Predicting the response to recombinant human growth hormone in Turner syndrome: KIGS models |
| |
Authors: | MB Ranke A Lindberg P chatelain P Wilton W Cutfield K Albertsson-Wikland DA Price |
| |
Affiliation: | Paediatric Endocrinology Section University Children's Hospital, Tübingen, Germany;Pharmacia &Upjohn Stockholm, Sweden, Service de Pédiatrie;endocrinologie et Diabétologie Infantiles, UniversitéClaude Bernard, Hôpital Debrousse, Lyon, France;Department of Pediatrics University of Auckland, Auckland, New Zealand;Department of Pediatrics East Hospital, Göteborg, Sweden, UK;Department of Pediatrics St Mary's Hospital, Manchester, UK |
| |
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 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. |
| |
Keywords: | Growth hormone KIGS prediction models Turner syndrome |
|
|