AB0820 Psoriatic Arthritis Mutilans Cohort Attending St. Vincent'S University Hospital: Demographics and Clinical Characteristics

BackgroundPsoriatic Arthritis (PsA) affects about 30% of individual with psoriasis after an average interval of 10 years (1,2). The most common classification of PsA by Moll and Wright still remains widely in use (3). The criteria include five clinical subgroups of PsA according to the pattern of jo...

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Veröffentlicht in:Annals of the rheumatic diseases 2015-06, Vol.74 (Suppl 2), p.1173-1174
Hauptverfasser: Elmamoun, M., Haroon, M., Gallagher, P., FitzGerald, O.
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Haroon, M.
Gallagher, P.
FitzGerald, O.
description BackgroundPsoriatic Arthritis (PsA) affects about 30% of individual with psoriasis after an average interval of 10 years (1,2). The most common classification of PsA by Moll and Wright still remains widely in use (3). The criteria include five clinical subgroups of PsA according to the pattern of joint involvement: oligoarthritis, polyarthritis, distal small joint arthritis, spondylarthritis, and Arthritis Mutilans (AM). AM is a rare type of PsA. In the literature the prevalence of AM has been estimated to range from zero or just 1% (4,5) up to 8% (6) of the PsA population.ObjectivesTo determine the demographic and clinical characteristics of psoriatic AM in an Irish cohort attending a rheumatology unit.MethodsPatients with a diagnosis of PsA, fulfilling the CASPAR criteria, who have AM, defined by digital shortening, erosion involving entire articular surfaces on both sides of the joint and/or pencil-in-cup change and/or osteolysis, aged >18 years were recruited. 23 patients were included after clinical and radiological examinations.ResultsThe female to male ratio was close to 2:1. The mean age was 56.52. The mean age of skin disease onset was 24 years and the mean age of onset of joint disease was 30 years. At inclusion, the mean duration of arthritis was 25.8 years ±9.9 years. The only pattern of arthritis was that of polyarticular disease; with 48% of patients exhibiting concomitant axial disease. Enthesitis was found in 8 patients (35%), while 13 patients (57%) had dactylitis. 8 patients (35%) had sacroiliitis on plain films, 6 of these patients (75%) had asymmetrical sacroiliitis. 21 patients (91%) had nail disease. None of the patients in this cohort had uveitis. At the time of inclusion, 70% of patients were found to have clear or almost clear skin. 16 patients were on biologics (75%). The most frequent joints that showed AM were the MTP joints on the fourth toe on the left foot (n=10), followed by MTP joints on the fourth toe on the right (n=9). Further characteristics are outlined table 1.ConclusionsThe prevalence of AM in our psoriatic arthritis cohort is approximately 8%. The majority of patients present with nail disease, and mild skin disease. The average interval between skin and joint disease is approximately 6 years. AM occurs in the setting of poly articular disease and frequent axial involvement. The axial disease in these patients tends to be asymmetrical sacroiliitis. Many patients require biologics to control their disease.ReferencesM
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The most common classification of PsA by Moll and Wright still remains widely in use (3). The criteria include five clinical subgroups of PsA according to the pattern of joint involvement: oligoarthritis, polyarthritis, distal small joint arthritis, spondylarthritis, and Arthritis Mutilans (AM). AM is a rare type of PsA. In the literature the prevalence of AM has been estimated to range from zero or just 1% (4,5) up to 8% (6) of the PsA population.ObjectivesTo determine the demographic and clinical characteristics of psoriatic AM in an Irish cohort attending a rheumatology unit.MethodsPatients with a diagnosis of PsA, fulfilling the CASPAR criteria, who have AM, defined by digital shortening, erosion involving entire articular surfaces on both sides of the joint and/or pencil-in-cup change and/or osteolysis, aged &gt;18 years were recruited. 