Objectives: To evaluate the construct validity of the European Scleroderma Study Group (EScSG) activity index and to propose modifications if necessary.
Methods: One hundred and thirty-one consecutive patients were investigated and re-evaluated 1 year later. Modified Rodnan skin score (MRSS), skin ulcers and joint contracture numbers, hand anatomic index (HAI), BMI, spirometry, carbon monoxide diffusing capacity (DL(CO)), left ventricular ejection fraction, pulmonary arterial hypertension, HAQ Disability Index (HAQ-DI), patient skin self-assessment questionnaire and several biomarkers were recorded, in addition to the data required for the EScSG activity index. Statistical analysis was performed by categorical principal component analysis (CATPCA).
Results: The EScSG activity index appeared in the same dimension as the HAQ-DI, ulcer score and joint contractures, MRSS, patient-reported skin score and HAI by CATPCA. Parameters of lung involvement appeared in another dimension. We constructed a 12-point activity index that was equally associated with both dimensions, by adding the forced vital capacity/DL(CO), change in DL(CO), change in the ulcer scores, HAQ-DI and patient-reported skin score. Biomarkers including vascular endothelial growth factor, soluble P-selectin glycoprotein ligand-1, CRP and albumin were related to both the EScSG and the 12-point index, though they did not improve the total variance of the model.
Conclusion: The construct validity of the EScSG activity index is good, though the lung-related disease activity may not be sufficiently represented. Further validation steps may be required for both the EScSG and our 12-point activity index.
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http://dx.doi.org/10.1093/rheumatology/keq022 | DOI Listing |
Arch Rheumatol
June 2023
Rheumatology and Clinical Immunology Unit of Internal Medicine Department, Cairo University, Cairo, Egypt.
Objectives: This study aims to investigate proprotein convertase subtilisin/kexin 9 (PCSK9) in patients with diffuse systemic sclerosis (d-SSc) and its relation to disease activity, severity and subclinical atherosclerosis in such group of patients.
Patients And Methods: Between December 2019 and July 2021, a total of 41 patients with d-SSc (17 males, 24 females; mean age: 36.1±1.
Semin Arthritis Rheum
April 2022
McGill University, Jewish General Hospital, Montreal, Canada. Electronic address:
Objective: Diffuse cutaneous systemic sclerosis (dcSSc) is a multifaceted disease for which the Composite Response Index in dcSSc (CRISS) was developed as a global outcome measure. We aimed to further validate the CRISS by examining its association with other disease measures, patient reported quality of life (QoL), and mortality.
Methods: DcSSc patients with ≤5 year disease duration were recruited from multinational registries.
Curr Rheumatol Rev
April 2022
Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Background: No fully validated index is available for assessing overall disease activity in systemic sclerosis (SSc).
Objectives: To estimate the effect of disease activity as measured by different disease activity indices on the risk of subsequent organ damage.
Methods: The European Systemic sclerosis study group activity index (EScSG AI), the European Scleroderma Trials and Research Group Activity Index (r-EUSTAR AI), 12 point activity index proposed by Minier (12point AI) were calculated for 91 patients; the CRISS (The Composite Response Index for Systemic Sclerosis) for patients included after 2016.
Exp Ther Med
October 2020
Department of Internal Medicine and Rheumatology, Cantacuzino Clinical Hospital, 'Carol Davila' University of Medicine and Pharmacy, 020475 Bucharest, Romania.
Capillary density on nailfold capillaroscopy (NFC) is considered a promising instrument for assessing disease characteristics in patients with systemic sclerosis (SSc), however, there is no agreement yet over how to analyze and interpret the results. The objective of this study was to investigate the possible associations of the mean number of capillaries with disease characteristics, disease activity [measured by the European Scleroderma Study Group (EScSG) disease activity score] and survival in a single-center cohort of patients with SSc. Sixty-eight patients were included; 54 had follow-up at 6 months.
View Article and Find Full Text PDFClin Rheumatol
December 2020
Department of Medicine, The University of Melbourne at St Vincent's Hospital, Melbourne, Australia.
Assessment of disease activity in systemic sclerosis (SSc) is limited by the absence of a fully validated, multisystem measure of disease activity. The European Scleroderma Trials and Research Group (EUSTAR) SSc activity index (EScSG-AI) was recently revised, and a validation study within the EUSTAR cohort was performed. In this study, we evaluated the performance of the revised EScSG-AI in an external Australian cohort.
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