AB0231 Elevation of Serum Matrix Metalloproteinase-3 in A Group of Rheumatoid Arthritis Algerian Patients
Background Matrix metalloproteinase-3 (MMP-3) is a protease induced by inflammatory cytokines in rheumatoid synovium and degrades a number of extracellular matrix components of cartilage and bone. Its central role in rheumatoid joint destruction was especially highlighted from both pathophysiologica...
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description | Background Matrix metalloproteinase-3 (MMP-3) is a protease induced by inflammatory cytokines in rheumatoid synovium and degrades a number of extracellular matrix components of cartilage and bone. Its central role in rheumatoid joint destruction was especially highlighted from both pathophysiological and clinical studies. In addition, serum MMP-3 level is a clinically useful maker for predicting joint destruction and for disease activity in rheumatoid arthritis (RA). Objectives The aim of our study is to evaluate the serum matrix metalloproteinase 3 (MMP-3) levels in a group of algerian patients with early and advanced rheumatoid arthritis (RA) compared to healthy subjects. Methods The study group consisted of 50 patients with RA, including 81.6% women, mean age 45,0±15,0 years, mean duration 4,3±4,2 years, Forty healthy subjects served as a control group (71.4% women, mean age 33,0±13,0 years). Analysis of serum concentrations of MMP-3 was based on a quantitative sandwich ELISA (Aeskulisa DF MMP-3, Aesku.Diagnostics, Wendelsheim, Germany). A cut-off point of 120 ng/ml (men) and 60 ng/ml (women) was used for MMP-3 positive/negative categorization. Results First of all, 61,3% of patients were rheumatoid factor (RF)-positive and 93,8% anti-CCP positive. MMP-3 is significantly higher in sera of RA patients (Mean value: 175,8±178,2 ng/ml) than in those of control group (Mean value: 23,0±17,8 ng/ml) (p |
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Its central role in rheumatoid joint destruction was especially highlighted from both pathophysiological and clinical studies. In addition, serum MMP-3 level is a clinically useful maker for predicting joint destruction and for disease activity in rheumatoid arthritis (RA). Objectives The aim of our study is to evaluate the serum matrix metalloproteinase 3 (MMP-3) levels in a group of algerian patients with early and advanced rheumatoid arthritis (RA) compared to healthy subjects. Methods The study group consisted of 50 patients with RA, including 81.6% women, mean age 45,0±15,0 years, mean duration 4,3±4,2 years, Forty healthy subjects served as a control group (71.4% women, mean age 33,0±13,0 years). Analysis of serum concentrations of MMP-3 was based on a quantitative sandwich ELISA (Aeskulisa DF MMP-3, Aesku.Diagnostics, Wendelsheim, Germany). A cut-off point of 120 ng/ml (men) and 60 ng/ml (women) was used for MMP-3 positive/negative categorization. Results First of all, 61,3% of patients were rheumatoid factor (RF)-positive and 93,8% anti-CCP positive. MMP-3 is significantly higher in sera of RA patients (Mean value: 175,8±178,2 ng/ml) than in those of control group (Mean value: 23,0±17,8 ng/ml) (p<0,001). The mean value in female and male patients was 161,9±174,7 ng/ml and 237,6±203,8 ng/ml respectively. Further, MMP-3 is higher (188,1±183,7 ng/ml) in sera of patients with early (<2 years duration) than advanced disease (between 3 and 8 years duration) (Mean value: 154,0±153,1 ng/ml) (p<0,05). Interestingly, there is no statistically significant difference between RF-positive patients and RF-negative patients concerning MMP-3 concentration (180,2±196,6 ng/ml vs. 183,3±201,4 ng/ml respectively). Conclusions In conclusion, patients with RA are characterized by high serum concentrations of MMP-3, particularly in early stages for both female and male affected patients regardless for RF positiviy. Serum concentration of MMP-3 is a useful marker of inflammation in the early stage of RA. References Tchetverikov,I. et al. (2003) Matrix metalloproteinases-3, -8, -9 as markers of disease activity and joint damage progression in early rheumatoid arthritis. Ann. Rheum. Dis. 62, 1094-1099. Shinozaki,M. et al. (2007) Elevation of serum matrix metalloproteinase-3 as a predictive marker for the long-term disability of rheumatoid arthritis patients in a prospective observational cohort IORRA. Mod. Rheumatol. 17, 403-408. Fiedorczyk,M. et al. (2006) Serum matrix metalloproteinases and tissue inhibitors of metalloproteinases in patients with early rheumatoid arthritis. J. Rheumatol. 