Literature DB >> 29709244

SCN5A mutation type and topology are associated with the risk of ventricular arrhythmia by sodium channel blockers.

Ahmad S Amin1, Yolan J Reckman2, Elena Arbelo3, Anne M Spanjaart2, Pieter G Postema2, Rafik Tadros4, Michael W Tanck2, Maarten P Van den Berg5, Arthur A M Wilde6, Hanno L Tan2.   

Abstract

BACKGROUND: Ventricular fibrillation in patients with Brugada syndrome (BrS) is often initiated by premature ventricular contractions (PVCs). Presence of SCN5A mutation increases the risk of PVCs upon exposure to sodium channel blockers (SCB) in patients with baseline type-1 ECG. In patients without baseline type-1 ECG, however, the effect of SCN5A mutation on the risk of SCB-induced arrhythmia is unknown. We aimed to establish whether presence/absence, type, and topology of SCN5A mutation correlates with PVC occurrence during ajmaline infusion. METHODS AND
RESULTS: We investigated 416 patients without baseline type-1 ECG who underwent ajmaline testing and SCN5A mutation analysis. A SCN5A mutation was identified in 88 patients (S+). Ajmaline-induced PVCs occurred more often in patients with non-missense mutations (Snon-missense) or missense mutations in transmembrane or pore regions of SCN5A-encoded channel protein (Smissense-TP) than patients with missense mutations in intra-/extracellular channel regions (Smissense-IE) and patients without SCN5A mutation (S-) (29%, 24%, 9%, and 3%, respectively; P<0.001). The proportion of patients with ajmaline-induced BrS was similar in different mutation groups but lower in S- (71% Snon-missense, 63% Smissense-TP, 70% Smissense-IE, and 34% S-; P<0.001). Logistic regression indicated Snon-missense and Smissense-TP as predictors of ajmaline-induced PVCs.
CONCLUSIONS: SCN5A mutation is associated with an increased risk of drug-induced ventricular arrhythmia in patients without baseline type-1 ECG. In particular, Snon-missense and Smissense-TP are at high risk.
Copyright © 2017 The Authors. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Ajmaline; Arrhythmia; Brugada syndrome; Mutation; PVC; SCN5A

Mesh:

Substances:

Year:  2018        PMID: 29709244     DOI: 10.1016/j.ijcard.2017.09.010

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  4 in total

1.  Catheter ablation in highly symptomatic Brugada patients: a Dutch case series.

Authors:  D M Haanschoten; A Elvan; P G Postema; J J J Smit; A Adiyaman; R M A Ter Bekke; N Asaad; W T J Aanhaanen; A R Ramdat Misier; P P H M Delnoy; H J G M Crijns; A A M Wilde
Journal:  Clin Res Cardiol       Date:  2019-09-02       Impact factor: 5.460

Review 2.  ArrhythmoGenoPharmacoTherapy.

Authors:  Arpad Tosaki
Journal:  Front Pharmacol       Date:  2020-05-12       Impact factor: 5.810

3.  Sudden cardiac death in families with premature cardiovascular disease.

Authors:  Caroline Bruikman; Maurice W J de Ronde; Ahmed Amin; Sonja Levy; Pien Lof; Ursula de Ruijter; Kees Hovingh; Hanno L Tan; Sara-Joan Pinto-Sietsma
Journal:  Heart       Date:  2019-08-17       Impact factor: 5.994

4.  Predicting cardiac electrical response to sodium-channel blockade and Brugada syndrome using polygenic risk scores.

Authors:  Rafik Tadros; Hanno L Tan; Sulayman El Mathari; Jan A Kors; Pieter G Postema; Najim Lahrouchi; Leander Beekman; Milena Radivojkov-Blagojevic; Ahmad S Amin; Thomas Meitinger; Michael W Tanck; Arthur A Wilde; Connie R Bezzina
Journal:  Eur Heart J       Date:  2019-10-01       Impact factor: 29.983

  4 in total

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