CineECG analysis provides new insights into Familial ST-segment Depression Syndrome

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CineECG analysis provides new insights into Familial ST-segment Depression Syndrome. / Frosted, Rasmus; Paludan-Mueller, Christian; Vad, Oliver Bundgaard; Olesen, Morten Salling; Bundgaard, Henning; van Dam, Peter; Christensen, Alex Horby.

I: Europace, Bind 25, Nr. 5, euad116, 2023.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Frosted, R, Paludan-Mueller, C, Vad, OB, Olesen, MS, Bundgaard, H, van Dam, P & Christensen, AH 2023, 'CineECG analysis provides new insights into Familial ST-segment Depression Syndrome', Europace, bind 25, nr. 5, euad116. https://doi.org/10.1093/europace/euad116

APA

Frosted, R., Paludan-Mueller, C., Vad, O. B., Olesen, M. S., Bundgaard, H., van Dam, P., & Christensen, A. H. (2023). CineECG analysis provides new insights into Familial ST-segment Depression Syndrome. Europace, 25(5), [euad116]. https://doi.org/10.1093/europace/euad116

Vancouver

Frosted R, Paludan-Mueller C, Vad OB, Olesen MS, Bundgaard H, van Dam P o.a. CineECG analysis provides new insights into Familial ST-segment Depression Syndrome. Europace. 2023;25(5). euad116. https://doi.org/10.1093/europace/euad116

Author

Frosted, Rasmus ; Paludan-Mueller, Christian ; Vad, Oliver Bundgaard ; Olesen, Morten Salling ; Bundgaard, Henning ; van Dam, Peter ; Christensen, Alex Horby. / CineECG analysis provides new insights into Familial ST-segment Depression Syndrome. I: Europace. 2023 ; Bind 25, Nr. 5.

Bibtex

@article{f9e9bc0d8c5c4924b47323e21e164410,
title = "CineECG analysis provides new insights into Familial ST-segment Depression Syndrome",
abstract = "Aims Familial ST-segment Depression Syndrome (Fam-STD) is a novel inherited cardiac disease associated with arrhythmias and sudden cardiac death. This study aimed at investigating the cardiac activation pathway in patients with Fam-STD, modelling the electrocardiogram (ECG) phenotype, and performing in-depth ST-segment analyses. Methods and results CineECG analysis of patients with Fam-STD and age- and sex-matched controls. The groups were compared using the CineECG software which included the trans-cardiac ratio and the electrical activation pathway. We simulated the Fam-STD ECG phenotype by adjusting action potential duration (APD) and action potential amplitude (APA) in specific cardiac regions. High-resolution ST-segment analyses were performed per lead by dividing the ST-segment into nine 10 ms subintervals. Twenty-seven Fam-STD patients (74% females, mean age 51.6 +/- 6.2 years) and 83 matched controls were included. Among Fam-STD patients, electrical activation pathway analysis in the anterior-basal orientation showed significantly abnormal direction toward the basal areas of the heart starting from QRS 60-89 ms until Tpeak-Tend (all P < 0.001). Simulations with shortened APD and reduced APA in the left ventricle basal regions recapitulated the Fam-STD ECG phenotype. Detailed ST-segment analyses showed significant differences in all nine 10 ms subintervals (all P < 0.01), with the most prominent findings during the 70-79/80-89 ms intervals. Conclusion CineECG analyses indicated abnormal repolarization with basal directions, and the Fam-STD ECG phenotype was simulated by reducing APD and APA in the left ventricle basal regions. Detailed ST-analysis showed amplitudes consistent with the proposed diagnostic criteria for Fam-STD patients. Our findings provide new insight into the electrophysiological abnormalities of Fam-STD.",
keywords = "Familial ST-segment Depression Syndrome, CineECG, Electrocardiogram, Arrhythmia, Electrical activation pathway, ECGsim, HEART-DISEASE, ELEVATION",
author = "Rasmus Frosted and Christian Paludan-Mueller and Vad, {Oliver Bundgaard} and Olesen, {Morten Salling} and Henning Bundgaard and {van Dam}, Peter and Christensen, {Alex Horby}",
year = "2023",
doi = "10.1093/europace/euad116",
language = "English",
volume = "25",
journal = "Europace",
issn = "1099-5129",
publisher = "Oxford University Press",
number = "5",

