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.

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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
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article

Outcome of creatine supplementation therapy in phosphoglucomutase-1 deficiency associated congenital disorders of glycosylation: Novel insights

Peter Seres, Clara Hung, Iveta Sosova, Anastasia Ambrose et al.
1 citations
Molecular Genetics and Metabolism Reports
Glycogen Storage Diseases and Myoclonus
1.67
article

Outcome of creatine supplementation therapy in phosphoglucomutase-1 deficiency associated congenital disorders of glycosylation: Novel insights

Peter Seres, Clara Hung, Iveta Sosova, Anastasia Ambrose, Saadet Mercimek‐Andrews, Marshall E. McCabe
article en
1 citations

Abstract

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.

Molecular Genetics and Metabolism ReportsVol. 43
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)
Zero hunger
Openalex Percentile: Top 19%
Glycogen Storage Diseases and Myoclonus
1.67
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Outcome of creatine supplementation therapy in phosphoglucomutase-1 deficiency associated congenital disorders of glycosylation: Novel insights — Peter Seres, Clara Hung, et al. · Molecular Genetics and Metabolism Reports (2025) | TGRS Research Map | TGRS