Evidence map›Paper›PMID 41906395›Full record

ArticleProteomics. Clinical applications2026

Proteomic Analysis of Cervicovaginal Fluid for Diagnostic Endometriosis Biomarker Discovery.

Emily S J Paterson, Simon Scheck, Torsten Kleffmann, Roopi Gill, Nicholas Bedford, Simon McDowell, Jane E Girling, Claire E Henry

Abstract read
In one paragraph

Article in Proteomics. Clinical applications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Emily S J PatersonDepartment of Surgery and Anaesthesia, University of Otago, Ōtākou Whakaihu Waka, Wellington, Aotearoa, New Zealand.ORCID 0000-0002-6257-0135
Simon ScheckDepartment of Obstetrics, Gynaecology and Women's Health, University of Otago, Ōtākou Whakaihu Waka, Wellington, Aotearoa, New Zealand.
Torsten KleffmannDepartment of Biochemistry, University of Otago, Ōtākou Whakaihu Waka, Dunedin, Aotearoa, New Zealand.
Roopi GillDepartment of Obstetrics, Gynaecology and Women's Health, University of Otago, Ōtākou Whakaihu Waka, Wellington, Aotearoa, New Zealand.
Nicholas BedfordDepartment of Obstetrics and Gynaecology, Wellington Hospital, Te Whatu Ora - Capital, Coast and Hutt Valley, Wellington, Aotearoa, New Zealand.
Simon McDowellDepartment of Obstetrics and Gynaecology, Wellington Hospital, Te Whatu Ora - Capital, Coast and Hutt Valley, Wellington, Aotearoa, New Zealand.
Jane E GirlingDepartment of Anatomy, University of Otago, Ōtākou Whakaihu Waka, Dunedin, Aotearoa, New Zealand.
Claire E HenryDepartment of Surgery and Anaesthesia, University of Otago, Ōtākou Whakaihu Waka, Wellington, Aotearoa, New Zealand.

Funding

Royal Australian and New Zealand College of Obstetricians and Gynaecologists
6 · The paper itself

Abstract

purposeEndometriosis is a prevalent inflammatory condition characterised by the presence of endometrial-like tissue outside the uterus and is associated with significant challenges, including diagnostic delays and continued reliance on laparoscopy. Although extensive research has investigated potential biomarkers in various biofluids, none have been validated for clinical use. EXPERIMENTAL

designThis pilot study explored the proteome of cervicovaginal fluid to identify biomarkers of endometriosis. SWATH-MS was performed over two experiments on cervicovaginal fluid sampled via a low vaginal swab, from people with (n = 20) and without (n = 19) surgically confirmed endometriosis. STRING, OPLS-DA modelling and ingenuity pathway analysis were used to interrogate the data. ELISA was performed validate SWATH-MS findings.

resultsThere were 29 proteins in experiment one and 47 proteins in experiment two identified as differentially abundant between cases and controls. No proteins were identified as differentially abundant in both experiments. Legumain (LGMN) measured via ELISA was significantly increased in the cervicovaginal fluid of people with endometriosis. CONCLUSIONS AND CLINICAL RELEVANCE: Cervicovaginal fluid proteins sampled via vaginal swab may have limited biomarker potential for endometriosis. A larger and more diverse cohort would be required to confirm the promise of cervicovaginal fluid LGMN as a candidate biomarker of endometriosis.

Indexed as

Body FluidsCervix UteriEndometriosisProteomeProteomicsVaginaAdultBiomarkersFemaleHumansPilot ProjectsBiomarkersProteomebiomarkerscervicovaginal fluidendometriosisvaginal swab

Identifiers

PMID41906395
PMCPMC13033910

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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.