An integrative correlation of myopathology, phenotype and genotype in late onset Pompe disease

  • Aims: Pompe disease is caused by pathogenic mutations in the alpha 1,4‐glucosidase (GAA) gene and in patients with late onset Pome disease (LOPD), genotype–phenotype correlations are unpredictable. Skeletal muscle pathology includes glycogen accumulation and altered autophagy of various degrees. A correlation of the muscle morphology with clinical features and the genetic background in GAA may contribute to the understanding of the phenotypic variability. Methods: Muscle biopsies taken before enzyme replacement therapy were analysed from 53 patients with LOPD. On resin sections, glycogen accumulation, fibrosis, autophagic vacuoles and the degree of muscle damage (morphology‐score) were analysed and the results were compared with clinical findings. Additional autophagy markers microtubule‐associated protein 1A/1B‐light chain 3, p62 and Bcl2‐associated athanogene 3 were analysed on cryosections from 22 LOPD biopsies. Results: The myopathology showed a high variability with, in most patients, a moderate glycogen accumulation and a low morphology‐score. High morphology‐scores were associated with increased fibrosis and autophagy highlighting the role of autophagy in severe stages of skeletal muscle damage. The morphology‐score did not correlate with the patient's age at biopsy, disease duration, nor with the residual GAA enzyme activity or creatine‐kinase levels. In 37 patients with LOPD, genetic analysis identified the most frequent mutation, c.‐32‐13T>G, in 95%, most commonly in combination with c.525delT (19%). No significant correlation was found between the different GAA genotypes and muscle morphology type. Conclusions: Muscle morphology in LOPD patients shows a high variability with, in most cases, moderate pathology. Increased pathology is associated with more fibrosis and autophagy.

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Author:Martin Kulessa, Iris Weyer‐Menkhoff, Lara Viergutz, Cornelia Kornblum, Kristl G. Claeys, Ilka Schneider, Ursula Plöckinger, Peter Young, Matthias Boentert, Stefan Vielhaber, Christian Mawrin, Markus Bergmann, Joachim Weis, Athanasia Ziagaki, Werner Stenzel, Marcus Deschauer, Dagmar Nolte, Andreas Hahn, Benedikt Schoser, Anne Schänzer
URN:urn:nbn:de:hebis:30:3-570305
DOI:https://doi.org/10.1111/nan.12580
ISSN:1365-2990
ISSN:0305-184
Parent Title (English):Neuropathology & applied neurobiology
Publisher:Wiley-Blackwell
Place of publication:Oxford [u.a.]
Document Type:Article
Language:English
Date of Publication (online):2019/09/23
Date of first Publication:2019/09/23
Publishing Institution:Universitätsbibliothek Johann Christian Senckenberg
Release Date:2020/12/08
Volume:46.2020
Page Number:16
First Page:359–374
Last Page:359–374
HeBIS-PPN:476273803
Institutes:Medizin / Medizin
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Sammlungen:Universitätspublikationen
Licence (German):License LogoCreative Commons - Namensnennung 4.0