Differential expression levels of plasma microRNA in Hashimoto's disease

小RNA 生物 实时聚合酶链反应 逆转录聚合酶链式反应 分子生物学 阶段(地层学) 聚合酶链反应 逆转录酶 接收机工作特性 内科学 基因表达 基因 免疫学 遗传学 医学 古生物学
作者
Lijuan Zhao,Xin Zhou,Xia Shan,Lian‐Wen Qi,Tongshan Wang,Jun Zhu,Danxia Zhu,Zebo Huang,Lan Zhang,Huo Zhang,Yin Yin,Zhiyan Wang,Wei Zhu,Wen‐Fang Cheng,Lin Jiang
出处
期刊:Gene [Elsevier BV]
卷期号:642: 152-158 被引量:17
标识
DOI:10.1016/j.gene.2017.10.053
摘要

The altered expression of circulating miRNAs has been discovered in many autoimmune diseases (ADs). With rare existing research, it is still unclear in Hashimoto's thyroiditis (HT). We detected plasma miRNA expression of HT patients in this three-stage designed study. Differently expressed miRNAs (4 HT pools vs. 1 normal control pool) were identified using quantitative reverse transcription polymerase chain reaction (qRT-PCR) based Exiqon panel (miRCURY-Ready-to-Use- PCR-Human- panel-I + II-V1.M) in the initial discovery stage. These miRNAs were then confirmed in the training stage and further validated in the testing stage using qRT-PCR with 64 (32 HT vs. 32 NCs) and 136 samples (68 HT vs. 68 NCs), respectively. A total of 10 miRNAs showed differential expression through the training stage. For further validation in the testing stage, expression of 6 miRNAs (miR-205, miR-20a-3p, miR-375, miR-296, miR-451, miR-500a) were consistent with those in the training stage. Combination results showed that these 6 miRNAs were significantly up-regulated in peripheral plasma of HT patients compared with normal controls (P < 0.05). In addition, the six-miRNA signature was evaluated to be a potential diagnostic marker of HT. The areas under the receiver operating characteristic curve of the signature were 0.80, 0.75 and 0.69 for the training, testing and the combined stages, respectively. Three miRNAs were associated with TSH levels in HT patients (miR-451, P = 0.043; miR-375, P = 0.043; miR-500a, P = 0.043). Additionally, miR-20a-3p was related with TgAb level (P = 0.046). We identified a miRNA signature including six dysregulated plasma miRNAs which could act as a diagnostic marker in plasma of HT, providing more evidence and better understanding for the association between circulating miRNAs and autoimmune diseases.
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