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Recognizing rheumatoid arthritis: oncoprotein survivin opens new possibilities: a population-based case-control study
Too Chun-Lai1, Shahnaz Murad, Malin C Erlandsson
1From the Allergy and Immunology Research Center, Institute of Medical Research, Kuala Lumpur, Malaysia (TCL, SM, JSD); Department of Medicine, Rheumatology Unit, Karolinska University Hospital, Karolinska Institutet, Stockholm (TCL); Department of Rheumatology and Inflammation Research, Institute of Medicine, the University of Gothenburg, Göteborg, Sweden (ME, MIB); Department of Medicine, Putrajaya Hospital, Putrajaya (HH); and Department of Medicine, Raja Perempuan Bainun Hospital, Ipoh, Perak, Malaysia (WS).
High survivin levels in blood show high specificity for rheumatoid arthritis (RA) diagnosis. This simple test improves RA predictability, especially when combined with other biomarkers.
Area of Science:
- Immunology
- Rheumatology
- Biomarker Research
Background:
- Survivin, a known cancer biomarker, is implicated in non-cancer pathologies like rheumatoid arthritis (RA).
- Elevated survivin levels in blood and synovial fluid correlate with joint damage and poor treatment response in RA patients.
- The Malaysian epidemiological investigation of rheumatoid arthritis (MyEIRA) study provides a cohort for investigating RA biomarkers.
Purpose of the Study:
- To evaluate the diagnostic value of blood survivin measurements for rheumatoid arthritis (RA).
- To assess the association of survivin levels with RA risk, considering ACPA and HLA-DRB1 SE alleles.
Main Methods:
- Enzyme-linked immunosorbent assay (ELISA) was used to measure survivin levels in 1233 RA patients and 1566 healthy controls.
- Antibodies against cyclic citrullinated peptides (ACPA) were detected by ELISA.
- HLA-DRB1 shared epitope (SE) alleles were identified using polymerase chain reaction (PCR).
Main Results:
- High survivin levels were found in 50.7% of RA cases versus 5.4% of controls, indicating high specificity.
- Survivin was associated with increased RA risk, particularly in patients lacking SE alleles and ACPA (OR=5.40).
- Combined analysis of survivin, SE, and ACPA significantly elevated RA risk (OR=16.21) compared to survivin-negative individuals with SE and ACPA.
Conclusions:
- Blood survivin detection offers a straightforward method to enhance RA diagnosis.
- Survivin measurement improves the predictability of RA, especially in conjunction with ACPA and SE allele status.
- This study highlights survivin's potential as a valuable biomarker in RA diagnostics within the Malaysian population.
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