Literature DB >> 28888851

Long term longitudinal study of muscle function in patients with glycogen storage disease type IIIa.

Valérie Decostre1, Pascal Laforêt2, Marie De Antonio3, Kahina Kachetel4, Aurélie Canal5, Gwenn Ollivier5, Aleksandra Nadaj-Pakleza4, François M Petit6, Karim Wahbi7, Abdallah Fayssoil5, Bruno Eymard4, Anthony Behin4, Philippe Labrune8, Jean-Yves Hogrel5.   

Abstract

Glycogen storage disease type III (GSDIII) is an autosomal recessive disorder caused by mutations in the AGL gene coding for the glycogen debranching enzyme. Current therapy is based on dietary adaptations but new preclinical therapies are emerging. The identification of outcome measures which are sensitive to disease progression becomes critical to assess the efficacy of new treatments in upcoming clinical trials. In order to prepare future longitudinal studies or therapeutic trials with large cohorts, information about disease progression is required. In this study we present preliminary longitudinal data of Motor Function Measure (MFM), timed tests, Purdue pegboard test, and handgrip strength collected over 5 to 9years of follow-up in 13 patients with GSDIII aged between 13 and 56years old. Follow-up for nine of the 13 patients was up to 9years. Similarly to our previous cross-sectional retrospective study, handgrip strength significantly decreased with age in patients older than 37years. MFM scores started to decline after the age of 35. The Purdue pegboard score also significantly reduced with increasing age (from 13years of age) but with large inter-visit variations. The time to stand up from a chair or to climb 4 stairs increased dramatically in some but not all patients older than 30years old. In conclusion, this preliminary longitudinal study suggests that MFM and handgrip strength are the most sensitive muscle function outcome measures in GSDIII patients from the end of their third decade. Sensitive muscle outcome measures remain to be identified in younger GSDIII patients but is challenging as muscle symptoms remain discrete and often present as accumulated fatigue.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Debranching enzyme deficiency; Glycogen storage disease type III; Metabolic myopathy; Outcome measures

Mesh:

Year:  2017        PMID: 28888851     DOI: 10.1016/j.ymgme.2017.08.010

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  3 in total

Review 1.  Physical therapy assessment and whole-body magnetic resonance imaging findings in children with glycogen storage disease type IIIa: A clinical study and review of the literature.

Authors:  Anna Paschall; Aleena A Khan; Syed Faaiz Enam; Tracy Boggs; Ghada Hijazi; Michael Bowling; Stephanie Austin; Laura E Case; Priya Kishnani
Journal:  Mol Genet Metab       Date:  2021-10-09       Impact factor: 4.797

2.  Glycogen storage disease type IIIa in pregnant women: A guide to management.

Authors:  Demi Beneru; Michel C Tchan; Kate Billmore; Roshini Nayyar
Journal:  JIMD Rep       Date:  2022-03-22

3.  Deep morphological analysis of muscle biopsies from type III glycogenesis (GSDIII), debranching enzyme deficiency, revealed stereotyped vacuolar myopathy and autophagy impairment.

Authors:  Pascal Laforêt; Michio Inoue; Evelyne Goillot; Claire Lefeuvre; Umut Cagin; Nathalie Streichenberger; Sarah Leonard-Louis; Guy Brochier; Angeline Madelaine; Clemence Labasse; Carola Hedberg-Oldfors; Thomas Krag; Louisa Jauze; Julien Fabregue; Philippe Labrune; Jose Milisenda; Aleksandra Nadaj-Pakleza; Sabrina Sacconi; Federico Mingozzi; Giuseppe Ronzitti; François Petit; Benedikt Schoser; Anders Oldfors; John Vissing; Norma B Romero; Ichizo Nishino; Edoardo Malfatti
Journal:  Acta Neuropathol Commun       Date:  2019-10-28       Impact factor: 7.801

  3 in total

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