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The role of postprandial very-low-density lipoprotein in the development of atrial remodeling in metabolic syndrome

BACKGROUND: Negatively charged very-low-density lipoprotein (VLDL-χ) in metabolic syndrome (MetS) patients exerts cytotoxic effects on endothelial cells and atrial myocytes. Atrial cardiomyopathy, manifested by atrial remodeling with a dilated diameter, contributes to atrial fibrillation pathogenesi...

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Autores principales: Lee, Hsiang-Chun, Shin, Shyi-Jang, Huang, Jih-Kai, Lin, Ming-Yen, Lin, Yu-Hsun, Ke, Liang-Yin, Jiang, He-Jiun, Tsai, Wei-Chung, Chao, Min-Fang, Lin, Yi-Hsiung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507670/
https://www.ncbi.nlm.nih.gov/pubmed/32962696
http://dx.doi.org/10.1186/s12944-020-01386-5
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author Lee, Hsiang-Chun
Shin, Shyi-Jang
Huang, Jih-Kai
Lin, Ming-Yen
Lin, Yu-Hsun
Ke, Liang-Yin
Jiang, He-Jiun
Tsai, Wei-Chung
Chao, Min-Fang
Lin, Yi-Hsiung
author_facet Lee, Hsiang-Chun
Shin, Shyi-Jang
Huang, Jih-Kai
Lin, Ming-Yen
Lin, Yu-Hsun
Ke, Liang-Yin
Jiang, He-Jiun
Tsai, Wei-Chung
Chao, Min-Fang
Lin, Yi-Hsiung
author_sort Lee, Hsiang-Chun
collection PubMed
description BACKGROUND: Negatively charged very-low-density lipoprotein (VLDL-χ) in metabolic syndrome (MetS) patients exerts cytotoxic effects on endothelial cells and atrial myocytes. Atrial cardiomyopathy, manifested by atrial remodeling with a dilated diameter, contributes to atrial fibrillation pathogenesis and predicts atrial fibrillation development. The correlation of VLDL-χ with atrial remodeling is unknown. This study investigated the association between VLDL-χ and remodeling of left atrium. METHODS: Consecutively, 87 MetS and 80 non-MetS individuals between 23 and 74 years old (50.6% men) without overt cardiovascular diseases were included in the prospective cohort study. Blood samples were collected while fasting and postprandially (at 0.5, 1, 2, and 4 h after a unified meal). VLDL was isolated by ultracentrifugation; the percentile concentration of VLDL-χ (%) was determined by ultra-performance liquid chromatography. The correlations of left atrium diameter (LAD) with variables including VLDL-χ, LDL-C, HDL-C, triglycerides, glucose, and blood pressure, were analyzed by multiple linear regression models. A hierarchical linear model was conducted to test the independencies of each variable’s correlation with LAD. RESULTS: The mean LAD was 3.4 ± 0.5 cm in non-MetS subjects and 3.9 ± 0.5 cm in MetS patients (P < 0.01). None of the fasting lipid profiles were associated with LAD. VLDL-χ, BMI, waist circumference, hip circumference, and blood pressure were positively correlated with LAD (all P < 0.05) after adjustment for age and sex. Significant interactions between VLDL-χ and blood pressure, waist circumference, and hip circumference were observed. When adjusted for obesity- and blood pressure-related variables, 2-h postprandial VLDL-χ (mean 1.30 ± 0.61%) showed a positive correlation with LAD in MetS patients. Each 1% VLDL-χ increase was estimated to increase LAD by 0.23 cm. CONCLUSIONS: Postprandial VLDL-χ is associated with atrial remodeling particularly in the MetS group. VLDL-χ is a novel biomarker and may be a therapeutic target for atrial cardiomyopathy in MetS patients. TRIAL REGISTRATION: ISRCTN 69295295. Retrospectively registered 9 June 2020.
