Literature DB >> 28336205

Andersen-Tawil syndrome: Clinical presentation and predictors of symptomatic arrhythmias - Possible role of polymorphisms K897T in KCNH2 and H558R in SCN5A gene.

Michalina Krych1, Elżbieta Katarzyna Biernacka2, Joanna Ponińska3, Piotr Kukla4, Artur Filipecki5, Robert Gajda6, Can Hasdemir7, Charles Antzelevitch8, Agnieszka Kosiec3, Małgorzata Szperl3, Rafał Płoski9, Maria Trusz-Gluza5, Katarzyna Mizia-Stec5, Piotr Hoffman2.   

Abstract

BACKGROUND: Andersen-Tawil syndrome (ATS) is rare channelopathy caused by KCNJ2 mutation and probably KCNJ5. It is characterized by arrhythmias, neurological symptoms, and dysmorphic features. The present study retrospectively examined the characteristics of 11 unrelated families with ATS.
METHODS: This study consisted of 11 probands positive for KCNJ2 variants and 33 family members (mean age 30.0±17.3 years, female n=31). Additional genetic screening of 3 LQTS genes (KCNQ1, KCNH2, SCN5A) was performed in 9 families. Predictors of arrhythmias [premature ventricular beats>2000/24h, biventricular and polymorphic ventricular tachycardia (VT)], syncope, and/or cardiac arrest (CA) were evaluated.
RESULTS: In KCNJ2 mutation carriers vs non-carriers (n=25 vs n=19) significant differences were observed in U-wave manifestations in V2-V4, Tpeak-Tend duration, QTUc duration (p<0.0001), dysmorphic features, and neurological symptoms. Compared to asymptomatic carriers (n=9), in those with arrhythmias and/or syncope and/or CA (n=16) micrognathia (p=0.004), periodic paralysis (p=0.019), palpitation (p=0.005), U-wave n V2-V4 (p=0.049) were more frequent; QTU (p=0.045) and Tpeak-Tend (p=0.014) were also longer (n=9). In the subgroup of carriers with syncope and/or cardiac arrest (n=10, 90% women), K897T-KCNH2 polymorphism (p=0.02), periodic paralysis (p=0.004), muscle weakness (p=0.04), palpitations (p=0.04), arrhythmias (biventricular VT, p=0.003; polymorphic VT, p=0.009) were observed more frequently. Tpeak-Tend duration was longer (p=0.007) and the percentage of patients with premature ventricular contraction >2000/24h was higher (p=0.005).
CONCLUSION: A higher risk of arrhythmia, syncope, and/or CA is associated with the presence of micrognathia, periodic paralysis, and prolonged Tpeak-Tend time. Our findings suggest that K897T may contribute to the occurrence of syncope.
Copyright © 2017 Japanese College of Cardiology. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Andersen-Tawil syndrome; Arrhythmia; K897T polymorphism; Long QT syndrome

Mesh:

Substances:

Year:  2017        PMID: 28336205      PMCID: PMC5607087          DOI: 10.1016/j.jjcc.2017.01.009

Source DB:  PubMed          Journal:  J Cardiol        ISSN: 0914-5087            Impact factor:   3.159


  19 in total

Review 1.  Congenital long QT syndrome: considerations for primary care physicians.

Authors:  Ethan Levine; Spencer Z Rosero; Adam S Budzikowski; Arthur J Moss; Wojciech Zareba; James P Daubert
Journal:  Cleve Clin J Med       Date:  2008-08       Impact factor: 2.321

2.  Coexistence of Andersen-Tawil Syndrome with Polymorphisms in hERG1 Gene (K897T) and SCN5A Gene (H558R) in One Family.

Authors:  Michalina Jagodzińska; Małgorzata Szperl; Joanna Ponińska; Agnieszka Kosiec; Robert Gajda; Piotr Kukla; Elżbieta Katarzyna Biernacka
Journal:  Ann Noninvasive Electrocardiol       Date:  2015-06-24       Impact factor: 1.468

3.  Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features.

Authors:  R Tawil; L J Ptacek; S G Pavlakis; D C DeVivo; A S Penn; C Ozdemir; R C Griggs
Journal:  Ann Neurol       Date:  1994-03       Impact factor: 10.422

4.  Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome.

Authors:  N M Plaster; R Tawil; M Tristani-Firouzi; S Canún; S Bendahhou; A Tsunoda; M R Donaldson; S T Iannaccone; E Brunt; R Barohn; J Clark; F Deymeer; A L George; F A Fish; A Hahn; A Nitu; C Ozdemir; P Serdaroglu; S H Subramony; G Wolfe; Y H Fu; L J Ptácek
Journal:  Cell       Date:  2001-05-18       Impact factor: 41.582

5.  Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype.

