Evidence map›Paper›PMID 42732072›Full record

ArticleBMC microbiology2026

Inferred functional microbiome features are associated with clinical trajectories of low-grade cervical lesions.

Milan Stosic, Mariano A Molina, Dhananjay Mukhedkar, Sadaf Sakina Hassan, Anna Sahlin, Cristina Ruiz Ballester, Jiangrong Wang, Laila Sara Arroyo Mühr

Abstract read
In one paragraph

Article in BMC microbiology, 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.

Milan Stosic *Norwegian HPV Reference Laboratory, Department of Microbiology and Infection Control, Akershus University Hospital, Lørenskog, 1478, Norway.
Mariano A Molina *Department of Laboratory Medicine, Karolinska Institutet, Huddinge, 141 52, Sweden. mariano.molina.beitia@ki.se.ORCID https://orcid.org/0000-0003-4260-0509
Dhananjay MukhedkarCenter for Cervical Cancer Elimination, F56, Karolinska University Hospital Huddinge, Karolinska Institutet, Huddinge, 141 86, Sweden.
Sadaf Sakina HassanCenter for Cervical Cancer Elimination, F56, Karolinska University Hospital Huddinge, Karolinska Institutet, Huddinge, 141 86, Sweden.
Anna SahlinDepartment of Laboratory Medicine, Karolinska Institutet, Huddinge, 141 52, Sweden.
Cristina Ruiz BallesterCenter for Cervical Cancer Elimination, F56, Karolinska University Hospital Huddinge, Karolinska Institutet, Huddinge, 141 86, Sweden.
Jiangrong WangCenter for Cervical Cancer Elimination, F56, Karolinska University Hospital Huddinge, Karolinska Institutet, Huddinge, 141 86, Sweden.
Laila Sara Arroyo MührCenter for Cervical Cancer Elimination, F56, Karolinska University Hospital Huddinge, Karolinska Institutet, Huddinge, 141 86, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe cervicovaginal microbiome has been associated with human papillomavirus (HPV)-related cervical disease, but its role in determining the clinical trajectory of low-grade squamous intraepithelial lesions (LSIL) remains unclear. We investigated whether microbial taxonomic, ecological, and inferred functional features could distinguish LSIL regression from progression and improve risk stratification.

resultsThe cervicovaginal microbiome of 90 women with LSIL and known clinical outcomes was profiled using 16S rRNA gene sequencing. Overall microbiome diversity and composition did not differ significantly between regression and progression groups. Instead, microbial profiles clustered primarily by community state type (CST), with CST I-B nominally more frequent among regression cases. Within Lactobacillus-dominated communities, CST I-B exhibited distinct inferred functional profiles characterized by enrichment of carbohydrate metabolism and fermentation pathways and relative depletion of nucleotide biosynthesis pathways compared with CST I-A. Exploratory logistic regression models based on age, or microbiome taxa alone, showed limited discriminatory performance, whereas an integrated model incorporating age, microbiome, and inferred functional pathway features improved apparent discrimination between regression and progression in this cohort (AUC = 0.76, 95% CI 0.66-0.86).

conclusionsDifferences in microbial community organization and inferred functional profiles were observed to be associated with LSIL clinical trajectories, whereas taxonomic composition alone showed limited discriminatory value. Integrating microbial taxonomic, ecological, and functional features modestly improved the apparent discrimination of LSIL outcomes, suggesting that inferred functional features may provide complementary information that warrants future research.

Indexed as

BacteriaMicrobiotaSquamous Intraepithelial LesionsUterine Cervical NeoplasmsAdultCervix UteriDisease ProgressionDNA, BacterialFemaleHuman Papillomavirus VirusesHumansLactobacillusPapillomavirus InfectionsPhylogenyRNA, Ribosomal, 16SSequence Analysis, DNADNA, BacterialRNA, Ribosomal, 16S16S rRNA sequencingCervicovaginal microbiomeClinical outcomeCommunity state typesHuman papillomavirusLow-grade squamous intraepithelial lesionsMicrobial function

Identifiers

PMID42732072
PMCPMC13570522

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.