Evidence map›Paper›PMID 39455640›Full record

ArticleScientific reports2024

Endometriosis specific vaginal microbiota links to urine and serum N-glycome.

John MacSharry, Zsuzsanna Kovács, Yongjing Xie, Barbara Adamczyk, Caitriona Walsh, Fiona Reidy, Fionnuala M McAuliffe, Mark T Kilbane, Patrick J Twomey, Pauline M Rudd and 5 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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

15 authors.

John MacSharry *School of Microbiology, University College Cork, Cork, Ireland.
Zsuzsanna Kovács *National Institute for Bioprocessing Research and Training (NIBRT), Belfield, Blackrock, Co. Dublin, Ireland.
Yongjing XieNational Institute for Bioprocessing Research and Training (NIBRT), Belfield, Blackrock, Co. Dublin, Ireland.
Barbara AdamczykNational Institute for Bioprocessing Research and Training (NIBRT), Belfield, Blackrock, Co. Dublin, Ireland.
Caitriona WalshNational Institute for Bioprocessing Research and Training (NIBRT), Belfield, Blackrock, Co. Dublin, Ireland.
Fiona ReidyMerrion Fertility Clinic and National Maternity Hospital, Dublin, Ireland.
Fionnuala M McAuliffeUCD Perinatal Research Centre, University College Dublin, National Maternity Hospital, Dublin, Ireland.
Mark T KilbaneDepartment of Clinical Chemistry, St. Vincent's University Hospital, Dublin, Ireland.
Patrick J TwomeyDepartment of Clinical Chemistry, St. Vincent's University Hospital, Dublin, Ireland.
Pauline M RuddNational Institute for Bioprocessing Research and Training (NIBRT), Belfield, Blackrock, Co. Dublin, Ireland.
Mary WingfieldMerrion Fertility Clinic and National Maternity Hospital, Dublin, Ireland.
Michael ButlerNational Institute for Bioprocessing Research and Training (NIBRT), Belfield, Blackrock, Co. Dublin, Ireland.
Douwe van SinderenSchool of Microbiology, University College Cork, Cork, Ireland.
Louise GloverMerrion Fertility Clinic and National Maternity Hospital, Dublin, Ireland.
Radka SaldovaNational Institute for Bioprocessing Research and Training (NIBRT), Belfield, Blackrock, Co. Dublin, Ireland. radka.fahey@nibrt.ie.

Funding

European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie 843862
6 · The paper itself

Abstract

Endometriosis is a chronic systemic disease, which results in endometrial-type tissue growing outside the uterus, and affects approximately 10% of reproductive-aged women worldwide. Its aetiology is poorly understood, and there is currently no long-term cure. Development and persistence of the disease depend on several coexisting factors including the vaginal microbiome. However, the role played by this important entity in endometriosis and its systemic involvement is not fully understood. Here, we investigated the vaginal microbiota, the serum and urine glycome, and antibody glycosylation in endometriosis patients. We reveal an endometriosis-specific vaginal microbiota in patients, being distinct from that present in a control group. Endometriosis patients were typified by a loss of the dominant Lactobacillus species, i.e. Lactobacillus iners, increased bacterial diversity and the presence of species such as Anaerococcus senegalensis, Prevotella jejuni, Porphyromonas bennonis and Anaerococcus octavius. The presence of trigalactosylated and triantennary serum glycans and urine core fucosylated mono-antennary glycans from IgG correlated with the vaginal presence of the bacterium A. senegalensis in endometriosis patients. Urine glycans did not differ in endometriosis, but urine IgG identified four novel sulfated glycans differing from serum IgG indicating functional relevance. Our findings contribute to understanding the relationships between the vaginal microbiota and the serum and urine glycome on the one hand, and endometriosis on the other. Further functional studies are warranted.

Indexed as

EndometriosisMicrobiotaPolysaccharidesVaginaAdultFemaleGlycosylationHumansImmunoglobulin GImmunoglobulin GPolysaccharidesBiomarkersEndometriosisMicrobiotaN-glycansSerumUrine

Identifiers

PMID39455640
PMCPMC11511964

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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.