Paulo Solberg; Christian Strasburger; Peter Trainer; Kevin C J Yuen; Kerstin Wickstrom; Jens O L Jorgensen
Journal:  Endocr Connect       Date:  2018-02-26       Impact factor: 3.335

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.