Phenomapping in Atrioventricular Nodal Reentrant Tachycardia: Mechanistic Insights and Therapeutic Implications.
Traditional classifications of atrioventricular nodal reentrant tachycardia (AVNRT) based on cardiac symptomatology, electrocardiographic findings, and reentrant circuits do not capture the full heterogeneity of AVNRT.
This study sought to identify distinct phenotypes among patients with AVNRT by using two-step cluster analysis and to determine differential effects of phenotypes on clinical and procedural outcomes.
All patients (n = 305) underwent catheter ablation and ajmaline challenge testing. A two-step cluster analysis was conducted using 17 demographic/clinical, anthropometric, electrocardiographic, echocardiographic, and anatomic variables.
Three distinct clinically and mechanistically relevant clusters were identified. Cluster 1 (Metabolic/Structural Phenotype, n = 44) patients were characterized by older age of onset of AVNRT (53.5 ± 8.5, 43.5 ± 15, and 24.7 ± 10.5 years, p = 4.9 × 10-31), shorter distance between coronary sinus floor and His bundle potential (22.7 ± 6.1, 24.7 ± 6.8, and 29 ± 7.5 mm, p = 1.3 × 10-7), higher prevalence of "correlated" (diagnosed ≥ 4 years before AVNRT onset) type 2 diabetes (100%, 0%, and 0%, p = 5.9 × 10-67) and "correlated" (diagnosed ≥ 6 years before AVNRT onset) structural heart disease (86.4%, 100%, 0%, p = 3.5 × 10-62) compared to Cluster 2 (Structural Phenotype, n = 78) and Cluster 3 (Anatomic/Genetic Phenotype, n = 183) patients, respectively. Cluster 1 patients had higher prevalence of "pro-arrhythmia" (new-onset and/or symptom worsening/intolerance) with anti-arrhythmic therapy and/or non-cardiac drugs (74.2%, 46.5%, and 31.6%, p = 1.5 × 10-4), AH prolongation/AV-VA block (20.5%, 7.7%, and 2.2%, p = 8.9 × 10-5) and aborted ablation (11.4%, 1.3%, and 0%, p = 8.6 × 10-5) during EP study compared to Clusters 2 and 3 patients, respectively.
Phenomapping identified three clinically and mechanistically relevant phenotypes of AVNRT associated with clinical and procedural outcomes, underscoring the considerable heterogeneity of AVNRT and the importance of comorbidities and substrates.
This study sought to identify distinct phenotypes among patients with AVNRT by using two-step cluster analysis and to determine differential effects of phenotypes on clinical and procedural outcomes.
All patients (n = 305) underwent catheter ablation and ajmaline challenge testing. A two-step cluster analysis was conducted using 17 demographic/clinical, anthropometric, electrocardiographic, echocardiographic, and anatomic variables.
Three distinct clinically and mechanistically relevant clusters were identified. Cluster 1 (Metabolic/Structural Phenotype, n = 44) patients were characterized by older age of onset of AVNRT (53.5 ± 8.5, 43.5 ± 15, and 24.7 ± 10.5 years, p = 4.9 × 10-31), shorter distance between coronary sinus floor and His bundle potential (22.7 ± 6.1, 24.7 ± 6.8, and 29 ± 7.5 mm, p = 1.3 × 10-7), higher prevalence of "correlated" (diagnosed ≥ 4 years before AVNRT onset) type 2 diabetes (100%, 0%, and 0%, p = 5.9 × 10-67) and "correlated" (diagnosed ≥ 6 years before AVNRT onset) structural heart disease (86.4%, 100%, 0%, p = 3.5 × 10-62) compared to Cluster 2 (Structural Phenotype, n = 78) and Cluster 3 (Anatomic/Genetic Phenotype, n = 183) patients, respectively. Cluster 1 patients had higher prevalence of "pro-arrhythmia" (new-onset and/or symptom worsening/intolerance) with anti-arrhythmic therapy and/or non-cardiac drugs (74.2%, 46.5%, and 31.6%, p = 1.5 × 10-4), AH prolongation/AV-VA block (20.5%, 7.7%, and 2.2%, p = 8.9 × 10-5) and aborted ablation (11.4%, 1.3%, and 0%, p = 8.6 × 10-5) during EP study compared to Clusters 2 and 3 patients, respectively.
Phenomapping identified three clinically and mechanistically relevant phenotypes of AVNRT associated with clinical and procedural outcomes, underscoring the considerable heterogeneity of AVNRT and the importance of comorbidities and substrates.
Authors
Hasdemir Hasdemir, Kocabaş Kocabaş, Yağmur Yağmur, Bulut Bulut, Hakverdi Hakverdi, Orman Orman, Antzelevitch Antzelevitch
View on Pubmed