Outcome of creatine supplementation therapy in phosphoglucomutase-1 deficiency associated congenital disorders of glycosylation: Novel insights
PGM1-CDG associated myopathy is likely due to combination of several factors including abnormal muscle carbohydrate metabolism, abnormal N-glycosylation of proteins involved in the muscle functions and creatine transport and altered muscle energy homeostasis. It was previously shown that creatine supplementation therapy improves myopathy in patients with mitochondrial cytopathies. We think that the use of creatine supplementation therapy coincided with improvements in fatigue and exercise intolerance subjectively and objectively in our patient.
Authors
- Peter Seres (ORCID: https://orcid.org/0000-0002-8812-2234)
- Clara Hung (ORCID: https://orcid.org/0009-0004-7036-0914)
- Iveta Sosova (ORCID: https://orcid.org/0000-0002-5537-5892)
- Anastasia Ambrose
- Saadet Mercimek‐Andrews (ORCID: https://orcid.org/0000-0001-8396-6764)
- Marshall E. McCabe
Institutions
- Alberta Health Services (CA)
- University of Alberta (CA)
- Alberta Hospital Edmonton (CA)
- University of Alberta Hospital (CA)
- Women and Children’s Health Research Institute (CA)
Publication Details
- Journal
- Molecular Genetics and Metabolism Reports
- Published
- 2025-04-06
- DOI
- https://doi.org/10.1016/j.ymgmr.2025.101212
- Citations
- 1
- Primary Topic
- Glycogen Storage Diseases and Myoclonus
- Type
- article
- Field-Weighted Citation Impact
- 1.67