Literature DB >> 20071715

Utility of treadmill testing in identification and genotype prediction in long-QT syndrome.

Jorge A Wong1, Lorne J Gula, George J Klein, Raymond Yee, Allan C Skanes, Andrew D Krahn.   

Abstract

BACKGROUND: The clinical diagnosis of long-QT syndrome (LQTS) remains challenging when ECG abnormalities are borderline or intermittent. Despite issues with access, cost, and heterogeneity of LQTS mutations, genetic testing remains the diagnostic gold standard for diagnosis of LQTS. We sought to develop a provocative testing strategy to unmask the LQTS phenotype and relate this to the results of genetic testing. METHODS AND
RESULTS: From 1995 to 2008, 159 consecutive patients with suspected LQTS underwent provocative testing that consisted of a modified Bruce protocol treadmill exercise test, with ECGs recorded supine at rest, immediately on standing, and at 1-minute intervals during exercise, at peak exercise, and at 1-minute intervals during the recovery phase. Similar testing was carried out on a stationary bike in a gradual and burst exercise fashion. LQTS was confirmed with genotyping in all 95 affected LQTS patients and excluded with negative family screening in 64 control subjects. Patients were studied before and after initiation of beta-blockers. Of 159 patients, 50 had an LQT1 mutation and 45 had an LQT2 mutation. In the LQTS group, 44.3% of patients had a normal-to-borderline resting QTc interval. LQTS patients exhibited a greater prolongation in QTc with postural change than unaffected patients (LQT1: 40 ms [IQR, 42]; LQT2: 35 ms [IQR, 46]; and LQTS-negative: 21 ms [IQR, 37]; P=0.029). During exercise, LQT1 patients had marked QTc prolongation compared with LQT2 and LQTS-negative patients (LQT1: 65 ms [60], LQT2: 3 ms [46], LQTS negative: 5 ms [41]; P<0.0001). QT hysteresis was more pronounced in patients with LQT2 mutations compared with LQT1 and LQT-negative patients (LQT2: 40 ms [10], LQT1: 15 ms [40]; LQTS-negative: 20 ms [20]; P<0.001). beta-Blockade normalized the QTc changes seen with standing and QT hysteresis.
CONCLUSIONS: The presence and genotype of LQTS can be predicted by a combination of postural and exercise changes in the QT/RR relationship. beta-Blockade normalized these changes. Routine exercise testing is useful in predicting and directing genetic testing in LQTS.

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Year:  2010        PMID: 20071715     DOI: 10.1161/CIRCEP.109.907865

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


  32 in total

1.  β-blockers protect against dispersion of repolarization during exercise in congenital long-QT syndrome type 1.

Authors:  Lee W Gemma; Gregory M Ward; Mary M Dettmer; Jennifer L Ball; Peter J Leo; Danielle N Doria; Elizabeth S Kaufman
Journal:  J Cardiovasc Electrophysiol       Date:  2011-06-02

2.  The phenomenon of "QT stunning": the abnormal QT prolongation provoked by standing persists even as the heart rate returns to normal in patients with long QT syndrome.

Authors:  Arnon Adler; Christian van der Werf; Pieter G Postema; Raphael Rosso; Zahir A Bhuiyan; Jonathan M Kalman; Jitendra K Vohra; Milton E Guevara-Valdivia; Manlio F Marquez; Amir Halkin; Jesaia Benhorin; Charles Antzelevitch; Arthur A M Wilde; Sami Viskin
Journal:  Heart Rhythm       Date:  2012-01-31       Impact factor: 6.343

3.  Genotype- and mutation site-specific QT adaptation during exercise, recovery, and postural changes in children with long-QT syndrome.

Authors:  Peter F Aziz; Tammy S Wieand; Jamie Ganley; Jacqueline Henderson; Akash R Patel; V Ramesh Iyer; R Lee Vogel; Michael McBride; Victoria L Vetter; Maully J Shah
Journal:  Circ Arrhythm Electrophysiol       Date:  2011-09-28

4.  Experience with bisoprolol in long-QT1 and long-QT2 syndrome.

Authors:  Christian Steinberg; Gareth J Padfield; Basil Al-Sabeq; Arnon Adler; John A Yeung-Lai-Wah; Charles R Kerr; Marc W Deyell; Jason G Andrade; Matthew T Bennett; Raymond Yee; George J Klein; Martin Green; Zachary W M Laksman; Andrew D Krahn; Santabhanu Chakrabarti
Journal:  J Interv Card Electrophysiol       Date:  2016-07-09       Impact factor: 1.900

Review 5.  Genotype- and phenotype-guided management of congenital long QT syndrome.

Authors:  John R Giudicessi; Michael J Ackerman
Journal:  Curr Probl Cardiol       Date:  2013-10       Impact factor: 5.200

6.  Postexercise recovery phase T-wave notching in concealed long QT syndrome.

Authors:  B Sensoy; O Ozeke; U Canpolat; S Cay; F Oksuz; S Topaloglu; D Aras; S Aydogdu
Journal:  Herz       Date:  2013-10-25       Impact factor: 1.443

Review 7.  Clinical applications of QT/RR hysteresis assessment: A systematic review.

Authors:  Hugo Gravel; Vincent Jacquemet; Nagib Dahdah; Daniel Curnier
Journal:  Ann Noninvasive Electrocardiol       Date:  2017-10-30       Impact factor: 1.468

8.  QT Dynamics During Exercise in Asymptomatic Children with Long QT Syndrome Type 3.

Authors:  Kazuhiro Takahashi; Taisuke Nabeshima; Mami Nakayashiro; Hitoshi Ganaha
Journal:  Pediatr Cardiol       Date:  2016-02-26       Impact factor: 1.655

Review 9.  Categorization and theoretical comparison of quantitative methods for assessing QT/RR hysteresis.

Authors:  Hugo Gravel; Daniel Curnier; Nagib Dahdah; Vincent Jacquemet
Journal:  Ann Noninvasive Electrocardiol       Date:  2017-05-16       Impact factor: 1.468

10.  Assessment of ventricular repolarization variability with the DeltaT50 method improves identification of patients with congenital long QT syndromes.

Authors:  Christina Abrahamsson; Corina Dota; Bo Skallefell; Leif Carlsson; Lars Frison; Anders Berggren; Nils Edvardsson; Göran Duker
Journal:  Ann Noninvasive Electrocardiol       Date:  2012-11-22       Impact factor: 1.468

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