}

RIS

TY - JOUR

T1 - CineECG analysis provides new insights into Familial ST-segment Depression Syndrome

AU - Frosted, Rasmus

AU - Paludan-Mueller, Christian

AU - Vad, Oliver Bundgaard

AU - Olesen, Morten Salling

AU - Bundgaard, Henning

AU - van Dam, Peter

AU - Christensen, Alex Horby

PY - 2023

Y1 - 2023

N2 - Aims Familial ST-segment Depression Syndrome (Fam-STD) is a novel inherited cardiac disease associated with arrhythmias and sudden cardiac death. This study aimed at investigating the cardiac activation pathway in patients with Fam-STD, modelling the electrocardiogram (ECG) phenotype, and performing in-depth ST-segment analyses. Methods and results CineECG analysis of patients with Fam-STD and age- and sex-matched controls. The groups were compared using the CineECG software which included the trans-cardiac ratio and the electrical activation pathway. We simulated the Fam-STD ECG phenotype by adjusting action potential duration (APD) and action potential amplitude (APA) in specific cardiac regions. High-resolution ST-segment analyses were performed per lead by dividing the ST-segment into nine 10 ms subintervals. Twenty-seven Fam-STD patients (74% females, mean age 51.6 +/- 6.2 years) and 83 matched controls were included. Among Fam-STD patients, electrical activation pathway analysis in the anterior-basal orientation showed significantly abnormal direction toward the basal areas of the heart starting from QRS 60-89 ms until Tpeak-Tend (all P < 0.001). Simulations with shortened APD and reduced APA in the left ventricle basal regions recapitulated the Fam-STD ECG phenotype. Detailed ST-segment analyses showed significant differences in all nine 10 ms subintervals (all P < 0.01), with the most prominent findings during the 70-79/80-89 ms intervals. Conclusion CineECG analyses indicated abnormal repolarization with basal directions, and the Fam-STD ECG phenotype was simulated by reducing APD and APA in the left ventricle basal regions. Detailed ST-analysis showed amplitudes consistent with the proposed diagnostic criteria for Fam-STD patients. Our findings provide new insight into the electrophysiological abnormalities of Fam-STD.

AB - Aims Familial ST-segment Depression Syndrome (Fam-STD) is a novel inherited cardiac disease associated with arrhythmias and sudden cardiac death. This study aimed at investigating the cardiac activation pathway in patients with Fam-STD, modelling the electrocardiogram (ECG) phenotype, and performing in-depth ST-segment analyses. Methods and results CineECG analysis of patients with Fam-STD and age- and sex-matched controls. The groups were compared using the CineECG software which included the trans-cardiac ratio and the electrical activation pathway. We simulated the Fam-STD ECG phenotype by adjusting action potential duration (APD) and action potential amplitude (APA) in specific cardiac regions. High-resolution ST-segment analyses were performed per lead by dividing the ST-segment into nine 10 ms subintervals. Twenty-seven Fam-STD patients (74% females, mean age 51.6 +/- 6.2 years) and 83 matched controls were included. Among Fam-STD patients, electrical activation pathway analysis in the anterior-basal orientation showed significantly abnormal direction toward the basal areas of the heart starting from QRS 60-89 ms until Tpeak-Tend (all P < 0.001). Simulations with shortened APD and reduced APA in the left ventricle basal regions recapitulated the Fam-STD ECG phenotype. Detailed ST-segment analyses showed significant differences in all nine 10 ms subintervals (all P < 0.01), with the most prominent findings during the 70-79/80-89 ms intervals. Conclusion CineECG analyses indicated abnormal repolarization with basal directions, and the Fam-STD ECG phenotype was simulated by reducing APD and APA in the left ventricle basal regions. Detailed ST-analysis showed amplitudes consistent with the proposed diagnostic criteria for Fam-STD patients. Our findings provide new insight into the electrophysiological abnormalities of Fam-STD.

KW - Familial ST-segment Depression Syndrome

KW - CineECG

KW - Electrocardiogram

KW - Arrhythmia

KW - Electrical activation pathway

KW - ECGsim

KW - HEART-DISEASE

KW - ELEVATION

U2 - 10.1093/europace/euad116

DO - 10.1093/europace/euad116

M3 - Journal article

C2 - 37140072

VL - 25

JO - Europace

JF - Europace

SN - 1099-5129

IS - 5

M1 - euad116

ER -

ID: 347814491