AB0476 Superoxide dismutase is associated to large vessels involvement in behcet syndrome
Background In Behçet’s Syndrome (BS), all polymorphonuclear cells (PMN) capacities are enhanced: chemoattraction, phagocytosis and free radicals (FR) production (1, 2). The excess of FR, responsible for an oxidative stress (OS) state, could present an endothelial toxicity (3) and could be implicated...
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Veröffentlicht in: | Annals of the rheumatic diseases 2013-06, Vol.72 (Suppl 3), p.A934-A934 |
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description | Background In Behçet’s Syndrome (BS), all polymorphonuclear cells (PMN) capacities are enhanced: chemoattraction, phagocytosis and free radicals (FR) production (1, 2). The excess of FR, responsible for an oxidative stress (OS) state, could present an endothelial toxicity (3) and could be implicated in tissue lesions genesis in BS. Objectives The aim of our work was to analyze the correlation between oxidative stress biological markers and main vessels involvement in BS. Methods 40 BD patients (27 males, 13 females; mean age: 38.8 years) were prospectively enrolled in the study. Plasma malondialdehyde (MDA), erythrocyte superoxide dismutase (SOD), catalase and glutathione peroxidase (GSH-PX) were analyzed. Levels of these parameters were compared between patients having or not neurological (NI), ocular (OI) and large vascular involvement (LVI). Results There were 16 patients with large vessels involvement (LVI), 10 with neurological involvement and 13 having Behçet’s eye disease. Patients with LVI were: 14 with deep venous thromboses and 2 with arterial aneurysms. Only SOD was significantly decreased (p = 0.01) in patients having LVI when compared to patients without LVI (table 1). There were any differences in MDA, SOD, catalase and GSH-PX levels when comparing patients with and without ocular; with and without neurological involvement. Conclusions SOD is decreased in patients with LVI in BS. This preliminary result deserves further investigation by other studies with larger samples. However, it probably indicates that SOD, the first line anti-oxidant enzymatic defense, has a probable role in the endothelial membrane protection against free radicals aggression in BS. References Takeno M, Kariyone AI, Yamashita N et al. Excessive functions of peripheral blood neutrophils frompatients with Behçet’s disease and from HLA B51 transgenic mice. Arthritis Rheum 1995; 3:426 –33 Harzallah O, Kerkeni A, Baati T. Oxidative stress: Correlation with Behçet’s activity and severity European Journal of Internal Medicine 2008; 19: 541– 7 Niwa Y, Miyake S, Sakane T. Autooxidative damage in Behçet’s disease-endothelial cell damage following the elevated oxygen radicals generated by stimulated neutrophils. Clin Exp Immunol 1982; 49: 247–55 Disclosure of Interest None Declared |
doi_str_mv | 10.1136/annrheumdis-2013-eular.2798 |
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The excess of FR, responsible for an oxidative stress (OS) state, could present an endothelial toxicity (3) and could be implicated in tissue lesions genesis in BS. Objectives The aim of our work was to analyze the correlation between oxidative stress biological markers and main vessels involvement in BS. Methods 40 BD patients (27 males, 13 females; mean age: 38.8 years) were prospectively enrolled in the study. Plasma malondialdehyde (MDA), erythrocyte superoxide dismutase (SOD), catalase and glutathione peroxidase (GSH-PX) were analyzed. Levels of these parameters were compared between patients having or not neurological (NI), ocular (OI) and large vascular involvement (LVI). Results There were 16 patients with large vessels involvement (LVI), 10 with neurological involvement and 13 having Behçet’s eye disease. Patients with LVI were: 14 with deep venous thromboses and 2 with arterial aneurysms. Only SOD was significantly decreased (p = 0.01) in patients having LVI when compared to patients without LVI (table 1). There were any differences in MDA, SOD, catalase and GSH-PX levels when comparing patients with and without ocular; with and without neurological involvement. Conclusions SOD is decreased in patients with LVI in BS. This preliminary result deserves further investigation by other studies with larger samples. However, it probably indicates that SOD, the first line