23 patients were included after clinical and radiological examinations.ResultsThe female to male ratio was close to 2:1. The mean age was 56.52. The mean age of skin disease onset was 24 years and the mean age of onset of joint disease was 30 years. At inclusion, the mean duration of arthritis was 25.8 years ±9.9 years. The only pattern of arthritis was that of polyarticular disease; with 48% of patients exhibiting concomitant axial disease. Enthesitis was found in 8 patients (35%), while 13 patients (57%) had dactylitis. 8 patients (35%) had sacroiliitis on plain films, 6 of these patients (75%) had asymmetrical sacroiliitis. 21 patients (91%) had nail disease. None of the patients in this cohort had uveitis. At the time of inclusion, 70% of patients were found to have clear or almost clear skin. 16 patients were on biologics (75%). The most frequent joints that showed AM were the MTP joints on the fourth toe on the left foot (n=10), followed by MTP joints on the fourth toe on the right (n=9). Further characteristics are outlined table 1.ConclusionsThe prevalence of AM in our psoriatic arthritis cohort is approximately 8%. The majority of patients present with nail disease, and mild skin disease. The average interval between skin and joint disease is approximately 6 years. AM occurs in the setting of poly articular disease and frequent axial involvement. The axial disease in these patients tends to be asymmetrical sacroiliitis. Many patients require biologics to control their disease.ReferencesMease PJ, Gladman DD, et al: Prevalence of rheumatologist-diagnosed psoriatic arthritis in patients with psoriasis in European/North American dermatology clinics, J Am Acad Dermatol. 69(5):729-35, 2013Gladman DD, et al. Psoriatic arthritis (PSA): an analysis of 220 patients. Q J Med 1987;62:127–41Moll JMH, Wright V. Psoriatic arthritis. Semin Arthritis Rheum. 1973;3:55–78.Tam LS, Leung YY, Li EK. Psoriatic arthritis in Asia. Rheumatology (Oxford) 2009;48:1473–7.Scarpa R. Clinical manifestation and diagnosis of psoriatic arthritis. Rheumatology in Europe 1998;27:130–2.Koo T, Nagy Z, et al. Subsets in psoriatic arthritis by cluster analysis. Clin Rheumatol 2001;20:36–43.Disclosure of InterestNone declared</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2015-eular.5098</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><ispartof>Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.1173-1174</ispartof><rights>2015, 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: 2015 (c) 2015, 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/74/Suppl_2/1173.2.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/74/Suppl_2/1173.2.full$$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>Elmamoun, M.</creatorcontrib><creatorcontrib>Haroon, M.</creatorcontrib><creatorcontrib>Gallagher, P.</creatorcontrib><creatorcontrib>FitzGerald, O.</creatorcontrib><title>AB0820 Psoriatic Arthritis Mutilans Cohort Attending St. Vincent'S University Hospital: Demographics and Clinical Characteristics</title><title>Annals of the rheumatic diseases</title><description>BackgroundPsoriatic Arthritis (PsA) affects about 30% of individual with psoriasis after an average interval of 10 years (1,2). The most common classification of PsA by Moll and Wright still remains widely in use (3). The criteria include five clinical subgroups of PsA according to the pattern of joint involvement: oligoarthritis, polyarthritis, distal small joint arthritis, spondylarthritis, and Arthritis Mutilans (AM). AM is a rare type of PsA. In the literature the prevalence of AM has been estimated to range from zero or just 1% (4,5) up to 8% (6) of the PsA population.ObjectivesTo determine the demographic and clinical characteristics of psoriatic AM in an Irish cohort attending a rheumatology unit.MethodsPatients with a diagnosis of PsA, fulfilling the CASPAR criteria, who have AM, defined by digital shortening, erosion involving entire articular surfaces on both sides of the joint and/or pencil-in-cup change and/or osteolysis, aged &gt;18 years were recruited. 