Ethnic and racial differences in Asian populations with ion channelopathies associated with sudden cardiac death

被引:2
作者
Zaveri, Sahil [1 ,2 ]
Qu, Yongxia Sarah [1 ,2 ,3 ]
Chahine, Mohamed [4 ,5 ]
Boutjdir, Mohamed [1 ,2 ,6 ]
机构
[1] SUNY Downstate Hlth Sci Univ, Dept Med Cell Biol & Pharmacol, Brooklyn, NY 11203 USA
[2] VA New York Harbor Healthcare Syst, Cardiovasc Res Program, New York, NY 11425 USA
[3] New York Presbyterian Brooklyn Methodist Hosp, Dept Cardiol, New York, NY USA
[4] Inst Univ Sante Mentale Quebec, CERVO Brain Res Ctr, Quebec City, PQ, Canada
[5] Univ Laval, Fac Medecine, Dept Med, Quebec City, PQ, Canada
[6] NYU Grossman Sch Med, Dept Med, Div Cardiol, New York, NY 10016 USA
基金
加拿大健康研究院;
关键词
ethnicity; race; brugada syndrome (BrS); long QT syndrome (LQTS); cardiac arrhythmia; sudden cardiac death; ion channels; LONG-QT SYNDROME; BRUGADA SYNDROME; ELECTROCARDIOGRAPHIC CHARACTERISTICS; CARDIOVASCULAR-DISEASE; CLINICAL-FEATURES; JAPANESE PATIENTS; SCN5A MUTATIONS; MORTALITY; HEART; RISK;
D O I
10.3389/fcvm.2023.1253479
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiovascular diseases are associated with several morbidities and are the most common cause of worldwide disease-related fatalities. Studies show that treatment and outcome-related differences for cardiovascular diseases disproportionately affect minorities in the United States. The emergence of ethnic and racial differences in sudden cardiac death (SCD) and related ion channelopathies complicates cardiovascular disease prevention, diagnosis, management, prognosis, and treatment objectives for patients and physicians alike. This review compiles and synthesizes current research in cardiac ion channelopathies and genetic disorders in Asian populations, an underrepresented population in cardiovascular literature. We first present a brief introduction to SCD, noting relevant observations and statistics from around the world, including Asian populations. We then examined existing differences between Asian and White populations in research, treatment, and outcomes related to cardiac ion channelopathies and SCD, showing progression in thought and research over time for each ion channelopathy. The review also identifies research that explored phenotypic abnormalities, device usage, and risk of death in Asian patients. We touch upon the unique genetic risk factors in Asian populations that lead to cardiac ion channelopathies and SCD while comparing them to White and Western populations, particularly in the United States, where Asians comprise approximately 7% of the total population. We also propose potential solutions such as improving early genetic screening, addressing barriers affecting access to medical care and device utilization, physician training, and patient education on risks.
引用
收藏
页数:15
相关论文
共 78 条
[1]   Human cardiac ryanodine receptor mutations in ion channel disorders in Japan [J].
Aizawa, Yoshiyasu ;
Mitsuma, Wataru ;
Ikrar, Taruna ;
Komura, Satoru ;
Hanawa, Haruo ;
Miyajima, Seiichi ;
Miyoshi, Fumito ;
Kobayashi, Youichi ;
Chinushi, Masaomi ;
Kimura, Akinori ;
Hiraoka, Masayasu ;
Aizawa, Yoshifusa .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2007, 116 (02) :263-265
[2]   RYR2 Sequencing Reveals Novel Missense Mutations in a Kazakh Idiopathic Ventricular Tachycardia Study Cohort [J].
Akilzhanova, Ainur ;
Guelly, Christian ;
Nuralinov, Omirbek ;
Nurkina, Zhannur ;
Nazhat, Dinara ;
Smagulov, Shalkhar ;
Tursunbekov, Azat ;
Alzhanova, Anar ;
Rashbayeva, Gulzhaina ;
Abdrakhmanov, Ayan ;
Dosmagambet, Sholpan ;
Trajanoski, Slave ;
Zhumadilov, Zhaxybay ;
Sharman, Almaz ;
Bekbosynova, Mahabbat .
PLOS ONE, 2014, 9 (06)
[3]  
Akimoto K, 1998, HUM MUTAT, pS184
[4]   Novel mechanism forBrugada syndrome -: Defective surface localization of an SCN5A mutant (R1432G) [J].
Baroudi, G ;
Pouliot, V ;
Denjoy, I ;
Guicheney, P ;
Shrier, A ;
Chahine, M .
CIRCULATION RESEARCH, 2001, 88 (12) :E78-E83
[5]   Common sodium channel promoter haplotype in Asian subjects underlies variability in cardiac conduction [J].
Bezzina, CR ;
Shimizu, W ;
Yang, P ;
Koopmann, TT ;
Tanck, MWT ;
Miyamoto, Y ;
Kamakura, S ;
Roden, DM ;
Wilde, AAM .
CIRCULATION, 2006, 113 (03) :338-344
[6]  
Bureau USC, 2021, Race and Ethnicity in the United States: 2010 Census and 2020 Census
[7]   The Genetics of Brugada Syndrome [J].
Cerrone, Marina ;
Costa, Sarah ;
Delmar, Mario .
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, 2022, 23 :255-274
[8]   Racial Disparities in Ion Channelopathies and Inherited Cardiovascular Diseases Associated With Sudden Cardiac Death [J].
Chahine, Mohamed ;
Fontaine, John M. ;
Boutjdir, Mohamed .
JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2022, 11 (06)
[9]   Brugada syndrome with SCN5A mutations exhibits more pronounced electrophysiological defects and more severe prognosis: A meta-analysis [J].
Chen, Chen ;
Tan, Zhaochong ;
Zhu, Wengen ;
Fu, Linghua ;
Kong, Qiling ;
Xiong, Qinmei ;
Yu, Jianhua ;
Hong, Kui .
CLINICAL GENETICS, 2020, 97 (01) :198-208
[10]   Cardiac sodium channel mutation associated with epinephrine-induced QT prolongation and sinus node dysfunction [J].
Chen, Jiarong ;
Makiyama, Takeru ;
Wuriyanghai, Yimin ;
Ohno, Seiko ;
Sasaki, Kenichi ;
Hayano, Mamoru ;
Harita, Takeshi ;
Nishiuchi, Suguru ;
Yamamoto, Yuta ;
Ueyama, Takeshi ;
Shimizu, Akihiko ;
Horie, Minoru ;
Kimura, Takeshi .
HEART RHYTHM, 2016, 13 (01) :289-298