Developing endpoints for the cardiac burden in myotonic dystrophy type 1: A workshop report

Cardiac disease is a well-established manifestation of myotonic dystrophy type 1 (DM1), characterized by progressive cardiac conduction slowing with increased risk of atrial and ventricular arrhythmias, heart block, and sudden cardiac death. Multiple disease modifying therapies are in clinical trials for DM1 and show promise in improving skeletal muscle weakness and myotonia. Testing the effects of these medicines, or others, in the heart is of critical importance, but requires identification of endpoints of cardiac function that accurately reflect the state of DM1 cardiac disease. To better define cardiac endpoints, the Myotonic Dystrophy Clinical Research Network (DMCRN) and the Myotonic Dystrophy Foundation (MDF) convened a workshop entitled ''Cardiac Endpoint Workshop'' in May 2025 at the Myotonic Dystrophy Foundation International Conference. Here, we summarize the discussion at the workshop and perform secondary analysis of cardiac outcomes in the published literature to evaluate cardiac endpoints for clinical impact and trial feasibility. This analysis demonstrates that major cardiac events are too infrequent (<1% annual incidence), and alternatives such as composite endpoints or progression of cardiac conduction prolongation would likely be underpowered in a conventional clinical trial. Given these limitations, we identify areas for further natural history study to better describe longitudinal cardiac structural and functional changes to inform specialized patient selection or identify alternative measures with sensitivity to detect therapeutic impact in a trial.

Authors

Institutions

Publication Details

Journal
Journal of Neuromuscular Diseases
Published
2026-04-07
DOI
https://doi.org/10.1177/22143602261433484
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Developing endpoints for the cardiac burden in myotonic dystrophy type 1: A workshop report

Jordana Kron, Thomas A. Cooper, J Hartman, Samuel Carrell et al.
Journal of Neuromuscular Diseases
Genetic Neurodegenerative Diseases
article

Developing endpoints for the cardiac burden in myotonic dystrophy type 1: A workshop report

Jordana Kron, Thomas A. Cooper, J Hartman, Samuel Carrell, Greg Hundley, J. H. Jordan, Man Hung, Amy Ladd, Nicholas E Johnson
article en

Abstract

Cardiac disease is a well-established manifestation of myotonic dystrophy type 1 (DM1), characterized by progressive cardiac conduction slowing with increased risk of atrial and ventricular arrhythmias, heart block, and sudden cardiac death. Multiple disease modifying therapies are in clinical trials for DM1 and show promise in improving skeletal muscle weakness and myotonia. Testing the effects of these medicines, or others, in the heart is of critical importance, but requires identification of endpoints of cardiac function that accurately reflect the state of DM1 cardiac disease. To better define cardiac endpoints, the Myotonic Dystrophy Clinical Research Network (DMCRN) and the Myotonic Dystrophy Foundation (MDF) convened a workshop entitled ''Cardiac Endpoint Workshop'' in May 2025 at the Myotonic Dystrophy Foundation International Conference. Here, we summarize the discussion at the workshop and perform secondary analysis of cardiac outcomes in the published literature to evaluate cardiac endpoints for clinical impact and trial feasibility. This analysis demonstrates that major cardiac events are too infrequent (<1% annual incidence), and alternatives such as composite endpoints or progression of cardiac conduction prolongation would likely be underpowered in a conventional clinical trial. Given these limitations, we identify areas for further natural history study to better describe longitudinal cardiac structural and functional changes to inform specialized patient selection or identify alternative measures with sensitivity to detect therapeutic impact in a trial.

Journal of Neuromuscular Diseases
Medical University of South Carolina (US), Baylor College of Medicine (US), Virginia Commonwealth University (US), Roseman University of Health Sciences (US)
Myotonic Dystrophy Foundation, Pfizer, Novartis, Muscular Dystrophy Association, Vertex Pharmaceuticals, Takeda Medical Research Foundation, U.S. Food and Drug Administration, Sanofi Genzyme
Openalex Percentile: Top 28%
Genetic Neurodegenerative Diseases
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.