Evaluation of the endothelial glycocalyx damage in patients with acute coronary syndrome

Abstract Background Endothelial glycocalyx (EG) is sugar-based cell-bound surface molecules linked to transmembrane proteins observed on the endothelial surface of the vessels. Damage to this structure causes an increase in platelet and leucocyte adhesion and shear stress in the vessel. We hypothesi...

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Veröffentlicht in:Atherosclerosis 2016-04, Vol.247, p.184-188
Hauptverfasser: Miranda, Carlos Henrique, de Carvalho Borges, Marcos, Schmidt, André, Marin-Neto, José Antônio, Pazin-Filho, Antônio
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container_end_page 188
container_issue
container_start_page 184
container_title Atherosclerosis
container_volume 247
creator Miranda, Carlos Henrique
de Carvalho Borges, Marcos
Schmidt, André
Marin-Neto, José Antônio
Pazin-Filho, Antônio
description Abstract Background Endothelial glycocalyx (EG) is sugar-based cell-bound surface molecules linked to transmembrane proteins observed on the endothelial surface of the vessels. Damage to this structure causes an increase in platelet and leucocyte adhesion and shear stress in the vessel. We hypothesized a possible link between EG damage and acute coronary syndrome (ACS). Methods We measured the syndecan-1 levels (a biomarker of EG damage) in 141 patients (99 men) with ACS and compared to those of 45 patients (24 men) with non-coronary chest pain (NCCP) and of 24 (14 men) healthy individuals (CONTROL). Results The baseline characteristics of the ACS and NCCP groups were similar. Syndecan-1 levels were significantly higher in the ACS group than in the NCCP (p = 0.01) and CONTROL (p = 0.001) groups but did not differ between the NCCP and CONTROL groups (p = 0.83). In analysis according to gender category, the difference among the groups remained significant only for men (p = 0.0009). A syndecan-1 level higher than 148 ng/ml was associated with ACS diagnosis with an odds ratio of 14 (95% confidence interval (CI): 1.8 to 102), p = 0.011. After adjusting for gender, age and current or past tobacco use, this syndecan-1 level remained positively associated with ACS diagnosis with an odds ratio of 12 (95% CI: 1.6 to 93), p = 0.016. Conclusion Higher syndecan-1 levels were observed during ACS, mostly in men, suggesting that EG damage could participate in the atherosclerotic plaque vulnerability process in these patients.
doi_str_mv 10.1016/j.atherosclerosis.2016.02.023
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Damage to this structure causes an increase in platelet and leucocyte adhesion and shear stress in the vessel. We hypothesized a possible link between EG damage and acute coronary syndrome (ACS). Methods We measured the syndecan-1 levels (a biomarker of EG damage) in 141 patients (99 men) with ACS and compared to those of 45 patients (24 men) with non-coronary chest pain (NCCP) and of 24 (14 men) healthy individuals (CONTROL). Results The baseline characteristics of the ACS and NCCP groups were similar. Syndecan-1 levels were significantly higher in the ACS group than in the NCCP (p = 0.01) and CONTROL (p = 0.001) groups but did not differ between the NCCP and CONTROL groups (p = 0.83). In analysis according to gender category, the difference among the groups remained significant only for men (p = 0.0009). A syndecan-1 level higher than 148 ng/ml was associated with ACS diagnosis with an odds ratio of 14 (95% confidence interval (CI): 1.8 to 102), p = 0.011. After adjusting for gender, age and current or past tobacco use, this syndecan-1 level remained positively associated with ACS diagnosis with an odds ratio of 12 (95% CI: 1.6 to 93), p = 0.016. Conclusion Higher syndecan-1 levels were observed during ACS, mostly in men, suggesting that EG damage could participate in the atherosclerotic plaque vulnerability process in these patients.