SAT0125 Tocilizumab Achieves Rapid Reduction of Disease Activity and Has Beneficial Effects on Bone Mineral Density in Patients with Rheumatoid Arthritis – Results of A Prospective 5- Year Study
BackgroundTocilizumab (TCZ) leads to a rapid improvement of the clinical course in patients with highly active rheumatoid arthritis (RA). However, a residual rheumatic activity can still be detected.1 RA is a known risk factor for osteoporosis related bone fractures.2 It is well established that TCZ...
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description | BackgroundTocilizumab (TCZ) leads to a rapid improvement of the clinical course in patients with highly active rheumatoid arthritis (RA). However, a residual rheumatic activity can still be detected.1 RA is a known risk factor for osteoporosis related bone fractures.2 It is well established that TCZ has beneficial effects on bone remodeling.3ObjectivesThe aim of this analysis was to investigate the effects of TCZ on bone mineral density in a real world patient population.Methods50 rheumatoid factor positive patients with RA (17 male, age 20–72 years) who received TCZ as monotherapy since 2008 were prospectively investigated. At baseline and the following 4–6 clinical visits, DAS28 was determined and ultrasound performed. At baseline and every 6 months thereafter, biochemical parameters for bone metabolism and protein diagnostics were recorded. Once a year, the subjects underwent MRI, CT and DXA scan.ResultsIn all 50 patients the DAS28 normalized at the latest by the 3rd infusion cycle of TCZ. The initial RAMRIS score of >5 was reduced to 2.7. 2 patients presented with pustular dermatosis in the palms. No allergic reactions were observed.ConclusionsTreatment with TCZ leads to a rapid decline of inflammatory activity of the affected joints in patients with RA and minimizes cartilage destruction. TCZ showed a positive effect on bone remodeling and therefore BMD. Thus, the risk for the development of osteoporosis and its related fractures can be minimized by TCZ treatment. Furthermore, TCZ has a positiv |
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However, a residual rheumatic activity can still be detected.1 RA is a known risk factor for osteoporosis related bone fractures.2 It is well established that TCZ has beneficial effects on bone remodeling.3ObjectivesThe aim of this analysis was to investigate the effects of TCZ on bone mineral density in a real world patient population.Methods50 rheumatoid factor positive patients with RA (17 male, age 20–72 years) who received TCZ as monotherapy since 2008 were prospectively investigated. At baseline and the following 4–6 clinical visits, DAS28 was determined and ultrasound performed. At baseline and every 6 months thereafter, biochemical parameters for bone metabolism and protein diagnostics were recorded. Once a year, the subjects underwent MRI, CT and DXA scan.ResultsIn all 50 patients the DAS28 normalized at the latest by the 3rd infusion cycle of TCZ. The initial RAMRIS score of >5 was reduced to <2 after 6–18 months. Ultrasound revealed a decline of synovialitis and tenodynovialitis after 8 weeks and 12 months, respectively. At baseline in 22 women with early RA, axial QCT/DXA values and lateral DXA values were within reference. 3 patients with early RA had osteopenia, 2 had osteoporosis. Patients with manifest RA had a BMD in the reference range, 3 had osteopenia and 2 were diagnosed with osteoporosis. In 6 male patients, BMD values were within the reference range. 2 men with early RA had osteopenia and 2 had manifest osteoporosis. In 1 male patient with manifest RA, normal BMD values were documented. 2 men with manifest RA hat osteopenia and 4 had osteoporosis. 10 patients had vitamin D3 deficiency and were treated with vitamin D3. 2 patients with osteoporosis were treated with antiresorptive medication. In all patients, BMD values were within the reference range after 1 year of treatment with TCZ, despite 18% of patients presenting with a DAS score >2.7. 2 patients presented with pustular dermatosis in the palms. No allergic reactions were observed.ConclusionsTreatment with TCZ leads to a rapid decline of inflammatory activity of the affected joints in patients with RA and minimizes cartilage destruction. TCZ showed a positive effect on bone remodeling and therefore BMD. Thus, the risk for the development of osteoporosis and its related fractures can be minimized by TCZ treatment. Furthermore, TCZ has a positive effect on BMD in manifest RA thus preventing sarcopenia. Temporary elevations of DAS28 during TCZ therapy do not negatively affect BMD.ReferencesHoehle M et al.; Synovialitis Plus Articular Cartilage Monitoring Via Magnetic Resonance Imaging and Ultrasound under Tocilizumab Therapy in Patients with Rheumatoid Arthritis. [abstract]. Arthritis Rheum 2012;64 Suppl 10:466Christiansen C et al.; Assessement of Tissue Turnover and Quality in Rheumatology. European Congress on Osteoporosis and Osteoarthritis, ESCE013-OF, SE 18 AbstractBriot K et al.; Positive Effects of Tocilizumab On Bone Remodeling in Patients withRheumatoid Arthritis. [abstract]. Arthritis Rheum 2012;64 Suppl 10:823Disclosure of InterestNone declared</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2016-eular.4890</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><ispartof>Annals of the rheumatic diseases, 2016-06, Vol.75 (Suppl 2), p.710-710</ispartof><rights>2016, 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: 2016 (c) 2016, 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/75/Suppl_2/710.2.