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The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations

OBJECTIVE: The histopathological features of malignant hyperthermia (MH) and non-anaesthetic (mostly exertional) rhabdomyolysis (RM) due to RYR1 mutations have only been reported in a few cases. METHODS: We performed a retrospective multi-centre cohort study focussing on the histopathological featur...

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Autores principales: Knuiman, G. J., Küsters, B., Eshuis, L., Snoeck, M., Lammens, M., Heytens, L., De Ridder, W., Baets, J., Scalco, R. S., Quinlivan, R., Holton, J., Bodi, I., Wraige, E., Radunovic, A., von Landenberg, C., Reimann, J., Kamsteeg, E.-J., Sewry, C., Jungbluth, H., Voermans, N. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420893/
https://www.ncbi.nlm.nih.gov/pubmed/30788618
http://dx.doi.org/10.1007/s00415-019-09209-z
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author Knuiman, G. J.
Küsters, B.
Eshuis, L.
Snoeck, M.
Lammens, M.
Heytens, L.
De Ridder, W.
Baets, J.
Scalco, R. S.
Quinlivan, R.
Holton, J.
Bodi, I.
Wraige, E.
Radunovic, A.
von Landenberg, C.
Reimann, J.
Kamsteeg, E.-J.
Sewry, C.
Jungbluth, H.
Voermans, N. C.
author_facet Knuiman, G. J.
Küsters, B.
Eshuis, L.
Snoeck, M.
Lammens, M.
Heytens, L.
De Ridder, W.
Baets, J.
Scalco, R. S.
Quinlivan, R.
Holton, J.
Bodi, I.
Wraige, E.
Radunovic, A.
von Landenberg, C.
Reimann, J.
Kamsteeg, E.-J.
Sewry, C.
Jungbluth, H.
Voermans, N. C.
author_sort Knuiman, G. J.
collection PubMed
description OBJECTIVE: The histopathological features of malignant hyperthermia (MH) and non-anaesthetic (mostly exertional) rhabdomyolysis (RM) due to RYR1 mutations have only been reported in a few cases. METHODS: We performed a retrospective multi-centre cohort study focussing on the histopathological features of patients with MH or RM due to RYR1 mutations (1987–2017). All muscle biopsies were reviewed by a neuromuscular pathologist. Additional morphometric and electron microscopic analysis were performed where possible. RESULTS: Through the six participating centres we identified 50 patients from 46 families, including patients with MH (n = 31) and RM (n = 19). Overall, the biopsy of 90% of patients showed one or more myopathic features including: increased fibre size variability (n = 44), increase in the number of fibres with internal nuclei (n = 30), and type I fibre predominance (n = 13). Abnormalities on oxidative staining, generally considered to be more specifically associated with RYR1-related congenital myopathies, were observed in 52%, and included unevenness (n = 24), central cores (n = 7) and multi-minicores (n = 3). Apart from oxidative staining abnormalities more frequently observed in MH patients, the histopathological spectrum was similar between the two groups. There was no correlation between the presence of cores and the occurrence of clinically detectable weakness or presence of (likely) pathogenic variants. CONCLUSIONS: Patients with RYR1-related MH and RM exhibit a similar histopathological spectrum, ranging from mild myopathic changes to cores and other features typical of RYR1-related congenital myopathies. Suggestive histopathological features may support RYR1 involvement, also in cases where the in vitro contracture test is not informative. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-019-09209-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-64208932019-04-03 The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations Knuiman, G. J. Küsters, B. Eshuis, L. Snoeck, M. Lammens, M. Heytens, L. De Ridder, W. Baets, J. Scalco, R. S. Quinlivan, R. Holton, J. Bodi, I. Wraige, E. Radunovic, A. von Landenberg, C. Reimann, J. Kamsteeg, E.-J. Sewry, C. Jungbluth, H. Voermans, N. C. J Neurol Original Communication OBJECTIVE: The histopathological features of malignant hyperthermia (MH) and non-anaesthetic (mostly exertional) rhabdomyolysis (RM) due to RYR1 mutations have only been reported in a few cases. METHODS: We performed a retrospective multi-centre cohort study focussing on the histopathological features of patients with MH or RM due to RYR1 mutations (1987–2017). All muscle biopsies were reviewed by a neuromuscular pathologist. Additional morphometric and electron microscopic analysis were performed where possible. RESULTS: Through the six participating centres we identified 50 patients from 46 families, including patients with MH (n = 31) and RM (n = 19). Overall, the biopsy of 90% of patients showed one or more myopathic features including: increased fibre size variability (n = 44), increase in the number of fibres with internal nuclei (n = 30), and type I fibre predominance (n = 13). Abnormalities on oxidative staining, generally considered to be more specifically associated with RYR1-related congenital myopathies, were observed in 52%, and included unevenness (n = 24), central cores (n = 7) and multi-minicores (n = 3). Apart from oxidative staining abnormalities more frequently observed in MH patients, the histopathological spectrum was similar between the two groups. There was no correlation between the presence of cores and the occurrence of clinically detectable weakness or presence of (likely) pathogenic variants. CONCLUSIONS: Patients with RYR1-related MH and RM exhibit a similar histopathological spectrum, ranging from mild myopathic changes to cores and other features typical of RYR1-related congenital myopathies. Suggestive histopathological features may support RYR1 involvement, also in cases where the in vitro contracture test is not informative. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-019-09209-z) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-02-20 2019 /pmc/articles/PMC6420893/ /pubmed/30788618 http://dx.doi.org/10.1007/s00415-019-09209-z Text en © The Author(s) 2019 Open AccessThis 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.
spellingShingle Original Communication
Knuiman, G. J.
Küsters, B.
Eshuis, L.
Snoeck, M.
Lammens, M.
Heytens, L.
De Ridder, W.
Baets, J.
Scalco, R. S.
Quinlivan, R.
Holton, J.
Bodi, I.
Wraige, E.
Radunovic, A.
von Landenberg, C.
Reimann, J.
Kamsteeg, E.-J.
Sewry, C.
Jungbluth, H.
Voermans, N. C.
The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations
title The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations
title_full The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations
title_fullStr The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations
title_full_unstemmed The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations
title_short The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations
title_sort histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to ryr1 mutations
topic Original Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420893/
https://www.ncbi.nlm.nih.gov/pubmed/30788618
http://dx.doi.org/10.1007/s00415-019-09209-z
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