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Abstract

Background/Objectives: Duchenne muscular dystrophy (DMD) is an X-linked inherited muscle disease. Patients with DMD demonstrate improved prognosis with angiotensin-converting enzyme inhibitors and beta-blockers at the time of cardiac dysfunction. However, most deaths due to DMD are due to cardiac dysfunction. Fragmented QRS (fQRS) is an abnormal finding that forms a notch in the QRS wave on electrocardiography (ECG) and is associated with fibrosis and scarring of the myocardium. Methods: Patients with DMD were examined for the number of leads of fQRS, their sites of appearance, changes in cardiac dysfunction, and age using the chest leads of a synthesized 18-ECG. A retrospective analysis of 184 patients under 20 years of age with DMD and known genetic mutations was performed; they were divided into three age groups: 3–10, 11–15, and 16–20 years. The chest leads of the ECG were defined as follows: V1-3, anterior leads; V4-6, lateral leads; V7-9, posterior leads; and V3R-V5R, right-sided chest leads. Cardiac dysfunction was defined as a left ventricular (LV) ejection fraction <53% on the same day, and echocardiography was performed. LV dilation was defined as dilation beyond the normal range, considering the body surface area. Results: In 167 of 184 patients (91%), fQRS was present in one or more chest leads. The number of fQRS leads in the anterior and lateral walls was significantly higher in 16–20-year-olds than in 3–10-year-olds. The total number of chest leads with fQRS was 4.9 ± 3.1 in the cardiac dysfunction group and 3.5 ± 2.5 in the preserved group. The cardiac dysfunction group had a significantly greater number of fQRS leads than did the preserved group (p = 0.003). The group with LV dilation had a significantly greater number of fQRS leads than did the non-dilation group (p = 0.009). Conclusions: The fQRS site is associated with age, cardiac dysfunction, and LV dilation. Multivariate regression analysis revealed that the number of anterior leads of the fQRS correlated with age and that of lateral leads of the fQRS with cardiac dysfunction and LV dilation. The number of fQRS leads on the lateral wall marks cardiac dysfunction and LV dilation.

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1009240
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Title
Fragmented QRS in Lateral Leads on Electrocardiography Is Associated with Cardiac Dysfunction and Left Ventricular Dilation in Duchenne Muscular Dystrophy
Author
Yamamoto Tetsushi 1 ; Ogawa Shuichiro 1   VIAFID ORCID Logo  ; Ide Yusuke 1   VIAFID ORCID Logo  ; Miyazaki Kokoro 1 ; Sunami Aiko 2 ; Nambu Yoshinori 3 ; Ryosuke, Bo 3 ; Matsuo Masafumi 4   VIAFID ORCID Logo  ; Awano Hiroyuki 5   VIAFID ORCID Logo 

 Department of Clinical Laboratory Science Course, Nagahama Institute of Bio-Science and Technology, Nagahama 526-0829, Japan 
 Department of Medical Laboratory Medicine, Faculty of Health Sciences, Kobe Tokiwa University, Kobe 653-0838, Japan, Department of Biophysics, Graduate School of Health Sciences, Kobe University, Kobe 657-0013, Japan 
 Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe 650-0047, Japan 
 Graduate School of Science, Technology and Innovation, Kobe University, Kobe 657-0013, Japan 
 Organization for Research Initiative and Promotion, Tottori University, Yonago 683-0826, Japan 
Publication title
Volume
13
Issue
4
First page
804
Publication year
2025
Publication date
2025
Publisher
MDPI AG
Place of publication
Basel
Country of publication
Switzerland
Publication subject
e-ISSN
22279059
Source type
Scholarly Journal
Language of publication
English
Document type
Journal Article
Publication history
 
 
Online publication date
2025-03-27
Milestone dates
2025-03-06 (Received); 2025-03-26 (Accepted)
Publication history
 
 
   First posting date
27 Mar 2025
ProQuest document ID
3194498553
Document URL
https://www.proquest.com/scholarly-journals/fragmented-qrs-lateral-leads-on/docview/3194498553/se-2?accountid=208611
Copyright
© 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Last updated
2025-04-25
Database
ProQuest One Academic