Evidence map›Paper›PMID 41254724›Full record

ArticleBMC medical genomics2025

Serum miR-141-3p serves as a biomarker for early-stage diagnosis of endometriosis.

Hao Tan, Dongbin Liu, Kan Zhang, Huan Li, Hougang Zhou

Abstract read
In one paragraph

Article in BMC medical genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Hao TanDepartment of Clinical Laboratory, Hunan Provincial Maternal and Child Health Care Hospital, No.53 Xiangchun Road, Changsha, 410008, Hunan, China.
Dongbin LiuDepartment of Clinical Laboratory, Hunan Provincial Maternal and Child Health Care Hospital, No.53 Xiangchun Road, Changsha, 410008, Hunan, China.
Kan ZhangDepartment of Clinical Laboratory, Hunan Provincial Maternal and Child Health Care Hospital, No.53 Xiangchun Road, Changsha, 410008, Hunan, China.
Huan LiDepartment of Clinical Laboratory, Hunan Provincial Maternal and Child Health Care Hospital, No.53 Xiangchun Road, Changsha, 410008, Hunan, China.
Hougang ZhouDepartment of Clinical Laboratory, Hunan Provincial Maternal and Child Health Care Hospital, No.53 Xiangchun Road, Changsha, 410008, Hunan, China. tead_81@163.com.

Funding

Hunan Provincial Natural Science Foundation of China No.2023JJ60286
6 · The paper itself

Abstract

objectiveThis study is conducted to investigate whether serum microRNA (miR)-141-3p can serve as a biomarker for early-stage diagnosis of endometriosis.

methodsA total of 246 patients who underwent laparoscopic examination and were diagnosed with endometriosis at our hospital between October 2020 and October 2022 were retrospectively enrolled as the Endometriosis group. This group was further allocated into Early-Endometriosis (Stage I-II) and Severe-Endometriosis (Stage III-IV) groups. Additionally, 87 healthy women with normal clinical parameters during the same period were selected as the control group. miR-141-3p expression in the serum of endometriosis patients were detected using RT-qPCR. The relationship of serum miR-141-3p expression with EHP-30 score in endometriosis patients was examined using Spearman. The diagnostic value of serum miR-141-3p for endometriosis was assessed by ROC analysis. Further ROC analysis was conducted to evaluate the diagnostic value of combined serum miR-141-3p and CA125 levels for early-stage endometriosis.

resultsSerum miR-141-3p expression was significantly lower in endometriosis patients and was negatively correlated with clinical staging. Serum miR-141-3p demonstrated excellent diagnostic performance for endometriosis (AUC = 0.916) and retained a high diagnostic value for early-stage endometriosis (AUC = 0.858). The diagnostic efficacy was further improved when combined with CA125 (AUC = 0.985).

conclusionSerum miR-141-3p expression decreases with disease progression in endometriosis patients and shows high clinical utility for the early-stage diagnosis of endometriosis. miR-141-3p expression may serve as a potential marker for diagnosis of endometriosis.

Indexed as

EndometriosisMicroRNAsAdultBiomarkersCA-125 AntigenCase-Control StudiesEarly DiagnosisFemaleHumansRetrospective StudiesROC CurveBiomarkersCA-125 AntigenMicroRNAsMIRN141 microRNA, humanClinical staging of endometriosisEarly-endometriosisEctopic cyst sizeEndometrial cycleEndometriosisSerum miR-141-3p expression

Identifiers

PMID41254724
PMCPMC12625237

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.