Abstract

Objective To investigate the potential possibilities of specific microRNA in plasma as novel biomarkers for the early diagnosis in juvenile idiopathic arthritis(JIA). Methods This research was be segmented into 4 stages.1. Screened candidate microRNAs: 5 candidate plasma microRNAs were detected by biochips of microRNAs, corresponding 5 JIA patients with onset of oligoarthritis, 5 JIA patients with onset of polyarthritis and 3 age-matched and sex-matched healthy controls individual.2. The feasibility of the microRNAs as novel biomarkers was validated by Real-time quantitative polymerase chain reaction (RT-PCR) in plasma on 80 JIA patients (43 oligoarthritis, 37 polyarthritis), 29 juvenile ankylosing spondylitis(JAS) patients and 30 healthy control individuals.3. The change of microRNAs was observed by RT-PCR in plasma from another 9 JIA patients before and 3 months after anti-rheumatic drug treatment.4. The correlation between the levels of candidate plasma microRNAs and clinical parameters of JIA patients was analyzed. Results Plasma concentrations of miR-16, miR-146a and miR-223 in JIA patients, including oligoarthritis and polyarthritis, were significantly higher than those in healthy subjects (all P 0.05). More importantly, it was found that the expression of miR-16 was considerably reduced in the post-treatment plasma samples when compared to the pre-treatment samples(P=0.061). In addition, the levels of miR-16 in JIA plasma inversely corrected with tender joint. Conclusions Plasma levels of miR-16 were well-discriminated between JIA patients and healthy subjects or JAS patients. It is suggested that plasma miR-16 might serve as a novel and potential biomarker for screening JIA. Furthermore, it might serve as a novel biomarker for joint inflammation but not specifically for differentiating the subtypes of JIA. Key words: MicroRNA; Juvenile idiopathic arthritis; Biomarker

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