33, 1523-1529. Disclosure of Interest None declared DOI 10.1136/annrheumdis-2014-eular.6019</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2014-eular.6019</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><ispartof>Annals of the rheumatic diseases, 2014-06, Vol.73 (Suppl 2), p.880-880</ispartof><rights>2014, 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: 2014 (c) 2014, 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/73/Suppl_2/880.1.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/73/Suppl_2/880.1.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,780,784,3196,23571,27924,27925,77600,77631</link.rule.ids></links><search><creatorcontrib>Fodil, D.</creatorcontrib><creatorcontrib>Salah, S.S.</creatorcontrib><creatorcontrib>Benidir, M.</creatorcontrib><creatorcontrib>Adjabi, S.</creatorcontrib><creatorcontrib>Abbadi, M.C.</creatorcontrib><creatorcontrib>Attal, N.</creatorcontrib><creatorcontrib>Bayou, M.</creatorcontrib><creatorcontrib>Mostefai, S.</creatorcontrib><title>AB0231 Elevation of Serum Matrix Metalloproteinase-3 in A Group of Rheumatoid Arthritis Algerian Patients</title><title>Annals of the rheumatic diseases</title><description>Background Matrix metalloproteinase-3 (MMP-3) is a protease induced by inflammatory cytokines in rheumatoid synovium and degrades a number of extracellular matrix components of cartilage and bone. Its central role in rheumatoid joint destruction was especially highlighted from both pathophysiological and clinical studies. In addition, serum MMP-3 level is a clinically useful maker for predicting joint destruction and for disease activity in rheumatoid arthritis (RA). Objectives The aim of our study is to evaluate the serum matrix metalloproteinase 3 (MMP-3) levels in a group of algerian patients with early and advanced rheumatoid arthritis (RA) compared to healthy subjects. Methods The study group consisted of 50 patients with RA, including 81.6% women, mean age 45,0±15,0 years, mean duration 4,3±4,2 years, Forty healthy subjects served as a control group (71.4% women, mean age 33,0±13,0 years). Analysis of serum concentrations of MMP-3 was based on a quantitative sandwich ELISA (Aeskulisa DF MMP-3, Aesku.Diagnostics, Wendelsheim, Germany). A cut-off point of 120 ng/ml (men) and 60 ng/ml (women) was used for MMP-3 positive/negative categorization. Results First of all, 61,3% of patients were rheumatoid factor (RF)-positive and 93,8% anti-CCP positive. MMP-3 is significantly higher in sera of RA patients (Mean value: 175,8±178,2 ng/ml) than in those of control group (Mean value: 23,0±17,8 ng/ml) (p<0,001). The mean value in female and male patients was 161,9±174,7 ng/ml and 237,6±203,8 ng/ml respectively. Further, MMP-3 is higher (188,1±183,7 ng/ml) in sera of patients with early (<2 years duration) than advanced disease (between 3 and 8 years duration) (Mean value: 154,0±153,1 ng/ml) (p<0,05). Interestingly, there is no statistically significant difference between RF-positive patients and RF-negative patients concerning MMP-3 concentration (180,2±196,6 ng/ml vs. 183,3±201,4 ng/ml respectively). Conclusions In conclusion, patients with RA are characterized by high serum concentrations of MMP-3, particularly in early stages for both female and male affected patients regardless for RF positiviy. Serum concentration of MMP-3 is a useful marker of inflammation in the early stage of RA. References Tchetverikov,I. et al. (2003) Matrix metalloproteinases-3, -8, -9 as markers of disease activity and joint damage progression in early rheumatoid arthritis. Ann. Rheum. Dis. 62, 1094-1099. Shinozaki,M. et al. (2007) Elevation of serum matrix metalloproteinase-3 as a predictive marker for the long-term disability of rheumatoid arthritis patients in a prospective observational cohort IORRA. Mod. Rheumatol. 17, 403-408. Fiedorczyk,M. et al. (2006) Serum matrix metalloproteinases and tissue inhibitors of metalloproteinases in patients with early rheumatoid arthritis. J. Rheumatol. 33, 1523-1529. Disclosure of Interest None declared DOI 10.1136/annrheumdis-2014-eular.6019</description><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</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>eNqVkM1OwzAQhC0EEqXwDpZ6TrET10nEKVRQkFqB-DlbTrKhLoldbAfBjQsvypPgUA5cOa12NTM7-hCaUDKlNOGnUmu7hr6rlYtiQlkEfSvtlBOa76ERZTwLZ0720YgQkkQs5-khOnJuE1aS0WyEnotzEif06-PzooVX6ZXR2DT4Hmzf4ZX0Vr3hFXjZtmZrjQelpYMowUrjAi-s6beD_G4oIb1RNS6sX1vllcNF-wRWSY1vQyxo747RQSNbBye_c4weLy8e5lfR8mZxPS-WUUnjNI8kr-s6zipGJSd1VZOkCpcYKhIzzqtSSplxAF4mPGNAZpWccVrRGYtT3lBWJmM02eWGxi89OC82prc6vBQ0TdM8pZzlQXW2U1XWOGehEVurOmnfBSVioCv-0BUDXfFDVwx0g5vv3GW3-ZfxG4oqh2g</recordid><startdate>201406</startdate><enddate>201406</enddate><creator>Fodil, D.</creator><creator>Salah, S.S.</creator><creator>Benidir, M.