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Identification and Evaluation of Serum Protein Biomarkers That Differentiate Psoriatic Arthritis From Rheumatoid Arthritis.
Mc Ardle, Angela; Kwasnik, Anna; Szentpetery, Agnes; Hernandez, Belinda; Parnell, Andrew; de Jager, Wilco; de Roock, Sytze; FitzGerald, Oliver; Pennington, Stephen R.
Affiliation
  • Mc Ardle A; University College Dublin, Dublin, Ireland.
  • Kwasnik A; University College Dublin, Dublin, Ireland.
  • Szentpetery A; University College Dublin, Dublin, Ireland.
  • Hernandez B; Trinity College Dublin and University College Dublin, Dublin, Ireland.
  • Parnell A; University College Dublin, Dublin, Ireland.
  • de Jager W; Wilhelmina Children Hospital and University Medical Centre Utrecht, Utrecht, The Netherlands.
  • de Roock S; University Medical Centre Utrecht, Utrecht, The Netherlands.
  • FitzGerald O; University College Dublin, Dublin, Ireland.
  • Pennington SR; University College Dublin, Dublin, Ireland.
Arthritis Rheumatol ; 74(1): 81-91, 2022 01.
Article in En | MEDLINE | ID: mdl-34114357
ABSTRACT

OBJECTIVE:

To identify serum protein biomarkers that might distinguish patients with early inflammatory arthritis (IA) with psoriatic arthritis (PsA) from those with rheumatoid arthritis (RA) and may be used to support appropriate early intervention.

METHODS:

The serum proteome of patients with PsA and patients with RA was interrogated using nano-liquid chromatography mass spectrometry (nano-LC-MS/MS) (n = 64 patients), an aptamer-based assay (SomaScan) targeting 1,129 proteins (n = 36 patients), and a multiplexed antibody assay (Luminex) for 48 proteins (n = 64 patients). Multiple reaction monitoring (MRM) assays were developed to evaluate the performance of putative markers using the discovery cohort (n = 60 patients) and subsequently an independent cohort of PsA and RA patients (n = 167).

RESULTS:

Multivariate machine learning analysis of the protein discovery data from the 3 platforms revealed that it was possible to differentiate PsA patients from RA patients with an area under the curve (AUC) of 0.94 for nano-LC-MS/MS, 0.69 for bead-based immunoassay measurements, and 0.73 for aptamer-based analysis. Subsequently, in the separate verification and evaluation studies, random forest models revealed that a subset of proteins measured by MRM could differentiate PsA and RA patients with AUCs of 0.79 and 0.85, respectively.

CONCLUSION:

We present a serum protein biomarker panel that can separate patients with early-onset IA with PsA from those with RA. With continued evaluation and refinement using additional and larger patient cohorts, including those with other arthropathies, we suggest that the panel identified here could contribute to improved clinical decision making.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arthritis, Rheumatoid / Blood Proteins / Arthritis, Psoriatic Type of study: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Arthritis Rheumatol Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arthritis, Rheumatoid / Blood Proteins / Arthritis, Psoriatic Type of study: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Arthritis Rheumatol Year: 2022 Document type: Article Affiliation country: