Literature DB >> 24721655

Personalized medicine to treat arrhythmias.

Dan M Roden1.   

Abstract

The efficacy of antiarrhythmic drug therapy is incomplete, with responses ranging from efficacy to no effect to severe adverse effects, including paradoxical drug-induced arrhythmia. Most antiarrhythmic drugs were developed at a time when the mechanisms underlying arrhythmias were not well understood. In the last decade, a range of experimental approaches have advanced our understanding of the molecular and genomic contributors to the generation of an arrhythmia-prone heart, and this information is directly informing targeted therapy with existing drugs or the development of new ones. The development of inexpensive whole genome sequencing holds the promise of identifying patients susceptible to arrhythmias in a presymptomatic phase, and thus implementing preventive therapies.
Copyright © 2013 Elsevier Ltd. All rights reserved.

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Year:  2013        PMID: 24721655      PMCID: PMC3984450          DOI: 10.1016/j.coph.2013.11.013

Source DB:  PubMed          Journal:  Curr Opin Pharmacol        ISSN: 1471-4892            Impact factor:   5.547


  56 in total

1.  KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.

Authors:  Lia Crotti; Andrew L Lundquist; Roberto Insolia; Matteo Pedrazzini; Chiara Ferrandi; Gaetano M De Ferrari; Alessandro Vicentini; Ping Yang; Dan M Roden; Alfred L George; Peter J Schwartz
Journal:  Circulation       Date:  2005-08-22       Impact factor: 29.690

2.  Safety and efficacy of flecainide in subjects with Long QT-3 syndrome (DeltaKPQ mutation): a randomized, double-blind, placebo-controlled clinical trial.

Authors:  Arthur J Moss; John R Windle; W Jackson Hall; Wojciech Zareba; Jennifer L Robinson; Scott McNitt; Patricia Severski; Spencer Rosero; James P Daubert; Ming Qi; Michael Cieciorka; Allan S Manalan
Journal:  Ann Noninvasive Electrocardiol       Date:  2005-10       Impact factor: 1.468

3.  The elusive link between LQT3 and Brugada syndrome: the role of flecainide challenge.

Authors:  S G Priori; C Napolitano; P J Schwartz; R Bloise; L Crotti; E Ronchetti
Journal:  Circulation       Date:  2000-08-29       Impact factor: 29.690

4.  Genetic susceptibility to acquired long QT syndrome: pharmacologic challenge in first-degree relatives.

Authors:  Prince J Kannankeril; Dan M Roden; Kris J Norris; S Patrick Whalen; Alfred L George; Katherine T Murray
Journal:  Heart Rhythm       Date:  2005-02       Impact factor: 6.343

Review 5.  Impact of genetics on the clinical management of channelopathies.

Authors:  Peter J Schwartz; Michael J Ackerman; Alfred L George; Arthur A M Wilde
Journal:  J Am Coll Cardiol       Date:  2013-05-15       Impact factor: 24.094

6.  Low penetrance in the long-QT syndrome: clinical impact.

Authors:  S G Priori; C Napolitano; P J Schwartz
Journal:  Circulation       Date:  1999-02-02       Impact factor: 29.690

7.  Familial atrial fibrillation is a genetically heterogeneous disorder.

Authors:  Dawood Darbar; Kathleen J Herron; Jeffrey D Ballew; Arshad Jahangir; Bernard J Gersh; Win-K Shen; Stephen C Hammill; Douglas L Packer; Timothy M Olson
Journal:  J Am Coll Cardiol       Date:  2003-06-18       Impact factor: 24.094

8.  Molecular mechanism for an inherited cardiac arrhythmia.

Authors:  P B Bennett; K Yazawa; N Makita; A L George
Journal:  Nature       Date:  1995-08-24       Impact factor: 49.962

9.  SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome.

Authors:  Q Wang; J Shen; I Splawski; D Atkinson; Z Li; J L Robinson; A J Moss; J A Towbin; M T Keating
Journal:  Cell       Date:  1995-03-10       Impact factor: 41.582

10.  A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome.

Authors:  M E Curran; I Splawski; K W Timothy; G M Vincent; E D Green; M T Keating
Journal:  Cell       Date:  1995-03-10       Impact factor: 41.582

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  1 in total

Review 1.  Personalized medicine for cardiovascular diseases.

Authors:  Hayato Tada; Noboru Fujino; Akihiro Nomura; Chiaki Nakanishi; Kenshi Hayashi; Masayuki Takamura; Masa-Aki Kawashiri
Journal:  J Hum Genet       Date:  2020-08-08       Impact factor: 3.172

  1 in total

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