Kamiya Yasuko, Kawada Jun-ichi, Kawano Yoshihiko, Torii Yuka, Kawabe Shinji, Iwata Naomi, Ito Yoshinori
Department of Pediatrics, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan.
Department of Infection and Immunology, Aichi Children's Health and Medical Center, 1-2 Osakada Morioka-cho, Obu, Aichi, 474-8710, Japan.
Clin Rheumatol. 2015 Oct;34(10):1705-12. doi: 10.1007/s10067-015-2922-1. Epub 2015 Apr 7.
MicroRNAs (miRNAs) are non-coding RNAs that regulate gene expression of targeted mRNAs, which are important in the pathogenesis of autoimmune diseases. MiRNAs may have the potential to serve as biomarkers of disease. We evaluated serum levels of selected miRNAs and their associations with disease activity in juvenile idiopathic arthritis (JIA). Sera and peripheral blood leukocytes were collected from patients with JIA (8 systemic onset, 16 polyarthritis) and healthy controls. Levels of miR-16, miR-132, miR-146a, miR-155, and miR-223 were quantified. Levels of miR-223 in sera were significantly higher in patients in the active phase of systemic onset JIA than in controls. MiRNAs of peripheral blood leukocytes did not exhibit any difference between patients with JIA and controls. In both systemic onset JIA and polyarthritis patients, levels of miR-223 and miR-16 correlated with erythrocyte sedimentation rate and matrix metalloproteinase-3, respectively. MiR-146a and miR-223 in polyarthritis showed correlations with matrix metalloproteinase-3. Expressions of miRNAs were altered in patients with JIA. Serum levels of miR-223 may be a potential disease biomarker. Investigation of miRNAs could be helpful in understanding the pathogenesis of JIA and could aid in the identification of additional disease biomarkers.
微小RNA(miRNA)是非编码RNA,可调节靶标mRNA的基因表达,这在自身免疫性疾病的发病机制中很重要。miRNA可能有潜力作为疾病的生物标志物。我们评估了青少年特发性关节炎(JIA)患者中选定miRNA的血清水平及其与疾病活动的关联。收集了JIA患者(8例全身型、16例多关节型)和健康对照者的血清及外周血白细胞。对miR-16、miR-132、miR-146a、miR-155和miR-223的水平进行了定量。全身型JIA活动期患者血清中miR-223的水平显著高于对照组。JIA患者和对照组外周血白细胞中的miRNA没有表现出任何差异。在全身型JIA和多关节型患者中,miR-223和miR-16的水平分别与红细胞沉降率和基质金属蛋白酶-3相关。多关节型患者中的miR-146a和miR-223与基质金属蛋白酶-3相关。JIA患者中miRNA的表达发生了改变。血清miR-223水平可能是一种潜在的疾病生物标志物。对miRNA的研究可能有助于理解JIA的发病机制,并有助于识别其他疾病生物标志物。