Literature DB >> 22682630

The insulin-like growth factors and growth disorders of childhood.

Philippe F Backeljauw1, Steven D Chernausek.   

Abstract

Specific lesions of the growth hormone (GH)/insulin-like growth factor (IGF) axis have been identified in humans, each of which has distinctive auxologic and biochemical features. Measures of circulating IGF-I are useful in diagnosing growth disorders in childhood and in evaluating response to GH therapy. Recombinant human IGF-I is an effective treatment of severe primary IGF deficiency, which is typical of patients with GH receptor defects (Laron syndrome). Such treatment has been limited to a few severely affected patients. Future studies will provide new insight into IGF-I as treatment and into the nature of growth disorders that involve the IGF axis.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22682630     DOI: 10.1016/j.ecl.2012.04.010

Source DB:  PubMed          Journal:  Endocrinol Metab Clin North Am        ISSN: 0889-8529            Impact factor:   4.741


  8 in total

Review 1.  Growth hormone insensitivity: diagnostic and therapeutic approaches.

Authors:  S Kurtoğlu; N Hatipoglu
Journal:  J Endocrinol Invest       Date:  2015-06-11       Impact factor: 4.256

2.  Severe growth deficiency is associated with STAT5b mutations that disrupt protein folding and activity.

Authors:  Benjamin Varco-Merth; Eva Feigerlová; Ujwal Shinde; Ron G Rosenfeld; Vivian Hwa; Peter Rotwein
Journal:  Mol Endocrinol       Date:  2012-11-16

3.  Imaging IGF-I uptake in growth plate cartilage using in vivo multiphoton microscopy.

Authors:  Maria A Serrat; Gabriela Ion
Journal:  J Appl Physiol (1985)       Date:  2017-08-10

4.  Altered IGF-I activity and accelerated bone elongation in growth plates precede excess weight gain in a mouse model of juvenile obesity.

Authors:  Allison L Machnicki; Cassaundra A White; Chad A Meadows; Darby McCloud; Sarah Evans; Dominic Thomas; John D Hurley; Daniel Crow; Habiba Chirchir; Maria A Serrat
Journal:  J Appl Physiol (1985)       Date:  2022-01-06

5.  Safety, pharmacokinetics, and preliminary assessment of efficacy of mecasermin (recombinant human IGF-1) for the treatment of Rett syndrome.

Authors:  Omar S Khwaja; Eugenia Ho; Katherine V Barnes; Heather M O'Leary; Luis M Pereira; Yaron Finkelstein; Charles A Nelson; Vanessa Vogel-Farley; Geneva DeGregorio; Ingrid A Holm; Umakanth Khatwa; Kush Kapur; Mark E Alexander; Deirdre M Finnegan; Nicole G Cantwell; Alexandra C Walco; Leonard Rappaport; Matt Gregas; Raina N Fichorova; Michael W Shannon; Mriganka Sur; Walter E Kaufmann
Journal:  Proc Natl Acad Sci U S A       Date:  2014-03-12       Impact factor: 11.205

6.  Illness Severity, Social and Cognitive Ability, and EEG Analysis of Ten Patients with Rett Syndrome Treated with Mecasermin (Recombinant Human IGF-1).

Authors:  Giorgio Pini; Laura Congiu; Alberto Benincasa; Pietro DiMarco; Stefania Bigoni; Adam H Dyer; Niall Mortimer; Andrea Della-Chiesa; Sean O'Leary; Rachel McNamara; Kevin J Mitchell; Michael Gill; Daniela Tropea
Journal:  Autism Res Treat       Date:  2016-01-26

7.  Placebo-controlled crossover assessment of mecasermin for the treatment of Rett syndrome.

Authors:  Heather M O'Leary; Walter E Kaufmann; Katherine V Barnes; Kshitiz Rakesh; Kush Kapur; Daniel C Tarquinio; Nicole G Cantwell; Katherine J Roche; Suzanne A Rose; Alexandra C Walco; Natalie M Bruck; Grace A Bazin; Ingrid A Holm; Mark E Alexander; Lindsay C Swanson; Lauren M Baczewski; Chi‐Sang Poon; Juan M Mayor Torres; Charles A Nelson; Mustafa Sahin
Journal:  Ann Clin Transl Neurol       Date:  2018-01-31       Impact factor: 4.511

8.  Severe growth failure associated with a novel heterozygous nonsense mutation in the GHR transmembrane domain leading to elevated growth hormone binding protein.

Authors:  Ankur Rughani; Dongsheng Zhang; Kanimozhi Vairamani; Andrew Dauber; Vivian Hwa; Sowmya Krishnan
Journal:  Clin Endocrinol (Oxf)       Date:  2020-01-22       Impact factor: 3.478

  8 in total

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