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/75/Suppl_2/710.2.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,780,784,3195,23570,27923,27924,77471,77502</link.rule.ids></links><search><creatorcontrib>Höhle, M.</creatorcontrib><title>SAT0125 Tocilizumab Achieves Rapid Reduction of Disease Activity and Has Beneficial Effects on Bone Mineral Density in Patients with Rheumatoid Arthritis – Results of A Prospective 5- Year Study</title><title>Annals of the rheumatic diseases</title><description>BackgroundTocilizumab (TCZ) leads to a rapid improvement of the clinical course in patients with highly active rheumatoid arthritis (RA). However, a residual rheumatic activity can still be detected.1 RA is a known risk factor for osteoporosis related bone fractures.2 It is well established that TCZ has beneficial effects on bone remodeling.3ObjectivesThe aim of this analysis was to investigate the effects of TCZ on bone mineral density in a real world patient population.Methods50 rheumatoid factor positive patients with RA (17 male, age 20–72 years) who received TCZ as monotherapy since 2008 were prospectively investigated. At baseline and the following 4–6 clinical visits, DAS28 was determined and ultrasound performed. At baseline and every 6 months thereafter, biochemical parameters for bone metabolism and protein diagnostics were recorded. Once a year, the subjects underwent MRI, CT and DXA scan.ResultsIn all 50 patients the DAS28 normalized at the latest by the 3rd infusion cycle of TCZ. The initial RAMRIS score of >5 was reduced to <2 after 6–18 months. Ultrasound revealed a decline of synovialitis and tenodynovialitis after 8 weeks and 12 months, respectively. At baseline in 22 women with early RA, axial QCT/DXA values and lateral DXA values were within reference. 3 patients with early RA had osteopenia, 2 had osteoporosis. Patients with manifest RA had a BMD in the reference range, 3 had osteopenia and 2 were diagnosed with osteoporosis. In 6 male patients, BMD values were within the reference range. 2 men with early RA had osteopenia and 2 had manifest osteoporosis. In 1 male patient with manifest RA, normal BMD values were documented. 2 men with manifest RA hat osteopenia and 4 had osteoporosis. 10 patients had vitamin D3 deficiency and were treated with vitamin D3. 2 patients with osteoporosis were treated with antiresorptive medication. In all patients, BMD values were within the reference range after 1 year of treatment with TCZ, despite 18% of patients presenting with a DAS score >2.7. 2 patients presented with pustular dermatosis in the palms. No allergic reactions were observed.ConclusionsTreatment with TCZ leads to a rapid decline of inflammatory activity of the affected joints in patients with RA and minimizes cartilage destruction. TCZ showed a positive effect on bone remodeling and therefore BMD. Thus, the risk for the development of osteoporosis and its related fractures can be minimized by TCZ treatment. Furthermore, TCZ has a positive effect on BMD in manifest RA thus preventing sarcopenia. Temporary elevations of DAS28 during TCZ therapy do not negatively affect BMD.ReferencesHoehle M et al.; Synovialitis Plus Articular Cartilage Monitoring Via Magnetic Resonance Imaging and Ultrasound under Tocilizumab Therapy in Patients with Rheumatoid Arthritis. [abstract]. Arthritis Rheum 2012;64 Suppl 10:466Christiansen C et al.; Assessement of Tissue Turnover and Quality in Rheumatology. European Congress on Osteoporosis and Osteoarthritis, ESCE013-OF, SE 18 AbstractBriot K et al.; Positive Effects of Tocilizumab On Bone Remodeling in Patients withRheumatoid Arthritis. [abstract]. Arthritis Rheum 2012;64 Suppl 10:823Disclosure of InterestNone declared</description><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</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>eNqVkc9u1DAQxi0EEkvhHUbqOcWOHScrTuk_WqmIars9cLK8zljrVdZZbKdoOfXCE_SdeJA-CQ7LgWslS5ZH32--8XyEHDN6whiXH7X3YY3jtnOxKCmTBY69DieimdNXZMaEbHJZ0tdkRinlhZjL-i15F-MmP2nDmhn5fdcuKSur58dfy8G43v0ct3oFrVk7fMAIC71zHSywG01yg4fBwrmLqCNmTXIPLu1B-w6udIRT9GidcbqHC2vRpAiZOB08whfnMeT6Ofo4Ic7DrU4Ofdb8cGkNi-kbOg3ZrA1pHVxyEZ4fn7J1HPupk4UWbsMQdzj5IlQFfEMd4C6N3f49eWN1H_HDv_uI3F9eLM-uipuvn6_P2ptixcqaFbYyZiWwkw3VtZwbU1Udp7qyvBZlp5HbjnJR500KJjXPxzLDhSybvN2aSX5Ejg99d2H4PmJMajOMwWdLxeaUNYJVJcuqTweVyfPGgFbtgtvqsFeMqik49V9wagpO_Q1OTcFlWh7o1XbzIvAPE1enhQ</recordid><startdate>201606</startdate><enddate>201606</enddate><creator>Höhle, M.