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微小RNA在强直性脊柱炎中的作用

The Role of MicroRNAS in Ankylosing Spondylitis.

作者信息

Li Zheng, Wong Sunny H, Shen Jianxiong, Chan Matthew T V, Wu William Ka Kei

机构信息

From the Department of Orthopedics Surgery Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College (ZL, JS); State Key Laboratory of Digestive Disease, LKS Institute of Health Sciences and Department of Medicine & Therapeutics (SHW, WKKW); and Department of Anaesthesia and Intensive Care (MTVC), The Chinese University of Hong Kong, Hong Kong, China.

出版信息

Medicine (Baltimore). 2016 Apr;95(14):e3325. doi: 10.1097/MD.0000000000003325.

Abstract

Ankylosing spondylitis (AS) is a common and genetically heterozygous inflammatory rheumatic disease characterized by new bone formation, ankylosis and inflammation of hip, sacroiliac joints and spine. Until now, there is no method for early diagnosis of AS and the effective treatment available for AS patients remain largely undefined.We searched articles indexed in PubMed (MEDLINE) database using Medical Subject Heading (MeSH) or Title/Abstract words ("microRNA" and "ankylosing spondylitis") from inception up to November 2015.Genetic polymorphisms of miRNAs and their targets might alter the risk of AS development whereas certain miRNAs exhibit correlation with inflammatory index.Let-7i and miR-124 were upregulated whereas miR-130a was downregulated in circulating immune cells of AS patients. These deregulated miRNAs could modulate key immune cell functions, such as cytokine response and T-cell survival.miRNA deregulation is key to AS pathogenesis. However, clinical utilization of miRNAs for management of AS patients requires further support from future translational studies.

摘要

强直性脊柱炎(AS)是一种常见的、基因杂合的炎性风湿性疾病,其特征为新骨形成、关节强直以及髋部、骶髂关节和脊柱的炎症。到目前为止,尚无AS的早期诊断方法,并且AS患者可用的有效治疗方法在很大程度上仍不明确。我们使用医学主题词(MeSH)或标题/摘要词(“微小RNA”和“强直性脊柱炎”)在PubMed(MEDLINE)数据库中检索了从建库至2015年11月的文章。微小RNA及其靶标的基因多态性可能会改变AS发生的风险,而某些微小RNA与炎症指标存在相关性。在AS患者的循环免疫细胞中,Let-7i和miR-124上调,而miR-130a下调。这些失调的微小RNA可调节关键免疫细胞功能,如细胞因子反应和T细胞存活。微小RNA失调是AS发病机制的关键。然而,微小RNA在AS患者管理中的临床应用需要未来转化研究的进一步支持。

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