</description><identifier>ISSN: 0021-9150</identifier><identifier>EISSN: 1879-1484</identifier><identifier>DOI: 10.1016/j.atherosclerosis.2016.02.023</identifier><identifier>PMID: 26926597</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Acute coronary syndrome ; Acute Coronary Syndrome - blood ; Acute Coronary Syndrome - diagnosis ; Acute Coronary Syndrome - pathology ; Adult ; Angina, Unstable - blood ; Angina, Unstable - diagnosis ; Angina, Unstable - pathology ; Biomarkers - blood ; Cardiovascular ; Case-Control Studies ; Cross-Sectional Studies ; Endothelial Cells - metabolism ; Endothelial Cells - pathology ; Endothelial glycocalyx ; Female ; Glycocalyx - metabolism ; Glycocalyx - pathology ; Humans ; Logistic Models ; Male ; Multivariate Analysis ; Myocardial infarction ; Myocardial Infarction - blood ; Myocardial Infarction - diagnosis ; Myocardial Infarction - pathology ; Odds Ratio ; Predictive Value of Tests ; Risk Factors ; Sex Factors ; Syndecan-1 ; Syndecan-1 - blood ; Up-Regulation</subject><ispartof>Atherosclerosis, 2016-04, Vol.247, p.184-188</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2016 Elsevier Ireland Ltd</rights><rights>Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c444t-85ea231153ebe5d6e5cbf40cc6155d5e0cdeb4ed116811a4f05c43955a73882c3</citedby><cites>FETCH-LOGICAL-c444t-85ea231153ebe5d6e5cbf40cc6155d5e0cdeb4ed116811a4f05c43955a73882c3</cites><orcidid>0000-0002-5968-4879</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.atherosclerosis.2016.02.023$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26926597$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miranda, Carlos Henrique</creatorcontrib><creatorcontrib>de Carvalho Borges, Marcos</creatorcontrib><creatorcontrib>Schmidt, André</creatorcontrib><creatorcontrib>Marin-Neto, José Antônio</creatorcontrib><creatorcontrib>Pazin-Filho, Antônio</creatorcontrib><title>Evaluation of the endothelial glycocalyx damage in patients with acute coronary syndrome</title><title>Atherosclerosis</title><addtitle>Atherosclerosis</addtitle><description>Abstract Background Endothelial glycocalyx (EG) is sugar-based cell-bound surface molecules linked to transmembrane proteins observed on the endothelial surface of the vessels. Damage to this structure causes an increase in platelet and leucocyte adhesion and shear stress in the vessel. We hypothesized a possible link between EG damage and acute coronary syndrome (ACS). Methods We measured the syndecan-1 levels (a biomarker of EG damage) in 141 patients (99 men) with ACS and compared to those of 45 patients (24 men) with non-coronary chest pain (NCCP) and of 24 (14 men) healthy individuals (CONTROL). Results The baseline characteristics of the ACS and NCCP groups were similar. Syndecan-1 levels were significantly higher in the ACS group than in the NCCP (p = 0.01) and CONTROL (p = 0.001) groups but did not differ between the NCCP and CONTROL groups (p = 0.83). In analysis according to gender category, the difference among the groups remained significant only for men (p = 0.0009). A syndecan-1 level higher than 148 ng/ml was associated with ACS diagnosis with an odds ratio of 14 (95% confidence interval (CI): 1.8 to 102), p = 0.011. After adjusting for gender, age and current or past tobacco use, this syndecan-1 level remained positively associated with ACS diagnosis with an odds ratio of 12 (95% CI: 1.6 to 93), p = 0.016. Conclusion Higher syndecan-1 levels were observed during ACS, mostly in men, suggesting that EG damage could participate in the atherosclerotic plaque vulnerability process in these patients.