Hedberg-Oldfors, C;
Glamuzina, E;
Ruygrok, P;
Anderson, LJ;
Elliott, P;
Watkinson, O;
Occleshaw, C;
... Oldfors, A; + view all
(2017)
Cardiomyopathy as presenting sign of glycogenin-1 deficiency-report of three cases and review of the literature.
Journal of Inherited Metabolic Disease
, 40
(1)
pp. 139-149.
10.1007/s10545-016-9978-1.
Preview |
Text
10.1007%2Fs10545-016-9978-1.pdf - Published Version Download (4MB) | Preview |
Abstract
We describe a new type of cardiomyopathy caused by a mutation in the glycogenin-1 gene (GYG1). Three unrelated male patients aged 34 to 52 years with cardiomyopathy and abnormal glycogen storage on endomyocardial biopsy were homozygous for the missense mutation p.Asp102His in GYG1. The mutated glycogenin-1 protein was expressed in cardiac tissue but had lost its ability to autoglucosylate as demonstrated by an in vitro assay and western blot analysis. It was therefore unable to form the primer for normal glycogen synthesis. Two of the patients showed similar patterns of heart dilatation, reduced ejection fraction and extensive late gadolinium enhancement on cardiac magnetic resonance imaging. These two patients were severely affected, necessitating cardiac transplantation. The cardiomyocyte storage material was characterized by large inclusions of periodic acid and Schiff positive material that was partly resistant to alpha-amylase treatment consistent with polyglucosan. The storage material had, unlike normal glycogen, a partly fibrillar structure by electron microscopy. None of the patients showed signs or symptoms of muscle weakness but a skeletal muscle biopsy in one case revealed muscle fibres with abnormal glycogen storage. Glycogenin-1 deficiency is known as a rare cause of skeletal muscle glycogen storage disease, usually without cardiomyopathy. We demonstrate that it may also be the cause of severe cardiomyopathy and cardiac failure without skeletal muscle weakness. GYG1 should be included in cardiomyopathy gene panels.
Type: | Article |
---|---|
Title: | Cardiomyopathy as presenting sign of glycogenin-1 deficiency-report of three cases and review of the literature |
Location: | Netherlands |
Open access status: | An open access version is available from UCL Discovery |
DOI: | 10.1007/s10545-016-9978-1 |
Publisher version: | http://doi.org/10.1007/s10545-016-9978-1 |
Language: | English |
Additional information: | Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http:// creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > Institute of Cardiovascular Science UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > Institute of Cardiovascular Science > Clinical Science |
URI: | https://discovery.ucl.ac.uk/id/eprint/1566870 |



1. | ![]() | 3 |
2. | ![]() | 2 |
3. | ![]() | 1 |
Archive Staff Only
![]() |
View Item |