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Comparison of QT peak and QT end interval responses to autonomic adaptation in asymptomatic LQT1 mutation carriers
BACKGROUND: LQT1 subtype of long QT syndrome is characterized by defective I(Ks), which is intrinsically stronger in the epicardium than in the midmyocardial region. Electrocardiographic QT peak and QT end intervals may reflect complete repolarization of epicardium and midmyocardial region of the ve...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121965/ https://www.ncbi.nlm.nih.gov/pubmed/21138517 http://dx.doi.org/10.1111/j.1475-097X.2010.01002.x |
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author | Haapalahti, Petri Viitasalo, Matti Perhonen, Merja Väänänen, Heikki Mäkijärvi, Markku Swan, Heikki Toivonen, Lauri |
author_facet | Haapalahti, Petri Viitasalo, Matti Perhonen, Merja Väänänen, Heikki Mäkijärvi, Markku Swan, Heikki Toivonen, Lauri |
author_sort | Haapalahti, Petri |
collection | PubMed |
description | BACKGROUND: LQT1 subtype of long QT syndrome is characterized by defective I(Ks), which is intrinsically stronger in the epicardium than in the midmyocardial region. Electrocardiographic QT peak and QT end intervals may reflect complete repolarization of epicardium and midmyocardial region of the ventricular wall, respectively. Repolarization abnormalities in LQT1 carriers may therefore be more easily detected in the QT peak intervals. METHODS: Asymptomatic KCNQ1 mutation carriers (LQT1, n = 9) and unaffected healthy controls (n = 8) were studied during Valsalva manoeuvre, mental stress, handgrip and supine exercise. Global QT peak and QT end intervals derived from 25 simultaneous electrocardiographic leads were measured beat to beat with an automated method. RESULTS: In unaffected subjects, the percentage shortening of QT peak was greater than that of QT end during mental stress and during the recovery phases of Valsalva and supine exercise. In LQT1 carriers, the percentage shortening of the intervals was similar. At the beginning of Valsalva strain under abrupt endogenous sympathetic activation, QT peak shortened in LQT1 but not in control patients yielding increased electrocardiographic transmural dispersion of repolarization in LQT1. CONCLUSIONS: In asymptomatic KCNQ1 mutation carriers, repolarization abnormalities are more evident in the QT peak than in the QT end interval during adrenergic adaptation, possibly related to transmural differences in the degree of I(Ks) block. |
format | Online Article Text |
id | pubmed-3121965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-31219652011-06-28 Comparison of QT peak and QT end interval responses to autonomic adaptation in asymptomatic LQT1 mutation carriers Haapalahti, Petri Viitasalo, Matti Perhonen, Merja Väänänen, Heikki Mäkijärvi, Markku Swan, Heikki Toivonen, Lauri Clin Physiol Funct Imaging Original Articles BACKGROUND: LQT1 subtype of long QT syndrome is characterized by defective I(Ks), which is intrinsically stronger in the epicardium than in the midmyocardial region. Electrocardiographic QT peak and QT end intervals may reflect complete repolarization of epicardium and midmyocardial region of the ventricular wall, respectively. Repolarization abnormalities in LQT1 carriers may therefore be more easily detected in the QT peak intervals. METHODS: Asymptomatic KCNQ1 mutation carriers (LQT1, n = 9) and unaffected healthy controls (n = 8) were studied during Valsalva manoeuvre, mental stress, handgrip and supine exercise. Global QT peak and QT end intervals derived from 25 simultaneous electrocardiographic leads were measured beat to beat with an automated method. RESULTS: In unaffected subjects, the percentage shortening of QT peak was greater than that of QT end during mental stress and during the recovery phases of Valsalva and supine exercise. In LQT1 carriers, the percentage shortening of the intervals was similar. At the beginning of Valsalva strain under abrupt endogenous sympathetic activation, QT peak shortened in LQT1 but not in control patients yielding increased electrocardiographic transmural dispersion of repolarization in LQT1. CONCLUSIONS: In asymptomatic KCNQ1 mutation carriers, repolarization abnormalities are more evident in the QT peak than in the QT end interval during adrenergic adaptation, possibly related to transmural differences in the degree of I(Ks) block. Blackwell Publishing Ltd 2011-05 /pmc/articles/PMC3121965/ /pubmed/21138517 http://dx.doi.org/10.1111/j.1475-097X.2010.01002.x Text en Clinical Physiology and Functional Imaging © 2011 Scandinavian Society of Clinical Physiology and Nuclear Medicine http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Articles Haapalahti, Petri Viitasalo, Matti Perhonen, Merja Väänänen, Heikki Mäkijärvi, Markku Swan, Heikki Toivonen, Lauri Comparison of QT peak and QT end interval responses to autonomic adaptation in asymptomatic LQT1 mutation carriers |
title | Comparison of QT peak and QT end interval responses to autonomic adaptation in asymptomatic LQT1 mutation carriers |
title_full | Comparison of QT peak and QT end interval responses to autonomic adaptation in asymptomatic LQT1 mutation carriers |
title_fullStr | Comparison of QT peak and QT end interval responses to autonomic adaptation in asymptomatic LQT1 mutation carriers |
title_full_unstemmed | Comparison of QT peak and QT end interval responses to autonomic adaptation in asymptomatic LQT1 mutation carriers |
title_short | Comparison of QT peak and QT end interval responses to autonomic adaptation in asymptomatic LQT1 mutation carriers |
title_sort | comparison of qt peak and qt end interval responses to autonomic adaptation in asymptomatic lqt1 mutation carriers |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121965/ https://www.ncbi.nlm.nih.gov/pubmed/21138517 http://dx.doi.org/10.1111/j.1475-097X.2010.01002.x |
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