Patterns and predictors of skin score change in early diffuse systemic sclerosis from the European Scleroderma Observational Study

被引:51
|
作者
Herrick, Ariane L. [1 ,2 ]
Peytrignet, Sebastien [3 ]
Lunt, Mark [3 ]
Pan, Xiaoyan [3 ]
Hesselstrand, Roger [4 ]
Mouthon, Luc [5 ]
Silman, Alan J. [6 ]
Dinsdale, Graham [1 ]
Brown, Edith [7 ]
Czirjak, Laszlo [8 ]
Distler, Joerg H. W. [9 ]
Distler, Oliver [10 ]
Fligelstone, Kim [11 ]
Gregory, William J. [12 ]
Ochiel, Rachel [11 ]
Vonk, Madelon C. [13 ]
Ancuta, Codrina [14 ]
Ong, Voon H. [15 ]
Farge, Dominique [16 ]
Hudson, Marie [17 ,18 ]
Matucci-Cerinic, Marco [19 ]
Balbir-Gurman, Alexandra [20 ]
Midtvedt, Oyvind [21 ]
Jobanputra, Paresh [22 ]
Jordan, Alison C. [22 ]
Stevens, Wendy [23 ]
Moinzadeh, Pia [24 ]
Hall, Frances C. [25 ]
Agard, Christian [26 ]
Anderson, Marina E. [27 ]
Diot, Elisabeth [28 ]
Madhok, Rajan [29 ]
Akil, Mohammed [30 ]
Buch, Maya H. [31 ,32 ]
Chung, Lorinda [33 ]
Damjanov, Nemanja S. [34 ]
Gunawardena, Harsha [35 ]
Lanyon, Peter [36 ,37 ]
Ahmad, Yasmeen [38 ]
Chakravarty, Kuntal [39 ]
Jacobsen, Soren [40 ]
MacGregor, Alexander J. [41 ]
McHugh, Neil [42 ]
Mueller-Ladner, Ulf [43 ]
Riemekasten, Gabriela [44 ]
Becker, Michael [45 ]
Roddy, Janet [46 ]
Carreira, Patricia E. [47 ]
Fauchais, Anne Laure [48 ]
Hachulla, Eric [49 ,50 ]
机构
[1] Univ Manchester, Manchester Acad Hlth Sci Ctr, Salford Royal NHS Fdn Trust, Ctr Musculoskeletal Res, Manchester, Lancs, England
[2] Cent Manchester NHS Fdn Trust, Manchester Acad Hlth Sci Ctr, NIHR Manchester Musculoskeletal Biomed Res Ctr, Manchester, Lancs, England
[3] Univ Manchester, Manchester Acad Hlth Sci Ctr, Ctr Musculoskeletal Res, Manchester, Lancs, England
[4] Lund Univ, Dept Rheumatol, Lund, Sweden
[5] Univ Paris 05, Hop Cochin, Ctr Reference Vasc Necrosantes & Sclerodermie Sys, Serv Med Interne, Paris, France
[6] Univ Oxford, Nuffield Dept Orthopaed Rheumatol & Musculoskelet, Oxford, England
[7] Univ Manchester, Manchester, Greater Manches, England
[8] Univ Pecs, Dept Rheumatol & Immunol, Med Ctr, Pecs, Hungary
[9] Univ Erlangen Nurnberg, Dept Internal Med 3, Erlangen, Germany
[10] Univ Zurich, Dept Rheumatol, Zurich, Switzerland
[11] Royal Free London NHS Fdn Trust, London, England
[12] Salford Royal NHS Fdn Trust, Rehabil Serv, Salford, Lancs, England
[13] Radboud Univ Nijmegen, Med Ctr, Dept Rheumat Dis, Nijmegen, Netherlands
[14] Grigore T Popa Univ Med & Pharm, Clin Rehabil Hosp, Rheumatol Dept 2, Iasi, Romania
[15] UCL Div Med, Ctr Rheumatol & Connect Tissue Dis, London, England
[16] Paris Denis Diderot Univ, Hop St Louis, AP HP,Malad Autoimmunes & Pathol Vasc, INSERM,UMRS 1160,Unite Clin Med Interne,UF 04, Paris, France
[17] Lady Davis Inst, Jewish Gen Hosp, Montreal, PQ, Canada
[18] McGill Univ, Montreal, PQ, Canada
[19] Univ Florence, AOUC, Dept Expt & Clin Med, Div Rheumatol, Florence, Italy
[20] Rambam Hlth Care Campus, Rappaport Fac Med, Shine Rheumatol Unit, Haifa, Israel
[21] Natl Hosp Norway, Oslo Univ Hosp, Rheumatol Unit, Oslo, Norway
[22] UHB Fdn Trust, Queen Elizabeth Hosp Birmingham, Birmingham, W Midlands, England
[23] St Vincents Hosp, Melbourne, Vic, Australia
[24] Univ Cologne, Dept Dermatol, Kerpener Str, Cologne, Germany
[25] Cambridge Univ NHS Hosp Fdn Trust, Cambridge, England
[26] Univ Nantes, Hotel Dieu Hosp, Dept Internal Med, Nantes, France
[27] Univ Liverpool, Aintree Univ Hosp, Liverpool, Merseyside, England
[28] Hop Bretonneau Tours, Serv Med Interne, Tours, France
[29] Royal Infirm, Ctr Rheumat Dis, Glasgow, Lanark, Scotland
