A Panel of Plasma miRNAs 199b-3p, 224-5p and Let-7d-3p as Non-Invasive Diagnostic Biomarkers for Endometriosis
Abstract
The objective of this study was to investigate whether the combination of miR-224-5p, miR-199-3p, and let-7d-3p is a suitable diagnostic panel for endometriosis. Twenty-five women with endometriosis (case) and twenty-five women without any sign of endometriosis (controls) were included. Peripheral blood specimens were collected from all these women who were a proper candidate for laparoscopy before surgery. Total RNA was isolated to synthesize complementary DNA. Expression of miR-199b-3p, miR-224-5p, and let-7d-3p was analyzed by RT-qPCR. To estimate the performance of the identified miRNAs for endometriosis diagnosis, we performed ROC curves analysis. There was an upregulation of miRNAs 199b-3p (P value < 0.001) and down-regulation of 224-5p (P value < 0.001) and miRNA let-7d-3p (P value < 0.05) in women with endometriosis compared to non-endometriosis women. The diagnostic accuracy of miRNAs 199b-3p, 224-5p, and let-7d-3p was measured by AUC which was 0.843 (sensitivity = 96% and specificity = 80%), 0.914 (sensitivity = 84% and specificity = 80%), and 0.696 (sensitivity = 80% and specificity = 56%) for miRNAs 199b-3p, 224-5p, and let-7d-3p, respectively. In combination, they showed the highest accuracy with the AUC 0.992 (sensitivity = 96% and specificity = 100%). In conclusion(s) the levels of miRNAs 199b-3p, 224-5p, and Let-7d-3p in plasma are potential diagnostic biomarkers for endometriosis patients.
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Levels of miRNAs 199b-3p, 224-5p, and Let-7d-3p in plasma are potential diagnostic biomarkers for endometriosis patients.
“Recent studies showed that the levels of miRNAs 199b-3p, 224-5p, and Let-7d-3p in plasma are potential diagnostic biomarkers for endometriosis patients [165].”
From Endometriosis: Epidemiology, Classification, Pathogenesis, Treatment and Genetics (Review of Literature) (2021) · cites this paper as [165]
A locus at 7p15.2 is associated with the development of endometriosis in British and Australian populations.
“On the basis of these studies, loci associated with the development of the disease–7p15.2–was established.”
From Endometriosis: Epidemiology, Classification, Pathogenesis, Treatment and Genetics (Review of Literature) (2021) · cites this paper as [165]
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- Authors
- Zafari, N., Tarafdari, A. M., Izadi, P., Noruzinia, M., Yekaninejad, M. S., Bahramy, A., & Mohebalian, A.
- Affiliations
- Tehran University of Medical Sciences (IR)
- Tarbiat Modares University (IR)
- Corresponding author
- Izadi, Pantea
- Venue
- Reproductive Sciences
- Published
- 2021-01-04
- Volume
- 28
- Issue
- 4
- Pages
- 991-999
- ISSN
- 1933-7191 (ISSN-L)
- 1933-7205
- OpenAlex
- W3121055841
- Cited by
- 36
- References
- 40
- Citations by year
- 2026: 4 · 2025: 8 · 2024: 7 · 2023: 7 · 2022: 5 · 2021: 5
- FWCI
- 5.17
- Type
- journal article
- Language
- en
- Update notices
- correction (2021-02-01)
- Open access
- closed
- Locations
- Reproductive Sciences (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Tehran University of Medical Sciences and Health Services (36424)
- Topics
- Health Sciences › Medicine › Reproductive Medicine › Endometriosis Research and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Keywords
- endometriosis, microRNA, miR-224-5p, plasma biomarkers, non-invasive diagnosis, diagnostic biomarker panel, diagnostic accuracy
- MeSH terms
- Adult, Endometriosis, Female, Humans, Biomarkers, Down-Regulation, Gene Expression Profiling, MicroRNAs
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