Rheumatology (Oxford, England) · 2026
Circulatory microRNA signature distinguishing rheumatoid arthritis and psoriatic arthritis.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Tynan Órla, Hanlon Megan M, Floudas Achilleas, Wade Siobhán, Fearon Ursula, Veale Douglas J
Аннотация
OBJECTIVES: Gene regulatory microRNAs (miRNAs) have emerged as promising biomarkers and therapeutic targets in autoimmunity pathology. This study examines circulatory miRNAs as cellular biomarkers that can distinguish rheumatoid arthritis (RA) from psoriatic arthritis (PsA) to evaluate the potential implications for disease pathogenesis.
METHODS: RA (n = 48) and PsA (n = 49) patients and healthy controls (HC) (n = 20) were recruited and serums obtained. Multiplex analysis of serum miRNAs was performed using the FirePlex miRNA Immunology-V2 panel (FirePlex Bioworks Inc.). DNA intelligent analysis (DIANA)-mirPath and STRING software were used to predict pathways targeted by the dysregulated miRNAs.
RESULTS: Seven miRNAs, miR-126-3p, miR-29b-3p, miR-22-3p, miR-223-3p, miR-320a, let-7e-5p and let-7g-5p, were significantly elevated in RA serum compared with PsA (all P < 0.05), in addition to HC (all P < 0.05), with high sensitivity and specificity as determined by receiver operating characteristic curve analysis. Principal component analysis and biplot analysis demonstrated differential miRNA clustering between both disease states with a dominant skew towards three specific miRNAs in RA vs PsA: miR-29b-3p, miR-22-3p and miR-223-3p. DIANA analysis and STRING visualization of this miRNA signature identified downstream target pathways including phosphoinositide 3-kinase-AKT and FoxO signalling, all importantly associated with aspects of RA pathogenesis including angiogenesis, invasion and cell death.
CONCLUSION: This study identified three key miRNAs demonstrating differential expression levels between RA and PsA, which potentially govern downstream inflammatory pathways regulating distinct disease mechanisms. Therefore, circulating miRNAs may be valuable as non-invasive diagnostic biomarkers that can distinguish RA from PsA and may additionally assist in elucidating differential disease pathogenesis.
METHODS: RA (n = 48) and PsA (n = 49) patients and healthy controls (HC) (n = 20) were recruited and serums obtained. Multiplex analysis of serum miRNAs was performed using the FirePlex miRNA Immunology-V2 panel (FirePlex Bioworks Inc.). DNA intelligent analysis (DIANA)-mirPath and STRING software were used to predict pathways targeted by the dysregulated miRNAs.
RESULTS: Seven miRNAs, miR-126-3p, miR-29b-3p, miR-22-3p, miR-223-3p, miR-320a, let-7e-5p and let-7g-5p, were significantly elevated in RA serum compared with PsA (all P < 0.05), in addition to HC (all P < 0.05), with high sensitivity and specificity as determined by receiver operating characteristic curve analysis. Principal component analysis and biplot analysis demonstrated differential miRNA clustering between both disease states with a dominant skew towards three specific miRNAs in RA vs PsA: miR-29b-3p, miR-22-3p and miR-223-3p. DIANA analysis and STRING visualization of this miRNA signature identified downstream target pathways including phosphoinositide 3-kinase-AKT and FoxO signalling, all importantly associated with aspects of RA pathogenesis including angiogenesis, invasion and cell death.
CONCLUSION: This study identified three key miRNAs demonstrating differential expression levels between RA and PsA, which potentially govern downstream inflammatory pathways regulating distinct disease mechanisms. Therefore, circulating miRNAs may be valuable as non-invasive diagnostic biomarkers that can distinguish RA from PsA and may additionally assist in elucidating differential disease pathogenesis.