T1 Mapping for Identifying the Substrate in Patients With Apparently Idiopathic Premature Ventricular Complexes
- PMID: 37380310
- DOI: 10.1016/j.jacep.2022.12.012
T1 Mapping for Identifying the Substrate in Patients With Apparently Idiopathic Premature Ventricular Complexes
Abstract
Background: Myocardial fibrosis is implicated as a potential substrate responsible for arrhythmias.
Objectives: This study aimed to investigate myocardial fibrosis assessed by T1 mapping in patients with apparently idiopathic premature ventricular complexes (PVCs), and to determine the relationship between this tissue biomarker and PVC features.
Methods: Patients with frequent PVC (>1,000/24 h) who underwent cardiac magnetic resonance imaging (MRI) between 2020 and 2021 were retrospectively evaluated. Patients were included if they had no indicator of known heart diseases on MRI. Sex- and age-matched healthy subjects underwent noncontrast MRI with native T1 mapping. High PVC burden was defined as the percentage of PVC >20%/24 h.
Results: A total of 70 patients and 70 healthy controls were included. Global T1 value was significantly higher in patients than in controls (P < 0.001). Extracellular volume was 26.03% ± 2.16% in the patients. Moreover, global T1 value showed a stepwise increase in PVC tertiles (P = 0.03) but not for extracellular volume (P = 0.85). Patients with a non-left bundle branch block (LBBB) inferior axis morphology showed higher global native T1 values than LBBB inferior axis pattern (P = 0.005). In addition, global T1 values correlated significantly with PVC burden (r = 0.28, P = 0.02). In the multivariate analysis, global T1 value independently correlated with high PVC burden (odds ratio: 1.22 per 10-ms increase, P = 0.02).
Conclusions: Increased global T1, a marker of interstitial fibrosis, was detected in patients with apparently idiopathic PVC and was significantly associated with non-LBBB inferior axis morphology and high PVC burden.
Keywords: T1 mapping; cardiac magnetic resonance; premature ventricular complexes.
Copyright © 2023 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Funding Support and Author Disclosures The study was funded by National Key Research and Development Program of China (2021YFF0501400 and 2021YFF0501404) and National Natural Science Foundation of China (No.81930044). All authors have reported that they have no relationships relevant to the contents of this paper to disclose.
Comment in
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Shifty Protons and the Compensatory Pause.JACC Clin Electrophysiol. 2023 Jun;9(6):762-764. doi: 10.1016/j.jacep.2023.01.027. Epub 2023 Mar 22. JACC Clin Electrophysiol. 2023. PMID: 37380311 No abstract available.
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