[30] Sheffield Teaching Hosp, Sheffield, S Yorkshire, England
[31] Univ Leeds, Leeds Inst Rheumat & Musculoskeletal Med, Leeds, W Yorkshire, England
[32] Leeds Teaching Hosp NHS Trust, NIHR Leeds Musculoskeletal Biomed Res Ctr, Leeds, W Yorkshire, England
[33] Stanford Univ, Stanford, CA 94305 USA
[34] Univ Belgrade, Sch Med, Inst Rheumatol, Belgrade, Serbia
[35] North Bristol NHS Trust, Clin & Acad Rheumatol, Bristol, Avon, England
[36] Nottingham Univ Hosp NHS Trust, Nottingham, England
[37] Nottingham NHS Treatment Ctr, Nottingham, England
[38] Peter Maddison Rheumatol Ctr, Llandudno, Wales
[39] Queens Hosp, Romford, Essex, England
[40] Univ Copenhagen, Rigshosp, Copenhagen Lupus & Vasculitis Clin, Ctr Rheumatol & Spine Dis, Copenhagen, Denmark
[41] Univ East Anglia, Norwich Med Sch, Norwich, Norfolk, England
[42] Royal Natl Hosp Rheumat Dis, Bath, Avon, England
[43] Justus Liebig Univ Giessen, Dept Rheumatol & Clin Immunol, Bad Nauheim, Germany
[44] Univ Lubeck, Dept Rheumatol, Lubeck, Germany
[45] Univ Hosp Charite Berlin, Dept Rheumatol & Clin Immunol, Berlin, Germany
[46] Royal Perth Hosp, Dept Rheumatol, Perth, WA, Australia
[47] Hosp Univ 12 Octubre, Serv Reumatol, Madrid, Spain
[48] Limoges Univ Hosp, Internal Med Unit, Limoges, France
[49] Univ Lille, Dept Med Interne, Ctr Natl Reference Malad Syst & Autoimmunes Rares, Lille, France
[50] Univ Lille, Immunol Clin, Lille, France
关键词
systemic sclerosis; autoantibodies; outcomes research; DOUBLE-BLIND; THICKNESS SCORE; D-PENICILLAMINE; PLACEBO; MULTICENTER; FIBROSIS; THERAPY; TRIAL;
D O I
10.1136/annrheumdis-2017-211912
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives Our aim was to use the opportunity provided by the European Scleroderma Observational Study to (1) identify and describe those patients with early diffuse cutaneous systemic sclerosis (dcSSc) with progressive skin thickness, and (2) derive prediction models for progression over 12 months, to inform future randomised controlled trials (RCTs). Methods The modified Rodnan skin score (mRSS) was recorded every 3months in 326 patients. Progressors' were defined as those experiencing a 5-unit and 25% increase in mRSS score over 12 months (3 months). Logistic models were fitted to predict progression and, using receiver operating characteristic (ROC) curves, were compared on the basis of the area under curve (AUC), accuracy and positive predictive value (PPV). Results 66 patients (22.5%) progressed, 227 (77.5%) did not (33 could not have their status assessed due to insufficient data). Progressors had shorter disease duration (median 8.1 vs 12.6 months, P=0.001) and lower mRSS (median 19 vs 21 units, P=0.030) than non-progressors. Skin score was highest, and peaked earliest, in the anti-RNA polymerase III (Pol3+) subgroup (n=50). A first predictive model (including mRSS, duration of skin thickening and their interaction) had an accuracy of 60.9%, AUC of 0.666 and PPV of 33.8%. By adding a variable for Pol3 positivity, the model reached an accuracy of 71%, AUC of 0.711 and PPV of 41%. Conclusions Two prediction models for progressive skin thickening were derived, for use both in clinical practice and for cohort enrichment in RCTs. These models will inform recruitment into the many clinical trials of dcSSc projected for the coming years. Trial registration number NCT02339441.
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收藏
页码:563 / 570
页数:8
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