Cardiac Conduction Disorders as Markers of Cardiac Events in Myotonic Dystrophy Type 1.
Activities of Daily Living
Adult
Aftercare
Arrhythmias, Cardiac
/ physiopathology
Atrioventricular Block
/ epidemiology
Cardiac Conduction System Disease
/ complications
Death, Sudden, Cardiac
/ epidemiology
Eating
Female
Health Status
Humans
Incidence
Japan
/ epidemiology
Male
Middle Aged
Myotonic Dystrophy
/ complications
Pacemaker, Artificial
/ statistics & numerical data
Proportional Hazards Models
Retrospective Studies
conduction disturbance
myotonic dystrophy
sudden death
ventricular tachycardia
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
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
e015709Références
Circulation. 2017 Sep 26;136(13):e200-e231
pubmed: 28838934
J Neurol. 2002 Jun;249(6):693-8
pubmed: 12111301
Eur Heart J Case Rep. 2019 Jun 1;3(2):
pubmed: 31449640
J Am Heart Assoc. 2020 Jan 21;9(2):e014004
pubmed: 31931688
JAMA. 2012 Mar 28;307(12):1292-301
pubmed: 22453570
J Am Coll Cardiol. 1995 Jan;25(1):239-45
pubmed: 7798509
N Engl J Med. 2008 Jun 19;358(25):2688-97
pubmed: 18565861
Circ Cardiovasc Genet. 2017 Jun;10(3):
pubmed: 28611030
Eur Heart J. 2017 Mar 7;38(10):751-758
pubmed: 27941019
Int J Cardiol. 2012 Oct 4;160(2):82-8
pubmed: 21917328
J Am Heart Assoc. 2020 Feb 18;9(4):e014006
pubmed: 32067592
Circulation. 1998 Aug 11;98(6):541-6
pubmed: 9714111
N Engl J Med. 2008 Oct 9;359(15):1626; author reply 1328-9
pubmed: 18843129
J Am Heart Assoc. 2020 Sep;9(17):e015709
pubmed: 32812471
Am J Cardiol. 2019 Dec 1;124(11):1770-1774
pubmed: 31586533