Evidence map›Paper›PMID 41591973›Full record

ArticlePloS one2026

S100-alarmins, antenatal corticosteroids and the risk of late-onset sepsis in preterm infants: A prospective cohort study.

Gloria Kessler, Thomas Ulas, Thomas Vogl, Johannes Roth, Fenja Albrecht, Gesine Hansen, Constantin S von Kaisenberg, Christoph Härtel, Bettina Bohnhorst, Dorothee Viemann and 1 more

Abstract read
In one paragraph

Article 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

11 authors.

Gloria KesslerDepartment of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
Thomas UlasGenomics and Immunoregulation, LIMES-Institute, University of Bonn, Bonn, Germany.
Thomas VoglInstitute of Immunology, University of Münster, Münster, Germany.
Johannes RothInstitute of Immunology, University of Münster, Münster, Germany.
Fenja AlbrechtDepartment of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
Gesine HansenDepartment of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
Constantin S von KaisenbergDepartment of Obstetrics, Gynecology and Reproductive Medicine, Hannover Medical School, Hannover, Germany.
Christoph HärtelDepartment of Pediatrics, University Hospital Würzburg, Würzburg, Germany.
Bettina BohnhorstDepartment of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
Dorothee ViemannDepartment of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
Sabine PirrDepartment of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.ORCID https://orcid.org/0000-0002-3624-6251

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAntenatal corticosteroids (aCS) are an important measure improving the outcome of preterm infants. Their influence on late-onset sepsis (LOS) risk remains inconclusive. The alarmin S100A8/A9 protects from LOS by regulating innate immune responses. We examined whether aCS impact on postnatal S100A8/A9 serum-levels and consequently on LOS risk. STUDY

designIn a prospective birth-cohort study of 162 preterm infants born before 32 gestational weeks, we determined postnatal S100A8/A9 serum-levels in relation to the timing of aCS and LOS incidence.

resultsaCS administration within 7 days before birth decreased LOS incidence in infants born via primary C-section compared to infants not exposed to aCS (5/69 (7.2%) vs. 4/27 (14.8%)). This effect was linked to increased S100A8/A9 levels, with nocturnal aCS administration being most effective. Opposite, S100A8/A9 levels were lower and the LOS incidence higher compared to unexposed infants (7/23 (30.4%) vs. 4/27 (14.8%)) when aCS were administered more than 14 days before delivery.

conclusionOur data suggest that aCS administration affects the risk of LOS in preterm infants in dependence of the timing of administration by influencing the infant's S100A8/A9 levels. This underlines the importance of optimal timing of aCS facing imminent preterm birth.

Indexed as

Adrenal Cortex HormonesCalgranulin ACalgranulin BInfant, PrematureSepsisFemaleGestational AgeHumansIncidenceInfant, NewbornMalePregnancyProspective StudiesRisk FactorsAdrenal Cortex HormonesCalgranulin ACalgranulin BS100A8 protein, human

Identifiers

PMID41591973
PMCPMC12843532

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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.