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Atrial fibrillation per se was a major determinant of global left ventricular longitudinal systolic strain

Atrial fibrillation (AF) may cause systolic abnormality via inadequate diastolic filling and tachycardia-induced cardiomyopathy. Global longitudinal strain (GLS) is a very sensitive method for detecting subtle left ventricular systolic dysfunction. Hence, this study aimed to evaluate whether AF pati...

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Autores principales: Lee, Hung-Hao, Lee, Meng-Kuang, Lee, Wen-Hsien, Hsu, Po-Chao, Chu, Chun-Yuan, Lee, Chee-Siong, Lin, Tsung-Hsien, Voon, Wen-Chol, Lai, Wen-Ter, Sheu, Sheng-Hsiung, Su, Ho-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937945/
https://www.ncbi.nlm.nih.gov/pubmed/27368031
http://dx.doi.org/10.1097/MD.0000000000004038
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author Lee, Hung-Hao
Lee, Meng-Kuang
Lee, Wen-Hsien
Hsu, Po-Chao
Chu, Chun-Yuan
Lee, Chee-Siong
Lin, Tsung-Hsien
Voon, Wen-Chol
Lai, Wen-Ter
Sheu, Sheng-Hsiung
Su, Ho-Ming
author_facet Lee, Hung-Hao
Lee, Meng-Kuang
Lee, Wen-Hsien
Hsu, Po-Chao
Chu, Chun-Yuan
Lee, Chee-Siong
Lin, Tsung-Hsien
Voon, Wen-Chol
Lai, Wen-Ter
Sheu, Sheng-Hsiung
Su, Ho-Ming
author_sort Lee, Hung-Hao
collection PubMed
description Atrial fibrillation (AF) may cause systolic abnormality via inadequate diastolic filling and tachycardia-induced cardiomyopathy. Global longitudinal strain (GLS) is a very sensitive method for detecting subtle left ventricular systolic dysfunction. Hence, this study aimed to evaluate whether AF patients had a more impaired GLS, AF was a major determinant of GLS, and determine the major correlates of GLS in AF patients. The study included 137 patients with persistent AF and left ventricular ejection fraction (LVEF) above 50% and 137 non-AF patients matched according to age, gender, and LVEF. Comprehensive echocardiography with GLS assessment was performed for all cases. Compared with non-AF patients, AF patients had a more impaired GLS, a larger left atrial volume index, higher transmitral E wave velocity (E), and early diastolic mitral velocity (Ea) (all P < 0.001) but comparable E/Ea. After adjustment for baseline and echocardiographic characteristics, the presence of AF remained significantly associated with impaired GLS (β = 0.533, P < 0.001). In addition, multivariate analysis of AF patients indicated that faster heart rates and decreased E, Ea, and LVEF were associated with more impaired GLS. This study demonstrated that AF patients had a more impaired GLS than non-AF patients, although LVEF was comparable between the 2 groups. AF was a major determinant of GLS even after adjustment for relevant clinical and echocardiographic parameters.
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spelling pubmed-49379452016-08-18 Atrial fibrillation per se was a major determinant of global left ventricular longitudinal systolic strain Lee, Hung-Hao Lee, Meng-Kuang Lee, Wen-Hsien Hsu, Po-Chao Chu, Chun-Yuan Lee, Chee-Siong Lin, Tsung-Hsien Voon, Wen-Chol Lai, Wen-Ter Sheu, Sheng-Hsiung Su, Ho-Ming Medicine (Baltimore) 3400 Atrial fibrillation (AF) may cause systolic abnormality via inadequate diastolic filling and tachycardia-induced cardiomyopathy. Global longitudinal strain (GLS) is a very sensitive method for detecting subtle left ventricular systolic dysfunction. Hence, this study aimed to evaluate whether AF patients had a more impaired GLS, AF was a major determinant of GLS, and determine the major correlates of GLS in AF patients. The study included 137 patients with persistent AF and left ventricular ejection fraction (LVEF) above 50% and 137 non-AF patients matched according to age, gender, and LVEF. Comprehensive echocardiography with GLS assessment was performed for all cases. Compared with non-AF patients, AF patients had a more impaired GLS, a larger left atrial volume index, higher transmitral E wave velocity (E), and early diastolic mitral velocity (Ea) (all P < 0.001) but comparable E/Ea. After adjustment for baseline and echocardiographic characteristics, the presence of AF remained significantly associated with impaired GLS (β = 0.533, P < 0.001). In addition, multivariate analysis of AF patients indicated that faster heart rates and decreased E, Ea, and LVEF were associated with more impaired GLS. This study demonstrated that AF patients had a more impaired GLS than non-AF patients, although LVEF was comparable between the 2 groups. AF was a major determinant of GLS even after adjustment for relevant clinical and echocardiographic parameters. Wolters Kluwer Health 2016-07-01 /pmc/articles/PMC4937945/ /pubmed/27368031 http://dx.doi.org/10.1097/MD.0000000000004038 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 3400
Lee, Hung-Hao
Lee, Meng-Kuang
Lee, Wen-Hsien
Hsu, Po-Chao
Chu, Chun-Yuan
Lee, Chee-Siong
Lin, Tsung-Hsien
Voon, Wen-Chol
Lai, Wen-Ter
Sheu, Sheng-Hsiung
Su, Ho-Ming
Atrial fibrillation per se was a major determinant of global left ventricular longitudinal systolic strain
title Atrial fibrillation per se was a major determinant of global left ventricular longitudinal systolic strain
title_full Atrial fibrillation per se was a major determinant of global left ventricular longitudinal systolic strain
title_fullStr Atrial fibrillation per se was a major determinant of global left ventricular longitudinal systolic strain
title_full_unstemmed Atrial fibrillation per se was a major determinant of global left ventricular longitudinal systolic strain
title_short Atrial fibrillation per se was a major determinant of global left ventricular longitudinal systolic strain
title_sort atrial fibrillation per se was a major determinant of global left ventricular longitudinal systolic strain
topic 3400
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937945/
https://www.ncbi.nlm.nih.gov/pubmed/27368031
http://dx.doi.org/10.1097/MD.0000000000004038
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