OP0242 Serum Indian Hedgehog (IHH) Levels Are Increased in Patients with Ankylosing Spondylitis (AS). Anti-TNF a Treatment Decreases Serum IHH Levels in Patients with as and Affects the Expression of Functional Target Genes in a Cell Line Model

Background The molecular pathways involved in the process of new bone formation in ankylosing spondylitis (AS) are not entirely known. However, data suggests that this process is linked to the reactivation of developmental pathways. It was recently shown that the Hedgehog pathway (HH) is involved in...

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Veröffentlicht in:Annals of the rheumatic diseases 2013-06, Vol.72 (Suppl 3), p.A134
Hauptverfasser: Filippopoulou, A., Daoussis, D., Liossis, S.-N., Bouris, P., Klavdianou, K., Karamanos, N., Andonopoulos, A.
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container_issue Suppl 3
container_start_page A134
container_title Annals of the rheumatic diseases
container_volume 72
creator Filippopoulou, A.
Daoussis, D.
Liossis, S.-N.
Bouris, P.
Klavdianou, K.
Karamanos, N.
Andonopoulos, A.
description Background The molecular pathways involved in the process of new bone formation in ankylosing spondylitis (AS) are not entirely known. However, data suggests that this process is linked to the reactivation of developmental pathways. It was recently shown that the Hedgehog pathway (HH) is involved in osteophyte formation in osteoarthritis. Moreover, it appears to be the main controller of endochondral ossification, a process already known to participate in new bone formation in AS. The ligand that activates the HH pathway in the skeleton is Indian Hedgehog (IHH). Objectives To assess i) serum levels of IHH in patients with AS compared to healthy subjects and patients with rheumatoid arthritis (RA) ii) the effect of anti-TNFα treatment on IHH levels in patients with AS and RA and iii) the effect of serum of patients with AS on HH pathway activation Methods Serum samples were obtained from 59 patients with AS (36 on anti-TNFα treatment), 70 patients with RA (30 on anti-TNFα treatment) and 53 healthy subjects. IHH levels were measured using an established solid phase immunoassay. The effect of serum from patients with AS on HH pathway activation was evaluated using an experimental model based on osteoblast-like, Saos-2 cells. On day 0, 2X106 Saos-2 cells were cultured in EMEM/10%FBS; on day 2, 10% of serum was added and on day 3 cells were lysed and mRNA was extracted. RT-PCR was used to assess the expression of two HH pathway target genes (Ptch-1 and glypican 3). Results IHH levels were significantly increased in AS patients not receiving anti TNF- treatment compared to healthy subjects (mean±SEM of OD: 0.37±0.02 vs 0.28±0.02, respectively, p=0.03). Patients with AS on anti-TNF treatment had significantly lower IHH levels compared to AS patients not on such treatment (mean±SEM: 0.28±0.02 vs 0.37±0.02, respectively, p=0.02). Interestingly, the exact opposite was true for patients with RA; patients on anti-TNF treatment had higher levels of IHH compared to patients not on such treatment (mean±SEM: 0.38±0.03 vs 0.27±0.02, respectively, p=0.01). In order to explore whether the differences in IHH levels found in AS patients have a functional effect, we assessed HH pathway activation in Saos2 cells following incubation with serum obtained form 2 AS patients prior to and 3 months following anti-TNF treatment. We found that the expression of both target genes (Ptch-1 and glypican 3) declined following anti-TNF treatment. Conclusions IHH levels are increased in patien
doi_str_mv 10.1136/annrheumdis-2013-eular.447
