Differences Sustained Between Diffuse and Limited Forms of Juvenile Systemic Sclerosis in an Expanded International Cohort
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
33787070
DOI
10.1002/acr.24609
Knihovny.cz E-zdroje
- MeSH
- difuzní sklerodermie * diagnóza MeSH
- intersticiální plicní nemoci * MeSH
- kožní vředy * MeSH
- lidé MeSH
- lokalizovaná sklerodermie MeSH
- průřezové studie MeSH
- systémová sklerodermie * diagnóza epidemiologie MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
OBJECTIVE: 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.
Asklepios Klnik Sankt Augustin Sankt Augustin Germany
Cerrahpasa Medical School Istanbul University Cerrahpasa Istanbul Turkey
Charité University Medicine and German Rheumatism Research Center Berlin Berlin Germany
Charles University Prague Czech Republic
Children's Hospital at Montefiore Bronx New York
Clinical Center Nis University of Niš Nis Serbia
German Rheumatism Research Center Berlin Germany
Ghent University and Ghent University Hospital Ghent Belgium
Great Ormond Street Hospital for Children NHS Foundation Trust London UK
Hamburg Centre for Pediatric and Adolescent Rheumatology Schön Klinik Hamburg Eilbek Hamburg Germany
Hospital de Niños Dr Orlando Alassia Santa Fe Argentina
Hospital de Pediatria J P Garrahan Buenos Aires Argentina
Hospital de Santa Maria Universidade de Lisboa Lisbon Portugal
Hospital for Special Surgery New York New York
Hospital Garcia de Orta Almada Portugal
Hospital Sant Joan de Déu Esplugues Universitat de Barcelona Barcelona Spain
Luzerner Kantonsspital Kinderspital Luzern Switzerland
Medical University Innsbruck Innsbruck Austria
Meir Medical Center Kfar Saba Tel Aviv University Tel Aviv Israel
Meyer Children's Hospital Florence Italy
Riga Stradins University University Children Hospital Riga Latvia
Rigshospitalet Copenhagen Denmark
Saint Petersburg State Pediatric Medical University Saint Petersburg Russia
School of Medical Science University of Campinas Sao Paulo Brazil
SickKids The Hospital for Sick Children Toronto Ontario Canada
Sir Ganga Ram Hospital Delhi India
Sri Ramachandra University Chennai India
Stony Brook Children's Hospital Stony Brook New York
Universidade do Estado Rio de Janeiro Brazil
Universidade Federal de São Paulo Sao Paulo Brazil
University Children's Hospital University Medical Center Ljubljana Ljubljana Slovenia
University Hospital Ramón y Cajal Madrid Spain
University of Missouri Columbia
University of Pittsburgh Children's Hospital of Pittsburgh Pittsburgh Pennsylvania
Zobrazit více v PubMed
Beukelman T, Xie F, Foeldvari I. Assessing the prevalence of juvenile systemic sclerosis in childhood using administrative claims data from the United States. J Scleroderma Relat Disord 2018;3:189-90.
Stevens BE, Torok KS, Li SC, Hershey N, Curran M, Higgins GC, et al. Clinical characteristics and factors associated with disability and impaired quality of life in children with juvenile systemic sclerosis: results from the Childhood Arthritis and Rheumatology Research Alliance Legacy Registry. Arthritis Care Res (Hoboken) 2018;70:1806-13.
Foeldvari I, Klotsche J, Torok KS, Kasapcopur O, Adrovic A, Stanevica V, et al. Characteristics of the first 80 patients at timepoint of first assessment included in the Juvenile Systemic Sclerosis Inception Cohort. J Scleroderma Relat Disord 2019;4:49-61.
Scalapino K, Arkachaisri T, Lucas M, Fertig N, Helfrich DJ, Londino AV Jr, et al. Childhood onset systemic sclerosis: classification, clinical and serologic features, and survival in comparison with adult onset disease. J Rheumatol 2006;33:1004-13.
Martini G, Foeldvari I, Russo R, Cuttica R, Eberhard A, Ravelli A, et al. Systemic sclerosis in childhood: clinical and immunologic features of 153 patients in an international database. Arthritis Rheum 2006;54:3971-8.
Foeldvari I, Zhavania M, Birdi N, Cuttica RJ, de Oliveira SH, Dent PB, et al. Favourable outcome in 135 children with juvenile systemic sclerosis: results of a multi-national survey. Rheumatology (Oxford) 2000;39:556-9.
LeRoy EC, Medsger TA Jr. Criteria for the classification of early systemic sclerosis. J Rheumatol 2001;28:1573-6.
Allanore Y. Limited cutaneous systemic sclerosis: the unfairly neglected subset. J Scleroderma Relat Disord 2016;1:241-6.
Foeldvari I, Nihtyanova SI, Wierk A, Denton CP. Characteristics of patients with juvenile onset systemic sclerosis in an adult single-center cohort. J Rheumatol 2010;37:2422-6.
