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Tissue kallikrein is related to the severity of coronary artery disease
The impairment of the tissue kallikrein (KLK1)–kinin system (KKS) may result in atheroma development. However, it remains unclear if the KKS correlates with coronary artery disease (CAD). KLK1, VEGF and hs-CRP plasma levels were measured in 100 patients newly diagnosed with CAD and 33 CAD-free contr...
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Published in: | Clinica chimica acta 2013-08, Vol.423, p.90-98 |
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creator | Yao, Yu-yu Fu, Cong Ma, Gen-shan Feng, Yi Shen, Cheng-xing Wu, Guo-qiu Zhang, Xiao-guo Ding, Jian-dong Tang, Cheng-chun Chen, Zhong Dai, Qi-ming Tong, Jia-yi Luo, Dan Zhu, Jian Zhi, Hong Li, Yong-jun Ju, Cheng-wei Lu, Jing Chao, Julie Chao, Lee |
description | The impairment of the tissue kallikrein (KLK1)–kinin system (KKS) may result in atheroma development. However, it remains unclear if the KKS correlates with coronary artery disease (CAD).
KLK1, VEGF and hs-CRP plasma levels were measured in 100 patients newly diagnosed with CAD and 33 CAD-free controls. Patients were followed-up for the incidence of major adverse cardiovascular events (MACE) for 8months to 2y. Gene expression of KLK1, CD105 and CD68 was assessed in human coronary endarterectomy specimens.
Patients with CAD and acute coronary syndrome (ACS) had significantly elevated KLK1 levels. In addition, the concentration of hs-CRP was increased in ACS patients. A strong positive correlation between plasma KLK1 and the severity of CAD was also demonstrated, suggesting that high KLK1 levels are an independent predictor for CAD. MACE during follow-up significantly correlated with KLK1 levels in the ACS group. Unstable coronary plaques demonstrated markedly increased KLK1 levels, macrophage infiltration and high microvessel density. Additionally, KLK1 staining primarily colocalized with macrophages.
In the present study, plasma KLK1 levels were a useful predictor for the presence and extent of CAD. More extensive studies are, however, necessary in order to validate these findings.
•A strong positive correlation between plasma KLK1 and the severity of CAD was demonstrated.•High KLK1 levels are an independent predictor for CAD.•KLK1 expression was primarily co-localized with intimal macrophages. |
doi_str_mv | 10.1016/j.cca.2013.04.017 |
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KLK1, VEGF and hs-CRP plasma levels were measured in 100 patients newly diagnosed with CAD and 33 CAD-free controls. Patients were followed-up for the incidence of major adverse cardiovascular events (MACE) for 8months to 2y. Gene expression of KLK1, CD105 and CD68 was assessed in human coronary endarterectomy specimens.
Patients with CAD and acute coronary syndrome (ACS) had significantly elevated KLK1 levels. In addition, the concentration of hs-CRP was increased in ACS patients. A strong positive correlation between plasma KLK1 and the severity of CAD was also demonstrated, suggesting that high KLK1 levels are an independent predictor for CAD. MACE during follow-up significantly correlated with KLK1 levels in the ACS group. Unstable coronary plaques demonstrated markedly increased KLK1 levels, macrophage infiltration and high microvessel density. Additionally, KLK1 staining primarily colocalized with macrophages.
In the present study, plasma KLK1 levels were a useful predictor for the presence and extent of CAD. More extensive studies are, however, necessary in order to validate these findings.
