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Brain tumors and circulating micrornas: a systematic review and diagnostic meta-analysis.
Aalami, Amir Hossein; Abdeahad, Hossein; Shoghi, Ali; Mesgari, Mohammad; Amirabadi, Amir; Sahebkar, Amirhossein.
Afiliación
  • Aalami AH; Department of Biology, Mashhad Branch, Islamic Azad University, Mashhad, Iran.
  • Abdeahad H; Department of Nutrition and Integrative Physiology, University of Utah, Salt Lake City, UT USA.
  • Shoghi A; Neurosurgery Department, Kermanshah University of Medical Sciences, Kermanshah, Iran.
  • Mesgari M; Department of Biology, Faculty of Science, Ferdowsi University of Mashhad, Mashhad Iran.
  • Amirabadi A; Department of Internal Medicine, Mashhad Medical Sciences Branch, Islamic Azad University, Mashhad, Iran.
  • Sahebkar A; Solid Tumors Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Expert Rev Mol Diagn ; 22(2): 201-211, 2022 Feb.
Article en En | MEDLINE | ID: mdl-34906021
ABSTRACT

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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / MicroARNs / MicroARN Circulante Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Expert Rev Mol Diagn Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Irán

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / MicroARNs / MicroARN Circulante Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Expert Rev Mol Diagn Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Irán
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