</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>Q9U</scope></search><sort><creationdate>201606</creationdate><title>SAT0125 Tocilizumab Achieves Rapid Reduction of Disease Activity and Has Beneficial Effects on Bone Mineral Density in Patients with Rheumatoid Arthritis – Results of A Prospective 5- Year Study</title><author>Höhle, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1271-f5ccb4ed680a769cc55d30a5f3742dae3fd0347016416a36a3f1c346282017163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Höhle, M.</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 Basic</collection><jtitle>Annals of the rheumatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Höhle, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SAT0125 Tocilizumab Achieves Rapid Reduction of Disease Activity and Has Beneficial Effects on Bone Mineral Density in Patients with Rheumatoid Arthritis – Results of A Prospective 5- Year Study</atitle><jtitle>Annals of the rheumatic diseases</jtitle><date>2016-06</date><risdate>2016</risdate><volume>75</volume><issue>Suppl 2</issue><spage>710</spage><epage>710</epage><pages>710-710</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>BackgroundTocilizumab (TCZ) leads to a rapid improvement of the clinical course in patients with highly active rheumatoid arthritis (RA). However, a residual rheumatic activity can still be detected.1 RA is a known risk factor for osteoporosis related bone fractures.2 It is well established that TCZ has beneficial effects on bone remodeling.3ObjectivesThe aim of this analysis was to investigate the effects of TCZ on bone mineral density in a real world patient population.Methods50 rheumatoid factor positive patients with RA (17 male, age 20–72 years) who received TCZ as monotherapy since 2008 were prospectively investigated. At baseline and the following 4–6 clinical visits, DAS28 was determined and ultrasound performed. At baseline and every 6 months thereafter, biochemical parameters for bone metabolism and protein diagnostics were recorded. Once a year, the subjects underwent MRI, CT and DXA scan.ResultsIn all 50 patients the DAS28 normalized at the latest by the 3rd infusion cycle of TCZ. The initial RAMRIS score of >5 was reduced to <2 after 6–18 months. Ultrasound revealed a decline of synovialitis and tenodynovialitis after 8 weeks and 12 months, respectively. At baseline in 22 women with early RA, axial QCT/DXA values and lateral DXA values were within reference. 3 patients with early RA had osteopenia, 2 had osteoporosis. Patients with manifest RA had a BMD in the reference range, 3 had osteopenia and 2 were diagnosed with osteoporosis. In 6 male patients, BMD values were within the reference range. 2 men with early RA had osteopenia and 2 had manifest osteoporosis. In 1 male patient with manifest RA, normal BMD values were documented. 2 men with manifest RA hat osteopenia and 4 had osteoporosis. 10 patients had vitamin D3 deficiency and were treated with vitamin D3. 2 patients with osteoporosis were treated with antiresorptive medication. In all patients, BMD values were within the reference range after 1 year of treatment with TCZ, despite 18% of patients presenting with a DAS score >2.7. 2 patients presented with pustular dermatosis in the palms. No allergic reactions were observed.ConclusionsTreatment with TCZ leads to a rapid decline of inflammatory activity of the affected joints in patients with RA and minimizes cartilage destruction. TCZ showed a positive effect on bone remodeling and therefore BMD. Thus, the risk for the development of osteoporosis and its related fractures can be minimized by TCZ treatment. Furthermore, TCZ has a positive effect on BMD in manifest RA thus preventing sarcopenia. Temporary elevations of DAS28 during TCZ therapy do not negatively affect BMD.ReferencesHoehle M et al.; Synovialitis Plus Articular Cartilage Monitoring Via Magnetic Resonance Imaging and Ultrasound under Tocilizumab Therapy in Patients with Rheumatoid Arthritis. [abstract]. Arthritis Rheum 2012;64 Suppl 10:466Christiansen C et al.; Assessement of Tissue Turnover and Quality in Rheumatology. European Congress on Osteoporosis and Osteoarthritis, ESCE013-OF, SE 18 AbstractBriot K et al.; Positive Effects of Tocilizumab On Bone Remodeling in Patients withRheumatoid Arthritis. [abstract]. Arthritis Rheum 2012;64 Suppl 10:823Disclosure of InterestNone declared</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/annrheumdis-2016-eular.4890</doi><tpages>1</tpages></addata></record> |
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