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dc.contributor.authorAnton, Jordi
dc.contributor.authorLehman, Thomas
dc.contributor.authorSifuentes-Giraldo, Walter-Alberto
dc.contributor.authorVasquez-Canizares, Natalia
dc.contributor.authorAppenzeller, Simone
dc.contributor.authorJanarthanan, Mahesh
dc.contributor.authorMoll, Monika
dc.contributor.authorNemcova, Dana
dc.contributor.authorPatwardhan, Anjali
dc.contributor.authorSantos, Maria Jose
dc.contributor.authorSawhney, Sujata
dc.contributor.authorSchonenberg-Meinema, Dieneke
dc.contributor.authorBattagliotti, Cristina
dc.contributor.authorBerntson, Lillemor
dc.contributor.authorBica, Blanca
dc.contributor.authorBrunner, Jurgen
dc.contributor.authorCosta-Reis, Patricia
dc.contributor.authorEleftheriou, Despina
dc.contributor.authorHarel, Liora
dc.contributor.authorHorneff, Gerd
dc.contributor.authorKaiser, Daniela
dc.contributor.authorKallinich, Tilmann
dc.contributor.authorLazarevic, Dragana
dc.contributor.authorMinden, Kirsten
dc.contributor.authorNielsen, Susan
dc.contributor.authorNuruzzaman, Farzana
dc.contributor.authorUziel, Yosef
dc.contributor.authorHelmus, Nicola
dc.contributor.authorTorok, Kathryn S.
dc.contributor.authorFoeldvari, Ivan
dc.contributor.authorKlotsche, Jens
dc.contributor.authorKASAPÇOPUR, ÖZGÜR
dc.contributor.authorAdrovic, Amra
dc.contributor.authorTerreri, Maria Teresa
dc.contributor.authorSakamoto, Ana Paula
dc.contributor.authorStanevicha, Valda
dc.contributor.authorSztajnbok, Flavio
dc.contributor.authorFeldman, Brian
dc.contributor.authorAlexeeva, Ekaterina
dc.contributor.authorKatsicas, Maria
dc.contributor.authorSmith, Vanessa
dc.contributor.authorAvcin, Tadej
dc.contributor.authorMarrani, Edoardo
dc.contributor.authorKostik, Mikhail
dc.date.accessioned2022-07-04T13:14:47Z
dc.date.available2022-07-04T13:14:47Z
dc.identifier.citationFoeldvari I., Klotsche J., KASAPÇOPUR Ö., Adrovic A., Terreri M. T. , Sakamoto A. P. , Stanevicha V., Sztajnbok F., Anton J., Feldman B., et al., "Differences Sustained Between Diffuse and Limited Forms of Juvenile Systemic Sclerosis in an Expanded International Cohort", ARTHRITIS CARE & RESEARCH, 2022
dc.identifier.issn2151-464X
dc.identifier.othervv_1032021
dc.identifier.otherav_40c83c2c-e631-4c9d-93ec-c793a388bd27
dc.identifier.urihttp://hdl.handle.net/20.500.12627/182461
dc.identifier.urihttps://avesis.istanbul.edu.tr/api/publication/40c83c2c-e631-4c9d-93ec-c793a388bd27/file
dc.identifier.urihttps://doi.org/10.1002/acr.24609
dc.description.abstractObjective To evaluate the baseline clinical characteristics of juvenile systemic sclerosis (SSc) patients in the international juvenile SSc inception cohort, and to compare these characteristics between the classically defined juvenile diffuse cutaneous SSc (dcSSc) and limited cutaneous SSc (lcSSc) subtypes and among those with overlap features. Methods A cross-sectional study was performed using baseline visit data. Information on demographic characteristics, organ system evaluation, treatment, and patient- and physician-reported outcomes was extracted and summary statistics applied. Comparisons between juvenile dcSSc and lcSSc subtypes and patients with and without overlap features were performed using chi-square and Mann-Whitney U tests. Results At data extraction, 150 juvenile SSc patients were enrolled across 42 centers; 83% were White, 80% were female, juvenile dcSSc predominated (72%), and 17% of the cohort had overlap features. Significant differences were found between juvenile dcSSc and juvenile lcSSc regarding modified Rodnan skin thickness score, the presence of Gottron's papules, digital tip ulceration, results of the 6-minute walk test, and composite pulmonary and cardiac involvement. All of these were more frequent in dcSSc except for cardiac involvement. Juvenile dcSSc patients had significantly worse scores for physician-rated disease activity and damage. A significantly higher occurrence of Gottron's papules and musculoskeletal and composite pulmonary involvement, and a significantly lower frequency of Raynaud's phenomenon, were seen in those with overlap features. Conclusion Results from a large international juvenile SSc cohort demonstrate significant differences between juvenile dcSSc and juvenile lcSSc patients, including more globally severe disease and increased frequency of interstitial lung disease in juvenile dcSSc patients, while those with lcSSc have more frequent cardiac involvement. Those with overlap features had an unexpected higher frequency of interstitial lung disease.
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectİmmünoloji ve Romatoloji
dc.subjectRheumatology
dc.subjectHealth Sciences
dc.subjectROMATOLOJİ
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.titleDifferences Sustained Between Diffuse and Limited Forms of Juvenile Systemic Sclerosis in an Expanded International Cohort
dc.typeMakale
dc.relation.journalARTHRITIS CARE & RESEARCH
dc.contributor.departmentSchon Klin Hamburg Eilbek , ,
dc.contributor.firstauthorID3432372


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