Cardiac Conduction Disorders as Markers of Cardiac Events in Myotonic Dystrophy Type 1.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
09 2020
Historique:
pubmed: 20 8 2020
medline: 10 3 2021
entrez: 20 8 2020
Statut: ppublish

Résumé

Background Myotonic dystrophy type 1 involves cardiac conduction disorders. Cardiac conduction disease can cause fatal arrhythmias or sudden death in patients with myotonic dystrophy type 1. Methods and Results This study enrolled 506 patients with myotonic dystrophy type 1 (aged ≥15 years; >50 cytosine-thymine-guanine repeats) and was treated in 9 Japanese hospitals for neuromuscular diseases from January 2006 to August 2016. We investigated genetic and clinical backgrounds including health care, activities of daily living, dietary intake, cardiac involvement, and respiratory involvement during follow-up. The cause of death or the occurrence of composite cardiac events (ie, ventricular arrhythmias, advanced atrioventricular blocks, and device implantations) were evaluated as significant outcomes. During a median follow-up period of 87 months (Q1-Q3, 37-138 months), 71 patients expired. In the univariate analysis, pacemaker implantations (hazard ratio [HR], 4.35; 95% CI, 1.22-15.50) were associated with sudden death. In contrast, PQ interval ≥240 ms, QRS duration ≥120 ms, nutrition, or respiratory failure were not associated with the incidence of sudden death. The multivariable analysis revealed that a PQ interval ≥240 ms (HR, 2.79; 95% CI, 1.9-7.19,

Identifiants

pubmed: 32812471
doi: 10.1161/JAHA.119.015709
pmc: PMC7660777
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e015709

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Auteurs

Hideki Itoh (H)

Department of Cardiovascular Medicine Shiga University of Medical Science Otsu Japan.
Division of Patient Safety Hiroshima University Hospital Hiroshima Japan.

Takashi Hisamatsu (T)

Department of Public Health Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama Japan.

Takuhisa Tamura (T)

Department of Neurology National Hospital Organization Higashisaitama National Hospital Saitama Japan.

Kazuhiko Segawa (K)

Department of Cardiology National Center Hospital National Center of Neurology and Psychiatry Tokyo Japan.

Toshiaki Takahashi (T)

Department of Neurology National Hospital Organization Sendai-Nishitaga Hospital Sendai Japan.

Hiroto Takada (H)

Department of Neurology National Hospital Organization Aomori National Hospital Aomori Japan.

Satoshi Kuru (S)

Department of Neurology National Hospital Organization Suzuka National Hospital Suzuka Japan.

Chizu Wada (C)

Department of Neurology National Hospital Organization Akita National Hospital Akita Japan.

Mikiya Suzuki (M)

Department of Neurology National Hospital Organization Higashisaitama National Hospital Saitama Japan.

Shugo Suwazono (S)

Division of Neurology and Center for Clinical Neuroscience National Hospital Organization Okinawa National Hospital Ginowan Japan.

Shingo Sasaki (S)

Department of Advanced Management of Cardiac Arrhythmias Hirosaki University Graduate School of Medicine Hirosaki Japan.

Ken Okumura (K)

Advanced Arrhythmia Therapeutic Branch Division of Cardiology Saiseikai Kumamoto Hospital Cardiovascular Center Kumamoto Japan.

Minoru Horie (M)

Department of Cardiovascular Medicine Shiga University of Medical Science Otsu Japan.
Center for Epidemiologic Research in Asia and Department of Cardiology Shiga University of Medical Science Otsu Japan.

Masanori P Takahashi (MP)

Department of Functional Diagnostic Science Osaka University Graduate School of Medicine Suita Japan.

Tsuyoshi Matumura (T)

Department of Neurology National Hospital Organization Osaka Toneyama Medical Center 5-1-1 Toyonaka Japan.

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Classifications MeSH