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Quantitative approach to fragmented QRS in arrhythmogenic cardiomyopathy: From disease towards asymptomatic carriers of pathogenic variants

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Abstract

Fragmented QRS complexes (fQRS) are common in patients with arrhythmogenic cardiomyopathy (ACM). A new method of fQRS quantification may aid early disease detection in pathogenic variant carriers and assessment of prognosis in patients with early stage ACM. Patients with definite ACM (n = 221, 66%), carriers of a pathogenic ACM-associated variant without a definite ACM diagnosis (n = 57, 17%) and control subjects (n = 58, 17%) were included. Quantitative fQRS (Q-fQRS) was defined as the total amount of deflections in the QRS complex in all 12 electrocardiography (ECG) leads. Q-fQRS was scored by a single observer and reproducibility was determined by three independent observers. Q-fQRS count was feasible with acceptable intra-and inter-observer agreement. Q-fQRS count is significantly higher in patients with definite ACM (54 ± 15) and pathogenic variant carriers (55 ± 10) compared to controls (35 ± 5) (p < 0.001). In patients with ACM, Q-fQRS was not associated with sustained ventricular arrhythmia (p = 0.701) at baseline or during follow-up (p = 0.335). Both definite ACM patients and pathogenic variant carriers not fulfilling ACM diagnosis have a higher Q-fQRS than controls. This may indicate that increased Q-fQRS is an early sign of disease penetrance. In concealed and early stages of ACM the role of Q-fQRS for risk stratification is limited.

Original languageEnglish
Article number545
Number of pages12
JournalJournal of Clinical medicine
Volume9
Issue number2
DOIs
Publication statusPublished - Feb 2020

Keywords

  • Arrhythmogenic cardiomyopathy
  • Electrocardiography
  • FQRS
  • Fragmented QRS
  • Genetics
  • Inherited cardiomyopathies
  • Sudden cardiac death
  • Ventricular arrhythmia

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