Literature DB >> 30055033

Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients.

Mark D Levin1, Sulagna C Saitta2, Karen W Gripp3, Tara L Wenger4, Jaya Ganesh5, Jennifer M Kalish6, Michael R Epstein7, Rosemarie Smith8, Richard J Czosek9, Stephanie M Ware10, Paula Goldenberg11, Angela Myers12, Kathryn C Chatfield13, Matthew J Gillespie14, Elaine H Zackai6, Angela E Lin11.   

Abstract

Multifocal atrial tachycardia (MAT) has a well-known association with Costello syndrome, but is rarely described with related RAS/MAPK pathway disorders (RASopathies). We report 11 patients with RASopathies (Costello, Noonan, and Noonan syndrome with multiple lentigines [formerly LEOPARD syndrome]) and nonreentrant atrial tachycardias (MAT and ectopic atrial tachycardia) demonstrating overlap in cardiac arrhythmia phenotype. Similar overlap is seen in RASopathies with respect to skeletal, musculoskeletal and cutaneous abnormalities, dysmorphic facial features, and neurodevelopmental deficits. Nonreentrant atrial tachycardias may cause cardiac compromise if sinus rhythm is not restored expeditiously. Typical first-line supraventricular tachycardia anti-arrhythmics (propranolol and digoxin) were generally not effective in restoring or maintaining sinus rhythm in this cohort, while flecainide or amiodarone alone or in concert with propranolol were effective anti-arrhythmic agents for acute and chronic use. Atrial tachycardia resolved in all patients. However, a 4-month-old boy from the cohort was found asystolic (with concurrent cellulitis) and a second patient underwent cardiac transplant for heart failure complicated by recalcitrant atrial arrhythmia. While propranolol alone frequently failed to convert or maintain sinus rhythm, fleccainide or amiodarone, occasionally in combination with propranolol, was effective for RASopathy patient treatment for nonreentrant atrial arrhythmia. Our analysis shows that RASopathy patients may have nonreentrant atrial tachycardia with and without associated cardiac hypertrophy. While nonreentrant arrhythmia has been traditionally associated with Costello syndrome, this work provides an expanded view of RASopathy cardiac arrhythmia phenotype as we demonstrate mutant proteins throughout this signaling pathway can also give rise to ectopic and/or MAT.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  Calcium; Costello syndrome; Noonan syndrome; Noonan syndrome with multiple lentigines; RAS/MAPK signaling pathway; ectopic atrial tachycardia; multifocal atrial tachycardia

Mesh:

Substances:

Year:  2018        PMID: 30055033      PMCID: PMC6107379          DOI: 10.1002/ajmg.a.38854

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  34 in total

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2.  Treatment of multifocal atrial tachycardia with verapamil.

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3.  Contemporary definitions and classification of the cardiomyopathies: an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention.

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Journal:  Circulation       Date:  2006-03-27       Impact factor: 29.690

4.  MEK-ERK pathway modulation ameliorates disease phenotypes in a mouse model of Noonan syndrome associated with the Raf1(L613V) mutation.

Authors:  Xue Wu; Jeremy Simpson; Jenny H Hong; Kyoung-Han Kim; Nirusha K Thavarajah; Peter H Backx; Benjamin G Neel; Toshiyuki Araki
Journal:  J Clin Invest       Date:  2011-02-21       Impact factor: 14.808

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Authors:  Xander H T Wehrens; Stephan E Lehnart; Steven R Reiken; Shi-Xian Deng; John A Vest; Daniel Cervantes; James Coromilas; Donald W Landry; Andrew R Marks
Journal:  Science       Date:  2004-04-09       Impact factor: 47.728

6.  Flecainide inhibits arrhythmogenic Ca2+ waves by open state block of ryanodine receptor Ca2+ release channels and reduction of Ca2+ spark mass.

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Journal:  J Mol Cell Cardiol       Date:  2009-10-14       Impact factor: 5.000

Review 7.  Hypertrophic cardiomyopathy.

Authors:  Perry Elliott; William J McKenna
Journal:  Lancet       Date:  2004-06-05       Impact factor: 79.321

8.  Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans.

