Ventricular Arrhythmia Substrate Distribution and Its Relation to Sympathetic Innervation in Nonischemic Cardiomyopathy Patients

• Published in: JACC. Clinical electrophysiology Vol. 8; no. 10; pp. 1234 - 1245
• Main Authors: Chen, H. Sophia, Jungen, Christiane, Kimura, Yoshitaka, Dibbets-Schneider, Petra, Piers, Sebastiaan R., Androulakis, Alexander F.A., van der Geest, Rob J., de Geus-Oei, Lioe-Fee, Scholte, Arthur J.H.A., Lamb, Hildo J., Jongbloed, Monique R.M., Zeppenfeld, Katja
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 01.10.2022
• Subjects: arrhythmogenicity; autonomic nervous system; dilated cardiomyopathy; electroanatomic voltage mapping; sympathetic denervation; ventricular tachycardia; NICM; IHD; LVEF; LV; arrhythmogenicity; SPECT; ILS; dilated cardiomyopathy; 123I MIBG; ASS; UV; autonomic nervous system; electroanatomic voltage mapping; LGE-CMR; CMR; sympathetic denervation; LGE; VA; HMR; 3D; EAVM; ventricular tachycardia; RF; RFCA; VT
• ISSN: 2405-500X; 2405-5018
• DOI: 10.1016/j.jacep.2022.07.006

Nonischemic cardiomyopathy patients referred for catheter ablation of ventricular arrhythmias (VAs) typically have either inferolateral (ILS) or anteroseptal (ASS) VA substrate locations, with poorer outcomes for ASS. Sympathetic denervation is an important determinant of arrhythmogenicity. Its relation to nonischemic fibrosis in general and to the different VA substrates is unknown. This study sought to evaluate the association between VA substrates, myocardial fibrosis, and sympathetic denervation. Thirty-five patients from the Leiden Nonischemic Cardiomyopathy Study, who underwent electroanatomic voltage mapping and iodine-123 metaiodobenzylguanidine imaging between 2011 and 2018 were included. Late gadolinium-enhanced cardiac magnetic resonance data were collected when available. The relation between global cardiac sympathetic innervation and area-weighted unipolar voltage (UV) as a surrogate for diffuse fibrosis was evaluated. For regional analysis, patients were categorized as ASS or ILS. The distribution of low UV, sympathetic denervation, and late gadolinium enhancement (LGE) scar were compared using the 17-segment model. Median area-weighted UV was 12.3 mV in patients with normal sympathetic innervation and 8.7 mV in patients with sympathetic denervation. Global sympathetic denervation correlated with diffuse myocardial fibrosis (R = 0.53; P = 0.02). ILS (n = 13) matched with low UV, sympathetic denervation, and LGE scar in all patients, whereas ASS (n = 11) matched with low UV in all patients, with LGE scar in 63% (P = 0.20), but with sympathetic denervation in only 27% of patients (P = 0.0002). Global cardiac sympathetic denervation is related to fibrosis in nonischemic cardiomyopathy patients with VA. The mismatch between regional fibrosis and preserved innervation for ASS may contribute to a VA substrate difficult to control by catheter ablation. [Display omitted]