دورية أكاديمية

QRS duration reflects underlying changes in conduction velocity during increased intraventricular pressure and heart failure

التفاصيل البيبلوغرافية
العنوان: QRS duration reflects underlying changes in conduction velocity during increased intraventricular pressure and heart failure
المؤلفون: Quintanilla, Jorge G., Moreno, Javier, Archondo, Tamara, Alfonso-Almazan, Jose M., Lillo-Castellano, Jose Maria, Usandizaga, Elena, García-Torrent, María Jesús, Rodríguez-Bobada, Cruz, González, Pablo, Borrego, Luis, Cañadas-Godoy, Victoria, González-Ferrer, Juan J, Pérez-Castellano, Nicasio, Pérez-Villacastín, Julián, Filgueiras-Rama, David
المساهمون: Ministerio de Economía, Industria y Competitividad (España), Unión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF), Instituto de Salud Carlos III, Fundación ProCNIC
بيانات النشر: Elsevier
سنة النشر: 2017
المجموعة: REPISALUD (REPositorio Institucional en SALUD del Instituto de Salud Carlos III - ISCIII)
مصطلحات موضوعية: Afterload, Heart failure, Intraventricular pressure, Optical mapping, Remodeling, Animals, Heart Conduction System, Swine, Electrocardiography, Ventricular Pressure
الوصف: Pressure overload and heart failure electrophysiological remodeling (HF-ER) in pigs are associated with decreased conduction velocity (CV) and dispersion of repolarization, which lead to higher risk of ventricular arrhythmia. This work aimed to establish the correlation between QRS complex duration and underlying changes in CV during increased intraventricular pressure (IVP) and/or HF-ER ex-vivo, and to determine whether QRS duration could be sensitive to an acute increase in left ventricular (LV) afterload in-vivo. HF-ER was induced in 7 pigs by high-rate ventricular pacing. Seven weight-matched animals were used as controls. Isolated Langendorff-perfused hearts underwent programmed ventricular stimulation to study QRS complex duration and CV under low/high IVP, using volume-conducted ECG and epicardial optical mapping, respectively. Four additional pigs underwent open-chest surgery to increase LV afterload by partially clamping the ascending aorta, while measuring QRS complex duration during sinus rhythm (SR). In 13 hearts included for analysis, both HF-ER and increased IVP showed significantly slower epicardial CV (-40% and -15%, p < 0.001 and p = 0.004, respectively), which correlated with similar widening of the QRS complex (+41% and +17%, p = 0.005 and p < 0.001, respectively). HF-ER hearts shower larger prolongation of the QRS complex than controls upon increasing the IVP (+21% vs. +12%, respectively. HF-ER*IVP interaction: p = 0.004). QRS complex widened after increasing LV afterload in-vivo (n=3), with correlation between QRS duration and aortic diastolic pressures (R = 0.58, p < 0.001). In conclusion, high IVP and/or HF-ER significantly decrease CV, which correlates with QRS widening on the ECG during ventricular pacing. Increased myocardial wall stress also widens the QRS complex during SR in-vivo. ; The CNIC is supported by the Ministry of Economy, Industry and Competitiveness and the Pro CNIC Foundation, and is a Severo Ochoa Center of Excellence (SEV-2015-0505). This study was supported by ...
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 0079-6107
1873-1732
العلاقة: Postprint; https://doi.org/10.1016/j.pbiomolbio.2017.08.003Test; info:eu-repo/grantAgreement/ES/SEV-2015-0505; info:eu-repo/grantAgreement/ES/CB16/11/00458; info:eu-repo/grantAgreement/ES/RD06/0003/0009; info:eu-repo/grantAgreement/ES/RD12/0042/0036; info:eu-repo/grantAgreement/ES/SAF2016-80324-R; Prog Biophys Mol Biol. 2017; 130(Pt B):394-403; http://hdl.handle.net/20.500.12105/9908Test; Progress in biophysics and molecular biology
DOI: 10.1016/j.pbiomolbio.2017.08.003
الإتاحة: https://doi.org/20.500.12105/9908Test
https://doi.org/10.1016/j.pbiomolbio.2017.08.003Test
https://hdl.handle.net/20.500.12105/9908Test
حقوق: http://creativecommons.org/licenses/by-nc-nd/4.0Test/ ; Attribution-NonCommercial-NoDerivatives 4.0 Internacional ; info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.EC4C1183
قاعدة البيانات: BASE
الوصف
تدمد:00796107
18731732
DOI:10.1016/j.pbiomolbio.2017.08.003