Evidence map›Paper›PMID 40625836›Full record

ArticleFrontiers in cellular and infection microbiology2025

Maternal and placental microbiome and immune crosstalk in pregnancies with small-for-gestational-age fetuses - a pilot case-control study.

Katarzyna Kosińska-Kaczyńska, Dominika Krawczyk, Martyna Bednorz, Katarzyna Chaberek, Agnieszka Czapska, Magdalena Zgliczyńska, Krzysztof Goryca, Magdalena Piątkowska, Aneta Bałabas, Paweł Czarnowski and 1 more

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 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

11 authors.

Katarzyna Kosińska-KaczyńskaDepartment of Obstetrics, Perinatology and Neonatology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Dominika KrawczykDepartment of Obstetrics, Perinatology and Neonatology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Martyna BednorzDepartment of Obstetrics, Perinatology and Neonatology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Katarzyna ChaberekDepartment of Obstetrics, Perinatology and Neonatology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Agnieszka CzapskaDepartment of Obstetrics, Perinatology and Neonatology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Magdalena ZgliczyńskaDepartment of Obstetrics, Perinatology and Neonatology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Krzysztof GorycaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Magdalena PiątkowskaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Aneta BałabasDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Paweł CzarnowskiDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Natalia Żeber-LubeckaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Pregnancies complicated by fetal growth restriction are associated with specific bacterial abundances and elevation of proinflammatory cytokines. The aim of the study was to simultaneously analyze the relation between the gut and placenta microbiome and cytokine profile in pregnant women with fetuses appropriate (AGA) and small for gestational age (SGA). Material and methods: Women with singleton pregnancies at or beyond 32 weeks of gestation were recruited. 11 delivered SGA newborns (study group) and 11 AGA newborns (control group). Samples of maternal venous blood, stool and placenta were collected perinatally. Results: In SGA group lower Chao index in placental samples collected from maternal side, while higher Chao index in placental samples collected from fetal side were observed. Taxonomic analysis identified four significantly less abundant genera in samples collected from maternal side. No taxa remained significant after correction in samples from fetal side, but several taxa showed trends of differing abundance. Conclusions: Specific changes in the gut microbiome and metabolome as well as placenta microbiome of women with SGA have been observed, with additional associations with inflammatory cytokine levels, suggesting a potential role of these factors in SGA development and highlighting the need for further research.

Indexed as

Fetal Growth RetardationGastrointestinal MicrobiomeInfant, Small for Gestational AgeMicrobiotaPlacentaAdultBacteriaCase-Control StudiesCytokinesFecesFemaleHumansInfant, NewbornPilot ProjectsPregnancyCytokinesfetal growth restrictionmicrobiomeplacentapregnancysmall-for-gestational-age

Identifiers

PMID40625836
PMCPMC12229884

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Registered trials

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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.