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Autoantibody status according to multiparametric assay accurately estimates connective tissue disease classification and identifies clinically relevant disease clusters. | LitMetric

AI Article Synopsis

  • The study aimed to assess how well a multiparametric assay can classify patients with different connective tissue diseases (CTDs) and distinguish them from healthy controls based purely on autoantibody levels.
  • The research involved testing serum from 908 subjects, resulting in a classification model with an accuracy of about 60.84% and high area under the curve scores, identifying distinct patient clusters based on their autoantibody profiles.
  • The findings concluded that this autoantibody assay effectively classifies CTD patients, revealing four distinct clusters, which may aid in understanding and predicting disease manifestations without relying on clinical features.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514657PMC
http://dx.doi.org/10.1136/rmdopen-2023-003365DOI Listing

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