Literature DB >> 24119082

Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.

Marco Merlo1, Gianfranco Sinagra, Elisa Carniel, Dobromir Slavov, Xiao Zhu, Giulia Barbati, Anita Spezzacatene, Federica Ramani, Ernesto Salcedo, Andrea Di Lenarda, Luisa Mestroni, Matthew R G Taylor.   

Abstract

BACKGROUND: In dilated cardiomyopathy (DCM), the clinical and prognostic implications of rare variants in sarcomeric genes remain poorly understood. To address this question, we analyzed the outcome of rare sarcomeric gene variants in patients enrolled in our Familial Cardiomyopathy Registry.
METHODS: DCM families harboring rare sarcomeric variants in MYH6, MYH7, MYBPC3, TNNT2, and TTN were identified. Genotype-phenotype association analysis was performed, and long-term survival-free from death or heart transplant was compared between carriers and noncarriers.
RESULTS: We found 24 rare variants (3 in MYH6, 3 in MYH7, 3 in MYBPC3, 2 in TNNT2, and 13 in TTN) affecting 52 subjects in 25 families. The phenotypes of variant carriers were severe (3 sudden deaths, 6 heart failure deaths, 8 heart transplants, 2 ventricular fibrillations). There was no difference in the overall long-term survival between carriers and the 33 noncarriers (p = 0.322). However after 50 years of age, the combined endpoint of death or transplant was decreased in carriers as compared to noncarriers (p = 0.026).
CONCLUSIONS: Patients with DCM carrying rare variants in sarcomeric genes manifest a poorer prognosis as compared to noncarriers after the age of 50 years. These data further support the role of genetic testing in DCM for risk stratification.
© 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  cardiomyopathy; genes; genetics; molecular genetics; phenotyping; prognosis

Mesh:

Substances:

Year:  2013        PMID: 24119082      PMCID: PMC3865161          DOI: 10.1111/cts.12116

Source DB:  PubMed          Journal:  Clin Transl Sci        ISSN: 1752-8054            Impact factor:   4.689


  33 in total

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Authors:  Elisa Carniel; Matthew R G Taylor; Gianfranco Sinagra; Andrea Di Lenarda; Lisa Ku; Pamela R Fain; Mark M Boucek; Jean Cavanaugh; Snjezana Miocic; Dobromir Slavov; Sharon L Graw; Jennie Feiger; Xiao Zhong Zhu; Dmi Dao; Debra A Ferguson; Michael R Bristow; Luisa Mestroni
Journal:  Circulation       Date:  2005-07-05       Impact factor: 29.690

2.  Arrhythmias and dilated cardiomyopathy common pathogenetic pathways?

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3.  Improved splice site detection in Genie.

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Review 4.  Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy.

Authors:  L Mestroni; B Maisch; W J McKenna; K Schwartz; P Charron; C Rocco; F Tesson; A Richter; A Wilke; M Komajda
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5.  Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene.

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Journal:  Eur Heart J       Date:  2005-03-15       Impact factor: 29.983

6.  Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy.

Authors:  Matthew R G Taylor; Dobromir Slavov; Andreas Gajewski; Sylvia Vlcek; Lisa Ku; Pamela R Fain; Elisa Carniel; Andrea Di Lenarda; Gianfranco Sinagra; Mark M Boucek; Jean Cavanaugh; Sharon L Graw; Patsy Ruegg; Jennie Feiger; Xiao Zhu; Debra A Ferguson; Michael R Bristow; Josef Gotzmann; Roland Foisner; Luisa Mestroni
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7.  Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.

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8.  Familial dilated cardiomyopathy: cardiac abnormalities are common in asymptomatic relatives and may represent early disease.

Authors:  M K Baig; J H Goldman; A L Caforio; A S Coonar; P J Keeling; W J McKenna
Journal:  J Am Coll Cardiol       Date:  1998-01       Impact factor: 24.094

9.  A method and server for predicting damaging missense mutations.

Authors:  Ivan A Adzhubei; Steffen Schmidt; Leonid Peshkin; Vasily E Ramensky; Anna Gerasimova; Peer Bork; Alexey S Kondrashov; Shamil R Sunyaev
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10.  Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.

Authors:  Ray E Hershberger; Sharie B Parks; Jessica D Kushner; Duanxiang Li; Susan Ludwigsen; Petra Jakobs; Deirdre Nauman; Donna Burgess; Julie Partain; Michael Litt
Journal:  Clin Transl Sci       Date:  2008-05       Impact factor: 4.689

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Authors:  Luisa Mestroni; Francesca Brun; Anita Spezzacatene; Gianfranco Sinagra; Matthew Rg Taylor
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Review 2.  Moving beyond simple answers to complex disorders in sarcomeric cardiomyopathies: the role of integrated systems.

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3.  Predicting Arrhythmia Risk in Dilated Cardiomyopathy Using Genetic Mutation Status.

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Review 4.  Clinical Implication of Genetic Testing in Dilated Cardiomyopathy.

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Review 5.  Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals.

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Journal:  Clin Res Cardiol       Date:  2016-08-30       Impact factor: 5.460

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7.  Targeted Next Generation Sequencing for Genetic Mutations of Dilated Cardiomyopathy.

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Review 8.  Personalizing Risk Stratification for Sudden Death in Dilated Cardiomyopathy: The Past, Present, and Future.

Authors:  Brian P Halliday; John G F Cleland; Jeffrey J Goldberger; Sanjay K Prasad
Journal:  Circulation       Date:  2017-07-11       Impact factor: 29.690

Review 9.  A Review of the Giant Protein Titin in Clinical Molecular Diagnostics of Cardiomyopathies.

Authors:  Marta Gigli; Rene L Begay; Gaetano Morea; Sharon L Graw; Gianfranco Sinagra; Matthew R G Taylor; Henk Granzier; Luisa Mestroni
Journal:  Front Cardiovasc Med       Date:  2016-07-21

10.  Role of Titin Missense Variants in Dilated Cardiomyopathy.

Authors:  Rene L Begay; Sharon Graw; Gianfranco Sinagra; Marco Merlo; Dobromir Slavov; Katherine Gowan; Kenneth L Jones; Giulia Barbati; Anita Spezzacatene; Francesca Brun; Andrea Di Lenarda; John E Smith; Henk L Granzier; Luisa Mestroni; Matthew Taylor
Journal:  J Am Heart Assoc       Date:  2015-11-13       Impact factor: 5.501

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