TY - JOUR
T1 - The European Scleroderma Trials and Research group (EUSTAR) task force for the development of revised activity criteria for systemic sclerosis: Derivation and validation of a preliminarily revised EUSTAR activity index
AU - Valentini, Gabriele
AU - Iudici, Michele
AU - Walker, Ulrich A.
AU - Jaeger, Veronika K.
AU - Baron, Murray
AU - Carreira, Patricia
AU - Czirják, László
AU - Denton, Christopher P.
AU - Distler, Oliver
AU - Hachulla, Eric
AU - Herrick, Ariane L.
AU - Kowal-Bielecka, Otylia
AU - Pope, Janet
AU - Möller-Ladner, Ulf
AU - Riemekasten, Gabriela
AU - Avouac, Jerome
AU - Frerix, Marc
AU - Jordan, Suzana
AU - Minier, Tönde
AU - Siegert, Elise
AU - Ong, Voon H.
AU - Vettori, Serena
AU - Allanore, Yannick
N1 - Funding Information:
Competing interests GV has received research funding in the area of systemic sclerosis from Abbvie, Actelion, Bayer, BMS, Merck SD, Pfizer and Roche. CPD has been a consultant to Roche, GSK, Actelion, Inventiva, CSL Behring, Takeda, Merck-Serono, MedImmune and Biogen. He has received research grants from Actelion, GSK, Novartis and CSL Behring. AH has undertaken consultancy work and received speaker’s fees and research funding from Actelion. She has undertaken consultancy work for Apricus. OD has/had a consultancy relationship and/or has received research funding in the area of systemic sclerosis and related conditions from 4 D Science, Actelion, Active Biotec, BMS, Boehringer Ingelheim, EpiPharm, BiogenIdec, Genentech/Roche, GSK, Inventiva, Lilly, Medac, Pfizer, Serodapharm, Sinoxa, Ergonex, Pharmacyclics and Sanofi. In addition, OD has a patent mir-29 for the treatment of systemic sclerosis licensed. YA has/had consultancy relationship and/or has received research funding in relationship with the treatment of systemic sclerosis from Actelion, Bayer, Biogen Idec, Bristol-Myers Squibb, Genentech/Roche, Inventiva, Medac, Pfizer, Sanofi/Genzyme, Servier and UCB. JP has consulted for Actelion, Bayer, BMS, Merck, Pfizer and Roche.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2017
Y1 - 2017
N2 - Background Validity of European Scleroderma Study Group (EScSG) activity indexes currently used to assess disease activity in systemic sclerosis (SSc) has been criticised. Methods Three investigators assigned an activity score on a 0-10 scale for 97 clinical charts. The median score served as gold standard. Two other investigators labelled the disease as inactive/moderately active or active/very active. Univariate-multivariate linear regression analyses were used to define variables predicting the 'gold standard', their weight and derive an activity index. The cut-off point of the index best separating active/very active from inactive/moderately active disease was identified by a receiver-operating curve analysis. The index was validated on a second set of 60 charts assessed by three different investigators on a 0-10 scale and defined as inactive/moderately active or active/very active by other two investigators. One hundred and twenty-Three were investigated for changes over time in the index and their relationships with those in the summed Medsger severity score (MSS). Results A weighted 10-point activity index was identified and validated: δ-skin=1.5 (δ=patient assessed worsening during the previous month), modified Rodnan skin score (mRss) >18=1.5, digital ulcers=1.5, tendon friction rubs=2.25, C-reactive protein >1 mg/dL=2.25 and diffusing capacity of the lung for CO (DLCO) % predicted <70%=1.0. A cut-off ≥2.5 was found to identify patients with active disease. Changes in the index paralleled those of MSS (p=0.0001). Conclusions A preliminarily revised SSc activity index has been developed and validated, providing a valuable tool for clinical practice and observational studies.
AB - Background Validity of European Scleroderma Study Group (EScSG) activity indexes currently used to assess disease activity in systemic sclerosis (SSc) has been criticised. Methods Three investigators assigned an activity score on a 0-10 scale for 97 clinical charts. The median score served as gold standard. Two other investigators labelled the disease as inactive/moderately active or active/very active. Univariate-multivariate linear regression analyses were used to define variables predicting the 'gold standard', their weight and derive an activity index. The cut-off point of the index best separating active/very active from inactive/moderately active disease was identified by a receiver-operating curve analysis. The index was validated on a second set of 60 charts assessed by three different investigators on a 0-10 scale and defined as inactive/moderately active or active/very active by other two investigators. One hundred and twenty-Three were investigated for changes over time in the index and their relationships with those in the summed Medsger severity score (MSS). Results A weighted 10-point activity index was identified and validated: δ-skin=1.5 (δ=patient assessed worsening during the previous month), modified Rodnan skin score (mRss) >18=1.5, digital ulcers=1.5, tendon friction rubs=2.25, C-reactive protein >1 mg/dL=2.25 and diffusing capacity of the lung for CO (DLCO) % predicted <70%=1.0. A cut-off ≥2.5 was found to identify patients with active disease. Changes in the index paralleled those of MSS (p=0.0001). Conclusions A preliminarily revised SSc activity index has been developed and validated, providing a valuable tool for clinical practice and observational studies.
UR - http://www.scopus.com/inward/record.url?scp=84987797058&partnerID=8YFLogxK
U2 - 10.1136/annrheumdis-2016-209768
DO - 10.1136/annrheumdis-2016-209768
M3 - Journal articles
C2 - 27621285
AN - SCOPUS:84987797058
SN - 0003-4967
VL - 76
SP - 270
EP - 276
JO - Annals of the Rheumatic Diseases
JF - Annals of the Rheumatic Diseases
IS - 1
ER -