Authors:  Li Zhang; D Woodrow Benson; Martin Tristani-Firouzi; Louis J Ptacek; Rabi Tawil; Peter J Schwartz; Alfred L George; Minoru Horie; Gregor Andelfinger; Gregory L Snow; Ying-Hui Fu; Michael J Ackerman; G Michael Vincent
Journal:  Circulation       Date:  2005-05-23       Impact factor: 29.690

6.  Efficacy and safety of flecainide for ventricular arrhythmias in patients with Andersen-Tawil syndrome with KCNJ2 mutations.

Authors:  Koji Miyamoto; Takeshi Aiba; Hiromi Kimura; Hideki Hayashi; Seiko Ohno; Chie Yasuoka; Yoshihito Tanioka; Takeshi Tsuchiya; Yoko Yoshida; Hiroshi Hayashi; Ippei Tsuboi; Ikutaro Nakajima; Kohei Ishibashi; Hideo Okamura; Takashi Noda; Masaharu Ishihara; Toshihisa Anzai; Satoshi Yasuda; Yoshihiro Miyamoto; Shiro Kamakura; Kengo Kusano; Hisao Ogawa; Minoru Horie; Wataru Shimizu
Journal:  Heart Rhythm       Date:  2014-12-10       Impact factor: 6.343

7.  Resuscitated sudden cardiac death in Andersen-Tawil syndrome.

Authors:  Kelly J Airey; Susan P Etheridge; Rabi Tawil; Martin Tristani-Firouzi
Journal:  Heart Rhythm       Date:  2009-08-29       Impact factor: 6.343

8.  A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1.

Authors:  Yosuke Kokunai; Tomohiko Nakata; Mitsuru Furuta; Souhei Sakata; Hiromi Kimura; Takeshi Aiba; Masao Yoshinaga; Yusuke Osaki; Masayuki Nakamori; Hideki Itoh; Takako Sato; Tomoya Kubota; Kazushige Kadota; Katsuro Shindo; Hideki Mochizuki; Wataru Shimizu; Minoru Horie; Yasushi Okamura; Kinji Ohno; Masanori P Takahashi
Journal:  Neurology       Date:  2014-02-26       Impact factor: 9.910

9.  Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation.

Authors:  Eric Delannoy; Frédéric Sacher; Philippe Maury; Philippe Mabo; Jacques Mansourati; Isabelle Magnin; Jean-Pierre Camous; Guillaume Tournant; Eric Rendu; Florence Kyndt; Michel Haïssaguerre; Stéphane Bézieau; Béatrice Guyomarch; Hervé Le Marec; Véronique Fressart; Isabelle Denjoy; Vincent Probst
Journal:  Europace       Date:  2013-07-17       Impact factor: 5.214

10.  Phenotype variability in patients carrying KCNJ2 mutations.

Authors:  Hiromi Kimura; Jun Zhou; Mihoko Kawamura; Hideki Itoh; Yuka Mizusawa; Wei-Guang Ding; Jie Wu; Seiko Ohno; Takeru Makiyama; Akashi Miyamoto; Nobu Naiki; Qi Wang; Yu Xie; Tsugutoshi Suzuki; Shigeru Tateno; Yoshihide Nakamura; Wei-Jin Zang; Makoto Ito; Hiroshi Matsuura; Minoru Horie
Journal:  Circ Cardiovasc Genet       Date:  2012-05-15
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  2 in total

1.  Variable Clinical Appearance of the Kir2.1 Rare Variants in Russian Patients with Long QT Syndrome.

Authors:  Elena Zaklyazminskaya; Margarita Polyak; Anna Shestak; Mariam Sadekova; Vera Komoliatova; Irina Kiseleva; Leonid Makarov; Dmitriy Podolyak; Grigory Glukhov; Han Zhang; Denis Abramochkin; Olga S Sokolova
Journal:  Genes (Basel)       Date:  2022-03-22       Impact factor: 4.141

2.  Amateur Athlete with Sinus Arrest and Severe Bradycardia Diagnosed through a Heart Rate Monitor: A Six-Year Observation-The Necessity of Shared Decision-Making in Heart Rhythm Therapy Management.

Authors:  Robert Gajda; Beat Knechtle; Anita Gębska-Kuczerowska; Jacek Gajda; Sebastian Stec; Michalina Krych; Magdalena Kwaśniewska; Wojciech Drygas
Journal:  Int J Environ Res Public Health       Date:  2022-08-19       Impact factor: 4.614

  2 in total

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