Left atrial remodeling in mitral regurgitation: A combined experimental-computational study

• Published in: PloS one Vol. 17; no. 7; p. e0271588
• Main Authors: Bouwmeester, Sjoerd, van Loon, Tim, Ploeg, Meike, Mast, Thomas P, Verzaal, Nienke J, van Middendorp, Lars B, Strik, Marc, van Nieuwenhoven, Frans A, Dekker, Lukas R, Prinzen, Frits W, Lumens, Joost, Houthuizen, Patrick
• Format: Journal Article
• Language: English
• Published: San Francisco Public Library of Science 15.07.2022; Public Library of Science (PLoS)
• Subjects: Ablation; Ablation (Surgery); Biology and Life Sciences; Care and treatment; Complications and side effects; Computer and Information Sciences; Computer applications; Contractility; Dilation; Echocardiography; Fibrosis; Gene expression; Hemodynamics; Histology; Mathematical models; Medicine and Health Sciences; Mitral valve insufficiency; Patient outcomes; Physical Sciences; Radio frequency; Regurgitation; Research and Analysis Methods; Simulation; Structure-function relationships; Netherlands; United States > US; Norway
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0271588

Progressive changes to left atrial (LA) structure and function following mitral regurgitation (MR) remain incompletely understood. This study aimed to demonstrate potential underlying mechanisms using experimental canine models and computer simulations. A canine model of MR was created by cauterization of mitral chordae followed by radiofrequency ablation-induced left bundle-branch block (LBBB) after 4 weeks (MR-LBBB group). Animals with LBBB alone served as control. Echocardiography was performed at baseline, acutely after MR induction, and at 4 and 20 weeks, and correlated with histology and computer simulations. Acute MR augmented LA reservoir and contractile strain (40±4 to 53±6% and -11±5 to -22±9% respectively, p<0.05). LA fractional area change increased significantly (47±4 to 56±4%, p<0.05) while LA end-systolic area remained unchanged (7.2±1.1 versus 7.9±1.1 cm.sup.2 respectively, p = 0.08). LA strain 'pseudonormalized' after 4 weeks and decompensated at 20 weeks with both strains decreasing to 25±6% and -3±2% respectively (p<0.05) together with a progressive increase in LA end-systolic area (7.2±1.1 to 14.0±6.3 cm.sup.2, p<0.05). In the LBBB-group, LA remodeling was less pronounced. Histology showed a trend towards increased interstitial fibrosis in the LA of the MR-LBBB group. Computer simulations indicated that the progressive changes in LA structure and function are a combination of progressive eccentric remodeling and fibrosis. MR augmented LA strain acutely to supranormal values without significant LA dilation. However, over time, LA strain gradually decreases (pseudornormal and decompensated) with LA dilation. Histology and computer simulations indicated a correlation to a varying degree of LA eccentric remodeling and fibrosis.