Carotid artery intima–media thickness, heat shock proteins and oxidized LDL autoantibodies in systemic necrotizing vasculitis
In this study we evaluate early atherosclerotic changes and determine whether anti-HSP-60, anti-HSP-65 and anti-oxLDL autoantibodies are elevated in systemic necrotizing vasculitis. Thirty-two patients having systemic necrotizing vasculitis were compared with normal controls and patients with system...
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Veröffentlicht in: | Rheumatology international 2008-09, Vol.28 (11), p.1099-1103 |
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description | In this study we evaluate early atherosclerotic changes and determine whether anti-HSP-60, anti-HSP-65 and anti-oxLDL autoantibodies are elevated in systemic necrotizing vasculitis. Thirty-two patients having systemic necrotizing vasculitis were compared with normal controls and patients with systemic lupus erythematosus (SLE). The antibodies against human HSP-60, HSP-65 and oxLDL were measured by antihuman ELISA kit. All patients underwent non-invasive measurements of carotid artery intima–media thickness (IMT). In a comparison between carotid IMT extent between vasculitis patients and SLE, no significant differences were noted. Levels of anti-HSP-60, anti-HSP-65 IgG and anti-oxLDL autoantibodies were similar among patients compared to controls. IgM anti-HSP-60 antibody levels were significantly lower in patients compared to controls and a similar trend was found regarding IgM anti-HSP-65. As a group, patients having various necrotizing vasculitis have similar extent of early atherosclerotic changes regardless of the vasculitis type, and these levels are similar to those found in SLE. |
doi_str_mv | 10.1007/s00296-008-0587-7 |
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Thirty-two patients having systemic necrotizing vasculitis were compared with normal controls and patients with systemic lupus erythematosus (SLE). The antibodies against human HSP-60, HSP-65 and oxLDL were measured by antihuman ELISA kit. All patients underwent non-invasive measurements of carotid artery intima–media thickness (IMT). In a comparison between carotid IMT extent between vasculitis patients and SLE, no significant differences were noted. Levels of anti-HSP-60, anti-HSP-65 IgG and anti-oxLDL autoantibodies were similar among patients compared to controls. IgM anti-HSP-60 antibody levels were significantly lower in patients compared to controls and a similar trend was found regarding IgM anti-HSP-65. As a group, patients having various necrotizing vasculitis have similar extent of early atherosclerotic changes regardless of the vasculitis type, and these levels are similar to those found in SLE.</description><identifier>ISSN: 0172-8172</identifier><identifier>EISSN: 1437-160X</identifier><identifier>DOI: 10.1007/s00296-008-0587-7</identifier><identifier>PMID: 18443794</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Adult ; Aged ; Autoantibodies - blood ; Autoimmune diseases ; Carotid Artery, Common - pathology ; Case-Control Studies ; Chaperonin 60 - immunology ; Female ; Heat-Shock Proteins - immunology ; Humans ; Immunoglobulin M ; Lipoproteins, LDL - immunology ; Lupus Erythematosus, Systemic ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Original Article ; Proteins ; Rheumatology ; Tunica Intima - pathology ; Tunica Media - pathology ; Vasculitis - immunology ; Vasculitis - pathology</subject><ispartof>Rheumatology international, 2008-09, Vol.28 (11), p.1099-1103</ispartof><rights>Springer-Verlag 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-170278faa7673e866522b56f7a9d8ef44da4878b8dfecdf0d75443bd893898763</citedby><cites>FETCH-LOGICAL-c369t-170278faa7673e866522b56f7a9d8ef44da4878b8dfecdf0d75443bd893898763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00296-008-0587-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00296-008-0587-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18443794$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sherer, Yaniv</creatorcontrib><creatorcontrib>Pagnoux, Christian</creatorcontrib><creatorcontrib>Chironi, Gilles</creatorcontrib><creatorcontrib>Simon, Alain</creatorcontrib><creatorcontrib>Guillevin, Loïc</creatorcontrib><creatorcontrib>Mouthon, Luc</creatorcontrib><creatorcontrib>Gilburd, Boris</creatorcontrib><creatorcontrib>Shoenfeld, Yehuda</creatorcontrib><title>Carotid artery intima–media thickness, heat shock proteins and oxidized LDL autoantibodies in systemic necrotizing vasculitis</title><title>Rheumatology international</title><addtitle>Rheumatol Int</addtitle><addtitle>Rheumatol Int</addtitle><description>In this study we evaluate early atherosclerotic changes and determine whether anti-HSP-60, anti-HSP-65 and anti-oxLDL autoantibodies are elevated in systemic necrotizing vasculitis. 