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dc.contributor.authorSsedyabane, Frank
dc.contributor.authorObuku, Ekwaro A.
dc.contributor.authorNamisango, Eve
dc.contributor.authorNgonzi, Joseph
dc.contributor.authorCastro, Cesar M.
dc.contributor.authorLeef, Hakho
dc.contributor.authorRandall, Thomas C.
dc.contributor.authorOcan, Moses
dc.contributor.authorApunyo, Robert
dc.contributor.authorKinengyere, Alison Annet
dc.contributor.authorKajabwangu, Rogers
dc.contributor.authorKisawe, Aziza Tahirah
dc.contributor.authorNajjuma, Josephine Nambi
dc.contributor.authorTusubira, Deusdedit
dc.contributor.authorNiyonzima, Nixon
dc.date.accessioned2024-08-28T13:23:29Z
dc.date.available2024-08-28T13:23:29Z
dc.date.issued2024
dc.identifier.citationSsedyabane, F., Obuku, E. A., Namisango, E., Ngonzi, J., Castro, C. M., Lee, H., ... & Niyonzima, N. (2024). The diagnostic accuracy of serum and plasma microRNAs in detection of cervical intraepithelial neoplasia and cervical cancer: A systematic review and meta-analysis. Gynecologic Oncology Reports, 101424.en_US
dc.identifier.urihttp://ir.must.ac.ug/xmlui/handle/123456789/3756
dc.description.abstractStudies suggest a need for new diagnostic approaches for cervical cancer including microRNA technology. In this review, we assessed the diagnostic accuracy of microRNAs in detecting cervical cancer and Cervical Intraepithelial Neoplasia (CIN). We performed a systematic review following the Preferred Reporting Items for Systematic Review and Meta- Analysis guideline for protocols (PRISMA-P). We searched for all articles in online databases and grey literature from 01st January 2012 to 16th August 2022. We used the quality assessment of diagnostic accuracy studies tool (QUADAS-2) to assess the risk of bias of included studies and then conducted a Random Effects Meta-analysis. We identified 297 articles and eventually extracted data from 24 studies. Serum/plasma concentration miR- 205, miR-21, miR-192, and miR-9 showed highest diagnostic accuracy (AUC of 0.750, 0.689, 0.980, and 0.900, respectively) for detecting CIN from healthy controls. MicroRNA panels (miR-21, miR-125b and miR-370) and (miR-9, miR-10a, miR-20a and miR-196a and miR-16–2) had AUC values of 0.897 and 0.886 respectively for detecting CIN from healthy controls. For detection of cervical cancer from healthy controls, the most promising microRNAs were miR-21, miR-205, miR-192 and miR-9 (AUC values of 0.723, 0.960, 1.00, and 0.99 respectively). We report higher diagnostic accuracy of upregulated microRNAs, especially miR-205, miR-9, miR-192, and miR-21. This highlights their potential as stand-alone screening or diagnostic tests, either with others, in a new algorithm, or together with other biomarkers for purposes of detecting cervical lesions. Future studies could standardize quantification methods, and also study microRNAs in higher prevalence populations like in sub- Saharan Africa and South Asia.en_US
dc.language.isoen_USen_US
dc.publisherGynecologic Oncology Reportsen_US
dc.subjectCervical Canceren_US
dc.subjectSerumen_US
dc.subjectPlasmaen_US
dc.subjectMicroRNAsen_US
dc.subjectDiagnostic utilityen_US
dc.subjectCervical Intraepithelial Neoplasiaen_US
dc.subjectSystematic reviewen_US
dc.titleThe diagnostic accuracy of serum and plasma microRNAs in detection of cervical intraepithelial neoplasia and cervical cancer: A systematic review and meta-analysisen_US
dc.typeArticleen_US


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