Literature DB >> 25465824

Cardiac manifestations of primary mitochondrial disorders.

Josef Finsterer1, Sonam Kothari2.   

Abstract

OBJECTIVES: One of the most frequently affected organs in mitochondrial disorders (MIDs), defined as hereditary diseases due to affection of the mitochondrial energy metabolism, is the heart. Cardiac involvement (CI) in MIDs has therapeutic and prognostic implications. This review aims at summarizing and discussing the various cardiac manifestations in MIDs.
METHODS: Data for this review were identified by searches of MEDLINE, Current Contents, and PubMed using appropriate search terms.
RESULTS: CI in MIDs may be classified according to various different criteria. In the present review cardiac abnormalities in MIDs are discussed according to their frequency with which they occur. CI in MIDs includes cardiomyopathy, arrhythmias, heart failure, pulmonary hypertension, dilation of the aortic root, pericardial effusion, coronary heart disease, autonomous nervous system dysfunction, congenital heart defects, or sudden cardiac death. The most frequent among the cardiomyopathies is hypertrophic cardiomyopathy, followed by dilated cardiomyopathy, and noncompaction.
CONCLUSIONS: CI in MID is more variable and prevalent than previously thought. All tissues of the heart may be variably affected. The most frequently affected tissue is the myocardium. MIDs should be included in the differential diagnoses of cardiac disease.
Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Arrhythmias; Cardiac involvement; Cardiomyopathy; Heart failure; Mitochondrial disorder; Myopathy; Neuropathy; Sudden cardiac death; Systolic dysfunction; Takotsubo

Mesh:

Year:  2014        PMID: 25465824     DOI: 10.1016/j.ijcard.2014.11.014

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  31 in total

Review 1.  MELAS syndrome and cardiomyopathy: linking mitochondrial function to heart failure pathogenesis.

Authors:  Ying-Han R Hsu; Haran Yogasundaram; Nirmal Parajuli; Lucas Valtuille; Consolato Sergi; Gavin Y Oudit
Journal:  Heart Fail Rev       Date:  2016-01       Impact factor: 4.214

Review 2.  Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology.

Authors:  Antoine Bondue; Eloisa Arbustini; Anna Bianco; Michele Ciccarelli; Dana Dawson; Matteo De Rosa; Nazha Hamdani; Denise Hilfiker-Kleiner; Benjamin Meder; Adelino F Leite-Moreira; Thomas Thum; Carlo G Tocchetti; Gilda Varricchi; Jolanda Van der Velden; Roddy Walsh; Stephane Heymans
Journal:  Cardiovasc Res       Date:  2018-08-01       Impact factor: 10.787

3.  Response to: Letter to the Editor regarding: The expanding phenotype of MELAS caused by the m.3291T > C tRNA mutation E. Kelland, C.A. Rupar, Asuri N. Prasad, A. Downie and C. Prasad (1) by Josef Finsterer, MD, PhD [1], Sinda Zarrouk-Mahjoub, PhD [2].

Authors: 
Journal:  Mol Genet Metab Rep       Date:  2016-06-01

Review 4.  Human-induced pluripotent stem cell approaches to model inborn and acquired metabolic heart diseases.

Authors:  Anita M Chanana; June-Wha Rhee; Joseph C Wu
Journal:  Curr Opin Cardiol       Date:  2016-05       Impact factor: 2.161

5.  Endurance Exercise Training in Young Adults with Barth Syndrome: A Pilot Study.

Authors:  W Todd Cade; Dominic N Reeds; Linda R Peterson; Kathryn L Bohnert; Rachel A Tinius; Paul B Benni; Barry J Byrne; Carolyn L Taylor
Journal:  JIMD Rep       Date:  2016-06-11

6.  Mitochondrial DNA mutations and cardiovascular disease.

Authors:  Alexander W Bray; Scott W Ballinger
Journal:  Curr Opin Cardiol       Date:  2017-05       Impact factor: 2.161

7.  Causes of Death in Adults with Mitochondrial Disease.

Authors:  Marlieke Barends; Lotte Verschuren; Eva Morava; Victoria Nesbitt; Doug Turnbull; Robert McFarland
Journal:  JIMD Rep       Date:  2015-09-10

8.  Rare Pathogenic Variants in Mitochondrial and Inflammation-Associated Genes May Lead to Inflammatory Cardiomyopathy in Chagas Disease.

Authors:  Edecio Cunha-Neto; Christophe Chevillard; Maryem Ouarhache; Sandrine Marquet; Amanda Farage Frade; Ariela Mota Ferreira; Barbara Ianni; Rafael Ribeiro Almeida; Joao Paulo Silva Nunes; Ludmila Rodrigues Pinto Ferreira; Vagner Oliveira-Carvalho Rigaud; Darlan Cândido; Charles Mady; Ricardo Costa Fernandes Zaniratto; Paula Buck; Magali Torres; Frederic Gallardo; Pauline Andrieux; Sergio Bydlowsky; Debora Levy; Laurent Abel; Clareci Silva Cardoso; Omar Ribeiro Santos-Junior; Lea Campos Oliveira; Claudia Di Lorenzo Oliveira; Maria Do Carmo Nunes; Aurelie Cobat; Jorge Kalil; Antonio Luiz Ribeiro; Ester Cerdeira Sabino
Journal:  J Clin Immunol       Date:  2021-03-03       Impact factor: 8.542

Review 9.  Molecular Epidemiology of Mitochondrial Cardiomyopathy: A Search Among Mitochondrial and Nuclear Genes.

Authors:  Cristina Mazzaccara; Bruno Mirra; Ferdinando Barretta; Martina Caiazza; Barbara Lombardo; Olga Scudiero; Nadia Tinto; Giuseppe Limongelli; Giulia Frisso
Journal:  Int J Mol Sci       Date:  2021-05-27       Impact factor: 6.208

Review 10.  Mitochondrial Bioenergetics and Dynamism in the Failing Heart.

Authors:  Giampaolo Morciano; Veronica Angela Maria Vitto; Esmaa Bouhamida; Carlotta Giorgi; Paolo Pinton
Journal:  Life (Basel)       Date:  2021-05-12
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.