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Augmented Oscillations in QT Interval Duration Predict Mortality Post Myocardial Infarction Independent of Heart Rate

OBJECTIVE: This study seeks to decompose QT variability (QTV) into physiological sources and assess their role for risk stratification in patients post myocardial infarction (MI). We hypothesize that the magnitude of QTV that cannot be explained by heart rate or respiration carries important prognos...

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Autores principales: El-Hamad, Fatima J., Bonabi, Safa Y., Müller, Alexander, Steger, Alexander, Schmidt, Georg, Baumert, Mathias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7680963/
https://www.ncbi.nlm.nih.gov/pubmed/33240101
http://dx.doi.org/10.3389/fphys.2020.578173
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author El-Hamad, Fatima J.
Bonabi, Safa Y.
Müller, Alexander
Steger, Alexander
Schmidt, Georg
Baumert, Mathias
author_facet El-Hamad, Fatima J.
Bonabi, Safa Y.
Müller, Alexander
Steger, Alexander
Schmidt, Georg
Baumert, Mathias
author_sort El-Hamad, Fatima J.
collection PubMed
description OBJECTIVE: This study seeks to decompose QT variability (QTV) into physiological sources and assess their role for risk stratification in patients post myocardial infarction (MI). We hypothesize that the magnitude of QTV that cannot be explained by heart rate or respiration carries important prognostic information. BACKGROUND: Elevated beat-to-beat QTV is predictive of cardiac mortality, but the underlying mechanisms, and hence its interpretation, remain opaque. METHODS: We decomposed the QTV of 895 patients post MI into contributions by heart rate, respiration, and unexplained sources. RESULTS: Cox proportional hazard analysis demonstrates that augmented oscillations in QTV and their level of dissociation from heart rate are associated with a higher 5-year mortality rate (18.4% vs. 4.7%, p < 0.0001). In patients with left ventricular ejection fraction (LVEF) > 35%, a higher QTV risk score was associated with a significantly higher 5-year mortality rate (16% vs. 4%, p < 0.0001). In patients with a GRACE score ≥ 120, a higher QTV risk score was associated with a significantly higher 5-year mortality (25% vs. 11%, p < 0.001). CONCLUSION: Augmented oscillations in QTV and discordance from heart rate, possibly indicative of excessive sympathetic outflow to the ventricular myocardium, predict high risk in patients post MI independent from established risk markers. CLINICAL TRIAL REGISTRATION: www.ClinicalTrials.gov, identifier NCT00196274.
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spelling pubmed-76809632020-11-24 Augmented Oscillations in QT Interval Duration Predict Mortality Post Myocardial Infarction Independent of Heart Rate El-Hamad, Fatima J. Bonabi, Safa Y. Müller, Alexander Steger, Alexander Schmidt, Georg Baumert, Mathias Front Physiol Physiology OBJECTIVE: This study seeks to decompose QT variability (QTV) into physiological sources and assess their role for risk stratification in patients post myocardial infarction (MI). We hypothesize that the magnitude of QTV that cannot be explained by heart rate or respiration carries important prognostic information. BACKGROUND: Elevated beat-to-beat QTV is predictive of cardiac mortality, but the underlying mechanisms, and hence its interpretation, remain opaque. METHODS: We decomposed the QTV of 895 patients post MI into contributions by heart rate, respiration, and unexplained sources. RESULTS: Cox proportional hazard analysis demonstrates that augmented oscillations in QTV and their level of dissociation from heart rate are associated with a higher 5-year mortality rate (18.4% vs. 4.7%, p < 0.0001). In patients with left ventricular ejection fraction (LVEF) > 35%, a higher QTV risk score was associated with a significantly higher 5-year mortality rate (16% vs. 4%, p < 0.0001). In patients with a GRACE score ≥ 120, a higher QTV risk score was associated with a significantly higher 5-year mortality (25% vs. 11%, p < 0.001). CONCLUSION: Augmented oscillations in QTV and discordance from heart rate, possibly indicative of excessive sympathetic outflow to the ventricular myocardium, predict high risk in patients post MI independent from established risk markers. CLINICAL TRIAL REGISTRATION: www.ClinicalTrials.gov, identifier NCT00196274. Frontiers Media S.A. 2020-11-09 /pmc/articles/PMC7680963/ /pubmed/33240101 http://dx.doi.org/10.3389/fphys.2020.578173 Text en Copyright © 2020 El-Hamad, Bonabi, Müller, Steger, Schmidt and Baumert. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
El-Hamad, Fatima J.
Bonabi, Safa Y.
Müller, Alexander
Steger, Alexander
Schmidt, Georg
Baumert, Mathias
Augmented Oscillations in QT Interval Duration Predict Mortality Post Myocardial Infarction Independent of Heart Rate
title Augmented Oscillations in QT Interval Duration Predict Mortality Post Myocardial Infarction Independent of Heart Rate
title_full Augmented Oscillations in QT Interval Duration Predict Mortality Post Myocardial Infarction Independent of Heart Rate
title_fullStr Augmented Oscillations in QT Interval Duration Predict Mortality Post Myocardial Infarction Independent of Heart Rate
title_full_unstemmed Augmented Oscillations in QT Interval Duration Predict Mortality Post Myocardial Infarction Independent of Heart Rate
title_short Augmented Oscillations in QT Interval Duration Predict Mortality Post Myocardial Infarction Independent of Heart Rate
title_sort augmented oscillations in qt interval duration predict mortality post myocardial infarction independent of heart rate
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7680963/
https://www.ncbi.nlm.nih.gov/pubmed/33240101
http://dx.doi.org/10.3389/fphys.2020.578173
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