The Receptor for Advanced Glycation End Products (Rage) and Its Ligands in Plasma and Infrainguinal Bypass Vein
Objective The aim was to investigate whether RAGE and its ligands are associated with infrainguinal bypass outcome in patients with and without diabetes. Methods This was a prospective observational cohort. Patients ( n = 68) with ( n = 38) and without ( n = 30) diabetes undergoing infrainguinal...
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description | Objective The aim was to investigate whether RAGE and its ligands are associated with infrainguinal bypass outcome in patients with and without diabetes. Methods This was a prospective observational cohort. Patients ( n = 68) with ( n = 38) and without ( n = 30) diabetes undergoing infrainguinal vein bypass for peripheral arterial disease were followed for 3 years. Endosecretory RAGE (esRAGE), S100A12, advanced glycation end products, and carboxymethyl-lysine (CML) were determined in plasma using ELISA. The influence of plasma levels on the main outcome (amputation free survival) was evaluated using Cox proportional hazard analysis. Plasma esRAGE, CML, and S100A12 in healthy controls ( n = 30) without cardiovascular disease matched for sex and age were compared with patients, using the Mann–Whitney U test. Veins from bypass surgery procedures were stained and S100A12, RAGE, AGE, and CML were determined using immunohistochemistry. Results Forty-six patients survived with an intact leg during follow up. Seventeen died (median survival time 702 days, IQR 188–899 day), and six had amputations. High plasma S100A12 was associated with reduced amputation free survival (hazard ratio [HR] 2.99; 95% CI 1.24–7.24) when comparing levels above the 75th percentile with levels below. The increased risk was unchanged adjusting for age, sex, and diabetes. Diabetic patients had higher plasma S100A12 (11.75 ng/mL; 95% CI 8.12–15.38 ng/mL) than non-diabetic patients (5.0141 ng/mL; 95% CI 3.62–6.41 ng/mL), whereas plasma CML, esRAGE, and AGE were similar. Plasma CML and S100A12 were higher in patients than in controls (1.25 μg/mL, 95% CI 1.18–1.32 μg/mL vs. 0.8925 μg/mL, 95% CI 0.82–0.96 μg/mL; and 8.7 μg/mL, 95% CI 6.52–10.95 μg/mL vs. 3.47 μg/mL, 95% CI 2.95–3.99 μg/mL, respectively). The proportion of vein tissue stained for AGE (21%), RAGE (5%), CML (9%) and S100A12 (3%), were similar in patients with and without diabetes. Conclusions Plasma S100A12 and CML are elevated in peripheral arterial disease and markers of RAGE and its ligands are found in vein used for bypass. This indicates a role for S100A12, CML, and RAGE in peripheral arterial disease complications by activation of the RAGE system. |
doi_str_mv | 10.1016/j.ejvs.2015.12.047 |
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Methods This was a prospective observational cohort. Patients ( n = 68) with ( n = 38) and without ( n = 30) diabetes undergoing infrainguinal vein bypass for peripheral arterial disease were followed for 3 years. Endosecretory RAGE (esRAGE), S100A12, advanced glycation end products, and carboxymethyl-lysine (CML) were determined in plasma using ELISA. The influence of plasma levels on the main outcome (amputation free survival) was evaluated using Cox proportional hazard analysis. Plasma esRAGE, CML, and S100A12 in healthy controls ( n = 30) without cardiovascular disease matched for sex and age were compared with patients, using the Mann–Whitney U test. Veins from bypass surgery procedures were stained and S100A12, RAGE, AGE, and CML were determined using immunohistochemistry. Results Forty-six patients survived with an intact leg during follow up. Seventeen died (median survival time 702 days, IQR 188–899 day), and six had amputations. High plasma S100A12 was