Literature DB >> 10626562

Predicting the response to recombinant human growth hormone in Turner syndrome: KIGS models. KIGS International Board. Kabi International Growth Study.

M B Ranke1, A Lindberg, P Chatelain, P Wilton, W Cutfield, K Albertsson-Wikland, D A Price.   

Abstract

A mathematical model for predicting the growth response in patients with Turner syndrome who received growth hormone (GH) therapy was developed by analysing data from KIGS, the Pharmacia & Upjohn International Growth Database. A model for year 1 of GH therapy explained 46% of the variability of the growth response, with GH dose being the most important of the predictors of height velocity. In years 2-4 of therapy, height velocity during the previous year was the most important predictor, suggesting that an individual's initial response to GH may determine the height outcome of treatment. Additional predictors of height velocity in years 1-4 of GH therapy included age (negative), weight SDS and additional treatment with oxandrolone. The predictions in all 4 years were highly accurate, as indicated by the low error SDs. However, relatively low predictive power (R) during years 2-4 of treatment suggests the models are missing other parameters that would explain more of the variability of the growth response. These growth prediction models could help clinicians to design individualized treatment regimens, provide realistic expectations of therapy outcomes, and adjust treatment on the basis of detected differences between observed and predicted height velocities.

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Year:  1999        PMID: 10626562     DOI: 10.1111/j.1651-2227.1999.tb14420.x

Source DB:  PubMed          Journal:  Acta Paediatr Suppl        ISSN: 0803-5326


  4 in total

Review 1.  Pharmacogenomics applied to recombinant human growth hormone responses in children with short stature.

Authors:  Adam Stevens; Reena Perchard; Terence Garner; Peter Clayton; Philip Murray
Journal:  Rev Endocr Metab Disord       Date:  2021-03-12       Impact factor: 6.514

2.  A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome.

Authors:  P Clayton; P Chatelain; L Tatò; H W Yoo; G R Ambler; A Belgorosky; S Quinteiro; C Deal; A Stevens; J Raelson; P Croteau; B Destenaves; C Olivier
Journal:  Eur J Endocrinol       Date:  2013-07-29       Impact factor: 6.664

3.  Validating genetic markers of response to recombinant human growth hormone in children with growth hormone deficiency and Turner syndrome: the PREDICT validation study.

Authors:  Adam Stevens; Philip Murray; Jerome Wojcik; John Raelson; Ekaterina Koledova; Pierre Chatelain; Peter Clayton
Journal:  Eur J Endocrinol       Date:  2016-09-20       Impact factor: 6.664

4.  Gene expression signatures predict response to therapy with growth hormone.

Authors:  Adam Stevens; Philip Murray; Chiara De Leonibus; Terence Garner; Ekaterina Koledova; Geoffrey Ambler; Klaus Kapelari; Gerhard Binder; Mohamad Maghnie; Stefano Zucchini; Elena Bashnina; Julia Skorodok; Diego Yeste; Alicia Belgorosky; Juan-Pedro Lopez Siguero; Regis Coutant; Eirik Vangsøy-Hansen; Lars Hagenäs; Jovanna Dahlgren; Cheri Deal; Pierre Chatelain; Peter Clayton
Journal:  Pharmacogenomics J       Date:  2021-05-27       Impact factor: 3.550

  4 in total

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