Serum exosome microRNA panel as a noninvasive biomarker for molecular diagnosis of fulminant myocarditis

被引:14
|
作者
Zhang, Yingying [1 ,2 ]
Li, Xueqin [1 ,3 ]
Wang, Deguo [4 ]
Jiang, Xiaogan [5 ]
Zhang, Mengying [1 ,3 ]
Lv, Kun [1 ,3 ]
机构
[1] Anhui Higher Educ Inst, Key Lab Noncoding RNA Transformat Res, Wuhu, Peoples R China
[2] Yijishan Hosp, Wannan Med Coll, Dept Lab Med, Affiliated Hosp 1, Wuhu, Peoples R China
[3] Yijishan Hosp, Wannan Med Coll, Affiliated Hosp 1, Dept Cent Lab, 2 Zheshan Western Rd, Wuhu 241001, Peoples R China
[4] Yijishan Hosp, Wannan Med Coll, Affiliated Hosp 1, Dept Gerontol, Wuhu, Peoples R China
[5] Yijishan Hosp, Wannan Med Coll, Affiliated Hosp 1, Dept Crit Care Med, Wuhu, Peoples R China
基金
中国国家自然科学基金;
关键词
CARDIAC TROPONIN-I; ENDOMYOCARDIAL BIOPSY; EUROPEAN-SOCIETY; ELEVATIONS; MANAGEMENT; INFARCTION; CARDIOLOGY; STATEMENT; KNOWLEDGE;
D O I
10.1016/j.omtm.2020.11.006
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Exosome-derivedmicroRNAs(miRNAs) are potential diagnostic biomarkers. However, little is known about their effectiveness as diagnostic biomarkers of fulminant myocarditis (FM). This study aimed to explore serumexosomalmiRNAs aspotential biomarkers for FM diagnosis. Peripheral blood samples were collected from 99 patients with FM, 32 patients with nonfulminant myocarditis (NFM), and 105 healthy controls (HCs). The miRNA expression profiles of serum exosomes were determined using next-generation sequencing, and differentially expressed miRNAs were further analyzed by quantitative reverse transcriptase polymerase chain reaction. A logistic regression model was constructed using a training cohort (n = 120) and then validated using an independent cohort (n = 106). The area under the receiver operating characteristic curvewas used to evaluate diagnostic accuracy. In FMpatients, hsa-miR-30a, hsa-miR192, hsa-miR-146a, hsa-miR-155, and hsa-miR-320a were validated as significantly and differentially expressed candidates that could serve as potentialmarkers for diagnosing FM. In addition, the miRNA panel (hsa-miR-155 and hsa-miR-320a) from themultivariate logistic regressionmodel demonstrated high accuracy in the diagnosis of FM and was able to distinguish FM from HCs and NFM. Moreover, the diagnostic value of the miRNA panel was greater than that of CRP and cTn alone or together. The miRNA panel provided the excellent diagnostic capability for FM.
引用
收藏
页码:142 / 151
页数:10
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