FRI0417 Prevalence of Osteoporosis in An Ankylosing Spondylitis Cohort
BackgroundThe Ankylosing Spondylitis Registry of Ireland (ASRI) is a web-based database established in 2013, the objectives of which are to provide descriptive epidemiological data on the ankylosing spondylitis (AS) population in Ireland and to establish a registry for potential future studies of ge...
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creator | Fitzgerald, G. Lundon, D.J. Gallagher, P. O'Rourke, K. Sheehy, C. Sullivan, C. Silke, C. Stafford, F. Haroon, M. Mullan, R. FitzGerald, O. O Shea, F. |
description | BackgroundThe Ankylosing Spondylitis Registry of Ireland (ASRI) is a web-based database established in 2013, the objectives of which are to provide descriptive epidemiological data on the ankylosing spondylitis (AS) population in Ireland and to establish a registry for potential future studies of genetics, aetiology and therapeutics. The prevalence of osteoporosis is higher in AS patients than age- and sex-matched controls, with potential for vertebral fractures increased. However, the true prevalence is unknown. There is no data on the prevalence of osteoporosis in an Irish cohort.ObjectivesTo determine the prevalence of low bone mineral density (BMD) in an Irish AS cohort.MethodsA standardised detailed clinical assessment was performed on each patient. Disease activity was assessed by Bath AS Disease Activity Index (BASDAI), function by the Bath AS Functional Index (BASFI) and Health Assessment Questionnaire (HAQ) and quality of life by AS Quality of Life (ASQoL). Structured interviews provided patient-reported data. Presence or absence of dual-energy x-ray absorptiometry (DXA) testing and result was recorded. Bone mineral density (BMD) was categorised according to the World Health Organisation criteria into normal BMD, osteopenia or osteoporosis. Statistical analysis was performed using SPSS.ResultsAs of October 2015, 416 patients are enrolled in ASRI: 78.1% males, mean age 47.95 (SD 12.4), mean disease duration 20.9 years (SD 12.2), average delay to diagnosis of 8.8 years (SD 8.3). Mean BASDAI is 3.8 (SD 2.5), BASFI 3.7 (SD 2.7), HAQ 0.53 (SD 0.51) and ASQoL 6.15 (SD 5.5). DXAs have been performed in 24.75% (n=103) of the cohort, of which 39.8% (n=41) have osteopenia and 10.7% (n=11) have osteoporosis. Low BMD is significantly correlated with men and advancing age. There is no association with disease activity or duration. Low BMD is more prevalent in patients treated with one or more biologics compared to those never treated. The self-reported prevalence of osteoporosis is 6.4% (n=27; 19 males).ConclusionsThere is an elevated prevalence of low BMD in this cohort, with no association with disease severity. The majority of affected patients were unaware, as demonstrated by the low self-reported prevalence. More research and education is needed.Disclosure of InterestNone declared |
doi_str_mv | 10.1136/annrheumdis-2016-eular.6012 |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1901808134</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4322510373</sourcerecordid><originalsourceid>FETCH-LOGICAL-b1274-d75336c5d080caca6117decea144ae075fc84ddd1d3151f3b57ac85d16dfacb33</originalsourceid><addsrcrecordid>eNqVkE1LAzEQhoMoWKv_YaHnrZkmm6R4KsXaQqHixzlkk6zdut2sya7Qmxf_qL_ErPXgVRgY5uOd4X0QGgEeAxB2rerab223N2VIJxhYartK-THDMDlBA6BMxDbDp2iAMSYpnTJ-ji5C2MUSCxADtFw8rDAF_vXxee_tu6psrW3iimQTWusa510oQ1LWyayP10MV6_oleWxcbQ5V2cbh3G2dby_RWaGqYK9-8xA9L26f5st0vblbzWfrNIcJp6nhGSFMZwYLrJVWDIAbq60CSpXFPCu0oMYYMAQyKEiecaVFZoCZQumckCEaHe823r11NrRy5zpfx5cSphhEtEVo3Lo5buloIHhbyMaXe-UPErDs0ck_6GSPTv6gkz26qGZHdb7f_Uv4DT1se1Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1901808134</pqid></control><display><type>article</type><title>FRI0417 Prevalence of Osteoporosis in An Ankylosing Spondylitis Cohort</title><source>BMJ Journals - NESLi2</source><creator>Fitzgerald, G. ; Lundon, D.J. ; Gallagher, P. ; O'Rourke, K. ; Sheehy, C. ; Sullivan, C. ; Silke, C. ; Stafford, F. ; Haroon, M. ; Mullan, R. ; FitzGerald, O. ; O Shea, F.