Autoantibody status according to multiparametric assay accurately estimates connective tissue disease classification and identifies clinically relevant disease clusters
Micaela Fredi,
Nicola Bizzaro,
Margherita Zen,
Chiara Baldini,
Ilaria Cavazzana,
Roberto Giacomelli,
Valeria Riccieri,
Marco Fornaro,
Franco Franceschini,
Roberto Gerli,
Anna Ghirardello,
Paola Migliorini,
Maurizio Benucci,
Maria Infantino,
Mariangela Manfredi,
Elena Bartoloni,
Antonella Fioravanti,
Amelia Rigon,
Silvia Piantoni,
Onelia Bistoni,
Francesca Bellisai,
Carlo Perricone,
Giacomo Cafaro,
Danilo Villalta,
Stefania Masneri,
Paola Parronchi,
Boaz Palterer,
Stefania Del Rosso,
Fabiana Topini,
Manuela Sebastiano,
Emirena Garrafa,
Sara Cheleschi,
Maria-Romana Bacarelli,
Marilina Tampoia,
Daniele Cammelli,
Luisa Arcarese,
Patrizia Rovere Querini,
Valentina Canti
Affiliations
Micaela Fredi
Nicola Bizzaro
Laboratory of Clinical Pathology, Azienda Sanitaria Universitaria Integrata, Udine, Italy
Margherita Zen
Chiara Baldini
Rheumatology Unit, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy
Ilaria Cavazzana
Roberto Giacomelli
Fondazione Policlinico Universitario, and Research Unit of Immuno-Rheumatology, Department of Medicine and Surgery, Campus Bio-Medico University, Via Alvaro del Portillo, 200, 00128 Roma, Italy, and Università Campus Bio-Medico di Roma, Via Alvaro del Portillo, 21, 00128 Roma, Italy, Roma, Italy
Valeria Riccieri
Rheumatology Unit, University of Rome La Sapienza, Rome, Italy
Marco Fornaro
Rheumatology Unit, Department of Precision and Regenerative Medicine and Ionian Area, University of Bari, Bari, Italy
Franco Franceschini
Unit of Rheumatology and Clinical Immunology, ASST Spedali Civili di Brescia, Brescia, Italy
Roberto Gerli
Rheumatology Unit, Department of Medicine and Surgery, University of Perugia, Perugia, Italy
Anna Ghirardello
Rheumatology Unit, Department of Medicine-DIMED, Padova University Hospital, Padova, Italy
Paola Migliorini
Maurizio Benucci
Maria Infantino
Laboratory of Immunology and Allergology, Ospedale San Giovanni di Dio, Firenze, Italy
Mariangela Manfredi
Elena Bartoloni
Rheumatology Unit, Department of Medicine and Surgery, University of Perugia, Perugia, Italy
Antonella Fioravanti
Rheumatology Unit, Department of Medicine, Surgery and Neuroscience, Azienda Ospedaliera Universitaria Senese - Policlinico Le Scotte, Siena, Italy
Amelia Rigon
Clinical Immunology and Rheumatology, Campus Bio-Medico University, Rome, Italy
Silvia Piantoni
Onelia Bistoni
Francesca Bellisai
Carlo Perricone
Giacomo Cafaro
Rheumatology Unit, Department of Medicine and Surgery, University of Perugia, Perugia, Italy
Danilo Villalta
Immunology and Allergology, Santa Maria degli Angeli Hospital, Pordenone, Italy
Stefania Masneri
Paola Parronchi
1 Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy
Boaz Palterer
Department of Clinical and Experimental Medicine, University of Florence, Firenze, Italy
Stefania Del Rosso
Autoimmunity Lab, IRCCS Ospedale San Raffaele, Milano, Italy
Objective Assessment of circulating autoantibodies represents one of the earliest diagnostic procedures in patients with suspected connective tissue disease (CTD), providing important information for disease diagnosis, identification and prediction of potential clinical manifestations. The purpose of this study was to evaluate the ability of multiparametric assay to correctly classify patients with multiple CTDs and healthy controls (HC), independent of clinical features, and to evaluate whether serological status could identify clusters of patients with similar clinical features.Methods Patients with systemic lupus erythematosus (SLE), systemic sclerosis (SSc), Sjogren’s syndrome (SjS), undifferentiated connective tissue disease (UCTD), idiopathic inflammatory myopathies (IIM) and HC were enrolled. Serum was tested for 29 autoantibodies. An XGBoost model, exclusively based on autoantibody titres was built and classification accuracy was evaluated. A hierarchical clustering model was subsequently developed and clinical/laboratory features compared among clusters.Results 908 subjects were enrolled. The classification model showed a mean accuracy of 60.84±4.05% and a mean area under the receiver operator characteristic curve of 88.99±2.50%, with significant discrepancies among groups. Cluster analysis identified four clusters (CL). CL1 included patients with typical features of SLE. CL2 included most patients with SjS, along with some SLE and UCTD patients with SjS-like features. CL4 included anti-Jo1 patients only. CL3 was the largest and most heterogeneous, including all the remaining subjects, overall characterised by low titre or lower-prevalence autoantibodies.Conclusion Extended multiparametric autoantibody assay allowed an accurate classification of CTD patients, independently of clinical features. Clustering according to autoantibody titres is able to identify clusters of CTD subjects with similar clinical features, independently of their final diagnosis.