Research
Print page Print page
Switch language
The Capital Region of Denmark - a part of Copenhagen University Hospital
Published

A New Glycogen Storage Disease Caused by a Dominant PYGM Mutation

Research output: Contribution to journalJournal articleResearchpeer-review

DOI

  1. Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Amylin Analog Pramlintide Induces Migraine-like Attacks in Patients

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. MRI in Neuromuscular Diseases: An Emerging Diagnostic Tool and Biomarker for Prognosis and Efficacy

    Research output: Contribution to journalReviewResearchpeer-review

  4. Optic Disc Classification by Deep Learning versus Expert Neuro-Ophthalmologists

    Research output: Contribution to journalJournal articleResearchpeer-review

  1. Quantitative Muscle MRI and Clinical Findings in Women With Pathogenic Dystrophin Gene Variants

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Myopathy can be a key phenotype of membrin (GOSR2) deficiency

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Fatigue, physical activity and associated factors in 779 patients with myasthenia gravis

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Cardiac Involvement in Women With Pathogenic Dystrophin Gene Variants

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Efficacy and Safety of Rozanolixizumab in Moderate to Severe Generalized Myasthenia Gravis: A Phase 2 Randomized Control Trial

    Research output: Contribution to journalJournal articleResearchpeer-review

  • Andoni Echaniz-Laguna
  • Xavière Lornage
  • Pascal Laforêt
  • Mette C Orngreen
  • Evelina Edelweiss
  • Guy Brochier
  • Mai T Bui
  • Roberto Silva-Rojas
  • Catherine Birck
  • Béatrice Lannes
  • Norma B Romero
  • John Vissing
  • Jocelyn Laporte
  • Johann Böhm
View graph of relations

Objective: Glycogen storage diseases (GSDs) are severe human disorders resulting from abnormal glucose metabolism, and all previously described GSDs segregate as autosomal recessive or X-linked traits. In this study, we aimed to molecularly characterize the first family with a dominant GSD. Methods: We describe a dominant GSD family with 13 affected members presenting with adult-onset muscle weakness, and we provide clinical, metabolic, histological, and ultrastructural data. We performed exome sequencing to uncover the causative gene, and functional experiments in the cell model and on recombinant proteins to investigate the pathogenic effect of the identified mutation. Results: We identified a heterozygous missense mutation in PYGM segregating with the disease in the family. PYGM codes for myophosphorylase, the enzyme catalyzing the initial step of glycogen breakdown. Enzymatic tests revealed that the PYGM mutation impairs the AMP-independent myophosphorylase activity, whereas the AMP-dependent activity was preserved. Further functional investigations demonstrated an altered conformation and aggregation of mutant myophosphorylase, and the concurrent accumulation of the intermediate filament desmin in the myofibers of the patients. Interpretation: Overall, this study describes the first example of a dominant glycogen storage disease in humans, and elucidates the underlying pathomechanisms by deciphering the sequence of events from the PYGM mutation to the accumulation of glycogen in the muscle fibers. ANN NEUROL 2020;88:274–282.

Original languageEnglish
JournalAnnals of Neurology
Volume88
Issue number2
Pages (from-to)274-282
Number of pages9
ISSN0364-5134
DOIs
Publication statusPublished - Aug 2020

    Research areas

  • Adult, Female, Glycogen Phosphorylase, Muscle Form/genetics, Glycogen Storage Disease/diagnosis, Humans, Male, Middle Aged, Mutation/genetics, Pedigree

ID: 61073864