Literature DB >> 31773301

Lamin A/C Cardiomyopathy: Implications for Treatment.

Suet Nee Chen1, Orfeo Sbaizero1,2, Matthew R G Taylor1, Luisa Mestroni3.   

Abstract

PURPOSE OF REVIEW: The purpose of this review is to provide an update on lamin A/C (LMNA)-related cardiomyopathy and discuss the current recommendations and progress in the management of this disease. LMNA-related cardiomyopathy, an inherited autosomal dominant disease, is one of the most common causes of dilated cardiomyopathy and is characterized by steady progression toward heart failure and high risks of arrhythmias and sudden cardiac death. RECENT
FINDINGS: We discuss recent advances in the understanding of the molecular mechanisms of the disease including altered cell biomechanics, which may represent novel therapeutic targets to advance the current management approach, which relies on standard heart failure recommendations. Future therapeutic approaches include repurposed molecularly directed drugs, siRNA-based gene silencing, and genome editing. LMNA-related cardiomyopathy is the focus of active in vitro and in vivo research, which is expected to generate novel biomarkers and identify new therapeutic targets. LMNA-related cardiomyopathy trials are currently underway.

Entities:  

Keywords:  Arrhythmias; CRISPR–Cas9 therapy; Heart failure; Lamin A/C gene; Laminopathy; Mechanotransduction; P53

Mesh:

Substances:

Year:  2019        PMID: 31773301     DOI: 10.1007/s11886-019-1224-7

Source DB:  PubMed          Journal:  Curr Cardiol Rep        ISSN: 1523-3782            Impact factor:   2.931


  72 in total

1.  Decreased WNT/β-catenin signalling contributes to the pathogenesis of dilated cardiomyopathy caused by mutations in the lamin a/C gene.

Authors:  Caroline Le Dour; Coline Macquart; Fusako Sera; Shunichi Homma; Gisele Bonne; John P Morrow; Howard J Worman; Antoine Muchir
Journal:  Hum Mol Genet       Date:  2017-01-15       Impact factor: 6.150

2.  2017 AHA/ACC/HRS Guideline for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society.

Authors:  Sana M Al-Khatib; William G Stevenson; Michael J Ackerman; William J Bryant; David J Callans; Anne B Curtis; Barbara J Deal; Timm Dickfeld; Michael E Field; Gregg C Fonarow; Anne M Gillis; Christopher B Granger; Stephen C Hammill; Mark A Hlatky; José A Joglar; G Neal Kay; Daniel D Matlock; Robert J Myerburg; Richard L Page
Journal:  Circulation       Date:  2018-09-25       Impact factor: 29.690

Review 3.  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

4.  Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice.

Authors:  Leslie C Mounkes; Serguei V Kozlov; Jeffrey N Rottman; Colin L Stewart
Journal:  Hum Mol Genet       Date:  2005-06-22       Impact factor: 6.150

Review 5.  'State-of-the-heart' of cardiac laminopathies.

Authors:  Marie-Elodie Cattin; Antoine Muchir; Gisèle Bonne
Journal:  Curr Opin Cardiol       Date:  2013-05       Impact factor: 2.161

6.  A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy.

Authors:  Satu Kärkkäinen; Tiina Heliö; Raija Miettinen; Petri Tuomainen; Paula Peltola; Juha Rummukainen; Kari Ylitalo; Maija Kaartinen; Johanna Kuusisto; Lauri Toivonen; Markku S Nieminen; Markku Laakso; Keijo Peuhkurinen
Journal:  Eur Heart J       Date:  2004-05       Impact factor: 29.983

7.  Modulation of LMNA splicing as a strategy to treat prelamin A diseases.

Authors:  John M Lee; Chika Nobumori; Yiping Tu; Catherine Choi; Shao H Yang; Hea-Jin Jung; Timothy A Vickers; Frank Rigo; C Frank Bennett; Stephen G Young; Loren G Fong
Journal:  J Clin Invest       Date:  2016-03-21       Impact factor: 14.808

8.  Rapamycin reverses elevated mTORC1 signaling in lamin A/C-deficient mice, rescues cardiac and skeletal muscle function, and extends survival.