•A strong positive correlation between plasma KLK1 and the severity of CAD was demonstrated.•High KLK1 levels are an independent predictor for CAD.•KLK1 expression was primarily co-localized with intimal macrophages.</description><identifier>ISSN: 0009-8981</identifier><identifier>EISSN: 1873-3492</identifier><identifier>DOI: 10.1016/j.cca.2013.04.017</identifier><identifier>PMID: 23639635</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Aged ; Angiogenesis ; C-Reactive Protein - analysis ; CAD ; Coronary Artery Disease - diagnosis ; Coronary Artery Disease - pathology ; Female ; Gene Expression Regulation ; Humans ; Immunohistochemistry ; Inflammation ; Macrophages - metabolism ; Male ; Middle Aged ; Plaque stability ; Reproducibility of Results ; Severity of Illness Index ; Tissue kallikrein ; Tissue Kallikreins - blood ; Tissue Kallikreins - genetics ; Tissue Kallikreins - metabolism ; Vascular Endothelial Growth Factor A - blood</subject><ispartof>Clinica chimica acta, 2013-08, Vol.423, p.90-98</ispartof><rights>2013 Elsevier B.V.</rights><rights>Copyright © 2013 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-62142db0547ddf2d38a3c99fef516bc9d97034c0003a9892fcfca8aa38b651cb3</citedby><cites>FETCH-LOGICAL-c353t-62142db0547ddf2d38a3c99fef516bc9d97034c0003a9892fcfca8aa38b651cb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23639635$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yao, Yu-yu</creatorcontrib><creatorcontrib>Fu, Cong</creatorcontrib><creatorcontrib>Ma, Gen-shan</creatorcontrib><creatorcontrib>Feng, Yi</creatorcontrib><creatorcontrib>Shen, Cheng-xing</creatorcontrib><creatorcontrib>Wu, Guo-qiu</creatorcontrib><creatorcontrib>Zhang, Xiao-guo</creatorcontrib><creatorcontrib>Ding, Jian-dong</creatorcontrib><creatorcontrib>Tang, Cheng-chun</creatorcontrib><creatorcontrib>Chen, Zhong</creatorcontrib><creatorcontrib>Dai, Qi-ming</creatorcontrib><creatorcontrib>Tong, Jia-yi</creatorcontrib><creatorcontrib>Luo, Dan</creatorcontrib><creatorcontrib>Zhu, Jian</creatorcontrib><creatorcontrib>Zhi, Hong</creatorcontrib><creatorcontrib>Li, Yong-jun</creatorcontrib><creatorcontrib>Ju, Cheng-wei</creatorcontrib><creatorcontrib>Lu, Jing</creatorcontrib><creatorcontrib>Chao, Julie</creatorcontrib><creatorcontrib>Chao, Lee</creatorcontrib><title>Tissue kallikrein is related to the severity of coronary artery disease</title><title>Clinica chimica acta</title><addtitle>Clin Chim Acta</addtitle><description>The impairment of the tissue kallikrein (KLK1)–kinin system (KKS) may result in atheroma development. However, it remains unclear if the KKS correlates with coronary artery disease (CAD).
KLK1, VEGF and hs-CRP plasma levels were measured in 100 patients newly diagnosed with CAD and 33 CAD-free controls. Patients were followed-up for the incidence of major adverse cardiovascular events (MACE) for 8months to 2y. Gene expression of KLK1, CD105 and CD68 was assessed in human coronary endarterectomy specimens.
Patients with CAD and acute coronary syndrome (ACS) had significantly elevated KLK1 levels. In addition, the concentration of hs-CRP was increased in ACS patients. A strong positive correlation between plasma KLK1 and the severity of CAD was also demonstrated, suggesting that high KLK1 levels are an independent predictor for CAD. MACE during follow-up significantly correlated with KLK1 levels in the ACS group. Unstable coronary plaques demonstrated markedly increased KLK1 levels, macrophage infiltration and high microvessel density. Additionally, KLK1 staining primarily colocalized with macrophages.
In the present study, plasma KLK1 levels were a useful predictor for the presence and extent of CAD. More extensive studies are, however, necessary in order to validate these findings.