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As a group, patients having various necrotizing vasculitis have similar extent of early atherosclerotic changes regardless of the vasculitis type, and these levels are similar to those found in SLE.</description><subject>Adult</subject><subject>Aged</subject><subject>Autoantibodies - blood</subject><subject>Autoimmune diseases</subject><subject>Carotid Artery, Common - pathology</subject><subject>Case-Control Studies</subject><subject>Chaperonin 60 - immunology</subject><subject>Female</subject><subject>Heat-Shock Proteins - immunology</subject><subject>Humans</subject><subject>Immunoglobulin M</subject><subject>Lipoproteins, LDL - immunology</subject><subject>Lupus Erythematosus, Systemic</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Original Article</subject><subject>Proteins</subject><subject>Rheumatology</subject><subject>Tunica Intima - pathology</subject><subject>Tunica Media - pathology</subject><subject>Vasculitis - immunology</subject><subject>Vasculitis - pathology</subject><issn>0172-8172</issn><issn>1437-160X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kc1q3DAUhUVJaKZpHyCbILroqm4lW5bkZZj-wkA2DWQnZOs6o2RGTnzl0MmmfYe8YZ6kd5iBQCEbCaHvnPtzGDuR4pMUwnxGIcpGF0LYQtTWFOYVm0lVmUJqcXnAZkKasrB0HLE3iNeC3lqL1-xIWkVYo2bsz9yPQ46B-zHDuOEx5bj2T38f1xCi53kZu5sEiB_5EnzmuBy6G35LEogJuU-BD79jiA8Q-OLLgvspD54s2iFEQHLjuMEM69jxBN220kNMV_zeYzetYo74lh32foXwbn8fs4tvX3_NfxSL8-8_52eLoqt0kwtpRGls773RpgKrdV2Wba1745tgoVcqeGWNbW3ooQu9CKamCdtgm8o21ujqmH3Y-VLvdxNgduuIHaxWPsEwodONKpVQksD3_4HXwzQm6s1Zq2RpRK0IkjuIRkIcoXe3I61t3Dgp3DYat4vGUTRuG40zpDndG08tLfdZsc-CgHIHIH2lKxifK7_s-g_X55yE</recordid><startdate>20080901</startdate><enddate>20080901</enddate><creator>Sherer, Yaniv</creator><creator>Pagnoux, Christian</creator><creator>Chironi, Gilles</creator><creator>Simon, Alain</creator><creator>Guillevin, Loïc</creator><creator>Mouthon, Luc</creator><creator>Gilburd, Boris</creator><creator>Shoenfeld, Yehuda</creator><general>Springer-Verlag</general><general>Springer Nature 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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20080901</creationdate><title>Carotid artery intima–media thickness, heat shock proteins and oxidized LDL autoantibodies in systemic necrotizing vasculitis</title><author>Sherer, Yaniv ; 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Thirty-two patients having systemic necrotizing vasculitis were compared with normal controls and patients with systemic lupus erythematosus (SLE). The antibodies against human HSP-60, HSP-65 and oxLDL were measured by antihuman ELISA kit. All patients underwent non-invasive measurements of carotid artery intima–media thickness (IMT). In a comparison between carotid IMT extent between vasculitis patients and SLE, no significant differences were noted. Levels of anti-HSP-60, anti-HSP-65 IgG and anti-oxLDL autoantibodies were similar among patients compared to controls. IgM anti-HSP-60 antibody levels were significantly lower in patients compared to controls and a similar trend was found regarding IgM anti-HSP-65. As a group, patients having various necrotizing vasculitis have similar extent of early atherosclerotic changes regardless of the vasculitis type, and these levels are similar to those found in SLE.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>18443794</pmid><doi>10.1007/s00296-008-0587-7</doi><tpages>5</tpages></addata></record> |
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subjects | Adult Aged Autoantibodies - blood Autoimmune diseases Carotid Artery, Common - pathology Case-Control Studies Chaperonin 60 - immunology Female Heat-Shock Proteins - immunology Humans Immunoglobulin M Lipoproteins, LDL - immunology Lupus Erythematosus, Systemic Male Medicine Medicine & Public Health Middle Aged Original Article Proteins Rheumatology Tunica Intima - pathology Tunica Media - pathology Vasculitis - immunology Vasculitis - pathology |
title | Carotid artery intima–media thickness, heat shock proteins and oxidized LDL autoantibodies in systemic necrotizing vasculitis |
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