Publication:
Comparison of clinical features between patients with anti-synthetase syndrome and dermatomyositis: Results from the MYONET registry.

cris.virtualsource.author-orcide918fa71-6dfb-4387-aeb5-77696cc9bc6c
datacite.rightsopen.access
dc.contributor.authorHum, Ryan Malcolm
dc.contributor.authorLilleker, James B
dc.contributor.authorLamb, Janine A
dc.contributor.authorOldroyd, Alexander G S
dc.contributor.authorWang, Guochun
dc.contributor.authorWedderburn, Lucy R
dc.contributor.authorDiederichsen, Louise P
dc.contributor.authorSchmidt, Jens
dc.contributor.authorDanieli, Maria Giovanna
dc.contributor.authorOakley, Paula
dc.contributor.authorGriger, Zoltan
dc.contributor.authorPhuong, Thuy Nguyen Thi
dc.contributor.authorKodishala, Chanakya
dc.contributor.authorMercado, Monica Vazquez-Del
dc.contributor.authorAndersson, Helena
dc.contributor.authorDe Paepe, Boel
dc.contributor.authorDe Bleecker, Jan L
dc.contributor.authorMaurer, Britta
dc.contributor.authorMcCann, Liza
dc.contributor.authorPipitone, Nicolo
dc.contributor.authorMcHugh, Neil
dc.contributor.authorNew, Robert Paul
dc.contributor.authorOllier, William E
dc.contributor.authorKrogh, Niels Steen
dc.contributor.authorVencovsky, Jiri
dc.contributor.authorLundberg, Ingrid E
dc.contributor.authorChinoy, Hector
dc.date.accessioned2024-10-25T18:06:07Z
dc.date.available2024-10-25T18:06:07Z
dc.date.issued2024-08-01
dc.description.abstractOBJECTIVES To compare clinical characteristics, including the frequency of cutaneous, extramuscular manifestations, and malignancy, between adults with anti-synthetase syndrome (ASyS) and dermatomyositis (DM). METHODS Using data regarding adults from the MYONET registry, a cohort of DM patients with anti-Mi2/-TIF1ɣ/-NXP2/-SAE/-MDA5 autoantibodies, and a cohort of ASyS patients with anti-tRNA synthetase autoantibodies (anti-Jo1/-PL7/-PL12/-OJ/-EJ/-Zo/-KS) were identified. Patients with DM sine dermatitis or with discordant dual autoantibody specificities were excluded. Sub-cohorts of patients with ASyS with or without skin involvement were defined based on presence of DM-type rashes (heliotrope rash, Gottron's papules/sign, violaceous rash, shawl sign, V sign, erythroderma, and/or periorbital rash). RESULTS In total 1,054 patients were included (DM, n = 405; ASyS, n = 649). In ASyS cohort, 31% (n = 203) had DM-type skin involvement (ASyS-DMskin). A higher frequency of extramuscular manifestations, including Mechanic's hands, Raynaud's phenomenon, arthritis, interstitial lung disease, and cardiac involvement differentiated ASyS-DMskin from DM (all p< 0.001), whereas higher frequency of any of four DM-type rashes: heliotrope rash (n = 248, 61% vs n = 90, 44%), violaceous rash (n = 166, 41% vs n = 57, 9%), V sign (n = 124, 31% vs n = 28, 4%), and shawl sign (n = 133, 33% vs n = 18, 3%) differentiated DM from ASyS-DMskin (all p< 0.005). Cancer-associated myositis (CAM) was more frequent in DM (n = 67, 17%) compared with ASyS (n = 21, 3%) and ASyS-DMskin (n = 7, 3%) cohorts (both p< 0.001). CONCLUSION DM-type rashes are frequent in patients with ASyS; however, distinct clinical manifestations differentiate these patients from classical DM. Skin involvement in ASyS does not necessitate increased malignancy surveillance. These findings will inform future ASyS classification criteria and patient management.
dc.description.numberOfPages8
dc.description.sponsorshipUniversitätsklinik für Rheumatologie und Immunologie - Fachbereich Rheumatologie
dc.identifier.doi10.48350/186271
dc.identifier.pmid37698987
dc.identifier.publisherDOI10.1093/rheumatology/kead481
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/169944
dc.language.isoen
dc.publisherOxford University Press
dc.relation.ispartofRheumatology
dc.relation.issn1462-0332
dc.relation.organizationClinic of Rheumatology and Immunology
dc.subjectAntisynthetase syndrome MYONET Raynaud’s phenomenon cutaneous dermatomyositis epidemiology extramuscular malignancy rashes skin
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleComparison of clinical features between patients with anti-synthetase syndrome and dermatomyositis: Results from the MYONET registry.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage2100
oaire.citation.issue8
oaire.citation.startPage2093
oaire.citation.volume63
oairecerif.author.affiliationUniversitätsklinik für Rheumatologie und Immunologie - Fachbereich Rheumatologie
oairecerif.author.affiliation2Universitätsklinik für Rheumatologie und Immunologie
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unibe.date.licenseChanged2023-09-14 09:30:19
unibe.description.ispublishedpub
unibe.eprints.legacyId186271
unibe.refereedtrue
unibe.subtype.articlejournal

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