Literature DB >> 20215590

Arrhythmogenic right ventricular dysplasia/cardiomyopathy diagnostic task force criteria: impact of new task force criteria.

Moniek G P J Cox1, Jasper J van der Smagt, Maartje Noorman, Ans C Wiesfeld, Paul G A Volders, Irene M van Langen, Douwe E Atsma, Dennis Dooijes, Arjan C Houweling, Peter Loh, Luc Jordaens, Yvonne Arens, Maarten J Cramer, Pieter A Doevendans, J Peter van Tintelen, Arthur A M Wilde, Richard N W Hauer.   

Abstract

BACKGROUND: Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C) Diagnostic Task Force Criteria (TFC) proposed in 1994 are highly specific but lack sensitivity. A new international task force modified criteria to improve diagnostic yield. A comparison of diagnosis by 1994 TFC versus newly proposed criteria in 3 patient groups was conducted. METHODS AND
RESULTS: In new TFC, scoring by major and minor criteria is maintained. Structural abnormalities are quantified and TFC highly specific for ARVD/C upgraded to major. Furthermore, new criteria are added: terminal activation duration of QRS > or = 55 ms, ventricular tachycardia with left bundle-branch block morphology and superior axis, and genetic criteria. Three groups were studied: (1) 105 patients with proven ARVD/C according to 1994 TFC, (2) 89 of their family members, and (3) 39 patients with probable ARVD/C (ie, 3 points by 1994 TFC). All were screened for pathogenic mutations in desmosomal genes. Three ARVD/C patients did not meet the new sharpened criteria on structural abnormalities and thereby did not fulfill new TFC. In 62 of 105 patients with proven ARVD/C, mutations were found: 58 in the gene encoding Plakophilin2 (PKP2), 3 in Desmoglein2, 3 in Desmocollin2, and 1 in Desmoplakin. Three patients had bigenic involvement. Ten additional relatives (11%) fulfilled new TFC: 9 (90%) were female, and all carried PKP2 mutations. No relatives lost diagnosis by application of new TFC. Of patients with probable ARVD/C, 25 (64%) fulfilled new TFC: 8 (40%) women and 14 (56%) carrying pathogenic mutations.
CONCLUSIONS: In this first study applying new TFC to patients suspected of ARVD/C, 64% of probable ARVD/C patients and 11% of family members were additionally diagnosed. ECG criteria and pathogenic mutations especially contributed to new diagnosis. Newly proposed TFC have a major impact in increasing diagnostic yield of ARVD/C.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20215590     DOI: 10.1161/CIRCEP.109.927202

Source DB:  PubMed          Journal:  Circ Arrhythm Electrophysiol        ISSN: 1941-3084


  23 in total

1.  Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise.

Authors:  Jamie D Kapplinger; Andrew P Landstrom; Benjamin A Salisbury; Thomas E Callis; Guido D Pollevick; David J Tester; Moniek G P J Cox; Zahir Bhuiyan; Hennie Bikker; Ans C P Wiesfeld; Richard N W Hauer; J Peter van Tintelen; Jan D H Jongbloed; Hugh Calkins; Daniel P Judge; Arthur A M Wilde; Michael J Ackerman
Journal:  J Am Coll Cardiol       Date:  2011-06-07       Impact factor: 24.094

2.  Clinico-radiological profile of arrhythmogenic right ventricular dysplasia at a tertiary care center: Two year experience.

Authors:  Feroze Shaheen; Khurshid Iqbal; Imran Hafeez; Naseer A Choh; Nisar A Tramboo; Ajaz Lone; Shamim Iqbal; Wasim Ahmed; Amit Gupta
Journal:  J Saudi Heart Assoc       Date:  2013-03-21

Review 3.  Cardiac MR findings and potential diagnostic pitfalls in patients evaluated for arrhythmogenic right ventricular cardiomyopathy.

Authors:  Neda Rastegar; Jeremy R Burt; Celia P Corona-Villalobos; Anneline S Te Riele; Cynthia A James; Brittney Murray; Hugh Calkins; Harikrishna Tandri; David A Bluemke; Stefan L Zimmerman; Ihab R Kamel
Journal:  Radiographics       Date:  2014-10       Impact factor: 5.333

Review 4.  Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a review and update.

Authors:  A Azaouagh; S Churzidse; T Konorza; R Erbel
Journal:  Clin Res Cardiol       Date:  2011-03-01       Impact factor: 5.460

5.  Mutation-positive arrhythmogenic right ventricular dysplasia/cardiomyopathy: the triangle of dysplasia displaced.

Authors:  Anneline S J M Te Riele; Cynthia A James; Binu Philips; Neda Rastegar; Aditya Bhonsale; Judith A Groeneweg; Brittney Murray; Crystal Tichnell; Daniel P Judge; Jeroen F Van Der Heijden; Maarten J M Cramer; Birgitta K Velthuis; David A Bluemke; Stefan L Zimmerman; Ihab R Kamel; Richard N W Hauer; Hugh Calkins; Harikrishna Tandri
Journal:  J Cardiovasc Electrophysiol       Date:  2013-07-25

Review 6.  Arrhythmogenic right ventricular cardiomyopathy. Contribution of cardiac magnetic resonance imaging to the diagnosis.

Authors:  M Perazzolo Marra; S Rizzo; B Bauce; M De Lazzari; K Pilichou; D Corrado; G Thiene; S Iliceto; C Basso
Journal:  Herz       Date:  2015-06       Impact factor: 1.443

Review 7.  Arrhythmogenic right ventricular cardiomyopathy: an update on pathophysiology, genetics, diagnosis, and risk stratification.

Authors:  M Paul; T Wichter; L Fabritz; J Waltenberger; E Schulze-Bahr; P Kirchhof
Journal:  Herzschrittmacherther Elektrophysiol       Date:  2012-09-26

8.  The use of cardiovascular magnetic resonance to identify adverse cardiac prognosis: an important step in reducing image-related heath care expenditures.

Authors:  W Gregory Hundley
Journal:  J Am Coll Cardiol       Date:  2010-10-05       Impact factor: 24.094

9.  Right ventricular sarcoidosis: is it time for updated diagnostic criteria?

Authors:  Kairav Vakil; Elina Minami; Daniel P Fishbein
Journal:  Tex Heart Inst J       Date:  2014-04-01

10.  Desmosomal molecules in and out of adhering junctions: normal and diseased States of epidermal, cardiac and mesenchymally derived cells.

Authors:  Sebastian Pieperhoff; Mareike Barth; Steffen Rickelt; Werner W Franke
Journal:  Dermatol Res Pract       Date:  2010-06-30
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.