Authors:  Fresnida J Ramos; Steven C Chen; Michael G Garelick; Dao-Fu Dai; Chen-Yu Liao; Katherine H Schreiber; Vivian L MacKay; Elroy H An; Randy Strong; Warren C Ladiges; Peter S Rabinovitch; Matt Kaeberlein; Brian K Kennedy
Journal:  Sci Transl Med       Date:  2012-07-25       Impact factor: 17.956

9.  Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity.

Authors:  Marie-Elodie Cattin; Anne T Bertrand; Saskia Schlossarek; Marie-Catherine Le Bihan; Søren Skov Jensen; Christiane Neuber; Claudia Crocini; Sophia Maron; Jeanne Lainé; Nathalie Mougenot; Shaïda Varnous; Yves Fromes; Arne Hansen; Thomas Eschenhagen; Valérie Decostre; Lucie Carrier; Gisèle Bonne
Journal:  Hum Mol Genet       Date:  2013-04-10       Impact factor: 6.150

10.  Development of a CRISPR/Cas9-based therapy for Hutchinson-Gilford progeria syndrome.

Authors:  Olaya Santiago-Fernández; Fernando G Osorio; Víctor Quesada; Francisco Rodríguez; Sammy Basso; Daniel Maeso; Loïc Rolas; Anna Barkaway; Sussan Nourshargh; Alicia R Folgueras; José M P Freije; Carlos López-Otín
Journal:  Nat Med       Date:  2019-02-18       Impact factor: 53.440

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  6 in total

Review 1.  SUMOylation targeting mitophagy in cardiovascular diseases.

Authors:  Hong Xiao; Hong Zhou; Gaofeng Zeng; Zhenjiang Mao; Junfa Zeng; Anbo Gao
Journal:  J Mol Med (Berl)       Date:  2022-09-26       Impact factor: 5.606

2.  BETs that cover the spread from acquired to heritable heart failure.

Authors:  Michael Alexanian; Saptarsi M Haldar
Journal:  J Clin Invest       Date:  2020-09-01       Impact factor: 14.808

3.  Role of Cdkn2a in the Emery-Dreifuss Muscular Dystrophy Cardiac Phenotype.

Authors:  Gloria Pegoli; Marika Milan; Pierluigi Giuseppe Manti; Andrea Bianchi; Federica Lucini; Philina Santarelli; Claudia Bearzi; Roberto Rizzi; Chiara Lanzuolo
Journal:  Biomolecules       Date:  2021-04-06

4.  Red herring pathogenic variants: a case report of premature ventricular contraction-triggered ventricular fibrillation with an incidental pathogenic LMNA variant.

Authors:  Ramin Garmany; Raquel Neves; Fatima Ali Ahmed; David J Tester; Bryan C Cannon; John R Giudicessi; Michael J Ackerman
Journal:  Eur Heart J Case Rep       Date:  2022-03-17

5.  Compromised Biomechanical Properties, Cell-Cell Adhesion and Nanotubes Communication in Cardiac Fibroblasts Carrying the Lamin A/C D192G Mutation.

Authors:  Veronique Lachaize; Brisa Peña; Catalin Ciubotaru; Dan Cojoc; Suet Nee Chen; Matthew R G Taylor; Luisa Mestroni; Orfeo Sbaizero
Journal:  Int J Mol Sci       Date:  2021-08-25       Impact factor: 5.923

6.  Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality.

Authors:  Jia Chen; Yuting Ma; Hong Li; Zhuo Lin; Zhe Yang; Qin Zhang; Feng Wang; Yanping Lin; Zebing Ye; Yubi Lin
Journal:  Orphanet J Rare Dis       Date:  2022-05-07       Impact factor: 4.123

  6 in total

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