Concordance and agreement between different activity scores in polymyalgia rheumatica
Bruno Fautrel,
Eric Toussirot,
Renaud Felten,
Emmanuel Nowak,
Christophe Richez,
Jacques-Eric Gottenberg,
Isabelle Chary-Valckenaere,
Alain Saraux,
Aleth Perdriger,
Emanuelle Dernis,
Thierry Marhadour,
Marie-Elise Truchetet,
Divi Cornec,
Valérie Devauchelle-Pensec,
Daniel Wendling,
Guillaume Direz,
Anne Lohse,
Laurent Chiche,
PASCAL HILLIQUIN,
Guillermo Carvajal Alegria,
Dewi Guellec,
Justine D'Agostino,
Aghiles Souki,
Catherine Le Henaff,
Benjamin Dervieux
Affiliations
Bruno Fautrel
1 Rheumatology, CEREMAIA Reference Center (ERN RITA) , Sorbonne Université – AP-HP, Pitié-Salpêtrière Hospital, Paris, France
Eric Toussirot
INSERM Clinical Investigation Center 1431, Centre Hospitalier Universitaire de Besancon, Besancon, France
Renaud Felten
1 Department of Rheumatology - Centre National de Référence des Maladies Systémiques Rares Est Sud-Ouest (RESO), Hôpitaux Universitaires de Strasbourg, Strasbourg, France
Emmanuel Nowak
Public Agency for Clinical Research and Innovation (DRCI), Brest University Hospital, Centre Hospitalier Universitaire de Brest, Brest, France
Christophe Richez
38Rheumatology Department, FHU ACRONIM, Pellegrin Hospital and UMR CNRS 5164, Bordeaux University, Bordeaux, France
Jacques-Eric Gottenberg
Rheumatology, Hopitaux universitaires de Strasbourg, Strasbourg, France
Isabelle Chary-Valckenaere
Department of Rheumatology, Centre Hospitalier Universitaire de Nancy, Nancy, France
Alain Saraux
Department of Rheumatology, Hopital Cavale Blanche, Brest, France
Aleth Perdriger
Polyclinique du Maine, Laval, France
Emanuelle Dernis
Rheumatology, Le Mans Hospital, Le Mans, France
Thierry Marhadour
Rheumatology Department, Centre National de Référence des Maladies Auto-Immunes Rares (CERAINOM), CHU Brest, Brest, France
Marie-Elise Truchetet
Service de Rhumatologie, CHU Bordeaux, Bordeaux, France
Divi Cornec
U1227, LBAI, Univ Brest, Inserm, and CHU Brest, Brest, France, Brest, France
Valérie Devauchelle-Pensec
Rheumatology, Brest University and La Cavale Blanche Hospital, Brest, France
Daniel Wendling
11 Rheumatology, CHU J Minjoz, Besancon, France
Guillaume Direz
19 Rheumatology Department, Le Mans General Hospital, Le Mans, France
Anne Lohse
4 Department of Rheumatology, Competence center FAI2R, Franche-Comte Hospital, Belfort, France
Laurent Chiche
1 Internal Medicine, European Hospital Marseille, Marseille, France
PASCAL HILLIQUIN
Department of Rhumatology, Centre Hospitalier Sud Francilien, Corbeil-Essonnes, France
Guillermo Carvajal Alegria
Rheumatology, CHU Tours, Tours, France
Dewi Guellec
Rheumatology Department, Centre National de Référence des Maladies Auto-Immunes Rares (CERAINOM), CHU Brest, Brest, France
Justine D'Agostino
Department of Rheumatology, Centre Hospitalier Universitaire de Brest, Brest, France
Aghiles Souki
Public Agency for Clinical Research and Innovation (DRCI), Brest University Hospital, Centre Hospitalier Universitaire de Brest, Brest, France
Catherine Le Henaff
Department of Rheumatology, Pays de Morlaix Hospital Centre, Morlaix, France
Benjamin Dervieux
Department of Rhuamtology, GHR Mulhouse Sud Alsace, Mulhouse, France
Objective The C reactive protein polymyalgia rheumatica activity score (CRP-PMR-AS) is a composite index that includes CRP levels and was developed specifically for PMR. As treatments such as interleukin-6 antagonists can normalise CRP levels, the erythrocyte sedimentation rate (ESR) of PMR-AS, the clinical (clin)-PMR-AS and the imputed-CRP (imp-CRP)-PMR-AS have been developed to avoid such bias. Our primary objective was to measure the correlation of these activity scores. Our secondary objective was to evaluate the concordance between different cutoffs of the PMR-ASs.Method Data from the Safety and Efficacy of tocilizumab versus Placebo in Polymyalgia rHeumatica With glucocORticoid dEpendence (SEMAPHORE) trial, a superiority randomised double-blind placebo-controlled trial, were subjected to post hoc analysis to compare the efficacy of tocilizumab versus placebo in patients with active PMR. The CRP-PMR-AS, ESR-PMR-AS, clin-PMR-AS and imp-CRP-PMR-AS were measured at every visit. The concordance and correlation between these scores were evaluated using kappa correlation coefficients, Bland-Altman correlations, intraclass correlation coefficients (ICCs) and scatter plots.Results A total of 101 patients were included in the SEMAPHORE trial, and 100 were analysed in this study. The correlation between the PMR-ASs was excellent, as the ICC and kappa were >0.85 from week 4 until week 24 (CRP-PMR-AS ≤10 or >10). Bland-Altman plots revealed that the differences between the CRP-PMR-AS and the other threescores were low. The cut-off values for the clin-PMR-AS were similar to those for the CRP-PMR-AS 86% of the time.Conclusion The correlation between all the PMR-ASs was excellent, reflecting the low weight of CRP. In clinical trials using drugs that have an impact on CRP, the derived activity scores can be used.Trial registration number NTC02908217.