Biomarker development for axial spondyloarthritis
Matthew A Brown1, Zhixiu Li2, Kim-Anh Lê Cao3
1Guy's and St Thomas' NHS Foundation Trust and King's College London NIHR Biomedical Research Centre, London, UK. matt.brown@kcl.ac.uk.
Nature Reviews. Rheumatology
|July 2, 2020
Summary
Improved biomarkers are needed for axial spondyloarthritis (axSpA) to aid early diagnosis and predict treatment success. Advanced
Area of Science:
- Rheumatology
- Immunology
- Genetics
Background:
- Axial spondyloarthritis (axSpA) is a diverse group of diseases with varied clinical presentations and treatment responses.
- Current biomarkers like HLA-B27 have limited diagnostic and predictive capabilities for axSpA.
- Understanding the interplay between host genetics and gut microbiota is crucial for axSpA pathogenesis.
Purpose of the Study:
- To highlight the need for improved biomarkers in axSpA for enhanced early diagnosis and treatment prediction.
- To explore the potential of advanced 'omics' technologies for developing novel axSpA biomarker sets.
- To emphasize the requirement for large, well-characterized datasets for biomarker discovery and validation.
Main Methods:
- Review of current diagnostic and predictive biomarkers for axSpA.
- Exploration of emerging 'omics' technologies including genomics, microbiome profiling, transcriptomics, proteomics, and metabolomics.
- Discussion of advanced statistical approaches for biomarker analysis and interpretation.
Main Results:
- Current biomarkers for axSpA offer only moderate diagnostic and predictive value.
- 'Omics' technologies offer potential for developing more informative biomarker sets.
- Future biomarker panels will likely involve combinations of markers analyzed with novel statistical methods.
Conclusions:
- Development of improved biomarkers is essential for better clinical management of axSpA.
- Integration of multi-omics data and advanced statistical analysis is key for future biomarker discovery.
- Large-scale, well-curated datasets are critical for validating new biomarkers in axSpA.