anti-oxidant enzymatic defense, has a probable role in the endothelial membrane protection against free radicals aggression in BS. References Takeno M, Kariyone AI, Yamashita N et al. Excessive functions of peripheral blood neutrophils frompatients with Behçet’s disease and from HLA B51 transgenic mice. Arthritis Rheum 1995; 3:426 –33 Harzallah O, Kerkeni A, Baati T. Oxidative stress: Correlation with Behçet’s activity and severity European Journal of Internal Medicine 2008; 19: 541– 7 Niwa Y, Miyake S, Sakane T. Autooxidative damage in Behçet’s disease-endothelial cell damage following the elevated oxygen radicals generated by stimulated neutrophils. Clin Exp Immunol 1982; 49: 247–55 Disclosure of Interest None Declared</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2013-eular.2798</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and European League Against Rheumatism</publisher><ispartof>Annals of the rheumatic diseases, 2013-06, Vol.72 (Suppl 3), p.A934-A934</ispartof><rights>2013, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>Copyright: 2013 (c) 2013, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://ard.bmj.com/content/72/Suppl_3/A934.3.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/72/Suppl_3/A934.3.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,315,782,786,3200,23580,27933,27934,77610,77641</link.rule.ids></links><search><creatorcontrib>Harzallah, O.</creatorcontrib><creatorcontrib>Klii, R.</creatorcontrib><creatorcontrib>Brahem, D.</creatorcontrib><creatorcontrib>Kechida, M.</creatorcontrib><creatorcontrib>Mahjoub, S.</creatorcontrib><title>AB0476 Superoxide dismutase is associated to large vessels involvement in behcet syndrome</title><title>Annals of the rheumatic diseases</title><addtitle>Ann Rheum Dis</addtitle><description>Background In Behçet’s Syndrome (BS), all polymorphonuclear cells (PMN) capacities are enhanced: chemoattraction, phagocytosis and free radicals (FR) production (1, 2). The excess of FR, responsible for an oxidative stress (OS) state, could present an endothelial toxicity (3) and could be implicated in tissue lesions genesis in BS. Objectives The aim of our work was to analyze the correlation between oxidative stress biological markers and main vessels involvement in BS. Methods 40 BD patients (27 males, 13 females; mean age: 38.8 years) were prospectively enrolled in the study. Plasma malondialdehyde (MDA), erythrocyte superoxide dismutase (SOD), catalase and glutathione peroxidase (GSH-PX) were analyzed. Levels of these parameters were compared between patients having or not neurological (NI), ocular (OI) and large vascular involvement (LVI). Results There were 16 patients with large vessels involvement (LVI), 10 with neurological involvement and 13 having Behçet’s eye disease. Patients with LVI were: 14 with deep venous thromboses and 2 with arterial aneurysms. Only SOD was significantly decreased (p = 0.01) in patients having LVI when compared to patients without LVI (table 1). There were any differences in MDA, SOD, catalase and GSH-PX levels when comparing patients with and without ocular; with and without neurological involvement. Conclusions SOD is decreased in patients with LVI in BS. This preliminary result deserves further investigation by other studies with larger samples. However, it probably indicates that SOD, the first line anti-oxidant enzymatic defense, has a probable role in the endothelial membrane protection against free radicals aggression in BS. References Takeno M, Kariyone AI, Yamashita N et al. Excessive functions of peripheral blood neutrophils frompatients with Behçet’s disease and from HLA B51 transgenic mice. Arthritis Rheum 1995; 3:426 –33 Harzallah O, Kerkeni A, Baati T. Oxidative stress: Correlation with Behçet’s activity and severity European Journal of Internal Medicine 2008; 19: 541– 7 Niwa Y, Miyake S, Sakane T. Autooxidative damage in Behçet’s disease-endothelial cell damage following the elevated oxygen radicals generated by stimulated neutrophils. Clin Exp Immunol 1982; 49: 247–55 Disclosure of Interest None Declared</description><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqVkLtOwzAUhi0EEqXwDpY6B-w4sRMxlUABqSoDl6EMlhOf0JRcip1U7cbCi_IkuAQhViZf9P3_OfoQGlFySinjZ6quzQK6ShfW8wllHnSlMqe-iKM9NKABj9w3J_toQAhhXhBzcYiOrF26J4loNEDP4wsSCP75_nHfrcA0m0IDdnVV1yoLuLBYWdtkhWpB47bBrv4F8BqshdLiol435RoqqFt3xyksMmix3dbaNBUco4NclRZOfs4hepxcPSQ33vTu-jYZT72U8pB4OYjQz6JIpZS5tXwVRz4B0IrRUBMRsjBwAFE8VyTytc8CpWPOmIAghDDQbIhGfe_KNG8d2FYum87UbqSkQoiYBpQTR533VGYaaw3kcmWKSpmtpETubMo_NuXOpvy2KXc2Xdrr04VtYfMbVeZVcsFEKGdPiSTzWTzxL-cycTzv-bRa_mvQF0MqkHQ</recordid><startdate>201306</startdate><enddate>201306</enddate><creator>Harzallah, O.