Risk of Cardiac Disease in a Population-Based Cohort of Myotonic Dystrophy Type 1 and Type 2 in the United States

This study confirms the increased risk of cardiac arrhythmias in individuals with DM and DM2 and identifies the development of cardiomyopathy as a low-frequency event. Notably, the risk of cardiac arrhythmias is particularly elevated in DM1. The study reaffirms the need for serial cardiac monitoring in individuals with DM1/DM2.

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Publication Details

Journal
Neurology Genetics
Published
2025-10-28
DOI
https://doi.org/10.1212/nxg.0000000000200322
Citations
1
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.91

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article

Risk of Cardiac Disease in a Population-Based Cohort of Myotonic Dystrophy Type 1 and Type 2 in the United States

Nicholas E. Johnson, Aida Soim, Treeva Jaff, Frank J. Raucci et al.
1 citations
Neurology Genetics
Genetic Neurodegenerative Diseases
0.91
article

Risk of Cardiac Disease in a Population-Based Cohort of Myotonic Dystrophy Type 1 and Type 2 in the United States

Nicholas E. Johnson, Aida Soim, Treeva Jaff, Frank J. Raucci, Emma Ciafaloni, Vinay Bhandaru, Yedatore Venkatesh, Madeline Murguia Rice, Jennifer Andrews
article en
1 citations

Abstract

This study confirms the increased risk of cardiac arrhythmias in individuals with DM and DM2 and identifies the development of cardiomyopathy as a low-frequency event. Notably, the risk of cardiac arrhythmias is particularly elevated in DM1. The study reaffirms the need for serial cardiac monitoring in individuals with DM1/DM2.

Neurology GeneticsVol. 11(6)
New York State Department of Health (US), University of Arizona (US), University of South Carolina (US), Virginia Commonwealth University (US), George Washington University (US), Children's Hospital of Richmond at VCU (US), University of Rochester (US)
Sanofi, Vertex Pharmaceuticals, Sarepta Therapeutics, Centers for Disease Control and Prevention, Sanofi Genzyme, National Heart, Lung, and Blood Institute, National Center for Advancing Translational Sciences
Openalex Percentile: Top 21%
Genetic Neurodegenerative Diseases
0.91
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