OP0178 Antibodies against Carbamylated Proteins (ANTI-CARP), A New Type of Autoantibody, in Spanish Patients with Rheumatoid Arthritis
Background Antibodies against carbamylated proteins (anti-CarP) are a new type of autoantibodies present in sera of patients with rheumatoid arthritis (RA). These antibodies, measured as the reactivity against carmabylated proteins from Fetal Calf Serum (FCS), do not show cross-reactivity with anti-...
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description | Background Antibodies against carbamylated proteins (anti-CarP) are a new type of autoantibodies present in sera of patients with rheumatoid arthritis (RA). These antibodies, measured as the reactivity against carmabylated proteins from Fetal Calf Serum (FCS), do not show cross-reactivity with anti-CCP antibodies, and are associated with radiologic progression both in anti-CCP+ and in anti-CCP– patients [1]. Objectives The aim of this study was to explore the presence of anti-CarP-FCS antibodies in our collection of patients with RA and their association with clinical and genetic characteristics of the disease. Methods Carbamylation of FCS proteins was performed as previously described [1]. IgG antibodies against carbamylated FCS were measured by ELISA in sera from 520 RA patients fulfilling 1987 ACR criteria and from 208 healthy donors. Anti-CarP FCS titre was obtained after subtracting reactivity to native FCS from the reactivity to carbamylated FCS. The cut-of for positivity was set as the mean ±2 SD of healthy donors. Association of anti-CarP-FCS with the presence of erosive arthritis, rheumatoid factor (RF), HLADRB1 alleles and the R620W SNP of PTPN22 was analyzed by logistic regression. The relationship between the titre of anti-CarP-FCS and anti-CCP was analyzed with Spearman correlation and the concordance between positivity of anti-CarP-FCS, anti-CCP and RF with the gamma coefficient. Results Anti-CarP-FCS antibodies were found in 36.1% (188/520) of the patients with RA, including 45.0% of the anti-CCP+ patients and 19.9% of the anti-CCP– patients. Presence and titres of anti-CarP-FCS and anti-CCP antibodies were significantly correlated (g =0.53, P=1.6×10-17 for status concordance, and r=0.27, P=2.1×10-10 for antibody titres, respectively). However, no association was found between anti-CarP-FCS and the risk alleles of HLADRB1 and PTPN22. Anti-CarP-FCS status showed also a significant association with RF status (OR=3.4, P=1.6×10-8) that remained after accounting for anti-CCP status (OR=2.2, P=0.001). In addition, we replicated the association of erosive arthritis with anti-CarP-FCS antibodies (OR=2.3, P=1.4×10-4) even accounting for the presence of anti-CCP (OR=1.6, P=0.026) Conclusions We have confirmed the presence of anti-CarP-FCS antibodies in RA patients (both anti-CCP+ and anti-CCP– patients) and their association with erosive arthritis as previously described in Dutch patients with RA. These associations indicate the interest of the anti-C |
doi_str_mv | 10.1136/annrheumdis-2014-eular.5427 |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1777976024</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4008685421</sourcerecordid><originalsourceid>FETCH-LOGICAL-b1854-ff0cd04fff306bec3c5487da0b48f4f1a359a5ebde6c6c908512a50e340334383</originalsourceid><addsrcrecordid>eNqVkM1KAzEUhYMoWH_eIeBGwdGbJpNJcTUU_6BoqXUd7swkNqWdqUkG6c6N4HP6JE6tC7euLvdwzrmXj5ATBheMcXmJde1npl1WLiR9YCIx7QL9RSr62Q7pMSFVJ0vYJT0A4IkYyGyfHIQw71ZQTPXI5-MYWKa-3j_yOrqiqZwJFF_Q1SHSIfoCl-sFRlPRsW-i6WR6mj9M75NhPhmfndOcPpg3Ol2vDG0szdvY4LZnfU5dTZ9WWLswo2OMztQx0DcXZ3Sy-Rlj4yqa-zjzLrpwRPYsLoI5_p2H5Pnmejq8S0aPt_fDfJQUTKUisRbKCoS1loMsTMnLVKisQiiEssIy5OkAU1NURpayHIBKWR9TMFwA54IrfkhOtr0r37y2JkQ9b1pfdyc1y7JskEnoi851tXWVvgnBG6tX3i3RrzUDvUGv_6DXG_T6B73eoO_ScpsulvN_Bb8B0zuQow</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1777976024</pqid></control><display><type>article</type><title>OP0178 Antibodies against Carbamylated Proteins (ANTI-CARP), A New Type of Autoantibody, in Spanish Patients with Rheumatoid Arthritis</title><source>BMJ Journals - NESLi2</source><creator>Montes, A. ; Perez-Pampín, E. ; Bόveda, M.D. ; Gόmez-Reino, J.J. ; González, A.</creator><creatorcontrib>Montes, A. ; Perez-Pampín, E. ; Bόveda, M.D. ; Gόmez-Reino, J.J. ; González, A.