Evidence map›Paper›PMID 42102051›Full record

SynthesisPloS one2026

Maternal body mass index and the risk of early-onset Group B Streptococcus disease in newborns: A systematic review and meta-analysis.

Elisabeth Emanuel Graae, Niels Uldbjerg, Flemming Skjøth, Marie Aunskjær Bech, Pernille Nathalie Nielsen, Susani Rothmann Karkov, Caroline Margaret Moos, Mohammed Rohi Khalil

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in PloS one, 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.

Elisabeth Emanuel GraaeDepartment of Gynecology and Obstetrics, Lillebælt University Hospital, Kolding, Denmark.ORCID https://orcid.org/0009-0009-8650-0738
Niels UldbjergDepartment of Obstetrics and Gynecology, Aarhus University Hospital, Skejby, Denmark.
Flemming SkjøthDepartment of Regional Health Research, University of Southern Denmark, Odense, Denmark.ORCID https://orcid.org/0000-0003-2975-647X
Marie Aunskjær BechDepartment of Gynecology and Obstetrics, Lillebælt University Hospital, Kolding, Denmark.ORCID https://orcid.org/0009-0005-6070-3466
Pernille Nathalie NielsenDepartment of Gynecology and Obstetrics, Lillebælt University Hospital, Kolding, Denmark.
Susani Rothmann KarkovDepartment of Gynecology and Obstetrics, Lillebælt University Hospital, Kolding, Denmark.
Caroline Margaret MoosDepartment of Clinical Research, Sønderjylland University Hospital, Aabenraa, Denmark.
Mohammed Rohi KhalilDepartment of Gynecology and Obstetrics, Lillebælt University Hospital, Kolding, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEarly-onset group B Streptococcus disease (EOGBS) remains a leading cause of neonatal morbidity and mortality. The incidence can be substantially reduced by intrapartum antibiotic prophylaxis in women with defined risk factors. However, the role of high prepregnancy body mass index (BMI) as a risk factor remains unclear. This systematic review and meta-analysis therefore aimed to evaluate the association between maternal BMI and the risk of EOGBS, as well as related proxy outcomes, including intrapartum vaginal GBS colonization and rectovaginal or urinary GBS colonization before term.

methodsWe systematically searched MEDLINE, Embase, and Cochrane CENTRAL on the 28th of January 2026, for studies examining the relationship between pregestational BMI and EOGBS or its proxy outcomes. Eligible studies included observational and interventional designs but not case reports and conference abstracts. Risk of bias was assessed using the QUIPS tool. Random-effects meta-regression and sensitivity analyses were performed.

resultsWe identified 19 eligible observational studies reporting data from a total of 3,707,047 women, encompassing 277,887 cases. For the risk of EOGBS and its proxy outcomes, assuming a log-linear association, our meta-regression showed a 2.4% increase in the odds ratio (OR) per unit increase in BMI. This corresponds to an OR of 1.4 (95% CI 1.1-1.6) for a BMI of 35 and 1.7 (95% CI 1.3-2.3) for a BMI of 45, compared to a normal BMI of 22.3. One very large study on 1,971,346 live singleton births with 780 EOGBS cases, found a hazard ratio of 2.4 (95% CI 1.7-3.4) for a BMI of 35.0-39.9 compared to normal BMI (18.5-24.9).

conclusionsAlthough the overall association appears modest, incorporating BMI may improve prevention strategies for EOGBS .

Indexed as

Body Mass IndexPregnancy Complications, InfectiousStreptococcal InfectionsStreptococcus agalactiaeFemaleHumansInfant, NewbornPregnancyRisk FactorsVagina

Identifiers

PMID42102051
PMCPMC13155626

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.