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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.3389/fphys.2023.1060919</dc:identifier><dc:language>eng</dc:language><dc:creator>Bukhari, Hassaan A.</dc:creator><dc:creator>Sánchez, Carlos</dc:creator><dc:creator>Laguna, Pablo</dc:creator><dc:creator>Potse, Mark</dc:creator><dc:creator>Pueyo, Esther</dc:creator><dc:title>Differences in ventricular wall composition may explain inter-patient variability in the ECG response to variations in serum potassium and calcium</dc:title><dc:identifier>ART-2023-134882</dc:identifier><dc:description>Objective: Chronic kidney disease patients have a decreased ability to maintain normal electrolyte concentrations in their blood, which increases the risk for ventricular arrhythmias and sudden cardiac death. Non-invasive monitoring of serum potassium and calcium concentration, [K + ] and [Ca 2+ ], can help to prevent arrhythmias in these patients. Electrocardiogram (ECG) markers that significantly correlate with [K + ] and [Ca 2+ ] have been proposed, but these relations are highly variable between patients. We hypothesized that inter-individual differences in cell type distribution across the ventricular wall can help to explain this variability.Methods: A population of human heart-torso models were built with different proportions of endocardial, midmyocardial and epicardial cells. Propagation of ventricular electrical activity was described by a reaction-diffusion model, with modified Ten Tusscher-Panfilov dynamics. [K + ] and [Ca 2+ ] were varied individually and in combination. Twelve-lead ECGs were simulated and the width, amplitude and morphological variability of T waves and QRS complexes were quantified.Results: Both simulations and patients data showed that most of the analyzed T wave and QRS complex markers correlated strongly with [K + ] (absolute median Pearson correlation coefficients, r, ranging from 0.68 to 0.98) and [Ca 2+ ] (ranging from 0.70 to 0.98). The same sign and similar magnitude of median r was observed in the simulations and the patients. Different cell type distributions in the ventricular wall led to variability in ECG markers that was accentuated at high [K + ] and low [Ca 2+ ], in agreement with the larger variability between patients measured at the onset of HD. The simulated ECG variability explained part of the measured inter-patient variability.</dc:description><dc:date>2023</dc:date><dc:source>http://zaguan.unizar.es/record/136061</dc:source><dc:doi>10.3389/fphys.2023.1060919</dc:doi><dc:identifier>http://zaguan.unizar.es/record/136061</dc:identifier><dc:identifier>oai:zaguan.unizar.es:136061</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/LMP141-21</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/DGA/LMP94_21</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/DGA/T39-23R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/PID2019-104881RB-I00</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/PID2019-105674RB-I00</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/PID2022-140556OB-I00</dc:relation><dc:relation>info:eu-repo/grantAgreement/EUR/MICINN/TED2021-130459B-I00</dc:relation><dc:identifier.citation>Frontiers in physiology 14 (2023), 1060919 [14 pp.]</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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