Literature DB >> 17998470

Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function.

Stephan E Lehnart1, Michael J Ackerman, D Woodrow Benson, Ramon Brugada, Colleen E Clancy, J Kevin Donahue, Alfred L George, Augustus O Grant, Stephen C Groft, Craig T January, David A Lathrop, W Jonathan Lederer, Jonathan C Makielski, Peter J Mohler, Arthur Moss, Jeanne M Nerbonne, Timothy M Olson, Dennis A Przywara, Jeffrey A Towbin, Lan-Hsiang Wang, Andrew R Marks.   

Abstract

The National Heart, Lung, and Blood Institute and Office of Rare Diseases at the National Institutes of Health organized a workshop (September 14 to 15, 2006, in Bethesda, Md) to advise on new research directions needed for improved identification and treatment of rare inherited arrhythmias. These included the following: (1) Na+ channelopathies; (2) arrhythmias due to K+ channel mutations; and (3) arrhythmias due to other inherited arrhythmogenic mechanisms. Another major goal was to provide recommendations to support, enable, or facilitate research to improve future diagnosis and management of inherited arrhythmias. Classifications of electric heart diseases have proved to be exceedingly complex and in many respects contradictory. A new contemporary and rigorous classification of arrhythmogenic cardiomyopathies is proposed. This consensus report provides an important framework and overview to this increasingly heterogeneous group of primary cardiac membrane channel diseases. Of particular note, the present classification scheme recognizes the rapid evolution of molecular biology and novel therapeutic approaches in cardiology, as well as the introduction of many recently described diseases, and is unique in that it incorporates ion channelopathies as a primary cardiomyopathy in consensus with a recent American Heart Association Scientific Statement.

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Year:  2007        PMID: 17998470     DOI: 10.1161/CIRCULATIONAHA.107.711689

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  77 in total

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7.  Novel chemical suppressors of long QT syndrome identified by an in vivo functional screen.

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Review 9.  New therapeutic targets in cardiology: arrhythmias and Ca2+/calmodulin-dependent kinase II (CaMKII).

Authors:  Adam G Rokita; Mark E Anderson
Journal:  Circulation       Date:  2012-10-23       Impact factor: 29.690

10.  High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation.

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Journal:  Biochemistry       Date:  2012-11-02       Impact factor: 3.162

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