Li SC. Scleroderma in children and adolescents: localized scleroderma and systemic sclerosis. Pediatr Clin North Am 2018;65:757-81.
Zulian F, Woo P, Athreya BH, Laxer RM, Medsger TA Jr, Lehman TJ, et al. The Pediatric Rheumatology European Society/American College of Rheumatology/European League Against Rheumatism provisional classification criteria for juvenile systemic sclerosis. Arthritis Rheum 2007;57:203-12.
Van den Hoogen F, Khanna D, Fransen J, Johnson SR, Baron M, Tyndall A, et al. 2013 classification criteria for systemic sclerosis: an American College of Rheumatology/European League Against Rheumatism collaborative initiative. Arthritis Rheum 2013;65:2737-47.
Rodnan GP, Lipinski E, Luksick J. Skin thickness and collagen content in progressive systemic sclerosis and localized scleroderma. Arthritis Rheum 1979;22:130-40.
Guedes M, Zilhao C, Almeida I, Silva I. Raynaud and digital ulcers in patients with juvenile systemic sclerosis: ambulatory iloprost protocol. A single center experience. Pediatr Rheumatol Online J 2014;12 Suppl 1:P308.
Bruni C, Ngcozana T, Braschi F, Pucci T, Piemonte G, Benelli L, et al. Preliminary validation of the digital ulcer clinical assessment score in systemic sclerosis. J Rheumatol 2019;46:603-8.
Hansmann G, Koestenberger M, Alastalo TP, Apitz C, Austin ED, Bonnet D, et al. 2019 updated consensus statement on the diagnosis and treatment of pediatric pulmonary hypertension: the European Pediatric Pulmonary Vascular Disease Network (EPPVDN), endorsed by AEPC, ESPR and ISHLT. J Heart Lung Transplant 2019;38:879-901.
Abman SH, Hansmann G, Archer SL, Ivy DD, Adatia I, Chung WK, et al. Pediatric pulmonary hypertension: guidelines from the American Heart Association and American Thoracic Society. Circulation 2015;132:2037-99.
Wollheim FA. Classification of systemic sclerosis: visions and reality. Rheumatology (Oxford) 2005;44:1212-6.
Kowal-Bielecka O, Fransen J, Avouac J, Becker M, Kulak A, Allanore Y, et al. Update of EULAR recommendations for the treatment of systemic sclerosis. Ann Rheum Dis 2017;76:1327-39.
Fernández-Codina A, Walker KM, Pope JE, Scleroderma Algorithm Group. Treatment algorithms for systemic sclerosis according to experts. Arthritis Rheumatol 2018;70:1820-8.
Roofeh D, Khanna D. Management of systemic sclerosis: the first five years. Curr Opin Rheumatol 2020;32:228-37.
Frantz C, Huscher D, Avouac J, Hachulla E, Balbir-Gurman A, Riemekasten G, et al. Outcomes of limited cutaneous systemic sclerosis patients: results on more than 12,000 patients from the EUSTAR database. Autoimmun Rev 2019:102452.
Dougherty DH, Kwakkenbos L, Carrier ME, Salazar G, Assassi S, Baron M, et al. The Scleroderma Patient-Centered Intervention Network cohort: baseline clinical features and comparison with other large scleroderma cohorts. Rheumatology (Oxford) 2018;57:1623-31.
Foeldvari I, Tyndall A, Zulian F, Muller-Ladner U, Czirjak L, Denton C, et al. Juvenile and young adult-onset systemic sclerosis share the same organ involvement in adulthood: data from the EUSTAR database. Rheumatology (Oxford) 2012;51:1832-7.
Pakozdi A, Nihtyanova S, Moinzadeh P, Ong VH, Black CM, Denton CP. Clinical and serological hallmarks of systemic sclerosis overlap syndromes. J Rheumatol 2011;38:2406-9.
Moinzadeh P, Aberer E, Ahmadi-Simab K, Blank N, Distler JH, Fierlbeck G, et al. Disease progression in systemic sclerosis-overlap syndrome is significantly different from limited and diffuse cutaneous systemic sclerosis. Ann Rheum Dis 2015;74:730-7.
Fairley JL, Hansen D, Proudman S, Sahhar J, Ngian GS, Walker J, et al. Clinical features of systemic sclerosis-mixed connective tissue disease and systemic sclerosis overlap syndromes. Arthritis Care Res (Hoboken) 2021;73:732-41.
Johnson S, Hinchcliff M, Asano Y. Controversies: molecular vs. clinical systemic sclerosis classification. J Scleroderma Relat Disord 2016;1:277-85.
Skaug B, Khanna D, Swindell WR, Hinchcliff ME, Frech TM, Steen VD, et al. Global skin gene expression analysis of early diffuse cutaneous systemic sclerosis shows a prominent innate and adaptive inflammatory profile. Ann Rheum Dis 2020;79:379-86.