</creator><creatorcontrib>Fitzgerald, G. ; Lundon, D.J. ; Gallagher, P. ; O'Rourke, K. ; Sheehy, C. ; Sullivan, C. ; Silke, C. ; Stafford, F. ; Haroon, M. ; Mullan, R. ; FitzGerald, O. ; O Shea, F.</creatorcontrib><description>BackgroundThe Ankylosing Spondylitis Registry of Ireland (ASRI) is a web-based database established in 2013, the objectives of which are to provide descriptive epidemiological data on the ankylosing spondylitis (AS) population in Ireland and to establish a registry for potential future studies of genetics, aetiology and therapeutics. The prevalence of osteoporosis is higher in AS patients than age- and sex-matched controls, with potential for vertebral fractures increased. However, the true prevalence is unknown. There is no data on the prevalence of osteoporosis in an Irish cohort.ObjectivesTo determine the prevalence of low bone mineral density (BMD) in an Irish AS cohort.MethodsA standardised detailed clinical assessment was performed on each patient. Disease activity was assessed by Bath AS Disease Activity Index (BASDAI), function by the Bath AS Functional Index (BASFI) and Health Assessment Questionnaire (HAQ) and quality of life by AS Quality of Life (ASQoL). Structured interviews provided patient-reported data. Presence or absence of dual-energy x-ray absorptiometry (DXA) testing and result was recorded. Bone mineral density (BMD) was categorised according to the World Health Organisation criteria into normal BMD, osteopenia or osteoporosis. Statistical analysis was performed using SPSS.ResultsAs of October 2015, 416 patients are enrolled in ASRI: 78.1% males, mean age 47.95 (SD 12.4), mean disease duration 20.9 years (SD 12.2), average delay to diagnosis of 8.8 years (SD 8.3). Mean BASDAI is 3.8 (SD 2.5), BASFI 3.7 (SD 2.7), HAQ 0.53 (SD 0.51) and ASQoL 6.15 (SD 5.5). DXAs have been performed in 24.75% (n=103) of the cohort, of which 39.8% (n=41) have osteopenia and 10.7% (n=11) have osteoporosis. Low BMD is significantly correlated with men and advancing age. There is no association with disease activity or duration. Low BMD is more prevalent in patients treated with one or more biologics compared to those never treated. The self-reported prevalence of osteoporosis is 6.4% (n=27; 19 males).ConclusionsThere is an elevated prevalence of low BMD in this cohort, with no association with disease severity. The majority of affected patients were unaware, as demonstrated by the low self-reported prevalence. More research and education is needed.Disclosure of InterestNone declared</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2016-eular.6012</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>Kidlington: Elsevier Limited</publisher><ispartof>Annals of the rheumatic diseases, 2016-06, Vol.75 (Suppl 2), p.586</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_2/586.1.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/75/Suppl_2/586.1.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,776,780,3183,23550,27901,27902,77342,77373</link.rule.ids></links><search><creatorcontrib>Fitzgerald, G.</creatorcontrib><creatorcontrib>Lundon, D.J.</creatorcontrib><creatorcontrib>Gallagher, P.</creatorcontrib><creatorcontrib>O'Rourke, K.</creatorcontrib><creatorcontrib>Sheehy, C.</creatorcontrib><creatorcontrib>Sullivan, C.</creatorcontrib><creatorcontrib>Silke, C.</creatorcontrib><creatorcontrib>Stafford, F.</creatorcontrib><creatorcontrib>Haroon, M.</creatorcontrib><creatorcontrib>Mullan, R.</creatorcontrib><creatorcontrib>FitzGerald, O.</creatorcontrib><creatorcontrib>O Shea, F.