Literature DB >> 12845244

Characteristics of Chinese patients with symptomatic Brugada syndrome in Taiwan.

Jyh-Ming Juang1, Shoei K Stephen Huang, Chia-Ti Tsai, Fu-Tien Chiang, Jiunn-Lee Lin, Ling-Ping Lai, Chun-Chieh Wang, Chi-Tai Kuo, Kwo-Chang Ueng, Chi-Woon Kong, Wen-Chin Ko, Meng-Huan Lei, Hsuan-Ming Tsao.   

Abstract

Since 1992, the Brugada syndrome has been increasingly recognized worldwide, although its incidence and distribution remain unclear. In Asia, several cases have been reported in Japan, Thailand, Singapore, and Vietnam. However, little information is available from the Chinese population. Since June 1997, we have identified 10 patients with the diagnosis of the Brugada syndrome from six hospitals in Taiwan. All patients were male with the mean age of 46 +/- 7 years (range 36-61). They all had a normal chemistry profile, coronary angiography and echocardiography. Clinical presentations varied from seizure and syncope to sudden cardiac death. MRI and ultrafast CT of the heart did not show any abnormalities. Sustained ventricular tachycardia/ventricular fibrillation (VF) was induced in 7 of 8 patients who underwent an electrophysiologic study. The pharmacological provocation test was positive in 4 of 5 patients. One of the 4 patients who had a genetic study showed SCN5A gene mutation. An implantable cardioverter defibrillator (ICD) was implanted in 8 patients. During a mean follow-up of 29 +/- 17 months (range 2-54), 3 of 8 patients who had an ICD received appropriate ICD discharges after implantation. These 3 patients who were subsequently treated with antiarrhythmic agents have had no further recurrent ICD discharges. Two patients who refused ICD implantation are alive and well without taking antiarrhythmic agents. Our study showed that the clinical characteristics of our patients are similar to those described in the literature and that ICD is an effective treatment modality for patients with recurrent VF. However, antiarrhythmic agents may be beneficial for suppressing arrhythmia recurrences in selected patients. Copyright 2003 S. Karger AG, Basel

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Year:  2003        PMID: 12845244     DOI: 10.1159/000071247

Source DB:  PubMed          Journal:  Cardiology        ISSN: 0008-6312            Impact factor:   1.869


  8 in total

1.  Management of patients with implantable cardioverter defibrillators at emergency departments.

Authors:  Chung-Pin Liu; Yi-Lwun Ho; Yen-Hung Lin; Yen-Bin Liu; Wei-Tien Chang; Chien-Hua Huang; Wen-Jone Chen
Journal:  Emerg Med J       Date:  2007-02       Impact factor: 2.740

2.  Identification of Novel SCN5A Single Nucleotide Variants in Brugada Syndrome: A Territory-Wide Study From Hong Kong.

Authors:  Gary Tse; Sharen Lee; Tong Liu; Ho Chuen Yuen; Ian Chi Kei Wong; Chloe Mak; Ngai Shing Mok; Wing Tak Wong
Journal:  Front Physiol       Date:  2020-09-18       Impact factor: 4.566

3.  Leaky Ca2+ release channel/ryanodine receptor 2 causes seizures and sudden cardiac death in mice.

Authors:  Stephan E Lehnart; Marco Mongillo; Andrew Bellinger; Nicolas Lindegger; Bi-Xing Chen; William Hsueh; Steven Reiken; Anetta Wronska; Liam J Drew; Chris W Ward; W J Lederer; Robert S Kass; Gregory Morley; Andrew R Marks
Journal:  J Clin Invest       Date:  2008-06       Impact factor: 14.808

4.  Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome.

Authors:  Jyh-Ming Jimmy Juang; Tzu-Pin Lu; Liang-Chuan Lai; Chia-Chuan Ho; Yen-Bin Liu; Chia-Ti Tsai; Lian-Yu Lin; Chih-Chieh Yu; Wen-Jone Chen; Fu-Tien Chiang; Shih-Fan Sherri Yeh; Ling-Ping Lai; Eric Y Chuang; Jiunn-Lee Lin
Journal:  Sci Rep       Date:  2014-10-23       Impact factor: 4.379

Review 5.  SCN5A gene mutations and the risk of ventricular fibrillation and syncope in Brugada syndrome patients: A meta-analysis.

Authors:  Sunu Budhi Raharjo; Rido Maulana; Irma Maghfirah; Fatimah Alzahra; Agnes Dinar Putrinarita; Dicky A Hanafy; Yoga Yuniadi
Journal:  J Arrhythm       Date:  2018-07-26

6.  GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death.

Authors:  Jyh-Ming Jimmy Juang; Anna Binda; Shyh-Jye Lee; Juey-Jen Hwang; Wen-Jone Chen; Yen-Bin Liu; Lian-Yu Lin; Chih-Chieh Yu; Li-Ting Ho; Hui-Chun Huang; Ching-Yu Julius Chen; Tzu-Pin Lu; Liang-Chuan Lai; Shih-Fan Sherri Yeh; Ling-Ping Lai; Eric Y Chuang; Ilaria Rivolta; Charles Antzelevitch
Journal:  EBioMedicine       Date:  2020-07-07       Impact factor: 8.143

7.  Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A.

Authors:  Yao-Bin Zhu; Jian-Hui Zhang; Yuan-Yuan Ji; Ya-Nan Hu; Han-Lu Wang; Dan-Dan Ruan; Xiao-Rong Meng; Xin-Fu Lin; Jie-Wei Luo; Wei Chen
Journal:  Cardiol Res Pract       Date:  2022-04-28       Impact factor: 1.990

8.  Meta-Analysis of Risk Stratification of SCN5A With Brugada Syndrome: Is SCN5A Always a Marker of Low Risk?

Authors:  Yihan Yang; Dan Hu; Frederic Sacher; Kengo F Kusano; Xinye Li; Hector Barajas-Martinez; Mélèze Hocini; Yanda Li; Yonghong Gao; Hongcai Shang; Yanwei Xing
Journal:  Front Physiol       Date:  2019-02-19       Impact factor: 4.566

  8 in total

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