23 patients were included after clinical and radiological examinations.ResultsThe female to male ratio was close to 2:1. The mean age was 56.52. The mean age of skin disease onset was 24 years and the mean age of onset of joint disease was 30 years. At inclusion, the mean duration of arthritis was 25.8 years ±9.9 years. The only pattern of arthritis was that of polyarticular disease; with 48% of patients exhibiting concomitant axial disease. Enthesitis was found in 8 patients (35%), while 13 patients (57%) had dactylitis. 8 patients (35%) had sacroiliitis on plain films, 6 of these patients (75%) had asymmetrical sacroiliitis. 21 patients (91%) had nail disease. None of the patients in this cohort had uveitis. At the time of inclusion, 70% of patients were found to have clear or almost clear skin. 16 patients were on biologics (75%). The most frequent joints that showed AM were the MTP joints on the fourth toe on the left foot (n=10), followed by MTP joints on the fourth toe on the right (n=9). Further characteristics are outlined table 1.ConclusionsThe prevalence of AM in our psoriatic arthritis cohort is approximately 8%. The majority of patients present with nail disease, and mild skin disease. The average interval between skin and joint disease is approximately 6 years. AM occurs in the setting of poly articular disease and frequent axial involvement. The axial disease in these patients tends to be asymmetrical sacroiliitis. Many patients require biologics to control their disease.ReferencesMease PJ, Gladman DD, et al: Prevalence of rheumatologist-diagnosed psoriatic arthritis in patients with psoriasis in European/North American dermatology clinics, J Am Acad Dermatol. 69(5):729-35, 2013Gladman DD, et al. Psoriatic arthritis (PSA): an analysis of 220 patients. Q J Med 1987;62:127–41Moll JMH, Wright V. Psoriatic arthritis. Semin Arthritis Rheum. 1973;3:55–78.Tam LS, Leung YY, Li EK. Psoriatic arthritis in Asia. Rheumatology (Oxford) 2009;48:1473–7.Scarpa R. Clinical manifestation and diagnosis of psoriatic arthritis. Rheumatology in Europe 1998;27:130–2.Koo T, Nagy Z, et al. Subsets in psoriatic arthritis by cluster analysis. Clin Rheumatol 2001;20:36–43.Disclosure of InterestNone declared</description><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</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>eNqVkM1KAzEURoMoWKvvEOjC1dTcyTST0VUdfypUFGrdhmSacVKmmZpkhO4E8UV9EqfWhVtXl3v5zv3gIDQAMgSg7Exa6yrdrhbGRzGBUaTbWrrhiGR8D_UgYbw7M7KPeoQQGiUZSw_RkffLbiUceA99jC8Jj8nX--ejb5yRwRR47ELlTDAe37fB1NJ6nDdV4wIeh6DtwtgXPAtD_GxsoW04neG5NW_aeRM2eNL4tQmyPsdXetW8OLmuTOGxtAuc18aaQtY4r6STRdDO-K7PH6ODUtZen_zOPprfXD_lk2j6cHuXj6eRgjgdRTFVi4JSrgBKTqHUUiumYhYnKmNJRpRiwGWmKAOI4xRKllBacp4VVHJNKe2jwe7v2jWvrfZBLJvW2a5SQEYgTYHCqEtd7FKFa7x3uhRrZ1bSbQQQsbUu_lgXW-vix7rYWu9otqPVavkv8BtQxY-7</recordid><startdate>201506</startdate><enddate>201506</enddate><creator>Elmamoun, M.</creator><creator>Haroon, M.</creator><creator>Gallagher, P.</creator><creator>FitzGerald, O.</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>201506</creationdate><title>AB0820 Psoriatic Arthritis Mutilans Cohort Attending St. Vincent'S University Hospital: Demographics and Clinical Characteristics</title><author>Elmamoun, M. ; Haroon, M. ; Gallagher, P. ; FitzGerald, O.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1275-23bdc338b11f831feaeb6b2624b96490bb618a9b36112271f6433f889c3a8e333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Elmamoun, M.</creatorcontrib><creatorcontrib>Haroon, M.</creatorcontrib><creatorcontrib>Gallagher, P.</creatorcontrib><creatorcontrib>FitzGerald, O.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Health &amp; Medical Complete</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)</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</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</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>ProQuest Family Health</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>ProQuest Biological Science Journals</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>Elmamoun, M.