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Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events: Insights From the SABRUS in 392 Probands

Authors :
Giulio Conte
Kengo Kusano
David C Johnson
P. Delise
Shingo Maeda
Domenico Corrado
Belinda Gray
Leonardo Calò
Gi-Byoung Nam
Ruben Casado-Arroyo
Georgia Sarquella-Brugada
Aviram Hochstadt
Jean-Baptiste Gourraud
Christian Veltmann
Jacob Tfelt-Hansen
Silvia G Priori
Camilla H Jespersen
Ramon Brugada
Kenzo Hirao
Anat Milman
Carla Giustetto
Yuka Mizusawa
Jimmy Jm Juang
Giuseppe Allocca
Vincent Probst
Antoine Leenhardt
Pieter G. Postema
Bernard Belhassen
Andrea Mazzanti
Pedro Brugada
Elijah R. Behr
Elena Arbelo
Josep Brugada
T Kamakura
Antoine Andorin
Masahiko Takagi
Isabelle Denjoy
Yoshihide Takahashi
Fiorenzo Gaita
Zhengrong Huang
Arthur A.M. Wilde
Sung Hwan Kim
Takeshi Aiba
Gan-Xin Yan
Cardiology
ACS - Heart failure & arrhythmias
Clinical sciences
Heartrhythmmanagement
Cardio-vascular diseases
Source :
Circulation. Genomic and precision medicine, 14(5). Lippincott Williams and Wilkins Ltd., Milman, A, Behr, E R, Gray, B, Johnson, D C, Andorin, A, Hochstadt, A, Gourraud, J-B, Maeda, S, Takahashi, Y, Jm Juang, J, Kim, S-H, Kamakura, T, Aiba, T, Postema, P G, Mizusawa, Y, Denjoy, I, Giustetto, C, Conte, G, Huang, Z, Sarquella-Brugada, G, Mazzanti, A, Jespersen, C H, Arbelo, E, Brugada, R, Calo, L, Corrado, D, Casado-Arroyo, R, Allocca, G, Takagi, M, Delise, P, Brugada, J, Tfelt-Hansen, J, Priori, S G, Veltmann, C, Yan, G-X, Brugada, P, Gaita, F, Leenhardt, A, Wilde, A A M, Kusano, K F, Nam, G-B, Hirao, K, Probst, V & Belhassen, B 2021, ' Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events : Insights From the SABRUS in 392 Probands ', Circulation. Genomic and precision medicine, vol. 14, no. 5, e003222 . https://doi.org/10.1161/CIRCGEN.120.003222, Circulation-Genomic and Precision Medicine, r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu, instname
Publication Year :
2021

Abstract

Background: Brugada syndrome (BrS) is associated with mutations in the cardiac sodium channel gene, SCN5A. However, genetic studies of patients with BrS with arrhythmic events have been limited. We sought to compare various clinical, ECG, and electrophysiological parameters according to SCN5A genotype in a large cohort of BrS probands with first arrhythmic event. Methods: Survey on Arrhythmic Events in Brugada Syndrome is a survey of 10 Western and 4 Asian countries, gathering 678 patients with BrS with first arrhythmic event. Only probands were included, and SCN5A genotype adjudicated. Patients without appropriate genetic data were excluded. Associations of genotype with clinical features were analyzed. Results: The study group comprised 392 probands: 92 (23.5%) SCN5A+ (44 pathogenic/likely pathogenic [P/LP] and 48 variants of unknown significance) and 300 (76.5%) SCN5A−. SCN5A missense variants and the patients hosting them were similar regardless of adjudication. A higher proportion of patients with P/LP were pediatric (SCN5A− (11.4% versus 3%, P =0.023). The proportion of females was higher among patients with P/LP compared with SCN5A − (18.2% versus 6.3%, P =0.013). P/LP probands were more likely to have a family history of sudden cardiac death compared with SCN5A − (41.9% versus 16.8%, P SCN5A− (87.5% versus 47%, P P P =0.009) were independent variables associated with P/LP genotype following logistic regression. Conclusions: The genetic basis of BrS has a complex relationship with gender, ethnicity, and age. Probands hosting a P/LP variant tended to experience their first arrhythmic event at a younger age and to have events triggered by fever compared with patients with SCN5A− . In addition, they were more likely to be White and to have family history of sudden cardiac death. Among females, a P/LP variant suggests an increased risk of being symptomatic. This association should be further studied on an ethnically specific basis in large prospectively collected international cohorts.

Details

Language :
English
ISSN :
25748300
Database :
OpenAIRE
Journal :
Circulation. Genomic and precision medicine, 14(5). Lippincott Williams and Wilkins Ltd., Milman, A, Behr, E R, Gray, B, Johnson, D C, Andorin, A, Hochstadt, A, Gourraud, J-B, Maeda, S, Takahashi, Y, Jm Juang, J, Kim, S-H, Kamakura, T, Aiba, T, Postema, P G, Mizusawa, Y, Denjoy, I, Giustetto, C, Conte, G, Huang, Z, Sarquella-Brugada, G, Mazzanti, A, Jespersen, C H, Arbelo, E, Brugada, R, Calo, L, Corrado, D, Casado-Arroyo, R, Allocca, G, Takagi, M, Delise, P, Brugada, J, Tfelt-Hansen, J, Priori, S G, Veltmann, C, Yan, G-X, Brugada, P, Gaita, F, Leenhardt, A, Wilde, A A M, Kusano, K F, Nam, G-B, Hirao, K, Probst, V & Belhassen, B 2021, ' Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events : Insights From the SABRUS in 392 Probands ', Circulation. Genomic and precision medicine, vol. 14, no. 5, e003222 . https://doi.org/10.1161/CIRCGEN.120.003222, Circulation-Genomic and Precision Medicine, r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu, instname
Accession number :
edsair.doi.dedup.....4996f0a0777debaf7d4e6c5402d63c04
Full Text :
https://doi.org/10.1161/CIRCGEN.120.003222