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Derivation and validation of adult Still Activity Score (SAS)

dc.contributor.authorKalyoncu, Umut
dc.contributor.authorKaşifoğlu, Timuçin
dc.contributor.authorOmma, Ahmet
dc.contributor.authorBeş, Cemal
dc.contributor.authorÇınar, Muhammet
dc.contributor.authorEmmungil, Hakan
dc.contributor.authorKüçükşahin, Orhan
dc.contributor.authorAkar, Servet
dc.contributor.authorAksu, Kenan
dc.contributor.authorYıldız, Fatih
dc.contributor.authorKanitez, Nilüfer Alpay
dc.contributor.authorErden, Abdulsamet
dc.contributor.authorBilgin, Emre
dc.contributor.authorDalkılıç, Ediz
dc.contributor.authorErmurat, Selime
dc.contributor.authorHayran, Mutlu
dc.contributor.buuauthorDALKILIÇ, HÜSEYİN EDİZ
dc.contributor.buuauthorErmurat, Selime
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentRomatoloji Bölümü
dc.contributor.researcheridABE-4424-2022
dc.contributor.researcheridCMF-4757-2022
dc.date.accessioned2024-11-29T10:38:18Z
dc.date.available2024-11-29T10:38:18Z
dc.date.issued2022-11-30
dc.description.abstractObjectives: Adult-onset Still's disease (AOSD) is a multi-systemic, autoinflammatory disorder. Several activity scores have been proposed but none of them have been adopted universally. Our aim was to create a clinician-friendly activity scoring system by using simple clinical and laboratory parameters.Methods: AODS patients, according to Yamaguchi criteria, were included in this cross-sectional, multi-center study. Derivation and validation cohorts were constituted. Demographic, clinical, and laboratory evaluation at the study visit; patients' and physicians' global assessments of disease activity (both VAS/Likert scale) were recorded. To develop the score, an ordinal logistic regression model was used to determine independent predictors of physicians' global assessments of disease activity. Clinically and statistically significant variables were weighted according to regression coefficients. Then, performance of the score was tested on the validation cohort. Results: A total of 197 consecutive AOSD patients (125 in derivation, 72 in validation cohorts) were included. Final Still Activity Score was fever (2 points), arthralgia (2 points, plus 1 point if arthritis was present in >= 2 joints), neutrophilia >= 65% (1 point) and ferritin >= 350 ng/mL (1 point) (maximum of 7 points). The SAS yielded an AUC value of 0.98 (0.96-1.00) in the derivation cohort and 0.91 (95%CI: 0.85-0.98) in the validation cohort to discriminate high AOSD activity from moderate-inactive AOSD. The correlation of SAS with PGA was 83% for the derivation cohort and 76% for the validation cohort. Conclusions: SAS has shown a good test performance to distinguish active AOSD patients from others. SAS may be a useful method for evaluating the disease activity of AOSD patients in daily practice.(c) 2022 Socie acute accent te acute accent franc , aise de rhumatologie. Published by Elsevier Masson SAS. All rights reserved.
dc.identifier.doi10.1016/j.jbspin.2022.105499
dc.identifier.eissn1778-7254
dc.identifier.issn1297-319X
dc.identifier.issue1
dc.identifier.scopus2-s2.0-85142832760
dc.identifier.urihttps://doi.org/10.1016/j.jbspin.2022.105499
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S1297319X22001592
dc.identifier.urihttps://hdl.handle.net/11452/48706
dc.identifier.volume90
dc.identifier.wos000902129000003
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherElsevier
dc.relation.journalJoint Bone Spine
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectClinical-manifestations
dc.subjectDisease course
dc.subjectMulticenter
dc.subjectAdult-onset still?s disease
dc.subjectDisease activity score
dc.subjectArthralgia
dc.subjectFerritin
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectRheumatology
dc.titleDerivation and validation of adult Still Activity Score (SAS)
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Romatoloji Bölümü
local.indexed.atWOS
local.indexed.atScopus
relation.isAuthorOfPublication1613225c-2f43-4052-9f82-210c854edcf4
relation.isAuthorOfPublication.latestForDiscovery1613225c-2f43-4052-9f82-210c854edcf4

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