</creatorcontrib><description>Background Antibodies against carbamylated proteins (anti-CarP) are a new type of autoantibodies present in sera of patients with rheumatoid arthritis (RA). These antibodies, measured as the reactivity against carmabylated proteins from Fetal Calf Serum (FCS), do not show cross-reactivity with anti-CCP antibodies, and are associated with radiologic progression both in anti-CCP+ and in anti-CCP– patients [1]. Objectives The aim of this study was to explore the presence of anti-CarP-FCS antibodies in our collection of patients with RA and their association with clinical and genetic characteristics of the disease. Methods Carbamylation of FCS proteins was performed as previously described [1]. IgG antibodies against carbamylated FCS were measured by ELISA in sera from 520 RA patients fulfilling 1987 ACR criteria and from 208 healthy donors. Anti-CarP FCS titre was obtained after subtracting reactivity to native FCS from the reactivity to carbamylated FCS. The cut-of for positivity was set as the mean ±2 SD of healthy donors. Association of anti-CarP-FCS with the presence of erosive arthritis, rheumatoid factor (RF), HLADRB1 alleles and the R620W SNP of PTPN22 was analyzed by logistic regression. The relationship between the titre of anti-CarP-FCS and anti-CCP was analyzed with Spearman correlation and the concordance between positivity of anti-CarP-FCS, anti-CCP and RF with the gamma coefficient. Results Anti-CarP-FCS antibodies were found in 36.1% (188/520) of the patients with RA, including 45.0% of the anti-CCP+ patients and 19.9% of the anti-CCP– patients. Presence and titres of anti-CarP-FCS and anti-CCP antibodies were significantly correlated (g =0.53, P=1.6×10-17 for status concordance, and r=0.27, P=2.1×10-10 for antibody titres, respectively). However, no association was found between anti-CarP-FCS and the risk alleles of HLADRB1 and PTPN22. Anti-CarP-FCS status showed also a significant association with RF status (OR=3.4, P=1.6×10-8) that remained after accounting for anti-CCP status (OR=2.2, P=0.001). In addition, we replicated the association of erosive arthritis with anti-CarP-FCS antibodies (OR=2.3, P=1.4×10-4) even accounting for the presence of anti-CCP (OR=1.6, P=0.026) Conclusions We have confirmed the presence of anti-CarP-FCS antibodies in RA patients (both anti-CCP+ and anti-CCP– patients) and their association with erosive arthritis as previously described in Dutch patients with RA. These associations indicate the interest of the anti-CarP antibodies in RA. In addition, our finding of lack of association of these antibodies with genetic risk factors for anti-CCP+ RA indicates that this is an independent autoantibody system in RA. We need to further study these antibodies to know if they define a new subgroup of patients with RA. References Shi J et al. Autoantibodies recognizing carbamylated proteins are present in sera of patients with rheumatoid arthritis and predict joint damage. Proc Natl Acad 108:17372-7. Disclosure of Interest None declared DOI 10.1136/annrheumdis-2014-eular.5427</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2014-eular.5427</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>Kidlington: Elsevier Limited</publisher><ispartof>Annals of the rheumatic diseases, 2014-06, Vol.73 (Suppl 2), p.129</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><citedby>FETCH-LOGICAL-b1854-ff0cd04fff306bec3c5487da0b48f4f1a359a5ebde6c6c908512a50e340334383</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://ard.bmj.com/content/73/Suppl_2/129.3.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/73/Suppl_2/129.3.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,776,780,3183,23550,27901,27902,77343,77374</link.rule.ids></links><search><creatorcontrib>Montes, A.</creatorcontrib><creatorcontrib>Perez-Pampín, E.</creatorcontrib><creatorcontrib>Bόveda, M.D.</creatorcontrib><creatorcontrib>Gόmez-Reino, J.J.</creatorcontrib><creatorcontrib>González, A.