Brain tumors and circulating micrornas: a systematic review and diagnostic meta-analysis

被引:15
作者
Aalami, Amir Hossein [1 ]
Abdeahad, Hossein [2 ]
Shoghi, Ali [3 ]
Mesgari, Mohammad [4 ]
Amirabadi, Amir [5 ,6 ]
Sahebkar, Amirhossein [7 ,8 ,9 ,10 ]
机构
[1] Islamic Azad Univ, Mashhad Branch, Dept Biol, Mashhad, Razavi Khorasan, Iran
[2] Univ Utah, Dept Nutr & Integrat Physiol, Salt Lake City, UT USA
[3] Kermanshah Univ Med Sci, Neurosurg Dept, Kermanshah, Iran
[4] Ferdowsi Univ Mashhad, Dept Biol, Fac Sci, Mashhad, Razavi Khorasan, Iran
[5] Islamic Azad Univ, Mashhad Med Sci Branch, Dept Internal Med, Mashhad, Razavi Khorasan, Iran
[6] Mashhad Univ Med Sci, Solid Tumors Res Ctr, Mashhad, Razavi Khorasan, Iran
[7] Mashhad Univ Med Sci, Applied Biomed Res Ctr, Mashhad, Razavi Khorasan, Iran
[8] Mashhad Univ Med Sci, Pharmaceut Technol Inst, Biotechnol Res Ctr, Mashhad, Razavi Khorasan, Iran
[9] Univ Western Australia, Sch Med, Perth, Australia
[10] Univ Med Sci, Sch Pharm, Mashhad, Razavi Khorasan, Iran
关键词
Circulating microRNAs; brain tumors; glioma; glioblastoma; diagnostic biomarker; CENTRAL-NERVOUS-SYSTEM; NONINVASIVE BIOMARKER; PROGNOSTIC INDICATOR; SERUM; SIGNATURE; EXPRESSION; IDENTIFICATION; EXOSOMES; GLIOMA; CURVE;
D O I
10.1080/14737159.2022.2019016
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Purpose Brain tumors (BT) are among the most prevalent cancers in recent years. Various studies have examined the diagnostic role of microRNAs in different diseases; however, their diagnostic role in BT has not been comprehensively investigated. This meta-analysis was performed to assess microRNAs in the blood of patients with BTs accurately. Methods Twenty-six eligible studies were included for analysis. The pooled sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR), diagnostic odds ratio (DOR), area under curve (AUC), Q*index, summary receiver-operating characteristic (SROC) were assessed using the Meta-Disc V.1.4 and Comprehensive Meta-Analysis V.3.3 software. Results The diagnostic accuracy of microRNA was high in identifying BT based on the pooled sensitivity 0.82 (95%CI: 0.816-0.84), specificity 0.82 (95%CI: 0.817-0.84), PLR 5.101 (95%CI: 3.99-6.51), NLR 0.187 (95%CI: 0.149-0.236), DOR 34.07 (95%CI: 22.56-51.43) as well as AUC (0.92), and Q*-index (0.86). Subgroup analyses were performed for sample types (serum/plasma), reference genes (RNU6, miR-39, and miR-24), and region to determine the diagnostic power of microRNAs in the diagnosis of BT using pooled sensitivity, specificity, PLR, NLR, AUC, and DOR. Conclusion This meta-analysis suggested that circulating microRNAs might be potential markers for noninvasive early detection of BT.
引用
收藏
页码:201 / 211
页数:11
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