Literature DB >> 27150113

Development of the ClinESSDAI: a clinical score without biological domain. A tool for biological studies.

Raphaèle Seror1, Petra Meiners2, Gabriel Baron3, Hendrika Bootsma4, Simon J Bowman5, Claudio Vitali6, Jacques-Eric Gottenberg7, Elke Theander8, Athanasios Tzioufas9, Salvatore De Vita10, Manel Ramos-Casals11, Thomas Dörner12, Luca Quartuccio10, Philippe Ravaud3, Xavier Mariette1.   

Abstract

OBJECTIVE: To develop and validate ClinESSDAI (Clinical European League Against Rheumatism Sjögren's Syndrome Disease Activity Index), ie, ESSDAI without the biological domain. PATIENTS AND METHODS: The 702 fictive vignettes derived from 96 real cases of primary Sjögren's syndrome of the ESSDAI development study were used. As for ESSDAI development, the physician assessment of disease activity (0-10 scale) was used as the 'gold standard' in a multivariate model for weighting domains, after removing the biological domain. The reliability, assessed by intraclass correlation coefficient (ICC) between ClinESSDAI and ESSDAI, explored if ClinESSDAI was equivalent to ESSDAI. Its psychometric (ie, measurement) properties were compared with that of ESSDAI in an independent cohort. Also, its use was evaluated on data of two clinical trials.
RESULTS: In multivariate modelling, all 11 domains remained significantly associated with disease activity, with slight modifications of some domain weights. Reliability between clinESSDAI and ESSDAI was excellent (ICC=0.98 and 0.99). Psychometric properties of clinESSDAI, disease activity levels and minimal clinically important improvement thresholds and its ability to detect change over time in clinical trials were very close to that of ESSDAI.
CONCLUSIONS: ClinESSDAI appears valid and very close to the original ESSDAI. This score provides an accurate evaluation of disease activity independent of B-cell biomarkers. It could be used in various circumstances: (i) in biological/clinical studies to avoid data collinearity, (ii) in clinical trials, as secondary endpoint, to detect change independent of biological effect of the drug, (iii) in clinical practice to assess disease activity for visits where immunological tests have not been done. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.

Entities:  

Keywords:  Disease Activity; Outcomes research; Sjøgren's Syndrome

Mesh:

Year:  2016        PMID: 27150113     DOI: 10.1136/annrheumdis-2015-208504

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  15 in total

Review 1.  Management of primary Sjögren's syndrome: recent developments and new classification criteria.

Authors:  Nicoletta Del Papa; Claudio Vitali
Journal:  Ther Adv Musculoskelet Dis       Date:  2018-01-01       Impact factor: 5.346

2.  Monoclonal gammopathy in rheumatic diseases.

Authors:  Yue Yang; Long Chen; Yuan Jia; Yang Liu; Lei Wen; Yaoxian Liang; Yuan An; Shi Chen; Yin Su; Zhanguo Li
Journal:  Clin Rheumatol       Date:  2018-03-13       Impact factor: 2.980

Review 3.  Dysregulation of gut microbiome is linked to disease activity of rheumatic diseases.

Authors:  Yanfeng Bao; Chen Dong; Juan Ji; Zhifeng Gu
Journal:  Clin Rheumatol       Date:  2020-06-09       Impact factor: 2.980

4.  Persistent serological activity in primary Sjögren's syndrome.

Authors:  Jorge López-Morales; Daniel Cortes-Muñoz; Miguel Astudillo-Ángel; Gabriela Hernández-Molina
Journal:  Clin Rheumatol       Date:  2019-12-14       Impact factor: 2.980

Review 5.  The Role of Interferons in the Pathogenesis of Sjögren's Syndrome and Future Therapeutic Perspectives.

Authors:  Nicoletta Del Papa; Antonina Minniti; Maurizio Lorini; Vincenzo Carbonelli; Wanda Maglione; Francesca Pignataro; Nicola Montano; Roberto Caporali; Claudio Vitali
Journal:  Biomolecules       Date:  2021-02-09

6.  Development and preliminary validation of the Sjögren's Tool for Assessing Response (STAR): a consensual composite score for assessing treatment effect in primary Sjögren's syndrome.

Authors:  Xavier Mariette; Raphael Porcher; Raphaele Seror; Gabriel Baron; Marine Camus; Divi Cornec; Elodie Perrodeau; Simon J Bowman; Michele Bombardieri; Hendrika Bootsma; Jacques-Eric Gottenberg; Benjamin Fisher; Wolfgang Hueber; Joel A van Roon; Valérie Devauchelle-Pensec; Peter Gergely
Journal:  Ann Rheum Dis       Date:  2022-04-07       Impact factor: 27.973

Review 7.  Epidemiology of Sjögren's Syndrome-from an Oral Perspective.

Authors:  Anne Isine Bolstad; Kathrine Skarstein
Journal:  Curr Oral Health Rep       Date:  2016-09-02

8.  Severe intestinal dysbiosis is prevalent in primary Sjögren's syndrome and is associated with systemic disease activity.

Authors:  Thomas Mandl; Jan Marsal; Peter Olsson; Bodil Ohlsson; Kristofer Andréasson
Journal:  Arthritis Res Ther       Date:  2017-10-24       Impact factor: 5.156

9.  Sjögren's syndrome: state of the art on clinical practice guidelines.

Authors:  Vasco C Romão; Rosaria Talarico; Carlo Alberto Scirè; Ana Vieira; Tobias Alexander; Chiara Baldini; Jacques-Eric Gottenberg; Heidi Gruner; Eric Hachulla; Luc Mouthon; Martina Orlandi; Cristina Pamfil; Marc Pineton de Chambrun; Marco Taglietti; Natasa Toplak; Paul van Daele; Jacob M van Laar; Stefano Bombardieri; Matthias Schneider; Vanessa Smith; Maurizio Cutolo; Marta Mosca; Xavier Mariette
Journal:  RMD Open       Date:  2018-10-18

10.  B-cell activity markers are associated with different disease activity domains in primary Sjögren's syndrome.

Authors:  Katherine James; Chimwemwe Chipeta; Antony Parker; Stephen Harding; Simon J Cockell; Colin S Gillespie; Jennifer Hallinan; Francesca Barone; Simon J Bowman; Wan-Fai Ng; Benjamin A Fisher
Journal:  Rheumatology (Oxford)       Date:  2018-07-01       Impact factor: 7.580

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