</creator><creator>Adjabi, S.</creator><creator>Abbadi, M.C.</creator><creator>Attal, N.</creator><creator>Bayou, M.</creator><creator>Mostefai, S.</creator><general>BMJ Publishing Group LTD</general><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>201406</creationdate><title>AB0231 Elevation of Serum Matrix Metalloproteinase-3 in A Group of Rheumatoid Arthritis Algerian Patients</title><author>Fodil, D. ; Salah, S.S. ; Benidir, M. ; Adjabi, S. ; Abbadi, M.C. ; Attal, N. ; Bayou, M. ; Mostefai, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1279-a6ddd28c41a60dcd03c6dd2ec02466cbaaa86ee6b3684e05ca561c154276f14b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fodil, D.</creatorcontrib><creatorcontrib>Salah, S.S.</creatorcontrib><creatorcontrib>Benidir, M.</creatorcontrib><creatorcontrib>Adjabi, S.</creatorcontrib><creatorcontrib>Abbadi, M.C.</creatorcontrib><creatorcontrib>Attal, N.</creatorcontrib><creatorcontrib>Bayou, M.</creatorcontrib><creatorcontrib>Mostefai, S.</creatorcontrib><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>Fodil, D.</au><au>Salah, S.S.</au><au>Benidir, M.</au><au>Adjabi, S.</au><au>Abbadi, M.C.</au><au>Attal, N.</au><au>Bayou, M.</au><au>Mostefai, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>AB0231 Elevation of Serum Matrix Metalloproteinase-3 in A Group of Rheumatoid Arthritis Algerian Patients</atitle><jtitle>Annals of the rheumatic diseases</jtitle><date>2014-06</date><risdate>2014</risdate><volume>73</volume><issue>Suppl 2</issue><spage>880</spage><epage>880</epage><pages>880-880</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>Background Matrix metalloproteinase-3 (MMP-3) is a protease induced by inflammatory cytokines in rheumatoid synovium and degrades a number of extracellular matrix components of cartilage and bone. Its central role in rheumatoid joint destruction was especially highlighted from both pathophysiological and clinical studies. In addition, serum MMP-3 level is a clinically useful maker for predicting joint destruction and for disease activity in rheumatoid arthritis (RA). Objectives The aim of our study is to evaluate the serum matrix metalloproteinase 3 (MMP-3) levels in a group of algerian patients with early and advanced rheumatoid arthritis (RA) compared to healthy subjects. Methods The study group consisted of 50 patients with RA, including 81.6% women, mean age 45,0±15,0 years, mean duration 4,3±4,2 years, Forty healthy subjects served as a control group (71.4% women, mean age 33,0±13,0 years). Analysis of serum concentrations of MMP-3 was based on a quantitative sandwich ELISA (Aeskulisa DF MMP-3, Aesku.Diagnostics, Wendelsheim, Germany). A cut-off point of 120 ng/ml (men) and 60 ng/ml (women) was used for MMP-3 positive/negative categorization. Results First of all, 61,3% of patients were rheumatoid factor (RF)-positive and 93,8% anti-CCP positive. MMP-3 is significantly higher in sera of RA patients (Mean value: 175,8±178,2 ng/ml) than in those of control group (Mean value: 23,0±17,8 ng/ml) (p<0,001). The mean value in female and male patients was 161,9±174,7 ng/ml and 237,6±203,8 ng/ml respectively. Further, MMP-3 is higher (188,1±183,7 ng/ml) in sera of patients with early (<2 years duration) than advanced disease (between 3 and 8 years duration) (Mean value: 154,0±153,1 ng/ml) (p<0,05). Interestingly, there is no statistically significant difference between RF-positive patients and RF-negative patients concerning MMP-3 concentration (180,2±196,6 ng/ml vs. 183,3±201,4 ng/ml respectively). Conclusions In conclusion, patients with RA are characterized by high serum concentrations of MMP-3, particularly in early stages for both female and male affected patients regardless for RF positiviy. Serum concentration of MMP-3 is a useful marker of inflammation in the early stage of RA. References Tchetverikov,I. et al. (2003) Matrix metalloproteinases-3, -8, -9 as markers of disease activity and joint damage progression in early rheumatoid arthritis. Ann. Rheum. Dis. 62, 1094-1099. Shinozaki,M. et al. (2007) Elevation of serum matrix metalloproteinase-3 as a predictive marker for the long-term disability of rheumatoid arthritis patients in a prospective observational cohort IORRA. Mod. Rheumatol. 17, 403-408. Fiedorczyk,M. et al. (2006) Serum matrix metalloproteinases and tissue inhibitors of metalloproteinases in patients with early rheumatoid arthritis. J. Rheumatol. 33, 1523-1529. Disclosure of Interest None declared DOI 10.1136/annrheumdis-2014-eular.6019</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/annrheumdis-2014-eular.6019</doi><tpages>1</tpages></addata></record> |
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