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Anti-TNF a Treatment Decreases Serum IHH Levels in Patients with as and Affects the Expression of Functional Target Genes in a Cell Line Model</title><source>BMJ Journals - NESLi2</source><creator>Filippopoulou, A. ; Daoussis, D. ; Liossis, S.-N. ; Bouris, P. ; Klavdianou, K. ; Karamanos, N. ; Andonopoulos, A.</creator><creatorcontrib>Filippopoulou, A. ; Daoussis, D. ; Liossis, S.-N. ; Bouris, P. ; Klavdianou, K. ; Karamanos, N. ; Andonopoulos, A.</creatorcontrib><description>Background The molecular pathways involved in the process of new bone formation in ankylosing spondylitis (AS) are not entirely known. However, data suggests that this process is linked to the reactivation of developmental pathways. It was recently shown that the Hedgehog pathway (HH) is involved in osteophyte formation in osteoarthritis. Moreover, it appears to be the main controller of endochondral ossification, a process already known to participate in new bone formation in AS. The ligand that activates the HH pathway in the skeleton is Indian Hedgehog (IHH). Objectives To assess i) serum levels of IHH in patients with AS compared to healthy subjects and patients with rheumatoid arthritis (RA) ii) the effect of anti-TNFα treatment on IHH levels in patients with AS and RA and iii) the effect of serum of patients with AS on HH pathway activation Methods Serum samples were obtained from 59 patients with AS (36 on anti-TNFα treatment), 70 patients with RA (30 on anti-TNFα treatment) and 53 healthy subjects. IHH levels were measured using an established solid phase immunoassay. The effect of serum from patients with AS on HH pathway activation was evaluated using an experimental model based on osteoblast-like, Saos-2 cells. On day 0, 2X106 Saos-2 cells were cultured in EMEM/10%FBS; on day 2, 10% of serum was added and on day 3 cells were lysed and mRNA was extracted. RT-PCR was used to assess the expression of two HH pathway target genes (Ptch-1 and glypican 3). Results IHH levels were significantly increased in AS patients not receiving anti TNF- treatment compared to healthy subjects (mean±SEM of OD: 0.37±0.02 vs 0.28±0.02, respectively, p=0.03). Patients with AS on anti-TNF treatment had significantly lower IHH levels compared to AS patients not on such treatment (mean±SEM: 0.28±0.02 vs 0.37±0.02, respectively, p=0.02). Interestingly, the exact opposite was true for patients with RA; patients on anti-TNF treatment had higher levels of IHH compared to patients not on such treatment (mean±SEM: 0.38±0.03 vs 0.27±0.02, respectively, p=0.01). In order to explore whether the differences in IHH levels found in AS patients have a functional effect, we assessed HH pathway activation in Saos2 cells following incubation with serum obtained form 2 AS patients prior to and 3 months following anti-TNF treatment. We found that the expression of both target genes (Ptch-1 and glypican 3) declined following anti-TNF treatment. Conclusions IHH levels are increased in patients with AS and decrease following anti-TNF treatment; taking into account the critical role of this pathway in the bone forming process this finding may have pathogenic and clinical implications. Disclosure of Interest None Declared</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2013-eular.447</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>Kidlington: BMJ Publishing Group Ltd and European League Against Rheumatism</publisher><ispartof>Annals of the rheumatic diseases, 2013-06, Vol.72 (Suppl 3), p.A134</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/A134.2.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/72/Suppl_3/A134.2.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,777,781,3183,23552,27905,27906,77349,77380</link.rule.ids></links><search><creatorcontrib>Filippopoulou, A.</creatorcontrib><creatorcontrib>Daoussis, D.</creatorcontrib><creatorcontrib>Liossis, S.-N.</creatorcontrib><creatorcontrib>Bouris, P.</creatorcontrib><creatorcontrib>Klavdianou, K.</creatorcontrib><creatorcontrib>Karamanos, N.</creatorcontrib><creatorcontrib>Andonopoulos, A.