•A strong positive correlation between plasma KLK1 and the severity of CAD was demonstrated.•High KLK1 levels are an independent predictor for CAD.•KLK1 expression was primarily co-localized with intimal macrophages.</description><subject>Aged</subject><subject>Angiogenesis</subject><subject>C-Reactive Protein - analysis</subject><subject>CAD</subject><subject>Coronary Artery Disease - diagnosis</subject><subject>Coronary Artery Disease - pathology</subject><subject>Female</subject><subject>Gene Expression Regulation</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Inflammation</subject><subject>Macrophages - metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Plaque stability</subject><subject>Reproducibility of Results</subject><subject>Severity of Illness Index</subject><subject>Tissue kallikrein</subject><subject>Tissue Kallikreins - blood</subject><subject>Tissue Kallikreins - genetics</subject><subject>Tissue Kallikreins - metabolism</subject><subject>Vascular Endothelial Growth Factor A - blood</subject><issn>0009-8981</issn><issn>1873-3492</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp9kE9LAzEUxIMotlY_gBfJ0cuuySb7J3gS0SoUvNRzyCYvmHa7W5Nsod_elFaPnoYHM8O8H0K3lOSU0OphlWut8oJQlhOeE1qfoSltapYxLopzNCWEiKwRDZ2gqxBW6eSkopdoUrCKiYqVUzRfuhBGwGvVdW7twfXYBeyhUxEMjgOOX4AD7MC7uMeDxXrwQ6_8HisfIYlxAVSAa3RhVRfg5qQz9Pn6snx-yxYf8_fnp0WmWcliVhWUF6YlJa-NsYVhjWJaCAu2pFWrhRE1YVynpUyJRhRWW60apVjTViXVLZuh-2Pv1g_fI4QoNy5o6DrVwzAGSVnFa1ILKpKVHq3aDyF4sHLr3SZNl5TIAz-5komfPPCThMvEL2XuTvVjuwHzl_gFlgyPRwOkJ3cOvAzaQa_BOA86SjO4f-p_AMzRgHc</recordid><startdate>20130823</startdate><enddate>20130823</enddate><creator>Yao, Yu-yu</creator><creator>Fu, Cong</creator><creator>Ma, Gen-shan</creator><creator>Feng, Yi</creator><creator>Shen, Cheng-xing</creator><creator>Wu, Guo-qiu</creator><creator>Zhang, Xiao-guo</creator><creator>Ding, Jian-dong</creator><creator>Tang, Cheng-chun</creator><creator>Chen, Zhong</creator><creator>Dai, Qi-ming</creator><creator>Tong, Jia-yi</creator><creator>Luo, Dan</creator><creator>Zhu, Jian</creator><creator>Zhi, Hong</creator><creator>Li, Yong-jun</creator><creator>Ju, Cheng-wei</creator><creator>Lu, Jing</creator><creator>Chao, Julie</creator><creator>Chao, Lee</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20130823</creationdate><title>Tissue kallikrein is related to the severity of coronary artery disease</title><author>Yao, Yu-yu ; 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However, it remains unclear if the KKS correlates with coronary artery disease (CAD).
KLK1, VEGF and hs-CRP plasma levels were measured in 100 patients newly diagnosed with CAD and 33 CAD-free controls. Patients were followed-up for the incidence of major adverse cardiovascular events (MACE) for 8months to 2y. Gene expression of KLK1, CD105 and CD68 was assessed in human coronary endarterectomy specimens.
Patients with CAD and acute coronary syndrome (ACS) had significantly elevated KLK1 levels. In addition, the concentration of hs-CRP was increased in ACS patients. A strong positive correlation between plasma KLK1 and the severity of CAD was also demonstrated, suggesting that high KLK1 levels are an independent predictor for CAD. MACE during follow-up significantly correlated with KLK1 levels in the ACS group. Unstable coronary plaques demonstrated markedly increased KLK1 levels, macrophage infiltration and high microvessel density. Additionally, KLK1 staining primarily colocalized with macrophages.
In the present study, plasma KLK1 levels were a useful predictor for the presence and extent of CAD. More extensive studies are, however, necessary in order to validate these findings.
•A strong positive correlation between plasma KLK1 and the severity of CAD was demonstrated.•High KLK1 levels are an independent predictor for CAD.•KLK1 expression was primarily co-localized with intimal macrophages.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>23639635</pmid><doi>10.1016/j.cca.2013.04.017</doi><tpages>9</tpages></addata></record> |
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subjects | Aged Angiogenesis C-Reactive Protein - analysis CAD Coronary Artery Disease - diagnosis Coronary Artery Disease - pathology Female Gene Expression Regulation Humans Immunohistochemistry Inflammation Macrophages - metabolism Male Middle Aged Plaque stability Reproducibility of Results Severity of Illness Index Tissue kallikrein Tissue Kallikreins - blood Tissue Kallikreins - genetics Tissue Kallikreins - metabolism Vascular Endothelial Growth Factor A - blood |
title | Tissue kallikrein is related to the severity of coronary artery disease |
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