</description><subject>Acute coronary syndrome</subject><subject>Acute Coronary Syndrome - blood</subject><subject>Acute Coronary Syndrome - diagnosis</subject><subject>Acute Coronary Syndrome - pathology</subject><subject>Adult</subject><subject>Angina, Unstable - blood</subject><subject>Angina, Unstable - diagnosis</subject><subject>Angina, Unstable - pathology</subject><subject>Biomarkers - blood</subject><subject>Cardiovascular</subject><subject>Case-Control Studies</subject><subject>Cross-Sectional Studies</subject><subject>Endothelial Cells - metabolism</subject><subject>Endothelial Cells - pathology</subject><subject>Endothelial glycocalyx</subject><subject>Female</subject><subject>Glycocalyx - metabolism</subject><subject>Glycocalyx - pathology</subject><subject>Humans</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Multivariate Analysis</subject><subject>Myocardial infarction</subject><subject>Myocardial Infarction - blood</subject><subject>Myocardial Infarction - diagnosis</subject><subject>Myocardial Infarction - pathology</subject><subject>Odds Ratio</subject><subject>Predictive Value of Tests</subject><subject>Risk Factors</subject><subject>Sex Factors</subject><subject>Syndecan-1</subject><subject>Syndecan-1 - blood</subject><subject>Up-Regulation</subject><issn>0021-9150</issn><issn>1879-1484</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9v1DAQxS0EotvCV0C-IHHJ4on_JDmAhKpSkCpxaJG4WV570npx4sVOCvn2dbSFQ09II49kvTdj_x4hb4FtgYF6v9-a6Q5TzDasp8_bulxvWV2KPyMbaJuuAtGK52TDWA1VB5KdkNOc94wx0UD7kpzUqquV7JoN-XFxb8JsJh9HGntaRlMcXSw9eBPobVhstCYsf6gzg7lF6kd6KHIcp0x_--mOGjtPSG1McTRpoXkZXYoDviIvehMyvn7sZ-T754ub8y_V1bfLr-efriorhJiqVqKpOYDkuEPpFEq76wWzVoGUTiKzDncCHYBqAYzombSCd1KahrdtbfkZeXece0jx14x50oPPFkMwI8Y5a2gaxVpVc1mkH45SW8DlhL0-JD-UR2tgeoWr9_oJXL3C1awuxYv_zeOqeTeg--f-S7MILo8CLB--95h0toWURecT2km76P971ccnk2zwoy9J_MQF8z7OaSxUNehcDPp6TXoNGhRnTCngD3Opq1g</recordid><startdate>20160401</startdate><enddate>20160401</enddate><creator>Miranda, Carlos Henrique</creator><creator>de Carvalho Borges, Marcos</creator><creator>Schmidt, André</creator><creator>Marin-Neto, José Antônio</creator><creator>Pazin-Filho, Antônio</creator><general>Elsevier Ireland Ltd</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><orcidid>https://orcid.org/0000-0002-5968-4879</orcidid></search><sort><creationdate>20160401</creationdate><title>Evaluation of the endothelial glycocalyx damage in patients with acute coronary syndrome</title><author>Miranda, Carlos Henrique ; de Carvalho Borges, Marcos ; Schmidt, André ; Marin-Neto, José Antônio ; Pazin-Filho, Antônio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c444t-85ea231153ebe5d6e5cbf40cc6155d5e0cdeb4ed116811a4f05c43955a73882c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acute coronary syndrome</topic><topic>Acute Coronary Syndrome - blood</topic><topic>Acute Coronary Syndrome - diagnosis</topic><topic>Acute Coronary Syndrome - pathology</topic><topic>Adult</topic><topic>Angina, Unstable - blood</topic><topic>Angina, Unstable - diagnosis</topic><topic>Angina, Unstable - pathology</topic><topic>Biomarkers - blood</topic><topic>Cardiovascular</topic><topic>Case-Control Studies</topic><topic>Cross-Sectional Studies</topic><topic>Endothelial Cells - metabolism</topic><topic>Endothelial Cells - pathology</topic><topic>Endothelial glycocalyx</topic><topic>Female</topic><topic>Glycocalyx - metabolism</topic><topic>Glycocalyx - pathology</topic><topic>Humans</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Multivariate Analysis</topic><topic>Myocardial infarction</topic><topic>Myocardial Infarction - blood</topic><topic>Myocardial Infarction - diagnosis</topic><topic>Myocardial Infarction - pathology</topic><topic>Odds Ratio</topic><topic>Predictive Value of Tests</topic><topic>Risk Factors</topic><topic>Sex Factors</topic><topic>Syndecan-1</topic><topic>Syndecan-1 - blood</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miranda, Carlos Henrique</creatorcontrib><creatorcontrib>de Carvalho Borges, Marcos</creatorcontrib><creatorcontrib>Schmidt, André</creatorcontrib><creatorcontrib>Marin-Neto, José Antônio</creatorcontrib><creatorcontrib>Pazin-Filho, Antônio</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Atherosclerosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miranda, Carlos Henrique</au><au>de Carvalho Borges, Marcos</au><au>Schmidt, André</au><au>Marin-Neto, José Antônio</au><au>Pazin-Filho, Antônio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of the endothelial glycocalyx damage in patients with acute coronary syndrome</atitle><jtitle>Atherosclerosis</jtitle><addtitle>Atherosclerosis</addtitle><date>2016-04-01</date><risdate>2016</risdate><volume>247</volume><spage>184</spage><epage>188</epage><pages>184-188</pages><issn>0021-9150</issn><eissn>1879-1484</eissn><abstract>Abstract Background Endothelial glycocalyx (EG) is sugar-based cell-bound surface molecules linked to transmembrane proteins observed on the endothelial surface of the vessels. Damage to this structure causes an increase in platelet and leucocyte adhesion and shear stress in the vessel. We hypothesized a possible link between EG damage and acute coronary syndrome (ACS). Methods We measured the syndecan-1 levels (a biomarker of EG damage) in 141 patients (99 men) with ACS and compared to those of 45 patients (24 men) with non-coronary chest pain (NCCP) and of 24 (14 men) healthy individuals (CONTROL). Results The baseline characteristics of the ACS and NCCP groups were similar. Syndecan-1 levels were significantly higher in the ACS group than in the NCCP (p = 0.01) and CONTROL (p = 0.001) groups but did not differ between the NCCP and CONTROL groups (p = 0.83). In analysis according to gender category, the difference among the groups remained significant only for men (p = 0.0009). A syndecan-1 level higher than 148 ng/ml was associated with ACS diagnosis with an odds ratio of 14 (95% confidence interval (CI): 1.8 to 102), p = 0.011. After adjusting for gender, age and current or past tobacco use, this syndecan-1 level remained positively associated with ACS diagnosis with an odds ratio of 12 (95% CI: 1.6 to 93), p = 0.016. Conclusion Higher syndecan-1 levels were observed during ACS, mostly in men, suggesting that EG damage could participate in the atherosclerotic plaque vulnerability process in these patients.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>26926597</pmid><doi>10.1016/j.atherosclerosis.2016.02.023</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-5968-4879</orcidid></addata></record>
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subjects Acute coronary syndrome
Acute Coronary Syndrome - blood
Acute Coronary Syndrome - diagnosis
Acute Coronary Syndrome - pathology
Adult
Angina, Unstable - blood
Angina, Unstable - diagnosis
Angina, Unstable - pathology
Biomarkers - blood
Cardiovascular
Case-Control Studies
Cross-Sectional Studies
Endothelial Cells - metabolism
Endothelial Cells - pathology
Endothelial glycocalyx
Female
Glycocalyx - metabolism
Glycocalyx - pathology
Humans
Logistic Models
Male
Multivariate Analysis
Myocardial infarction
Myocardial Infarction - blood
Myocardial Infarction - diagnosis
Myocardial Infarction - pathology
Odds Ratio
Predictive Value of Tests
Risk Factors
Sex Factors
Syndecan-1
Syndecan-1 - blood
Up-Regulation
title Evaluation of the endothelial glycocalyx damage in patients with acute coronary syndrome
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