</creatorcontrib><title>FRI0417 Prevalence of Osteoporosis in An Ankylosing Spondylitis Cohort</title><title>Annals of the rheumatic diseases</title><description>BackgroundThe Ankylosing Spondylitis Registry of Ireland (ASRI) is a web-based database established in 2013, the objectives of which are to provide descriptive epidemiological data on the ankylosing spondylitis (AS) population in Ireland and to establish a registry for potential future studies of genetics, aetiology and therapeutics. The prevalence of osteoporosis is higher in AS patients than age- and sex-matched controls, with potential for vertebral fractures increased. However, the true prevalence is unknown. There is no data on the prevalence of osteoporosis in an Irish cohort.ObjectivesTo determine the prevalence of low bone mineral density (BMD) in an Irish AS cohort.MethodsA standardised detailed clinical assessment was performed on each patient. Disease activity was assessed by Bath AS Disease Activity Index (BASDAI), function by the Bath AS Functional Index (BASFI) and Health Assessment Questionnaire (HAQ) and quality of life by AS Quality of Life (ASQoL). Structured interviews provided patient-reported data. Presence or absence of dual-energy x-ray absorptiometry (DXA) testing and result was recorded. Bone mineral density (BMD) was categorised according to the World Health Organisation criteria into normal BMD, osteopenia or osteoporosis. Statistical analysis was performed using SPSS.ResultsAs of October 2015, 416 patients are enrolled in ASRI: 78.1% males, mean age 47.95 (SD 12.4), mean disease duration 20.9 years (SD 12.2), average delay to diagnosis of 8.8 years (SD 8.3). Mean BASDAI is 3.8 (SD 2.5), BASFI 3.7 (SD 2.7), HAQ 0.53 (SD 0.51) and ASQoL 6.15 (SD 5.5). DXAs have been performed in 24.75% (n=103) of the cohort, of which 39.8% (n=41) have osteopenia and 10.7% (n=11) have osteoporosis. Low BMD is significantly correlated with men and advancing age. There is no association with disease activity or duration. Low BMD is more prevalent in patients treated with one or more biologics compared to those never treated. The self-reported prevalence of osteoporosis is 6.4% (n=27; 19 males).ConclusionsThere is an elevated prevalence of low BMD in this cohort, with no association with disease severity. The majority of affected patients were unaware, as demonstrated by the low self-reported prevalence. More research and education is needed.Disclosure 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>BENPR</sourceid><recordid>eNqVkE1LAzEQhoMoWKv_YaHnrZkmm6R4KsXaQqHixzlkk6zdut2sya7Qmxf_qL_ErPXgVRgY5uOd4X0QGgEeAxB2rerab223N2VIJxhYartK-THDMDlBA6BMxDbDp2iAMSYpnTJ-ji5C2MUSCxADtFw8rDAF_vXxee_tu6psrW3iimQTWusa510oQ1LWyayP10MV6_oleWxcbQ5V2cbh3G2dby_RWaGqYK9-8xA9L26f5st0vblbzWfrNIcJp6nhGSFMZwYLrJVWDIAbq60CSpXFPCu0oMYYMAQyKEiecaVFZoCZQumckCEaHe823r11NrRy5zpfx5cSphhEtEVo3Lo5buloIHhbyMaXe-UPErDs0ck_6GSPTv6gkz26qGZHdb7f_Uv4DT1se1Q</recordid><startdate>201606</startdate><enddate>201606</enddate><creator>Fitzgerald, G.</creator><creator>Lundon, D.J.</creator><creator>Gallagher, P.</creator><creator>O'Rourke, K.</creator><creator>Sheehy, C.</creator><creator>Sullivan, C.</creator><creator>Silke, C.</creator><creator>Stafford, F.</creator><creator>Haroon, M.</creator><creator>Mullan, R.</creator><creator>FitzGerald, O.</creator><creator>O Shea, F.</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>201606</creationdate><title>FRI0417 Prevalence of Osteoporosis in An Ankylosing Spondylitis Cohort</title><author>Fitzgerald, G. ; Lundon, D.J. ; Gallagher, P. ; O'Rourke, K. ; Sheehy, C. ; Sullivan, C. ; Silke, C. ; Stafford, F. ; Haroon, M. ; Mullan, R. ; FitzGerald, O. ; O Shea, F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1274-d75336c5d080caca6117decea144ae075fc84ddd1d3151f3b57ac85d16dfacb33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fitzgerald, G.