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DOI 10.1136/rmdopen-2025-006136

Медицинская библиотека · RMD open · 2026

Transcriptomic and proteomic analysis stratifies patients with axial spondyloarthritis based on disease activity, structural damage and radiographic progression.

Cuesta-López Laura, Arias-de la Rosa Iván, Pérez-Sánchez Carlos, Barbera-Betancour Ariana, Ruiz-Ponce Miriam, Barranco Antonio Manuel, Ortiz-Buitrago Pedro, Ladehesa-Pineda Lourdes, Puche-Larrubia María Ángeles, Martín-Salazar Jesus Eduardo, Moreno-Caño Elena, Ábalos-Aguilera María Carmen, Lopez-Pedrera Chary, Escudero-Contreras Alejandro, Collantes-Estévez Eduardo, López-Medina Clementina, Barbarroja Nuria

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Аннотация

OBJECTIVES

To identify clusters of highly correlated genes enriched in biological functions and specific molecular pathways involved in the pathogenesis of radiographic damage in axial spondyloarthritis (axSpA) and to discover molecular biomarkers of radiographic progression and disease severity.

METHODS

A total of 144 patients with axSpA were included. First, RNA from peripheral blood mononuclear cells was sequenced in a cohort of 24 patients with axSpA. Hub genes were measured in a n=60 validation cohort through microfluidic PCR. A 5-year follow-up enabled the classification of the patients into fast/moderate or slow progressors. Machine learning approaches were applied to identify a predictive biomarker of progression by integrating gene expression data with clinical variables. An independent cohort of 60 patients with axSpA, with spine radiographs taken 5 years prior, underwent serum proteomic analysis using a Proximity Extension Assay.

RESULTS

Unsupervised clustering analysis using transcriptomics revealed two distinct groups of patients with axSpA, differentiated by their clinical profiles. Weight gene correlation network analysis identified six gene modules differentially expressed between the two clusters. Patients in cluster 2 exhibited higher disease activity, greater functional impairment and more structural damage. Molecular alterations linked to structural damage revealed a specific circulating inflammatory proteome profile associated with disease severity. A predictive model composed of two genes and basal total modified Stoke Ankylosing Spondylitis Spinal Score emerged as a key biomarker for identifying moderate-to-fast radiographic progression.

CONCLUSIONS

This study identified molecular pathways involved in radiographic damage and discovered potential proteomic biomarkers of disease severity and transcriptomic predictors of radiographic progression in axSpA.

Для цитирования: Cuesta-López Laura, Arias-de la Rosa Iván, Pérez-Sánchez Carlos, Barbera-Betancour Ariana, Ruiz-Ponce Miriam, Barranco Antonio Manuel, Ortiz-Buitrago Pedro, Ladehesa-Pineda Lourdes, Puche-Larrubia María Ángeles, Martín-Salazar Jesus Eduardo, Moreno-Caño Elena, Ábalos-Aguilera María Carmen, Lopez-Pedrera Chary, Escudero-Contreras Alejandro, Collantes-Estévez Eduardo, López-Medina Clementina, Barbarroja Nuria. Transcriptomic and proteomic analysis stratifies patients with axial spondyloarthritis based on disease activity, structural damage and radiographic progression.. RMD open. 2026. DOI: 10.1136/rmdopen-2025-006136.

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