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Association Between Serum Leptin Level and Calcific Aortic Valve Disease
BACKGROUND: The pathophysiological process of calcific aortic valve disease (CAVD) is similar to that of atherosclerosis. Leptin accelerates the process of atherosclerosis. We sought to examine the relationship between leptin and CAVD. METHODS AND RESULTS: Serum leptin was measured in 397 consecutiv...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6806045/ https://www.ncbi.nlm.nih.gov/pubmed/31566104 http://dx.doi.org/10.1161/JAHA.119.012495 |
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author | Liu, Yehong Gu, Yuying Shen, Ying Lin, Bowen Li, Ying He, Xiaoyan Zhang, Yibo Lu, Lin Shen, Weifeng Zhang, Qi Yang, Ke |
author_facet | Liu, Yehong Gu, Yuying Shen, Ying Lin, Bowen Li, Ying He, Xiaoyan Zhang, Yibo Lu, Lin Shen, Weifeng Zhang, Qi Yang, Ke |
author_sort | Liu, Yehong |
collection | PubMed |
description | BACKGROUND: The pathophysiological process of calcific aortic valve disease (CAVD) is similar to that of atherosclerosis. Leptin accelerates the process of atherosclerosis. We sought to examine the relationship between leptin and CAVD. METHODS AND RESULTS: Serum leptin was measured in 397 consecutive patients undergoing standard transthoracic echocardiography and Doppler flow imaging. Multiple logistic regression analyses were used to assess the association between leptin and CAVD. Western blotting was performed to detect the expression of phosphorylated and total extracellular signal‐regulated kinase. Serum leptin (median) was higher in 200 patients with CAVD than that in 197 non‐CAVD controls (20.07 versus 9.03 ng/mL; P<0.01). Leptin correlated positively with age (r=0.37, P<0.01) and negatively with estimated glomerular filtration rate (r=−0.37, P<0.01). Multivariate analysis indicated that elevated leptin was an independent determinant for the presence of CAVD (P<0.01). Receiver‐operating characteristic curve analysis of leptin to detect the presence of CAVD showed that the area under the curve was 0.74 (95% CI, 0.69–0.79; P<0.01). The diagnostic value of leptin for the detection of CAVD was higher among younger patients (aged ≤65 years) or those with at least mildly reduced renal function (estimated glomerular filtration rate ≤82.06 mL/min per 1.73 m(2)). The activation of extracellular signal‐regulated kinase 1/2 was stronger in calcific aortic valves than in normal aortic valves. CONCLUSIONS: Elevated leptin is associated with the presence of CAVD, especially among younger patients or those with renal dysfunction. |
format | Online Article Text |
id | pubmed-6806045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68060452019-10-28 Association Between Serum Leptin Level and Calcific Aortic Valve Disease Liu, Yehong Gu, Yuying Shen, Ying Lin, Bowen Li, Ying He, Xiaoyan Zhang, Yibo Lu, Lin Shen, Weifeng Zhang, Qi Yang, Ke J Am Heart Assoc Original Research BACKGROUND: The pathophysiological process of calcific aortic valve disease (CAVD) is similar to that of atherosclerosis. Leptin accelerates the process of atherosclerosis. We sought to examine the relationship between leptin and CAVD. METHODS AND RESULTS: Serum leptin was measured in 397 consecutive patients undergoing standard transthoracic echocardiography and Doppler flow imaging. Multiple logistic regression analyses were used to assess the association between leptin and CAVD. Western blotting was performed to detect the expression of phosphorylated and total extracellular signal‐regulated kinase. Serum leptin (median) was higher in 200 patients with CAVD than that in 197 non‐CAVD controls (20.07 versus 9.03 ng/mL; P<0.01). Leptin correlated positively with age (r=0.37, P<0.01) and negatively with estimated glomerular filtration rate (r=−0.37, P<0.01). Multivariate analysis indicated that elevated leptin was an independent determinant for the presence of CAVD (P<0.01). Receiver‐operating characteristic curve analysis of leptin to detect the presence of CAVD showed that the area under the curve was 0.74 (95% CI, 0.69–0.79; P<0.01). The diagnostic value of leptin for the detection of CAVD was higher among younger patients (aged ≤65 years) or those with at least mildly reduced renal function (estimated glomerular filtration rate ≤82.06 mL/min per 1.73 m(2)). The activation of extracellular signal‐regulated kinase 1/2 was stronger in calcific aortic valves than in normal aortic valves. CONCLUSIONS: Elevated leptin is associated with the presence of CAVD, especially among younger patients or those with renal dysfunction. John Wiley and Sons Inc. 2019-09-28 /pmc/articles/PMC6806045/ /pubmed/31566104 http://dx.doi.org/10.1161/JAHA.119.012495 Text en © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Research Liu, Yehong Gu, Yuying Shen, Ying Lin, Bowen Li, Ying He, Xiaoyan Zhang, Yibo Lu, Lin Shen, Weifeng Zhang, Qi Yang, Ke Association Between Serum Leptin Level and Calcific Aortic Valve Disease |
title | Association Between Serum Leptin Level and Calcific Aortic Valve Disease |
title_full | Association Between Serum Leptin Level and Calcific Aortic Valve Disease |
title_fullStr | Association Between Serum Leptin Level and Calcific Aortic Valve Disease |
title_full_unstemmed | Association Between Serum Leptin Level and Calcific Aortic Valve Disease |
title_short | Association Between Serum Leptin Level and Calcific Aortic Valve Disease |
title_sort | association between serum leptin level and calcific aortic valve disease |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6806045/ https://www.ncbi.nlm.nih.gov/pubmed/31566104 http://dx.doi.org/10.1161/JAHA.119.012495 |
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