</creatorcontrib><creatorcontrib>Lundon, D.J.</creatorcontrib><creatorcontrib>Gallagher, P.</creatorcontrib><creatorcontrib>O'Rourke, K.</creatorcontrib><creatorcontrib>Sheehy, C.</creatorcontrib><creatorcontrib>Sullivan, C.</creatorcontrib><creatorcontrib>Silke, C.</creatorcontrib><creatorcontrib>Stafford, F.</creatorcontrib><creatorcontrib>Haroon, M.</creatorcontrib><creatorcontrib>Mullan, R.</creatorcontrib><creatorcontrib>FitzGerald, O.</creatorcontrib><creatorcontrib>O Shea, F.</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>Fitzgerald, G.</au><au>Lundon, D.J.</au><au>Gallagher, P.</au><au>O'Rourke, K.</au><au>Sheehy, C.</au><au>Sullivan, C.</au><au>Silke, C.</au><au>Stafford, F.</au><au>Haroon, M.</au><au>Mullan, R.</au><au>FitzGerald, O.</au><au>O Shea, F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>FRI0417 Prevalence of Osteoporosis in An Ankylosing Spondylitis Cohort</atitle><jtitle>Annals of the rheumatic diseases</jtitle><date>2016-06</date><risdate>2016</risdate><volume>75</volume><issue>Suppl 2</issue><spage>586</spage><pages>586-</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>BackgroundThe Ankylosing Spondylitis Registry of Ireland (ASRI) is a web-based database established in 2013, the objectives of which are to provide descriptive epidemiological data on the ankylosing spondylitis (AS) population in Ireland and to establish a registry for potential future studies of genetics, aetiology and therapeutics. The prevalence of osteoporosis is higher in AS patients than age- and sex-matched controls, with potential for vertebral fractures increased. However, the true prevalence is unknown. There is no data on the prevalence of osteoporosis in an Irish cohort.ObjectivesTo determine the prevalence of low bone mineral density (BMD) in an Irish AS cohort.MethodsA standardised detailed clinical assessment was performed on each patient. Disease activity was assessed by Bath AS Disease Activity Index (BASDAI), function by the Bath AS Functional Index (BASFI) and Health Assessment Questionnaire (HAQ) and quality of life by AS Quality of Life (ASQoL). Structured interviews provided patient-reported data. Presence or absence of dual-energy x-ray absorptiometry (DXA) testing and result was recorded. Bone mineral density (BMD) was categorised according to the World Health Organisation criteria into normal BMD, osteopenia or osteoporosis. Statistical analysis was performed using SPSS.ResultsAs of October 2015, 416 patients are enrolled in ASRI: 78.1% males, mean age 47.95 (SD 12.4), mean disease duration 20.9 years (SD 12.2), average delay to diagnosis of 8.8 years (SD 8.3). Mean BASDAI is 3.8 (SD 2.5), BASFI 3.7 (SD 2.7), HAQ 0.53 (SD 0.51) and ASQoL 6.15 (SD 5.5). DXAs have been performed in 24.75% (n=103) of the cohort, of which 39.8% (n=41) have osteopenia and 10.7% (n=11) have osteoporosis. Low BMD is significantly correlated with men and advancing age. There is no association with disease activity or duration. Low BMD is more prevalent in patients treated with one or more biologics compared to those never treated. The self-reported prevalence of osteoporosis is 6.4% (n=27; 19 males).ConclusionsThere is an elevated prevalence of low BMD in this cohort, with no association with disease severity. The majority of affected patients were unaware, as demonstrated by the low self-reported prevalence. More research and education is needed.Disclosure of InterestNone declared</abstract><cop>Kidlington</cop><pub>Elsevier Limited</pub><doi>10.1136/annrheumdis-2016-eular.6012</doi></addata></record> |
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title | FRI0417 Prevalence of Osteoporosis in An Ankylosing Spondylitis Cohort |
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