Serum MicroRNA Levels as a Noninvasive Diagnostic Biomarker for the Early Diagnosis of Hepatitis B Virus-Related Liver Fibrosis.
Serum MicroRNA Levels as a Noninvasive Diagnostic Biomarker for the Early Diagnosis of Hepatitis B Virus-Related Liver Fibrosis.
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血清 MicroRNA 水平作为乙型肝炎病毒相关肝纤维化早期诊断的无创诊断生物标志物
DOI:
10.5009/gnl16560
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发表时间:
2017-11-15
期刊:
影响因子:
3.4
通讯作者:
Shi G
中科院分区:
文献类型:
--
作者:
Bao S;Zheng J;Li N;Huang C;Chen M;Cheng Q;Yu K;Chen S;Zhu M;Shi G
To investigate the role of selected serum microRNA (miRNA) levels as potential noninvasive biomarkers for differentiating S0–S2 (early fibrosis) from S3–S4 (late fibrosis) in patients with a chronic hepatitis B virus (HBV) infection. One hundred twenty-three treatment-naive patients with a chronic HBV infection who underwent a liver biopsy were enrolled in this study. The levels of selected miRNAs were measured using a real-time quantitative polymerase chain reaction assay. A logistic regression analysis was performed to assess factors associated with fibrosis progression. Receiver operating characteristic (ROC) curve and discriminant analyses validated these the ability of these predicted variables to discriminate S0–S2 from S3–S4. Serum miR-29, miR-143, miR-223, miR-21, and miR-374 levels were significantly downregulated as fibrosis progressed from S0–S2 to S3–S4 (p<0.05), but not miR-16. The multivariate logistic regression analysis identified a panel of three miRNAs and platelets that were associated with a high diagnostic accuracy in discriminating S0–S2 from S3–S4, with an area under the curve of 0.936. The levels of the studied miRNAs, with the exception of miR-16, varied with fibrosis progression. A panel was identified that was capable of discriminating S0–S2 from S3–S4, indicating that serum miRNA levels could serve as a potential noninvasive biomarker of fibrosis progression.
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影响因子:
5.7
作者:
Naito Y;Sakamoto N;Oue N;Yashiro M;Sentani K;Yanagihara K;Hirakawa K;Yasui W
通讯作者:
Yasui W
影响因子:
3.2
作者:
Liu, Xiujuan;Hong, Quan;Xu, Lihong
通讯作者:
Xu, Lihong
影响因子:
64.8
作者:
Davis, Brandi N.;Hilyard, Aaron C.;Hata, Akiko
通讯作者:
Hata, Akiko
影响因子:
13.5
作者:
DESMET, VJ;GERBER, M;SCHEUER, PJ
通讯作者:
SCHEUER, PJ
影响因子:
25.7
作者:
Trebicka, Jonel;Anadol, Evrim;Odenthal, Margarete
通讯作者:
Odenthal, Margarete