-
Je něco špatně v tomto záznamu ?
Dyssynchronous Left Ventricular Activation is Insufficient for the Breakdown of Wringing Rotation
T. Gerach, S. Appel, J. Wilczek, KS. Golba, T. Jadczyk, A. Loewe
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2010
Free Medical Journals
od 2010
PubMed Central
od 2010
Europe PubMed Central
od 2010
Open Access Digital Library
od 2010-01-01
Open Access Digital Library
od 2010-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2010
- Publikační typ
- časopisecké články MeSH
Cardiac resynchronization therapy is a valuable tool to restore left ventricular function in patients experiencing dyssynchronous ventricular activation. However, the non-responder rate is still as high as 40%. Recent studies suggest that left ventricular torsion or specifically the lack thereof might be a good predictor for the response of cardiac resynchronization therapy. Since left ventricular torsion is governed by the muscle fiber orientation and the heterogeneous electromechanical activation of the myocardium, understanding the relation between these components and the ability to measure them is vital. To analyze if locally altered electromechanical activation in heart failure patients affects left ventricular torsion, we conducted a simulation study on 27 personalized left ventricular models. Electroanatomical maps and late gadolinium enhanced magnetic resonance imaging data informed our in-silico model cohort. The angle of rotation was evaluated in every material point of the model and averaged values were used to classify the rotation as clockwise or counterclockwise in each segment and sector of the left ventricle. 88% of the patient models (n = 24) were classified as a wringing rotation and 12% (n = 3) as a rigid-body-type rotation. Comparison to classification based on in vivo rotational NOGA XP maps showed no correlation. Thus, isolated changes of the electromechanical activation sequence in the left ventricle are not sufficient to reproduce the rotation pattern changes observed in vivo and suggest that further patho-mechanisms are involved.
Department of Electrocardiology and Heart Failure Medical University of Silesia Katowice Poland
Department of Electrocardiology Upper Silesian Heart Center Katowice Poland
Division of Cardiology and Structural Heart Diseases Medical University of Silesia Katowice Poland
Institute of Biomedical Engineering Karlsruhe Institute of Technology Karlsruhe Germany
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22017199
- 003
- CZ-PrNML
- 005
- 20220720100134.0
- 007
- ta
- 008
- 220718s2022 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3389/fphys.2022.838038 $2 doi
- 035 __
- $a (PubMed)35615669
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Gerach, Tobias $u Institute of Biomedical Engineering, Karlsruhe Institute of Technology (KIT), Karlsruhe, Germany
- 245 10
- $a Dyssynchronous Left Ventricular Activation is Insufficient for the Breakdown of Wringing Rotation / $c T. Gerach, S. Appel, J. Wilczek, KS. Golba, T. Jadczyk, A. Loewe
- 520 9_
- $a Cardiac resynchronization therapy is a valuable tool to restore left ventricular function in patients experiencing dyssynchronous ventricular activation. However, the non-responder rate is still as high as 40%. Recent studies suggest that left ventricular torsion or specifically the lack thereof might be a good predictor for the response of cardiac resynchronization therapy. Since left ventricular torsion is governed by the muscle fiber orientation and the heterogeneous electromechanical activation of the myocardium, understanding the relation between these components and the ability to measure them is vital. To analyze if locally altered electromechanical activation in heart failure patients affects left ventricular torsion, we conducted a simulation study on 27 personalized left ventricular models. Electroanatomical maps and late gadolinium enhanced magnetic resonance imaging data informed our in-silico model cohort. The angle of rotation was evaluated in every material point of the model and averaged values were used to classify the rotation as clockwise or counterclockwise in each segment and sector of the left ventricle. 88% of the patient models (n = 24) were classified as a wringing rotation and 12% (n = 3) as a rigid-body-type rotation. Comparison to classification based on in vivo rotational NOGA XP maps showed no correlation. Thus, isolated changes of the electromechanical activation sequence in the left ventricle are not sufficient to reproduce the rotation pattern changes observed in vivo and suggest that further patho-mechanisms are involved.
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Appel, Stephanie $u Institute of Biomedical Engineering, Karlsruhe Institute of Technology (KIT), Karlsruhe, Germany
- 700 1_
- $a Wilczek, Jacek $u Department of Electrocardiology, Upper-Silesian Heart Center, Katowice, Poland $u Department of Electrocardiology and Heart Failure, Medical University of Silesia, Katowice, Poland
- 700 1_
- $a Golba, Krzysztof S $u Department of Electrocardiology, Upper-Silesian Heart Center, Katowice, Poland $u Department of Electrocardiology and Heart Failure, Medical University of Silesia, Katowice, Poland
- 700 1_
- $a Jadczyk, Tomasz $u Division of Cardiology and Structural Heart Diseases, Medical University of Silesia, Katowice, Poland $u Interventional Cardiac Electrophysiology Group, International Clinical Research Center, St. Anne's University Hospital, Brno, Czech Republic
- 700 1_
- $a Loewe, Axel $u Institute of Biomedical Engineering, Karlsruhe Institute of Technology (KIT), Karlsruhe, Germany
- 773 0_
- $w MED00174601 $t Frontiers in physiology $x 1664-042X $g Roč. 13, č. - (2022), s. 838038
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/35615669 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20220718 $b ABA008
- 991 __
- $a 20220720100130 $b ABA008
- 999 __
- $a ind $b bmc $g 1816481 $s 1168441
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2022 $b 13 $c - $d 838038 $e 20220509 $i 1664-042X $m Frontiers in physiology $n Front. physiol. $x MED00174601
- LZP __
- $a Pubmed-20220718