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spelling pubmed-75076702020-09-23 The role of postprandial very-low-density lipoprotein in the development of atrial remodeling in metabolic syndrome Lee, Hsiang-Chun Shin, Shyi-Jang Huang, Jih-Kai Lin, Ming-Yen Lin, Yu-Hsun Ke, Liang-Yin Jiang, He-Jiun Tsai, Wei-Chung Chao, Min-Fang Lin, Yi-Hsiung Lipids Health Dis Research BACKGROUND: Negatively charged very-low-density lipoprotein (VLDL-χ) in metabolic syndrome (MetS) patients exerts cytotoxic effects on endothelial cells and atrial myocytes. Atrial cardiomyopathy, manifested by atrial remodeling with a dilated diameter, contributes to atrial fibrillation pathogenesis and predicts atrial fibrillation development. The correlation of VLDL-χ with atrial remodeling is unknown. This study investigated the association between VLDL-χ and remodeling of left atrium. METHODS: Consecutively, 87 MetS and 80 non-MetS individuals between 23 and 74 years old (50.6% men) without overt cardiovascular diseases were included in the prospective cohort study. Blood samples were collected while fasting and postprandially (at 0.5, 1, 2, and 4 h after a unified meal). VLDL was isolated by ultracentrifugation; the percentile concentration of VLDL-χ (%) was determined by ultra-performance liquid chromatography. The correlations of left atrium diameter (LAD) with variables including VLDL-χ, LDL-C, HDL-C, triglycerides, glucose, and blood pressure, were analyzed by multiple linear regression models. A hierarchical linear model was conducted to test the independencies of each variable’s correlation with LAD. RESULTS: The mean LAD was 3.4 ± 0.5 cm in non-MetS subjects and 3.9 ± 0.5 cm in MetS patients (P < 0.01). None of the fasting lipid profiles were associated with LAD. VLDL-χ, BMI, waist circumference, hip circumference, and blood pressure were positively correlated with LAD (all P < 0.05) after adjustment for age and sex. Significant interactions between VLDL-χ and blood pressure, waist circumference, and hip circumference were observed. When adjusted for obesity- and blood pressure-related variables, 2-h postprandial VLDL-χ (mean 1.30 ± 0.61%) showed a positive correlation with LAD in MetS patients. Each 1% VLDL-χ increase was estimated to increase LAD by 0.23 cm. CONCLUSIONS: Postprandial VLDL-χ is associated with atrial remodeling particularly in the MetS group. VLDL-χ is a novel biomarker and may be a therapeutic target for atrial cardiomyopathy in MetS patients. TRIAL REGISTRATION: ISRCTN 69295295. Retrospectively registered 9 June 2020. BioMed Central 2020-09-22 /pmc/articles/PMC7507670/ /pubmed/32962696 http://dx.doi.org/10.1186/s12944-020-01386-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Lee, Hsiang-Chun
Shin, Shyi-Jang
Huang, Jih-Kai
Lin, Ming-Yen
Lin, Yu-Hsun
Ke, Liang-Yin
Jiang, He-Jiun
Tsai, Wei-Chung
Chao, Min-Fang
Lin, Yi-Hsiung
The role of postprandial very-low-density lipoprotein in the development of atrial remodeling in metabolic syndrome
title The role of postprandial very-low-density lipoprotein in the development of atrial remodeling in metabolic syndrome
title_full The role of postprandial very-low-density lipoprotein in the development of atrial remodeling in metabolic syndrome
title_fullStr The role of postprandial very-low-density lipoprotein in the development of atrial remodeling in metabolic syndrome
title_full_unstemmed The role of postprandial very-low-density lipoprotein in the development of atrial remodeling in metabolic syndrome
title_short The role of postprandial very-low-density lipoprotein in the development of atrial remodeling in metabolic syndrome
title_sort role of postprandial very-low-density lipoprotein in the development of atrial remodeling in metabolic syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507670/
https://www.ncbi.nlm.nih.gov/pubmed/32962696
http://dx.doi.org/10.1186/s12944-020-01386-5
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