</creator><creator>Klii, R.</creator><creator>Brahem, D.</creator><creator>Kechida, M.</creator><creator>Mahjoub, S.</creator><general>BMJ Publishing Group Ltd and European League Against Rheumatism</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>201306</creationdate><title>AB0476 Superoxide dismutase is associated to large vessels involvement in behcet syndrome</title><author>Harzallah, O. ; Klii, R. ; Brahem, D. ; Kechida, M. ; Mahjoub, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1650-fe752c88ab130002a9820eeda315d0753547520a6fa082d234ad96337e45e54d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harzallah, O.</creatorcontrib><creatorcontrib>Klii, R.</creatorcontrib><creatorcontrib>Brahem, D.</creatorcontrib><creatorcontrib>Kechida, M.</creatorcontrib><creatorcontrib>Mahjoub, S.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Annals of the rheumatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harzallah, O.</au><au>Klii, R.</au><au>Brahem, D.</au><au>Kechida, M.</au><au>Mahjoub, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>AB0476 Superoxide dismutase is associated to large vessels involvement in behcet syndrome</atitle><jtitle>Annals of the rheumatic diseases</jtitle><addtitle>Ann Rheum Dis</addtitle><date>2013-06</date><risdate>2013</risdate><volume>72</volume><issue>Suppl 3</issue><spage>A934</spage><epage>A934</epage><pages>A934-A934</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>Background In Behçet’s Syndrome (BS), all polymorphonuclear cells (PMN) capacities are enhanced: chemoattraction, phagocytosis and free radicals (FR) production (1, 2). The excess of FR, responsible for an oxidative stress (OS) state, could present an endothelial toxicity (3) and could be implicated in tissue lesions genesis in BS. Objectives The aim of our work was to analyze the correlation between oxidative stress biological markers and main vessels involvement in BS. Methods 40 BD patients (27 males, 13 females; mean age: 38.8 years) were prospectively enrolled in the study. Plasma malondialdehyde (MDA), erythrocyte superoxide dismutase (SOD), catalase and glutathione peroxidase (GSH-PX) were analyzed. Levels of these parameters were compared between patients having or not neurological (NI), ocular (OI) and large vascular involvement (LVI). Results There were 16 patients with large vessels involvement (LVI), 10 with neurological involvement and 13 having Behçet’s eye disease. Patients with LVI were: 14 with deep venous thromboses and 2 with arterial aneurysms. Only SOD was significantly decreased (p = 0.01) in patients having LVI when compared to patients without LVI (table 1). There were any differences in MDA, SOD, catalase and GSH-PX levels when comparing patients with and without ocular; with and without neurological involvement. Conclusions SOD is decreased in patients with LVI in BS. This preliminary result deserves further investigation by other studies with larger samples. However, it probably indicates that SOD, the first line anti-oxidant enzymatic defense, has a probable role in the endothelial membrane protection against free radicals aggression in BS. References Takeno M, Kariyone AI, Yamashita N et al. Excessive functions of peripheral blood neutrophils frompatients with Behçet’s disease and from HLA B51 transgenic mice. Arthritis Rheum 1995; 3:426 –33 Harzallah O, Kerkeni A, Baati T. Oxidative stress: Correlation with Behçet’s activity and severity European Journal of Internal Medicine 2008; 19: 541– 7 Niwa Y, Miyake S, Sakane T. Autooxidative damage in Behçet’s disease-endothelial cell damage following the elevated oxygen radicals generated by stimulated neutrophils. Clin Exp Immunol 1982; 49: 247–55 Disclosure of Interest None Declared</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and European League Against Rheumatism</pub><doi>10.1136/annrheumdis-2013-eular.2798</doi></addata></record> |
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title | AB0476 Superoxide dismutase is associated to large vessels involvement in behcet syndrome |
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