Spontaneous improvement of carbohydrate-deficient transferrin in PMM2-CDG without mannose observed in CDG natural history study.

Peter Witters, Andrew C Edmondson, Christina Lam, Christin Johnsen, Marc C Patterson, Kimiyo M Raymond, Miao He, Hudson H Freeze, Eva Morava

Journal: Orphanet journal of rare diseases 2021;16(1):102

PMID: 33632285

Abstract

A recent report on long-term dietary mannose supplementation in phosphomannomutase 2 deficiency (PMM2-CDG) claimed improved glycosylation and called for double-blind randomized study of the dietary supplement in PMM2-CDG patients. A lack of efficacy of short-term mannose supplementation in multiple prior reports challenge this study's conclusions. Additionally, some CDG types have previously been reported to demonstrate spontaneous improvement in glycosylated biomarkers, including transferrin. We have likewise observed improvements in transferrin glycosylation without mannose supplementation. This observation questions the reliability of transferrin as a therapeutic outcome measure in clinical trials for PMM2-CDG. We are concerned that renewed focus on mannose therapy in PMM2-CDG will detract from clinical trials of more promising therapies. Approaches to increase efficiency of clinical trials and ultimately improve patients' lives requires prospective natural history studies and identification of reliable biomarkers linked to clinical outcomes in CDG. Collaborations with patients and families are essential to identifying meaningful study outcomes.

Address: Department of Paediatrics and Metabolic Center, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium. [email protected].; Department of Development and Regeneration, KU Leuven, Leuven, Belgium. [email protected].; Department of Pediatrics, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Pediatrics, Division of Genetic Medicine, University of Washington, Seattle, WA, USA.; Center of Integrated Brain Research, Seattle Children's Research Institute, Seattle, WA, USA.; Department of Clinical Genomics, Mayo Clinic, 200 First Street, SW, Rochester, MN, 55905, USA.; Department of Neurology, Mayo Clinic, Rochester, MN, USA.; Biochemical Genetics Laboratory, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.; Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Human Genetics Program, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.; Department of Clinical Genomics, Mayo Clinic, 200 First Street, SW, Rochester, MN, 55905, USA. [email protected].
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