Authors:  Hiroshi Watanabe; Nagesh Chopra; Derek Laver; Hyun Seok Hwang; Sean S Davies; Daniel E Roach; Henry J Duff; Dan M Roden; Arthur A M Wilde; Björn C Knollmann
Journal:  Nat Med       Date:  2009-03-29       Impact factor: 53.440

9.  The direct actions of flecainide on the human cardiac ryanodine receptor: keeping open the debate on the mechanism of action of local anesthetics in CPVT.

Authors:  Godfrey L Smith; Niall MacQuaide
Journal:  Circ Res       Date:  2015-04-10       Impact factor: 17.367

10.  Kinase-activating and kinase-impaired cardio-facio-cutaneous syndrome alleles have activity during zebrafish development and are sensitive to small molecule inhibitors.

Authors:  Corina Anastasaki; Anne L Estep; Richard Marais; Katherine A Rauen; E Elizabeth Patton
Journal:  Hum Mol Genet       Date:  2009-04-17       Impact factor: 6.150

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  8 in total

1.  Costello syndrome: Clinical phenotype, genotype, and management guidelines.

Authors:  Karen W Gripp; Lindsey A Morse; Marni Axelrad; Kathryn C Chatfield; Aaron Chidekel; William Dobyns; Daniel Doyle; Bronwyn Kerr; Angela E Lin; David D Schwartz; Barbara J Sibbles; Dawn Siegel; Suma P Shankar; David A Stevenson; Mihir M Thacker; K Nicole Weaver; Sue M White; Katherine A Rauen
Journal:  Am J Med Genet A       Date:  2019-06-20       Impact factor: 2.802

2.  Congenital heart defects in Noonan syndrome: Diagnosis, management, and treatment.

Authors:  Léa Linglart; Bruce D Gelb
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-02-05       Impact factor: 3.908

3.  RAF-1 Mutation Associated with a Risk for Ventricular Arrhythmias in a Child with Noonan Syndrome and Cardiovascular Pathology.

Authors:  Amalia Făgărășan; Hamida Al Hussein; Simina Elena Ghiragosian Rusu
Journal:  J Crit Care Med (Targu Mures)       Date:  2022-05-12

4.  Severe Lymphatic Disorder and Multifocal Atrial Tachycardia Treated with Trametinib in a Patient with Noonan Syndrome and SOS1 Mutation.

Authors:  Michele Lioncino; Adelaide Fusco; Emanuele Monda; Diego Colonna; Michelina Sibilio; Martina Caiazza; Daniela Magri; Angela Carla Borrelli; Barbara D'Onofrio; Maria Luisa Mazzella; Rossella Colantuono; Maria Rosaria Arienzo; Berardo Sarubbi; Maria Giovanna Russo; Giovanni Chello; Giuseppe Limongelli
Journal:  Genes (Basel)       Date:  2022-08-23       Impact factor: 4.141

Review 5.  Inside the Noonan "universe": Literature review on growth, GH/IGF axis and rhGH treatment: Facts and concerns.

Authors:  Stefano Stagi; Vittorio Ferrari; Marta Ferrari; Manuela Priolo; Marco Tartaglia
Journal:  Front Endocrinol (Lausanne)       Date:  2022-08-18       Impact factor: 6.055

6.  Noonan syndrome caused by RIT1 gene mutation: A case report and literature review.

Authors:  Ping Zha; Ying Kong; Lili Wang; Yujuan Wang; Qing Qing; Liying Dai
Journal:  Front Pediatr       Date:  2022-09-07       Impact factor: 3.569

7.  Male infant with Noonan syndrome with RAF-1 gene mutation who survived hypertrophic cardiomyopathy-induced fatal heart failure and uncontrollable arrhythmias.

Authors:  Mao Hagino; Chiharu Ota; Takehiko Onoki; Shinya Iwasawa
Journal:  BMJ Case Rep       Date:  2022-09-28

Review 8.  Complicated ventricular arrhythmia and hematologic myeloproliferative disorder in RIT1-associated Noonan syndrome: Expanding the phenotype and review of the literature.

Authors:  Safwat A Aly; Kenneth M Boyer; Brie-Ann A Muller; Davide Marini; Carolyn H Jones; Hoang H Nguyen
Journal:  Mol Genet Genomic Med       Date:  2020-05-12       Impact factor: 2.183

  8 in total

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