associated with reduced amputation free survival (hazard ratio [HR] 2.99; 95% CI 1.24–7.24) when comparing levels above the 75th percentile with levels below. The increased risk was unchanged adjusting for age, sex, and diabetes. Diabetic patients had higher plasma S100A12 (11.75 ng/mL; 95% CI 8.12–15.38 ng/mL) than non-diabetic patients (5.0141 ng/mL; 95% CI 3.62–6.41 ng/mL), whereas plasma CML, esRAGE, and AGE were similar. Plasma CML and S100A12 were higher in patients than in controls (1.25 μg/mL, 95% CI 1.18–1.32 μg/mL vs. 0.8925 μg/mL, 95% CI 0.82–0.96 μg/mL; and 8.7 μg/mL, 95% CI 6.52–10.95 μg/mL vs. 3.47 μg/mL, 95% CI 2.95–3.99 μg/mL, respectively). The proportion of vein tissue stained for AGE (21%), RAGE (5%), CML (9%) and S100A12 (3%), were similar in patients with and without diabetes. Conclusions Plasma S100A12 and CML are elevated in peripheral arterial disease and markers of RAGE and its ligands are found in vein used for bypass. This indicates a role for S100A12, CML, and RAGE in peripheral arterial disease complications by activation of the RAGE system.</description><identifier>ISSN: 1078-5884</identifier><identifier>EISSN: 1532-2165</identifier><identifier>DOI: 10.1016/j.ejvs.2015.12.047</identifier><identifier>PMID: 26905625</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adult ; Aged ; Amputation ; Amputation free survival ; Biomarkers - blood ; Bypass vein ; Diabetic Angiopathies - blood ; Diabetic Angiopathies - diagnosis ; Diabetic Angiopathies - mortality ; Diabetic Angiopathies - surgery ; Disease-Free Survival ; Female ; Glycation End Products, Advanced - blood ; Humans ; Infrainguinal bypass ; Kaplan-Meier Estimate ; Ligands ; Lysine - analogs & derivatives ; Lysine - blood ; Male ; Middle Aged ; Peripheral Arterial Disease - blood ; Peripheral Arterial Disease - diagnosis ; Peripheral Arterial Disease - mortality ; Peripheral Arterial Disease - surgery ; Proportional Hazards Models ; Prospective Studies ; Receptor for advanced glycation end products (RAGE) ; Receptor for Advanced Glycation End Products - blood ; Reoperation ; Risk Factors ; S100A12 Protein - blood ; Surgery ; Time Factors ; Treatment Outcome ; Up-Regulation ; Vascular Grafting - adverse effects ; Vascular Grafting - methods ; Vascular Grafting - mortality ; Veins - metabolism ; Veins - transplantation</subject><ispartof>European journal of vascular and endovascular surgery, 2016-04, Vol.51 (4), p.579-586</ispartof><rights>European Society for Vascular Surgery</rights><rights>2016 European Society for Vascular Surgery</rights><rights>Copyright © 2016 European Society for Vascular Surgery. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c559t-c1756a348767187d7ae158dfb581ef9cdc815434dd7b835f2094cd69447520633</citedby><cites>FETCH-LOGICAL-c559t-c1756a348767187d7ae158dfb581ef9cdc815434dd7b835f2094cd69447520633</cites><orcidid>0000-0002-2758-9623</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1078588415009259$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,550,776,780,881,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26905625$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:133382151$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Malmstedt, J</creatorcontrib><creatorcontrib>Frebelius, S</creatorcontrib><creatorcontrib>Lengquist, M</creatorcontrib><creatorcontrib>Jörneskog, G</creatorcontrib><creatorcontrib>Wang, J</creatorcontrib><creatorcontrib>Swedenborg, J</creatorcontrib><title>The Receptor for Advanced Glycation End Products (Rage) and Its Ligands in Plasma and Infrainguinal Bypass Vein</title><title>European journal of vascular and endovascular surgery</title><addtitle>Eur J Vasc Endovasc Surg</addtitle><description>Objective The aim was to investigate whether RAGE and its