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Narrative review on multi-omics for spondyloarthritis and psoriatic arthritis

Narrative review on multi-omics for spondyloarthritis and psoriatic arthritis
Photo by julien Tromeur / Unsplash
Key Takeaway
Consider multi-omics as a conceptual framework for spondyloarthritis research, not a proven clinical tool.

This is a narrative review that synthesizes existing literature on multi-omics strategies for spondyloarthritis and psoriatic arthritis. The scope covers the potential of integrating genomics, transcriptomics, proteomics, and microbiomics compared to single-omics approaches. The authors argue that such integration could help elucidate shared and distinct immunopathological mechanisms, facilitate differential diagnosis, discover novel biomarkers, advance early diagnosis, enable precision monitoring, predict treatment responses, and identify novel therapeutic targets. The review does not report a pooled effect size or specific study populations, as it is a qualitative synthesis. Key limitations noted by the authors include the absence of reported primary trial data and the conceptual nature of the hypotheses discussed. The authors acknowledge that the evidence base is preliminary and that clinical implementation requires further validation. Practice relevance is not reported, and the findings should be interpreted as mechanistic hypotheses rather than proven clinical strategies.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
Spondyloarthritis (SpA) and psoriatic arthritis (PsA) are interrelated, immune-mediated inflammatory diseases characterized by significant clinical heterogeneity. Early differential diagnosis, accurate disease activity assessment, and the development of personalized treatment strategies remain significant clinical challenges. Single-omics approaches have provided only a limited view of this complexity, highlighting the need for integrative strategies. This review systematically synthesizes findings from multi-omics studies—including genomics, transcriptomics, proteomics, and microbiomics—in SpA and PsA. We focus on their application in three key areas: (i) elucidating shared and distinct immunopathological mechanisms, (ii) facilitating differential diagnosis, and (iii) discovering novel biomarkers. By comparing their molecular landscapes, we explore the shared and distinct immunological foundations of SpA and PsA. Furthermore, we critically evaluate the translational potential of integrated multi-omics strategies for advancing early diagnosis, precision monitoring, predicting treatment responses, and identifying novel therapeutic targets. This integrated, multi-omics framework promises to refine disease taxonomy and guide personalized therapeutic decisions, paving the way for precision medicine in SpA and PsA.
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