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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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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