</creatorcontrib><title>OP0178 Antibodies against Carbamylated Proteins (ANTI-CARP), A New Type of Autoantibody, in Spanish Patients with Rheumatoid Arthritis</title><title>Annals of the rheumatic diseases</title><description>Background Antibodies against carbamylated proteins (anti-CarP) are a new type of autoantibodies present in sera of patients with rheumatoid arthritis (RA). These antibodies, measured as the reactivity against carmabylated proteins from Fetal Calf Serum (FCS), do not show cross-reactivity with anti-CCP antibodies, and are associated with radiologic progression both in anti-CCP+ and in anti-CCP– patients [1]. Objectives The aim of this study was to explore the presence of anti-CarP-FCS antibodies in our collection of patients with RA and their association with clinical and genetic characteristics of the disease. Methods Carbamylation of FCS proteins was performed as previously described [1]. IgG antibodies against carbamylated FCS were measured by ELISA in sera from 520 RA patients fulfilling 1987 ACR criteria and from 208 healthy donors. Anti-CarP FCS titre was obtained after subtracting reactivity to native FCS from the reactivity to carbamylated FCS. The cut-of for positivity was set as the mean ±2 SD of healthy donors. Association of anti-CarP-FCS with the presence of erosive arthritis, rheumatoid factor (RF), HLADRB1 alleles and the R620W SNP of PTPN22 was analyzed by logistic regression. The relationship between the titre of anti-CarP-FCS and anti-CCP was analyzed with Spearman correlation and the concordance between positivity of anti-CarP-FCS, anti-CCP and RF with the gamma coefficient. Results Anti-CarP-FCS antibodies were found in 36.1% (188/520) of the patients with RA, including 45.0% of the anti-CCP+ patients and 19.9% of the anti-CCP– patients. Presence and titres of anti-CarP-FCS and anti-CCP antibodies were significantly correlated (g =0.53, P=1.6×10-17 for status concordance, and r=0.27, P=2.1×10-10 for antibody titres, respectively). However, no association was found between anti-CarP-FCS and the risk alleles of HLADRB1 and PTPN22. Anti-CarP-FCS status showed also a significant association with RF status (OR=3.4, P=1.6×10-8) that remained after accounting for anti-CCP status (OR=2.2, P=0.001). In addition, we replicated the association of erosive arthritis with anti-CarP-FCS antibodies (OR=2.3, P=1.4×10-4) even accounting for the presence of anti-CCP (OR=1.6, P=0.026) Conclusions We have confirmed the presence of anti-CarP-FCS antibodies in RA patients (both anti-CCP+ and anti-CCP– patients) and their association with erosive arthritis as previously described in Dutch patients with RA. These associations indicate the interest of the anti-CarP antibodies in RA. In addition, our finding of lack of association of these antibodies with genetic risk factors for anti-CCP+ RA indicates that this is an independent autoantibody system in RA. We need to further study these antibodies to know if they define a new subgroup of patients with RA. References Shi J et al. Autoantibodies recognizing carbamylated proteins are present in sera of patients with rheumatoid arthritis and predict joint damage. Proc Natl Acad 108:17372-7. Disclosure of Interest None declared DOI 10.1136/annrheumdis-2014-eular.5427</description><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqVkM1KAzEUhYMoWH_eIeBGwdGbJpNJcTUU_6BoqXUd7swkNqWdqUkG6c6N4HP6JE6tC7euLvdwzrmXj5ATBheMcXmJde1npl1WLiR9YCIx7QL9RSr62Q7pMSFVJ0vYJT0A4IkYyGyfHIQw71ZQTPXI5-MYWKa-3j_yOrqiqZwJFF_Q1SHSIfoCl-sFRlPRsW-i6WR6mj9M75NhPhmfndOcPpg3Ol2vDG0szdvY4LZnfU5dTZ9WWLswo2OMztQx0DcXZ3Sy-Rlj4yqa-zjzLrpwRPYsLoI5_p2H5Pnmejq8S0aPt_fDfJQUTKUisRbKCoS1loMsTMnLVKisQiiEssIy5OkAU1NURpayHIBKWR9TMFwA54IrfkhOtr0r37y2JkQ9b1pfdyc1y7JskEnoi851tXWVvgnBG6tX3i3RrzUDvUGv_6DXG_T6B73eoO_ScpsulvN_Bb8B0zuQow</recordid><startdate>201406</startdate><enddate>201406</enddate><creator>Montes, A.</creator><creator>Perez-Pampín, E.</creator><creator>Bόveda, M.D.</creator><creator>Gόmez-Reino, J.J.</creator><creator>González, A.</creator><general>Elsevier Limited</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>OP0178 Antibodies against Carbamylated Proteins (ANTI-CARP), A New Type of Autoantibody, in Spanish Patients with Rheumatoid Arthritis</title><author>Montes, A. ; Perez-Pampín, E. ; Bόveda, M.D. ; Gόmez-Reino, J.J. ; González, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1854-ff0cd04fff306bec3c5487da0b48f4f1a359a5ebde6c6c908512a50e340334383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Montes, A.