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Leptin Expression in Human Epicardial Adipose Tissue Is Associated with Local Coronary Atherosclerosis

BACKGROUND: Leptin is an adipokine related to overweight and cardiovascular diseases. However, the leptin expression level in epicardial adipose tissue (EAT) of humans and its association with coronary atherosclerosis has never been investigated. MATERIAL/METHODS: Patients receiving cardiac surgery...

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Autores principales: Zhang, Tuowei, Yang, Pengkang, Li, Tonghua, Gao, Jianping, Zhang, Yuyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941777/
https://www.ncbi.nlm.nih.gov/pubmed/31872802
http://dx.doi.org/10.12659/MSM.918390
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author Zhang, Tuowei
Yang, Pengkang
Li, Tonghua
Gao, Jianping
Zhang, Yuyang
author_facet Zhang, Tuowei
Yang, Pengkang
Li, Tonghua
Gao, Jianping
Zhang, Yuyang
author_sort Zhang, Tuowei
collection PubMed
description BACKGROUND: Leptin is an adipokine related to overweight and cardiovascular diseases. However, the leptin expression level in epicardial adipose tissue (EAT) of humans and its association with coronary atherosclerosis has never been investigated. MATERIAL/METHODS: Patients receiving cardiac surgery were divided into a coronary artery disease group (CAD group) and a non-CAD group (NCAD group). Blood samples from coronary vein, biopsies of subcutaneous adipose tissue (SAT), and EAT were acquired during the surgery. Serum leptin level and leptin level in EAT and SAT were tested with ELISA, quantitative PCR, and immunohistochemistry and were compared between the CAD group and NCAD group, as well as between stenosis and non-stenosis subgroups. Logistic regression analysis was performed to explore the risk factors for coronary artery stenosis. RESULTS: No statistically significant differences were found in demographic and clinical data between groups (all P>0.05). Serum leptin concentration and leptin expression in EAT and SAT of the CAD group were much higher in than in the NCAD group (all P<0.05). In subgroup analysis, there was no difference in serum leptin and expression in SAT of stenosis and non-stenosis patients (All P>0.05). The leptin expression level in EAT of stenosis patients was significantly higher than in non-stenosis patients (P=0.0431). By multivariate logistic regression analysis, we demonstrated that leptin expression level in EAT was an independent risk factor for coronary artery stenosis [OR=1.09, 95%CI (1.01±1.18), P=0.031]. CONCLUSIONS: Leptin expression in EAT and SAT were both increased for CAD patients. Leptin expression in EAT was an independent risk factor for coronary atherosclerosis in the adjacent artery, while leptin in SAT was not associated.
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spelling pubmed-69417772020-01-10 Leptin Expression in Human Epicardial Adipose Tissue Is Associated with Local Coronary Atherosclerosis Zhang, Tuowei Yang, Pengkang Li, Tonghua Gao, Jianping Zhang, Yuyang Med Sci Monit Clinical Research BACKGROUND: Leptin is an adipokine related to overweight and cardiovascular diseases. However, the leptin expression level in epicardial adipose tissue (EAT) of humans and its association with coronary atherosclerosis has never been investigated. MATERIAL/METHODS: Patients receiving cardiac surgery were divided into a coronary artery disease group (CAD group) and a non-CAD group (NCAD group). Blood samples from coronary vein, biopsies of subcutaneous adipose tissue (SAT), and EAT were acquired during the surgery. Serum leptin level and leptin level in EAT and SAT were tested with ELISA, quantitative PCR, and immunohistochemistry and were compared between the CAD group and NCAD group, as well as between stenosis and non-stenosis subgroups. Logistic regression analysis was performed to explore the risk factors for coronary artery stenosis. RESULTS: No statistically significant differences were found in demographic and clinical data between groups (all P>0.05). Serum leptin concentration and leptin expression in EAT and SAT of the CAD group were much higher in than in the NCAD group (all P<0.05). In subgroup analysis, there was no difference in serum leptin and expression in SAT of stenosis and non-stenosis patients (All P>0.05). The leptin expression level in EAT of stenosis patients was significantly higher than in non-stenosis patients (P=0.0431). By multivariate logistic regression analysis, we demonstrated that leptin expression level in EAT was an independent risk factor for coronary artery stenosis [OR=1.09, 95%CI (1.01±1.18), P=0.031]. CONCLUSIONS: Leptin expression in EAT and SAT were both increased for CAD patients. Leptin expression in EAT was an independent risk factor for coronary atherosclerosis in the adjacent artery, while leptin in SAT was not associated. International Scientific Literature, Inc. 2019-12-24 /pmc/articles/PMC6941777/ /pubmed/31872802 http://dx.doi.org/10.12659/MSM.918390 Text en © Med Sci Monit, 2019 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Clinical Research
Zhang, Tuowei
Yang, Pengkang
Li, Tonghua
Gao, Jianping
Zhang, Yuyang
Leptin Expression in Human Epicardial Adipose Tissue Is Associated with Local Coronary Atherosclerosis
title Leptin Expression in Human Epicardial Adipose Tissue Is Associated with Local Coronary Atherosclerosis
title_full Leptin Expression in Human Epicardial Adipose Tissue Is Associated with Local Coronary Atherosclerosis
title_fullStr Leptin Expression in Human Epicardial Adipose Tissue Is Associated with Local Coronary Atherosclerosis
title_full_unstemmed Leptin Expression in Human Epicardial Adipose Tissue Is Associated with Local Coronary Atherosclerosis
title_short Leptin Expression in Human Epicardial Adipose Tissue Is Associated with Local Coronary Atherosclerosis
title_sort leptin expression in human epicardial adipose tissue is associated with local coronary atherosclerosis
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941777/
https://www.ncbi.nlm.nih.gov/pubmed/31872802
http://dx.doi.org/10.12659/MSM.918390
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