Liu Wei, Huang Lili, Zhang Cuiying, Liu Zuozhong
Department of Orthopedics, Yongchuan Hospital of Chongqing Medical University, Chongqing 402160, P.R. China.
Department of Infections, Yongchuan Hospital of Chongqing Medical University, Chongqing 402160, P.R. China.
Exp Ther Med. 2019 Jan;17(1):291-297. doi: 10.3892/etm.2018.6921. Epub 2018 Nov 2.
Long non-coding (lnc)RNA maternally expressed gene 3 (MEG3) has been proved to participate in osteoporosis, which features inverse pathological changes to those associated with spondylosis. The present study aimed to investigate the involvement of lncRNA MEG3 in ankylosing spondylitis. Blood and open sacroiliac joint biopsies were obtained from ankylosing spondylitis patients and healthy controls, and the expression of MEG3 in those tissues was detected by reverse-transcription-quantitative polymerase chain reaction analysis. Disease activity was evaluated according to the Ankylosing Spondylitis Disease Activity Score established by the International Association of Ankylosing Spondylitis. The diagnostic value of MEG3 expression for ankylosing spondylitis was evaluated by receiver operating characteristic curve analysis. The correlation between MEG3 expression and disease activity was assessed using Pearson correlation analysis. Furthermore, according to the median expression level of MEG3, patients were divided into high-level and low-level groups. The hospitalization time and re-hospitalization rate within 2 years after discharge were compared between these two groups and differences in clinicopathological parameters between the two groups were analyzed using the chi-square test. The results indicated that MEG3 was downregulated in ankylosing spondylitis patients compared with that in healthy controls. Furthermore, MEG3 expression levels may be used to effectively distinguish ankylosing spondylitis patients from healthy controls. The serum levels of MEG3 were not associated with the patients' age, sex or alcohol/tobacco consumption, but closely correlated with disease activity and disease duration. In addition, patients with higher expression levels of MEG3 had a shorter hospitalization time and a lower re-hospitalization rate within 2 years after discharge It was concluded that lncRNA MEG3 is downregulated in ankylosing spondylitis patients and is associated with disease activity, time of hospitalization and disease duration.
长链非编码(lnc)RNA母系表达基因3(MEG3)已被证明参与骨质疏松症,其病理变化与脊柱关节病相反。本研究旨在探讨lncRNA MEG3在强直性脊柱炎中的作用。从强直性脊柱炎患者和健康对照者中获取血液和开放性骶髂关节活检组织,通过逆转录-定量聚合酶链反应分析检测这些组织中MEG3的表达。根据国际强直性脊柱炎协会制定的强直性脊柱炎疾病活动评分评估疾病活动度。通过受试者工作特征曲线分析评估MEG3表达对强直性脊柱炎的诊断价值。采用Pearson相关分析评估MEG3表达与疾病活动度之间的相关性。此外,根据MEG3的中位表达水平,将患者分为高水平组和低水平组。比较两组患者出院后2年内的住院时间和再住院率,并使用卡方检验分析两组患者临床病理参数的差异。结果表明,与健康对照者相比,强直性脊柱炎患者中MEG3表达下调。此外,MEG3表达水平可有效区分强直性脊柱炎患者和健康对照者。MEG3的血清水平与患者的年龄、性别或烟酒消费无关,但与疾病活动度和病程密切相关。此外,MEG3表达水平较高的患者出院后2年内住院时间较短,再住院率较低。结论是,lncRNA MEG3在强直性脊柱炎患者中表达下调,且与疾病活动度、住院时间和病程相关。