Ascoli Christian, Huang Yue, Schott Cody, Turturice Benjamin A, Metwally Ahmed, Perkins David L, Finn Patricia W
Division of Pulmonary, Critical Care, Sleep, and Allergy, Department of Medicine.
Department of Microbiology and Immunology.
Am J Respir Cell Mol Biol. 2018 Jan;58(1):40-54. doi: 10.1165/rcmb.2017-0207OC.
MicroRNAs (miRNAs) act as post-transcriptional regulators of gene expression. In sarcoidosis, aberrant miRNA expression may enhance immune responses mounted against an unknown antigenic agent. We tested whether a distinct miRNA signature functions as a diagnostic biomarker and explored its role as an immune modulator in sarcoidosis. The expression of miRNAs in peripheral blood mononuclear cells from subjects who met clinical and histopathologic criteria for sarcoidosis was compared with that observed in matched controls in the ACCESS (A Case Controlled Etiologic Study of Sarcoidosis) study. Signature miRNAs were determined by miRNA microarray analysis and validated by quantitative RT-PCR. Microarray analysis identified 54 mature, human feature miRNAs that were differentially expressed between the groups. Significant feature miRNAs that distinguished subjects with sarcoidosis from controls were selected by means of probabilistic models adjusted for clinical variables. Eight signature miRNAs were chosen to verify the diagnosis of sarcoidosis in a validation cohort, and distinguished subjects with sarcoidosis from controls with a positive predictive value of 88%. We identified both novel and previously described genes and molecular pathways associated with sarcoidosis as targets of these signature miRNAs. Additionally, we demonstrate that signature miRNAs (hsa-miR-150-3p and hsa-miR-342-5p) are significantly associated with reduced lymphocytes and airflow limitations, both of which are known markers of a poor prognosis. Together, these findings suggest that a circulating miRNA signature serves as a noninvasive biomarker that supports the diagnosis of sarcoidosis. Future studies will test the miRNA signature as a prognostication tool to identify unfavorable changes associated with poor clinical outcomes in sarcoidosis.
微小RNA(miRNA)作为基因表达的转录后调节因子。在结节病中,异常的miRNA表达可能会增强针对未知抗原的免疫反应。我们测试了一种独特的miRNA特征是否可作为诊断生物标志物,并探讨了其在结节病中作为免疫调节剂的作用。在ACCESS(结节病病例对照病因研究)研究中,将符合结节病临床和组织病理学标准的受试者外周血单核细胞中miRNA的表达与匹配对照组中观察到的表达进行了比较。通过miRNA微阵列分析确定特征性miRNA,并通过定量逆转录-聚合酶链反应进行验证。微阵列分析鉴定出54种成熟的人类特征性miRNA在两组之间存在差异表达。通过针对临床变量进行调整的概率模型,选择了区分结节病患者与对照组的重要特征性miRNA。选择了8种特征性miRNA在验证队列中验证结节病的诊断,其区分结节病患者与对照组的阳性预测值为88%。我们确定了与结节病相关的新的和先前描述的基因以及分子途径作为这些特征性miRNA的靶标。此外,我们证明特征性miRNA(hsa-miR-150-3p和hsa-miR-342-5p)与淋巴细胞减少和气流受限显著相关,这两者都是已知的预后不良标志物。总之,这些发现表明循环miRNA特征可作为支持结节病诊断