ligands are associated with infrainguinal bypass outcome in patients with and without diabetes. Methods This was a prospective observational cohort. Patients ( n = 68) with ( n = 38) and without ( n = 30) diabetes undergoing infrainguinal vein bypass for peripheral arterial disease were followed for 3 years. Endosecretory RAGE (esRAGE), S100A12, advanced glycation end products, and carboxymethyl-lysine (CML) were determined in plasma using ELISA. The influence of plasma levels on the main outcome (amputation free survival) was evaluated using Cox proportional hazard analysis. Plasma esRAGE, CML, and S100A12 in healthy controls ( n = 30) without cardiovascular disease matched for sex and age were compared with patients, using the Mann–Whitney U test. Veins from bypass surgery procedures were stained and S100A12, RAGE, AGE, and CML were determined using immunohistochemistry. Results Forty-six patients survived with an intact leg during follow up. Seventeen died (median survival time 702 days, IQR 188–899 day), and six had amputations. High plasma S100A12 was associated with reduced amputation free survival (hazard ratio [HR] 2.99; 95% CI 1.24–7.24) when comparing levels above the 75th percentile with levels below. The increased risk was unchanged adjusting for age, sex, and diabetes. Diabetic patients had higher plasma S100A12 (11.75 ng/mL; 95% CI 8.12–15.38 ng/mL) than non-diabetic patients (5.0141 ng/mL; 95% CI 3.62–6.41 ng/mL), whereas plasma CML, esRAGE, and AGE were similar. Plasma CML and S100A12 were higher in patients than in controls (1.25 μg/mL, 95% CI 1.18–1.32 μg/mL vs. 0.8925 μg/mL, 95% CI 0.82–0.96 μg/mL; and 8.7 μg/mL, 95% CI 6.52–10.95 μg/mL vs. 3.47 μg/mL, 95% CI 2.95–3.99 μg/mL, respectively). The proportion of vein tissue stained for AGE (21%), RAGE (5%), CML (9%) and S100A12 (3%), were similar in patients with and without diabetes. Conclusions Plasma S100A12 and CML are elevated in peripheral arterial disease and markers of RAGE and its ligands are found in vein used for bypass. This indicates a role for S100A12, CML, and RAGE in peripheral arterial disease complications by activation of the RAGE system.</description><subject>Adult</subject><subject>Aged</subject><subject>Amputation</subject><subject>Amputation free survival</subject><subject>Biomarkers - blood</subject><subject>Bypass vein</subject><subject>Diabetic Angiopathies - blood</subject><subject>Diabetic Angiopathies - diagnosis</subject><subject>Diabetic Angiopathies - mortality</subject><subject>Diabetic Angiopathies - surgery</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Glycation End Products, Advanced - blood</subject><subject>Humans</subject><subject>Infrainguinal bypass</subject><subject>Kaplan-Meier Estimate</subject><subject>Ligands</subject><subject>Lysine - analogs & derivatives</subject><subject>Lysine - blood</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Peripheral Arterial Disease - blood</subject><subject>Peripheral Arterial Disease - diagnosis</subject><subject>Peripheral Arterial Disease - mortality</subject><subject>Peripheral Arterial Disease - surgery</subject><subject>Proportional Hazards Models</subject><subject>Prospective Studies</subject><subject>Receptor for advanced glycation end products (RAGE)</subject><subject>Receptor for Advanced Glycation End Products - blood</subject><subject>Reoperation</subject><subject>Risk Factors</subject><subject>S100A12 Protein - blood</subject><subject>Surgery</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Up-Regulation</subject><subject>Vascular Grafting - adverse effects</subject><subject>Vascular Grafting - methods</subject><subject>Vascular Grafting - mortality</subject><subject>Veins - metabolism</subject><subject>Veins - transplantation</subject><issn>1078-5884</issn><issn>1532-2165</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>D8T</sourceid><recordid>eNp9kkFv1DAQhSMEoqXwBzggH8shwXYycSIhpFKVUmklqlK4Wl57snibtVM7WbT_HkdZeuDAwfJ4_L0n2W-y7C2jBaOs_rAtcLuPBacMCsYLWoln2SmDkuec1fA81VQ0OTRNdZK9inFLKQVWwsvshNcthZrDaebvfyG5Q43D6APp0rowe-U0GnLdH7QarXfkyhlyG7yZ9BjJ-Z3a4HuiUu8mHVd2k8pIrCO3vYo7tdy4LijrNpN1qiefD4OKkfxE615nLzrVR3xz3M-yH1-u7i-_5qtv1zeXF6tcA7RjrpmAWpVVI2rBGmGEQgaN6dbQMOxabXTDoCorY8S6KaHjtK20qduqEsBpXZZnWb74xt84TGs5BLtT4SC9svLYekgVSqCCCpH484Ufgn-cMI5yZ6PGvlcO_RQlE2LmBOUJ5Quqg48xYPdkzqicg5FbOQcj52Ak4zIFk0Tvjv7TeofmSfI3iQR8XABMv7K3GGTUFucgbEA9SuPt__0__SPXvXVWq_4BDxi3fgopifQOGZNAfp9HY54MBpS2HNryDxsqswQ</recordid><startdate>20160401</startdate><enddate>20160401</enddate><creator>Malmstedt, J</creator><creator>Frebelius, S</creator><creator>Lengquist, M</creator><creator>Jörneskog, G</creator><creator>Wang, J</creator><creator>Swedenborg, J</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</scope><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><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0002-2758-9623</orcidid></search><sort><creationdate>20160401</creationdate><title>The Receptor for Advanced Glycation End Products (Rage) and Its Ligands in Plasma and Infrainguinal Bypass Vein</title><author>Malmstedt, J ; Frebelius, S ; Lengquist, M ; Jörneskog, G ; Wang, J ; Swedenborg, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c559t-c1756a348767187d7ae158dfb581ef9cdc815434dd7b835f2094cd69447520633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Amputation</topic><topic>Amputation free survival</topic><topic>Biomarkers - blood</topic><topic>Bypass vein</topic><topic>Diabetic Angiopathies - blood</topic><topic>Diabetic Angiopathies - diagnosis</topic><topic>Diabetic Angiopathies - mortality</topic><topic>Diabetic Angiopathies - surgery</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Glycation End Products, Advanced - blood</topic><topic>Humans</topic><topic>Infrainguinal bypass</topic><topic>Kaplan-Meier Estimate</topic><topic>Ligands</topic><topic>Lysine - analogs & derivatives</topic><topic>Lysine - blood</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Peripheral Arterial Disease - blood</topic><topic>Peripheral Arterial Disease - diagnosis</topic><topic>Peripheral Arterial Disease - mortality</topic><topic>Peripheral Arterial Disease - surgery</topic><topic>Proportional Hazards Models</topic><topic>Prospective Studies</topic><topic>Receptor for advanced glycation end products (RAGE)</topic><topic>Receptor for Advanced Glycation End Products - blood</topic><topic>Reoperation</topic><topic>Risk Factors</topic><topic>S100A12 Protein - blood</topic><topic>Surgery</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Up-Regulation</topic><topic>Vascular Grafting - adverse effects</topic><topic>Vascular Grafting - methods</topic><topic>Vascular Grafting - mortality</topic><topic>Veins - metabolism</topic><topic>Veins - transplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Malmstedt, J</creatorcontrib><creatorcontrib>Frebelius, S</creatorcontrib><creatorcontrib>Lengquist, M</creatorcontrib><creatorcontrib>Jörneskog, G</creatorcontrib><creatorcontrib>Wang, J</creatorcontrib><creatorcontrib>Swedenborg, J</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>European journal of vascular and endovascular surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Malmstedt, J</au><au>Frebelius, S</au><au>Lengquist, M</au><au>Jörneskog, G</au><au>Wang, J</au><au>Swedenborg, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Receptor for Advanced Glycation End Products (Rage) and Its Ligands in Plasma and Infrainguinal Bypass Vein</atitle><jtitle>European journal of vascular and endovascular surgery</jtitle><addtitle>Eur