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      Comparison of Four Computerized Models to Estimate 24-Hour Growth Hormone Secretion in Girls with Turner’s Syndrome

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          Abstract

          Daily pituitary growth hormone (GH) secretion can be estimated from a 24-hour GH profile by various methods. We have used four methods to assess GH secretion in 36 girls with Turner’s syndrome: the method described by Thompson et al., the Pulsar algorithm combined with the method of Hellman et al. and two deconvolution techniques. The number of detected peaks varied considerably among the methods. The mean ( ± SD) total daily secretion per square meter body surface was 0.53 (0.19) U/m<sup>2</sup>·day by deconvolution, in contrast to 0.31 (0.17) with the Hellman method and 1.06 (0.37) according to Thompson. The differences are explained by different assumptions about the metabolic clearance rate and various methodological aspects. Assuming a degradation rate of 50%, the growth hormone substitution dosage would be 1-2 IU/m<sup>2</sup>· day in GH-deficient children. The usual dosage in girls with Turner’s syndrome is expected to lead to serum GH levels approximately 4 times higher than in the untreated state.

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          Author and article information

          Journal
          HRE
          Horm Res Paediatr
          10.1159/issn.1663-2818
          Hormone Research in Paediatrics
          S. Karger AG
          1663-2818
          1663-2826
          1992
          1992
          03 December 2008
          : 38
          : 3-4
          : 125-133
          Affiliations
          aDivision of Endocrinology, Department of Pediatrics, Wilhelmina Childrens Hospital, State University, Utrecht, The Netherlands; bDivision of Endocrinology and Metabolism, Department of Internal Medicine, and cDepartment of Pharmacology, University of Virginia, Charlottesville, Va., USA
          Article
          182527 Horm Res 1992;38:125–133
          10.1159/000182527
          1306843
          3865d108-ea4d-4f47-a0c4-4668e7eb8bfc
          © 1992 S. Karger AG, Basel

          Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher. Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug. Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.

          History
          : 27 January 1992
          : 27 November 1992
          Page count
          Pages: 9
          Categories
          Original Paper

          Endocrinology & Diabetes,Neurology,Nutrition & Dietetics,Sexual medicine,Internal medicine,Pharmacology & Pharmaceutical medicine
          Deconvolution analysis,Growth,Turner’s syndrome,Growth failure,Growth hormone secretion

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