</creatorcontrib><title>OP0242 Serum Indian Hedgehog (IHH) Levels Are Increased in Patients with Ankylosing Spondylitis (AS). Anti-TNF a Treatment Decreases Serum IHH Levels in Patients with as and Affects the Expression of Functional Target Genes in a Cell Line Model</title><title>Annals of the rheumatic diseases</title><addtitle>Ann Rheum Dis</addtitle><description>Background The molecular pathways involved in the process of new bone formation in ankylosing spondylitis (AS) are not entirely known. However, data suggests that this process is linked to the reactivation of developmental pathways. It was recently shown that the Hedgehog pathway (HH) is involved in osteophyte formation in osteoarthritis. Moreover, it appears to be the main controller of endochondral ossification, a process already known to participate in new bone formation in AS. The ligand that activates the HH pathway in the skeleton is Indian Hedgehog (IHH). Objectives To assess i) serum levels of IHH in patients with AS compared to healthy subjects and patients with rheumatoid arthritis (RA) ii) the effect of anti-TNFα treatment on IHH levels in patients with AS and RA and iii) the effect of serum of patients with AS on HH pathway activation Methods Serum samples were obtained from 59 patients with AS (36 on anti-TNFα treatment), 70 patients with RA (30 on anti-TNFα treatment) and 53 healthy subjects. IHH levels were measured using an established solid phase immunoassay. The effect of serum from patients with AS on HH pathway activation was evaluated using an experimental model based on osteoblast-like, Saos-2 cells. On day 0, 2X106 Saos-2 cells were cultured in EMEM/10%FBS; on day 2, 10% of serum was added and on day 3 cells were lysed and mRNA was extracted. RT-PCR was used to assess the expression of two HH pathway target genes (Ptch-1 and glypican 3). Results IHH levels were significantly increased in AS patients not receiving anti TNF- treatment compared to healthy subjects (mean±SEM of OD: 0.37±0.02 vs 0.28±0.02, respectively, p=0.03). Patients with AS on anti-TNF treatment had significantly lower IHH levels compared to AS patients not on such treatment (mean±SEM: 0.28±0.02 vs 0.37±0.02, respectively, p=0.02). Interestingly, the exact opposite was true for patients with RA; patients on anti-TNF treatment had higher levels of IHH compared to patients not on such treatment (mean±SEM: 0.38±0.03 vs 0.27±0.02, respectively, p=0.01). In order to explore whether the differences in IHH levels found in AS patients have a functional effect, we assessed HH pathway activation in Saos2 cells following incubation with serum obtained form 2 AS patients prior to and 3 months following anti-TNF treatment. We found that the expression of both target genes (Ptch-1 and glypican 3) declined following anti-TNF treatment. Conclusions IHH levels are increased in patients with AS and decrease following anti-TNF treatment; taking into account the critical role of this pathway in the bone forming process this finding may have pathogenic and clinical implications. 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>eNqVkUFv0zAYhiMEEmXwHz7BZTuk2HESu9yqbl2KyjZo4Wq58ZfWXeIUO4H1xoU_yo_gjLsOhMQJX2x_ft_ntfRG0UtKhpSy_LWy1m2wb7TxcUIoi7GvlRumKX8UDWiaizDNyeNoQAhhcTrK-dPomffbcCWCikH08_qGJGny49v3Bbq-gZnVRlkoUK9x067hdFYUZzDHL1h7GDsMgtKh8qjBWLhRnUHbefhqug2M7e2-br2xa1jsWqv3temMh9Px4mwYHjsTL6-moGAZAF0TfHCOR5iHh_Si-J31D115UFbDuKqwDLNug3Bxt3PovWkttBVMe1t24axqWCq3xg4u0eI9ScEE6xrmxiK8azXWz6Mnlao9vnjYT6KP04vlpIjn15ezyXger2jO0lixtGRCkTLNVrzKCakyXo6EYGyU5HyFqhQirdSKJ8hQZEwLrROheFUJjTxL2Un06sjdufZzj76T27Z34YteUs75iKZhBdWbo6p0rfcOK7lzplFuLymRh57lXz3LQ8_yvmcZeg7m-Gg2vsO7P07lbmXOGc_k1aeJ_PB2siT0fSYPYdlRv2q2_5PzC33GxOc</recordid><startdate>201306</startdate><enddate>201306</enddate><creator>Filippopoulou, A.</creator><creator>Daoussis, D.</creator><creator>Liossis, S.-N.</creator><creator>Bouris, P.</creator><creator>Klavdianou, K.</creator><creator>Karamanos, N.</creator><creator>Andonopoulos, A.</creator><general>BMJ Publishing Group Ltd and European League Against Rheumatism</general><general>Elsevier Limited</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>OP0242 Serum Indian Hedgehog (IHH) Levels Are Increased in Patients with Ankylosing Spondylitis (AS). Anti-TNF a Treatment Decreases Serum IHH Levels in Patients with as and Affects the Expression of Functional Target Genes in a Cell Line Model</title><author>Filippopoulou, A. ; Daoussis, D. ; Liossis, S.-N. ; Bouris, P. ; Klavdianou, K. ; Karamanos, N. ; Andonopoulos, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1634-a34c38a0c45b7f600f57c988339267beac884fab72e3e853d8dd28a7ff8de7543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Filippopoulou, A.</creatorcontrib><creatorcontrib>Daoussis, D.