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Beyond conduction impairment: Unveiling the profound myocardial injury in left bundle branch block.
Wang, Xiaoxian; Ge, Beibei; Miao, Changqing; Lee, Christopher; Romero, Jorge E; Li, Peng; Wang, Fang; Xu, Di; Chen, Minglong; Li, Dianfu; Li, Dong; Li, Mingxia; Xu, Fang; Li, Yan; Gong, Chanjuan; Taub, Cynthia C; Yao, Jing.
Afiliación
  • Wang X; Department of Ultrasound Medicine, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, People's Republic of China.
  • Ge B; Department of Ultrasound Medicine, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, People's Republic of China.
  • Miao C; Department of Cardiology, Jiangyin People's Hospital, Jiangyin, People's Republic of China.
  • Lee C; Department of Cardiology, University of California, San Francisco, California.
  • Romero JE; Cardiac Arrhythmia Service, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Li P; Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
  • Wang F; Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
  • Xu D; Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
  • Chen M; Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
  • Li D; Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
  • Li D; Harbor-UCLA Medical Center, Torrance, California.
  • Li M; Department of Ultrasound Medicine, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, People's Republic of China.
  • Xu F; Department of Ultrasound Medicine, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, People's Republic of China.
  • Li Y; Department of Anesthesiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
  • Gong C; Department of Anesthesiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
  • Taub CC; Department of Medicine, Upstate Medical University, Norton College of Medicine, Syracuse, New York.
  • Yao J; Department of Ultrasound Medicine, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, People's Republic of China; Medical Imaging Center, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, People's Republic o
Heart Rhythm ; 21(8): 1370-1379, 2024 08.
Article en En | MEDLINE | ID: mdl-38490601
ABSTRACT

BACKGROUND:

Left bundle branch block (LBBB) represents a frequently encountered conduction system disorder. Despite its widespread occurrence, a continual dilemma persists regarding its intricate association with underlying cardiomyopathy and its pivotal role in the initiation of dilated cardiomyopathy. The pathologic alterations linked to LBBB-induced cardiomyopathy (LBBB-CM) have remained elusive.

OBJECTIVE:

This study sought to investigate the chronologic dynamics of LBBB to left ventricular dysfunction and the pathologic mechanism of LBBB-CM.

METHODS:

LBBB model was established through main left bundle branch trunk ablation in 14 canines. All LBBB dogs underwent transesophageal echocardiography and electrocardiography before ablation and at 1 month, 3 months, 6 months, and 12 months after LBBB induction. Single-photon emission computed tomography imaging was performed at 12 months. We then harvested the heart from all LBBB dogs and 14 healthy adult dogs as normal controls for anatomic observation, Purkinje fiber staining, histologic staining, and connexin43 protein expression quantitation.

RESULTS:

LBBB induction caused significant fibrotic changes in the endocardium and mid-myocardium. Purkinje fibers exhibited fatty degeneration, vacuolization, and fibrosis along with downregulated connexin43 protein expression. During a 12-month follow-up, left ventricular dysfunction progressively worsened, peaking at the end of the observation period. The association between myocardial dysfunction, hypoperfusion, and fibrosis was observed in the LBBB-afflicted canines.

CONCLUSION:

LBBB may lead to profound myocardial injury beyond its conduction impairment effects. The temporal progression of left ventricular dysfunction and the pathologic alterations observed shed light on the complex relationship between LBBB and cardiomyopathy. These findings offer insights into potential mechanisms and clinical implications of LBBB-CM.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Bloqueo de Rama / Modelos Animales de Enfermedad / Electrocardiografía Límite: Animals Idioma: En Revista: Heart Rhythm Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Bloqueo de Rama / Modelos Animales de Enfermedad / Electrocardiografía Límite: Animals Idioma: En Revista: Heart Rhythm Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos