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Association of serum leptin levels with central arterial stiffness in coronary artery disease patients
BACKGROUND: Serum adipokines have roles in the development of arterial stiffness. Our aim was to investigate the relationship of leptin and the surrogate marker carotid-femoral pulse wave velocity (cfPWV) in coronary artery disease (CAD) patients. METHODS: Fasting blood samples were obtained from 10...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857286/ https://www.ncbi.nlm.nih.gov/pubmed/27151106 http://dx.doi.org/10.1186/s12872-016-0268-5 |
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author | Tsai, Jen-Pi Wang, Ji-Hung Chen, Mei-Ling Yang, Chiu-Fen Chen, Yu-Chih Hsu, Bang-Gee |
author_facet | Tsai, Jen-Pi Wang, Ji-Hung Chen, Mei-Ling Yang, Chiu-Fen Chen, Yu-Chih Hsu, Bang-Gee |
author_sort | Tsai, Jen-Pi |
collection | PubMed |
description | BACKGROUND: Serum adipokines have roles in the development of arterial stiffness. Our aim was to investigate the relationship of leptin and the surrogate marker carotid-femoral pulse wave velocity (cfPWV) in coronary artery disease (CAD) patients. METHODS: Fasting blood samples were obtained from 105 CAD patients. cfPWV was measured with the SphygmoCor system. A cfPWV > 10 m/s was defined as high arterial stiffness, and ≤ 10 m/s as low arterial stiffness. RESULTS: Thirty-seven patients (35.2 %) had high arterial stiffness, and had a higher percentage of diabetes (P = 0.001), hypertension (P = 0.010), older age (P = 0.001), and higher systolic blood pressure (SBP) (P < 0.001), diastolic blood pressure (DBP) (P = 0.021), pulse pressure (P = 0.014), and serum leptin level (P = 0.002) compared to patients with low arterial stiffness. Serum leptin levels correlated with the number of angiographically documented stenotic coronary artery vessels (P < 0.001). After adjusting for factors significantly associated with arterial stiffness, multivariate logistic regression analysis showed that leptin (odds ratio = 1.026, 95 % confidence interval: 1.002–1.051, P = 0.037) was a significant independent predictor of arterial stiffness. CONCLUSIONS: Increasing serum concentration of leptin correlated positively with the total number of stenotic coronary arteries, and serum leptin level may predict the development of arterial stiffness in CAD patients. |
format | Online Article Text |
id | pubmed-4857286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48572862016-05-06 Association of serum leptin levels with central arterial stiffness in coronary artery disease patients Tsai, Jen-Pi Wang, Ji-Hung Chen, Mei-Ling Yang, Chiu-Fen Chen, Yu-Chih Hsu, Bang-Gee BMC Cardiovasc Disord Research Article BACKGROUND: Serum adipokines have roles in the development of arterial stiffness. Our aim was to investigate the relationship of leptin and the surrogate marker carotid-femoral pulse wave velocity (cfPWV) in coronary artery disease (CAD) patients. METHODS: Fasting blood samples were obtained from 105 CAD patients. cfPWV was measured with the SphygmoCor system. A cfPWV > 10 m/s was defined as high arterial stiffness, and ≤ 10 m/s as low arterial stiffness. RESULTS: Thirty-seven patients (35.2 %) had high arterial stiffness, and had a higher percentage of diabetes (P = 0.001), hypertension (P = 0.010), older age (P = 0.001), and higher systolic blood pressure (SBP) (P < 0.001), diastolic blood pressure (DBP) (P = 0.021), pulse pressure (P = 0.014), and serum leptin level (P = 0.002) compared to patients with low arterial stiffness. Serum leptin levels correlated with the number of angiographically documented stenotic coronary artery vessels (P < 0.001). After adjusting for factors significantly associated with arterial stiffness, multivariate logistic regression analysis showed that leptin (odds ratio = 1.026, 95 % confidence interval: 1.002–1.051, P = 0.037) was a significant independent predictor of arterial stiffness. CONCLUSIONS: Increasing serum concentration of leptin correlated positively with the total number of stenotic coronary arteries, and serum leptin level may predict the development of arterial stiffness in CAD patients. BioMed Central 2016-05-05 /pmc/articles/PMC4857286/ /pubmed/27151106 http://dx.doi.org/10.1186/s12872-016-0268-5 Text en © Tsai et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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. |
spellingShingle | Research Article Tsai, Jen-Pi Wang, Ji-Hung Chen, Mei-Ling Yang, Chiu-Fen Chen, Yu-Chih Hsu, Bang-Gee Association of serum leptin levels with central arterial stiffness in coronary artery disease patients |
title | Association of serum leptin levels with central arterial stiffness in coronary artery disease patients |
title_full | Association of serum leptin levels with central arterial stiffness in coronary artery disease patients |
title_fullStr | Association of serum leptin levels with central arterial stiffness in coronary artery disease patients |
title_full_unstemmed | Association of serum leptin levels with central arterial stiffness in coronary artery disease patients |
title_short | Association of serum leptin levels with central arterial stiffness in coronary artery disease patients |
title_sort | association of serum leptin levels with central arterial stiffness in coronary artery disease patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857286/ https://www.ncbi.nlm.nih.gov/pubmed/27151106 http://dx.doi.org/10.1186/s12872-016-0268-5 |
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