Evidence map›Paper›PMID 38019873›Full record

ArticlePloS one2023

Comparison of vaginal microbiota between women with inflammatory bowel disease and healthy controls.

Ofri Bar, Leanna S Sudhof, Laura J Yockey, Agnes Bergerat, Nadav Moriel, Elizabeth Andrews, Ashwin N Ananthakrishnan, Ramnik J Xavier, Moran Yassour, Caroline M Mitchell

Abstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Article
  4. Review
  5. Review
  6. Review
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

10 authors.

Ofri BarVincent Center for Reproductive Biology, Massachusetts General Hospital, Boston, MA, United States of America.
Leanna S SudhofHarvard Medical School, Boston, MA, United States of America.
Laura J YockeyDepartments of Medicine, Massachusetts General Hospital, Boston, MA, United States of America.
Agnes BergeratVincent Center for Reproductive Biology, Massachusetts General Hospital, Boston, MA, United States of America.
Nadav MorielDepartment of Microbiology and Molecular Genetics, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Elizabeth AndrewsDepartments of Gastroenterology, Massachusetts General Hospital, Boston, MA, United States of America.
Ashwin N AnanthakrishnanHarvard Medical School, Boston, MA, United States of America.
Ramnik J XavierHarvard Medical School, Boston, MA, United States of America.
Moran YassourThe Rachel and Selim Benin School of Computer Science and Engineering, Hebrew University of Jerusalem, Jerusalem, Israel.ORCID 0000-0002-7344-5188
Caroline M MitchellVincent Center for Reproductive Biology, Massachusetts General Hospital, Boston, MA, United States of America.ORCID 0000-0001-9924-2349

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
Novel mechanisms of pathogenesis in idiopathic vaginitisR21AI113439 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI MITCHELL, CAROLINE M · 2015 to 2016
$499k
NIAID NIH HHS R21 AI113439NIDDK NIH HHS P30 DK043351
6 · The paper itself

Abstract

backgroundThe gut microbiota in patients with inflammatory bowel disease are perturbed in both composition and function. The vaginal microbiome and its role in the reproductive health of women with inflammatory bowel disease is less well described.

objectiveWe aim to compare the vaginal microbiota of women with inflammatory bowel disease to healthy controls.

methodsWomen with inflammatory bowel disease enrolled in a longitudinal cohort study provided self-collected vaginal swabs. Healthy controls underwent provider-collected vaginal swabs at routine gynecologic exams. All participants completed surveys on health history, vulvovaginal symptoms and gastrointestinal symptoms, if applicable. Microbiota were characterized by sequencing the V4 region of the 16S rRNA gene. Associations between patient characteristics and microbial community composition were evaluated by PERMANOVA and Principal Components Analysis. Lactobacillus dominance of the microbial community was compared between groups using chi-square and Poisson regression.

resultsThe cohort included 54 women with inflammatory bowel disease (25 Ulcerative colitis, 25 Crohn's Disease) and 26 controls. A majority, 72 (90%) were White; 17 (31%) with inflammatory bowel disease and 7 (27%) controls were postmenopausal. The composition of the vaginal microbiota did not vary significantly by diagnosis or severity of inflammatory bowel disease but did vary by menopausal status (p = 0.042). There were no significant differences in Shannon Diversity Index between healthy controls and women with IBD in premenopausal participants. There was no difference in proportion of Lactobacillus dominance according to diagnosis in premenopausal participants. A subgroup of postmenopausal women with Ulcerative colitis showed a significant higher alpha diversity and a lack of Lactobacillus dominance in the vaginal microbiome.

conclusionsMenopausal status had a larger impact on vaginal microbial communities than inflammatory bowel disease diagnosis or severity.

Indexed as

Colitis, UlcerativeInflammatory Bowel DiseasesMicrobiotaFemaleHumansLactobacillusLongitudinal StudiesRNA, Ribosomal, 16SVaginaRNA, Ribosomal, 16S

Identifiers

PMID38019873
PMCPMC10686494

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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.