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Cardiomyopathy in limb girdle muscular dystrophy R9, FKRP related
INTRODUCTION: Reported frequencies of cardiomyopathy in limb girdle muscular dystrophy R9 (LGMDR9) vary. We describe the frequency and age at onset of cardiomyopathy in an LDMDR9 cohort. METHODS: Echocardiograms from 56 subjects (157 echocardiograms) with LGMDR9 were retrospectively reviewed. The cu...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693230/ https://www.ncbi.nlm.nih.gov/pubmed/32914449 http://dx.doi.org/10.1002/mus.27052 |
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author | Libell, Eric M. Richardson, Julia A. Lutz, Katie L. Ng, Benton Y. Mockler, Shelley R. H. Laubscher, Katie M. Stephan, Carrie M. Zimmerman, Bridget M. Edens, Erik R. Reinking, Benjamin E. Mathews, Katherine D. |
author_facet | Libell, Eric M. Richardson, Julia A. Lutz, Katie L. Ng, Benton Y. Mockler, Shelley R. H. Laubscher, Katie M. Stephan, Carrie M. Zimmerman, Bridget M. Edens, Erik R. Reinking, Benjamin E. Mathews, Katherine D. |
author_sort | Libell, Eric M. |
collection | PubMed |
description | INTRODUCTION: Reported frequencies of cardiomyopathy in limb girdle muscular dystrophy R9 (LGMDR9) vary. We describe the frequency and age at onset of cardiomyopathy in an LDMDR9 cohort. METHODS: Echocardiograms from 56 subjects (157 echocardiograms) with LGMDR9 were retrospectively reviewed. The cumulative probability of having an abnormal echocardiogram as a function of age was assessed by survival analysis for interval‐censored data by genotype. Correlations between cardiac and clinical function were evaluated. RESULTS: Twenty‐five (45%) participants had cardiomyopathy. The median age at first abnormal echocardiogram for subjects homozygous for the c.826C>A variant was 54.2 y compared to 18.1 y for all other fukutin‐related protein (FKRP) genotypes (P < .0001). There was a weak correlation between ejection fraction and 10‐Meter Walk Test speed (r = 0.25), but no correlation with forced vital capacity (r = 0.08). DISCUSSION: Cardiomyopathy is prevalent among those with LGMDR9 and occurs later in subjects homozygous for the c.826C>A mutation. These data will help to guide surveillance and management. |
format | Online Article Text |
id | pubmed-7693230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76932302020-12-11 Cardiomyopathy in limb girdle muscular dystrophy R9, FKRP related Libell, Eric M. Richardson, Julia A. Lutz, Katie L. Ng, Benton Y. Mockler, Shelley R. H. Laubscher, Katie M. Stephan, Carrie M. Zimmerman, Bridget M. Edens, Erik R. Reinking, Benjamin E. Mathews, Katherine D. Muscle Nerve Clinical Research Articles INTRODUCTION: Reported frequencies of cardiomyopathy in limb girdle muscular dystrophy R9 (LGMDR9) vary. We describe the frequency and age at onset of cardiomyopathy in an LDMDR9 cohort. METHODS: Echocardiograms from 56 subjects (157 echocardiograms) with LGMDR9 were retrospectively reviewed. The cumulative probability of having an abnormal echocardiogram as a function of age was assessed by survival analysis for interval‐censored data by genotype. Correlations between cardiac and clinical function were evaluated. RESULTS: Twenty‐five (45%) participants had cardiomyopathy. The median age at first abnormal echocardiogram for subjects homozygous for the c.826C>A variant was 54.2 y compared to 18.1 y for all other fukutin‐related protein (FKRP) genotypes (P < .0001). There was a weak correlation between ejection fraction and 10‐Meter Walk Test speed (r = 0.25), but no correlation with forced vital capacity (r = 0.08). DISCUSSION: Cardiomyopathy is prevalent among those with LGMDR9 and occurs later in subjects homozygous for the c.826C>A mutation. These data will help to guide surveillance and management. John Wiley & Sons, Inc. 2020-09-10 2020-11 /pmc/articles/PMC7693230/ /pubmed/32914449 http://dx.doi.org/10.1002/mus.27052 Text en © 2020 The Authors. Muscle & Nerve published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Clinical Research Articles Libell, Eric M. Richardson, Julia A. Lutz, Katie L. Ng, Benton Y. Mockler, Shelley R. H. Laubscher, Katie M. Stephan, Carrie M. Zimmerman, Bridget M. Edens, Erik R. Reinking, Benjamin E. Mathews, Katherine D. Cardiomyopathy in limb girdle muscular dystrophy R9, FKRP related |
title | Cardiomyopathy in limb girdle muscular dystrophy R9, FKRP related |
title_full | Cardiomyopathy in limb girdle muscular dystrophy R9, FKRP related |
title_fullStr | Cardiomyopathy in limb girdle muscular dystrophy R9, FKRP related |
title_full_unstemmed | Cardiomyopathy in limb girdle muscular dystrophy R9, FKRP related |
title_short | Cardiomyopathy in limb girdle muscular dystrophy R9, FKRP related |
title_sort | cardiomyopathy in limb girdle muscular dystrophy r9, fkrp related |
topic | Clinical Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693230/ https://www.ncbi.nlm.nih.gov/pubmed/32914449 http://dx.doi.org/10.1002/mus.27052 |
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