Literature DB >> 20541041

Long QT syndrome with compound mutations is associated with a more severe phenotype: a Japanese multicenter study.

Hideki Itoh1, Wataru Shimizu, Kenshi Hayashi, Kenichiro Yamagata, Tomoko Sakaguchi, Seiko Ohno, Takeru Makiyama, Masaharu Akao, Tomohiko Ai, Takashi Noda, Aya Miyazaki, Yoshihiro Miyamoto, Masakazu Yamagishi, Shiro Kamakura, Minoru Horie.   

Abstract

BACKGROUND: Long QT syndrome (LQTS) can be caused by mutations in the cardiac ion channels. Compound mutations occur at a frequency of 4% to 11% among genotyped LQTS cases.
OBJECTIVE: The purpose of this study was to determine the clinical characteristics and manner of onset of cardiac events in Japanese patients with LQTS and compound mutations.
METHODS: Six hundred three genotyped LQTS patients (310 probands and 293 family members) were divided into two groups: those with a single mutation (n = 568) and those with two mutations (n = 35). Clinical phenotypes were compared between the two groups.
RESULTS: Of 310 genotyped probands, 26 (8.4%) had two mutations in the same or different LQTS-related genes (compound mutations). Among the 603 LQTS patients, compound mutation carriers had significantly longer QTc interval (510 ± 56 ms vs 478± 53 ms, P = .001) and younger age at onset of cardiac events (10 ± 8 years vs 18 ± 16 years, P = .043) than did single mutation carriers. The incidence rate of cardiac events before age 40 years and use of beta-blocker therapy among compound mutation carriers also were different than in single mutation carriers. Subgroup analysis showed more cardiac events in LQTS type 1 (LQT1) and type 2 (LQT2) compound mutations compared to single LQT1 and LQT2 mutations.
CONCLUSION: Compound mutation carriers are associated with a more severe phenotype than single mutation carriers.
Copyright © 2010 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20541041     DOI: 10.1016/j.hrthm.2010.06.013

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN: 1547-5271            Impact factor:   6.343


  37 in total

1.  Coexisting mutations/polymorphisms of the long QT syndrome genes in patients with repaired Tetralogy of Fallot are associated with the risks of life-threatening events.

Authors:  Shuenn-Nan Chiu; Mei-Hwan Wu; Ming-Jai Su; Jou-Kou Wang; Ming-Tai Lin; Chien-Chih Chang; Hui-Wen Hsu; Ching-Tsuen Shen; Olivier Thériault; Mohamed Chahine
Journal:  Hum Genet       Date:  2012-03-11       Impact factor: 4.132

Review 2.  Genotype- and phenotype-guided management of congenital long QT syndrome.

Authors:  John R Giudicessi; Michael J Ackerman
Journal:  Curr Probl Cardiol       Date:  2013-10       Impact factor: 5.200

Review 3.  Genetics of sudden cardiac death.

Authors:  Alon Barsheshet; Andrew Brenyo; Arthur J Moss; Ilan Goldenberg
Journal:  Curr Cardiol Rep       Date:  2011-10       Impact factor: 2.931

4.  A high-risk patient with long-QT syndrome with no response to cardioselective beta-blockers.

Authors:  Naoki Toyota; Aya Miyazaki; Heima Sakaguchi; Wataru Shimizu; Hideo Ohuchi
Journal:  Heart Vessels       Date:  2014-06-11       Impact factor: 2.037

5.  Congenital long QT syndrome with compound mutations in the KCNH2 gene.

Authors:  Sachiko Bando; Takeshi Soeki; Tomomi Matsuura; Toshiyuki Niki; Takayuki Ise; Koji Yamaguchi; Yoshio Taketani; Takashi Iwase; Hirotsugu Yamada; Tetsuzo Wakatsuki; Masashi Akaike; Takeshi Aiba; Wataru Shimizu; Masataka Sata
Journal:  Heart Vessels       Date:  2013-09-22       Impact factor: 2.037

Review 6.  Current perspectives in genetic cardiovascular disorders: from basic to clinical aspects.

Authors:  Masa-aki Kawashiri; Kenshi Hayashi; Tetsuo Konno; Noboru Fujino; Hidekazu Ino; Masakazu Yamagishi
Journal:  Heart Vessels       Date:  2013-08-02       Impact factor: 2.037

Review 7.  Long-QT syndrome: from genetics to management.

Authors:  Peter J Schwartz; Lia Crotti; Roberto Insolia
Journal:  Circ Arrhythm Electrophysiol       Date:  2012-08-01

Review 8.  Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.

Authors:  David N Cooper; Michael Krawczak; Constantin Polychronakos; Chris Tyler-Smith; Hildegard Kehrer-Sawatzki
Journal:  Hum Genet       Date:  2013-07-03       Impact factor: 4.132

9.  An Interdomain KCNH2 Mutation Produces an Intermediate Long QT Syndrome.

Authors:  Marika L Osterbur; Renjian Zheng; Robert Marion; Christine Walsh; Thomas V McDonald
Journal:  Hum Mutat       Date:  2015-06-13       Impact factor: 4.878

Review 10.  Genetic etiology and evaluation of sudden cardiac death.

Authors:  Elena Dolmatova; Saagar Mahida; Patrick T Ellinor; Steven A Lubitz
Journal:  Curr Cardiol Rep       Date:  2013-08       Impact factor: 2.931

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