</creatorcontrib><creatorcontrib>Liossis, S.-N.</creatorcontrib><creatorcontrib>Bouris, P.</creatorcontrib><creatorcontrib>Klavdianou, K.</creatorcontrib><creatorcontrib>Karamanos, N.</creatorcontrib><creatorcontrib>Andonopoulos, A.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health &amp; 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>Filippopoulou, A.</au><au>Daoussis, D.</au><au>Liossis, S.-N.</au><au>Bouris, P.</au><au>Klavdianou, K.</au><au>Karamanos, N.</au><au>Andonopoulos, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>OP0242 Serum Indian Hedgehog (IHH) Levels Are Increased in Patients with Ankylosing Spondylitis (AS). Anti-TNF a Treatment Decreases Serum IHH Levels in Patients with as and Affects the Expression of Functional Target Genes in a Cell Line Model</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>A134</spage><pages>A134-</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>Background The molecular pathways involved in the process of new bone formation in ankylosing spondylitis (AS) are not entirely known. However, data suggests that this process is linked to the reactivation of developmental pathways. It was recently shown that the Hedgehog pathway (HH) is involved in osteophyte formation in osteoarthritis. Moreover, it appears to be the main controller of endochondral ossification, a process already known to participate in new bone formation in AS. The ligand that activates the HH pathway in the skeleton is Indian Hedgehog (IHH). Objectives To assess i) serum levels of IHH in patients with AS compared to healthy subjects and patients with rheumatoid arthritis (RA) ii) the effect of anti-TNFα treatment on IHH levels in patients with AS and RA and iii) the effect of serum of patients with AS on HH pathway activation Methods Serum samples were obtained from 59 patients with AS (36 on anti-TNFα treatment), 70 patients with RA (30 on anti-TNFα treatment) and 53 healthy subjects. IHH levels were measured using an established solid phase immunoassay. The effect of serum from patients with AS on HH pathway activation was evaluated using an experimental model based on osteoblast-like, Saos-2 cells. On day 0, 2X106 Saos-2 cells were cultured in EMEM/10%FBS; on day 2, 10% of serum was added and on day 3 cells were lysed and mRNA was extracted. RT-PCR was used to assess the expression of two HH pathway target genes (Ptch-1 and glypican 3). Results IHH levels were significantly increased in AS patients not receiving anti TNF- treatment compared to healthy subjects (mean±SEM of OD: 0.37±0.02 vs 0.28±0.02, respectively, p=0.03). Patients with AS on anti-TNF treatment had significantly lower IHH levels compared to AS patients not on such treatment (mean±SEM: 0.28±0.02 vs 0.37±0.02, respectively, p=0.02). Interestingly, the exact opposite was true for patients with RA; patients on anti-TNF treatment had higher levels of IHH compared to patients not on such treatment (mean±SEM: 0.38±0.03 vs 0.27±0.02, respectively, p=0.01). In order to explore whether the differences in IHH levels found in AS patients have a functional effect, we assessed HH pathway activation in Saos2 cells following incubation with serum obtained form 2 AS patients prior to and 3 months following anti-TNF treatment. We found that the expression of both target genes (Ptch-1 and glypican 3) declined following anti-TNF treatment. Conclusions IHH levels are increased in patients with AS and decrease following anti-TNF treatment; taking into account the critical role of this pathway in the bone forming process this finding may have pathogenic and clinical implications. Disclosure of Interest None Declared</abstract><cop>Kidlington</cop><pub>BMJ Publishing Group Ltd and European League Against Rheumatism</pub><doi>10.1136/annrheumdis-2013-eular.447</doi></addata></record>
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title OP0242 Serum Indian Hedgehog (IHH) Levels Are Increased in Patients with Ankylosing Spondylitis (AS). Anti-TNF a Treatment Decreases Serum IHH Levels in Patients with as and Affects the Expression of Functional Target Genes in a Cell Line Model
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