J Vasc Endovasc Surg</addtitle><date>2016-04-01</date><risdate>2016</risdate><volume>51</volume><issue>4</issue><spage>579</spage><epage>586</epage><pages>579-586</pages><issn>1078-5884</issn><eissn>1532-2165</eissn><abstract>Objective The aim was to investigate whether RAGE and its ligands are associated with infrainguinal bypass outcome in patients with and without diabetes. Methods This was a prospective observational cohort. Patients ( n = 68) with ( n = 38) and without ( n = 30) diabetes undergoing infrainguinal vein bypass for peripheral arterial disease were followed for 3 years. Endosecretory RAGE (esRAGE), S100A12, advanced glycation end products, and carboxymethyl-lysine (CML) were determined in plasma using ELISA. The influence of plasma levels on the main outcome (amputation free survival) was evaluated using Cox proportional hazard analysis. Plasma esRAGE, CML, and S100A12 in healthy controls ( n = 30) without cardiovascular disease matched for sex and age were compared with patients, using the Mann–Whitney U test. Veins from bypass surgery procedures were stained and S100A12, RAGE, AGE, and CML were determined using immunohistochemistry. Results Forty-six patients survived with an intact leg during follow up. Seventeen died (median survival time 702 days, IQR 188–899 day), and six had amputations. High plasma S100A12 was associated with reduced amputation free survival (hazard ratio [HR] 2.99; 95% CI 1.24–7.24) when comparing levels above the 75th percentile with levels below. The increased risk was unchanged adjusting for age, sex, and diabetes. Diabetic patients had higher plasma S100A12 (11.75 ng/mL; 95% CI 8.12–15.38 ng/mL) than non-diabetic patients (5.0141 ng/mL; 95% CI 3.62–6.41 ng/mL), whereas plasma CML, esRAGE, and AGE were similar. Plasma CML and S100A12 were higher in patients than in controls (1.25 μg/mL, 95% CI 1.18–1.32 μg/mL vs. 0.8925 μg/mL, 95% CI 0.82–0.96 μg/mL; and 8.7 μg/mL, 95% CI 6.52–10.95 μg/mL vs. 3.47 μg/mL, 95% CI 2.95–3.99 μg/mL, respectively). The proportion of vein tissue stained for AGE (21%), RAGE (5%), CML (9%) and S100A12 (3%), were similar in patients with and without diabetes. Conclusions Plasma S100A12 and CML are elevated in peripheral arterial disease and markers of RAGE and its ligands are found in vein used for bypass. This indicates a role for S100A12, CML, and RAGE in peripheral arterial disease complications by activation of the RAGE system.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>26905625</pmid><doi>10.1016/j.ejvs.2015.12.047</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-2758-9623</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Amputation Amputation free survival Biomarkers - blood Bypass vein Diabetic Angiopathies - blood Diabetic Angiopathies - diagnosis Diabetic Angiopathies - mortality Diabetic Angiopathies - surgery Disease-Free Survival Female Glycation End Products, Advanced - blood Humans Infrainguinal bypass Kaplan-Meier Estimate Ligands Lysine - analogs & derivatives Lysine - blood Male Middle Aged Peripheral Arterial Disease - blood Peripheral Arterial Disease - diagnosis Peripheral Arterial Disease - mortality Peripheral Arterial Disease - surgery Proportional Hazards Models Prospective Studies Receptor for advanced glycation end products (RAGE) Receptor for Advanced Glycation End Products - blood Reoperation Risk Factors S100A12 Protein - blood Surgery Time Factors Treatment Outcome Up-Regulation Vascular Grafting - adverse effects Vascular Grafting - methods Vascular Grafting - mortality Veins - metabolism Veins - transplantation |
title | The Receptor for Advanced Glycation End Products (Rage) and Its Ligands in Plasma and Infrainguinal Bypass Vein |
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