</au><au>Haroon, M.</au><au>Gallagher, P.</au><au>FitzGerald, O.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>AB0820 Psoriatic Arthritis Mutilans Cohort Attending St. Vincent'S University Hospital: Demographics and Clinical Characteristics</atitle><jtitle>Annals of the rheumatic diseases</jtitle><date>2015-06</date><risdate>2015</risdate><volume>74</volume><issue>Suppl 2</issue><spage>1173</spage><epage>1174</epage><pages>1173-1174</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>BackgroundPsoriatic Arthritis (PsA) affects about 30% of individual with psoriasis after an average interval of 10 years (1,2). The most common classification of PsA by Moll and Wright still remains widely in use (3). The criteria include five clinical subgroups of PsA according to the pattern of joint involvement: oligoarthritis, polyarthritis, distal small joint arthritis, spondylarthritis, and Arthritis Mutilans (AM). AM is a rare type of PsA. In the literature the prevalence of AM has been estimated to range from zero or just 1% (4,5) up to 8% (6) of the PsA population.ObjectivesTo determine the demographic and clinical characteristics of psoriatic AM in an Irish cohort attending a rheumatology unit.MethodsPatients with a diagnosis of PsA, fulfilling the CASPAR criteria, who have AM, defined by digital shortening, erosion involving entire articular surfaces on both sides of the joint and/or pencil-in-cup change and/or osteolysis, aged &gt;18 years were recruited. 23 patients were included after clinical and radiological examinations.ResultsThe female to male ratio was close to 2:1. The mean age was 56.52. The mean age of skin disease onset was 24 years and the mean age of onset of joint disease was 30 years. At inclusion, the mean duration of arthritis was 25.8 years ±9.9 years. The only pattern of arthritis was that of polyarticular disease; with 48% of patients exhibiting concomitant axial disease. Enthesitis was found in 8 patients (35%), while 13 patients (57%) had dactylitis. 8 patients (35%) had sacroiliitis on plain films, 6 of these patients (75%) had asymmetrical sacroiliitis. 21 patients (91%) had nail disease. None of the patients in this cohort had uveitis. At the time of inclusion, 70% of patients were found to have clear or almost clear skin. 16 patients were on biologics (75%). The most frequent joints that showed AM were the MTP joints on the fourth toe on the left foot (n=10), followed by MTP joints on the fourth toe on the right (n=9). Further characteristics are outlined table 1.ConclusionsThe prevalence of AM in our psoriatic arthritis cohort is approximately 8%. The majority of patients present with nail disease, and mild skin disease. The average interval between skin and joint disease is approximately 6 years. AM occurs in the setting of poly articular disease and frequent axial involvement. The axial disease in these patients tends to be asymmetrical sacroiliitis. Many patients require biologics to control their disease.ReferencesMease PJ, Gladman DD, et al: Prevalence of rheumatologist-diagnosed psoriatic arthritis in patients with psoriasis in European/North American dermatology clinics, J Am Acad Dermatol. 69(5):729-35, 2013Gladman DD, et al. Psoriatic arthritis (PSA): an analysis of 220 patients. Q J Med 1987;62:127–41Moll JMH, Wright V. Psoriatic arthritis. Semin Arthritis Rheum. 1973;3:55–78.Tam LS, Leung YY, Li EK. Psoriatic arthritis in Asia. Rheumatology (Oxford) 2009;48:1473–7.Scarpa R. Clinical manifestation and diagnosis of psoriatic arthritis. Rheumatology in Europe 1998;27:130–2.Koo T, Nagy Z, et al. Subsets in psoriatic arthritis by cluster analysis. Clin Rheumatol 2001;20:36–43.Disclosure of InterestNone declared</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/annrheumdis-2015-eular.5098</doi><tpages>2</tpages></addata></record>
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