</creatorcontrib><creatorcontrib>Perez-Pampín, E.</creatorcontrib><creatorcontrib>Bόveda, M.D.</creatorcontrib><creatorcontrib>Gόmez-Reino, J.J.</creatorcontrib><creatorcontrib>González, A.</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>Montes, A.</au><au>Perez-Pampín, E.</au><au>Bόveda, M.D.</au><au>Gόmez-Reino, J.J.</au><au>González, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>OP0178 Antibodies against Carbamylated Proteins (ANTI-CARP), A New Type of Autoantibody, in Spanish Patients with Rheumatoid Arthritis</atitle><jtitle>Annals of the rheumatic diseases</jtitle><date>2014-06</date><risdate>2014</risdate><volume>73</volume><issue>Suppl 2</issue><spage>129</spage><pages>129-</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>Background Antibodies against carbamylated proteins (anti-CarP) are a new type of autoantibodies present in sera of patients with rheumatoid arthritis (RA). These antibodies, measured as the reactivity against carmabylated proteins from Fetal Calf Serum (FCS), do not show cross-reactivity with anti-CCP antibodies, and are associated with radiologic progression both in anti-CCP+ and in anti-CCP– patients [1]. Objectives The aim of this study was to explore the presence of anti-CarP-FCS antibodies in our collection of patients with RA and their association with clinical and genetic characteristics of the disease. Methods Carbamylation of FCS proteins was performed as previously described [1]. IgG antibodies against carbamylated FCS were measured by ELISA in sera from 520 RA patients fulfilling 1987 ACR criteria and from 208 healthy donors. Anti-CarP FCS titre was obtained after subtracting reactivity to native FCS from the reactivity to carbamylated FCS. The cut-of for positivity was set as the mean ±2 SD of healthy donors. Association of anti-CarP-FCS with the presence of erosive arthritis, rheumatoid factor (RF), HLADRB1 alleles and the R620W SNP of PTPN22 was analyzed by logistic regression. The relationship between the titre of anti-CarP-FCS and anti-CCP was analyzed with Spearman correlation and the concordance between positivity of anti-CarP-FCS, anti-CCP and RF with the gamma coefficient. Results Anti-CarP-FCS antibodies were found in 36.1% (188/520) of the patients with RA, including 45.0% of the anti-CCP+ patients and 19.9% of the anti-CCP– patients. Presence and titres of anti-CarP-FCS and anti-CCP antibodies were significantly correlated (g =0.53, P=1.6×10-17 for status concordance, and r=0.27, P=2.1×10-10 for antibody titres, respectively). However, no association was found between anti-CarP-FCS and the risk alleles of HLADRB1 and PTPN22. Anti-CarP-FCS status showed also a significant association with RF status (OR=3.4, P=1.6×10-8) that remained after accounting for anti-CCP status (OR=2.2, P=0.001). In addition, we replicated the association of erosive arthritis with anti-CarP-FCS antibodies (OR=2.3, P=1.4×10-4) even accounting for the presence of anti-CCP (OR=1.6, P=0.026) Conclusions We have confirmed the presence of anti-CarP-FCS antibodies in RA patients (both anti-CCP+ and anti-CCP– patients) and their association with erosive arthritis as previously described in Dutch patients with RA. These associations indicate the interest of the anti-CarP antibodies in RA. In addition, our finding of lack of association of these antibodies with genetic risk factors for anti-CCP+ RA indicates that this is an independent autoantibody system in RA. We need to further study these antibodies to know if they define a new subgroup of patients with RA. References Shi J et al. Autoantibodies recognizing carbamylated proteins are present in sera of patients with rheumatoid arthritis and predict joint damage. Proc Natl Acad 108:17372-7. Disclosure of Interest None declared DOI 10.1136/annrheumdis-2014-eular.5427</abstract><cop>Kidlington</cop><pub>Elsevier Limited</pub><doi>10.1136/annrheumdis-2014-eular.5427</doi></addata></record> |
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title | OP0178 Antibodies against Carbamylated Proteins (ANTI-CARP), A New Type of Autoantibody, in Spanish Patients with Rheumatoid Arthritis |
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