Evidence map›Paper›PMID 38407648›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2024

Associations of the placental metabolome with immune maturation up to one year of age in the Swedish NICE-cohort.

Olle Hartvigsson, Malin Barman, Hardis Rabe, Anna Sandin, Agnes E Wold, Carl Brunius, Ann-Sofie Sandberg

Open access · hybridAbstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2024. 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
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0citing papers in PubMed
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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, 0 citations in OpenAlex.

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

7 authors at 3 institutions in 1 country.

Olle HartvigssonFood and Nutrition Science, Department of Life Sciences, Chalmers University of Technology, Göteborg, Sweden.
Malin BarmanFood and Nutrition Science, Department of Life Sciences, Chalmers University of Technology, Göteborg, Sweden. malin.barman@chalmers.se.ORCID 0000-0002-5317-2768
Hardis RabeInstitute of Biomedicine, Department of Infectious Diseases, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0003-1184-6135
Anna SandinDepartment of Clinical Sciences, Unit of Pediatrics, Umeå University, Umeå, Sweden.
Agnes E WoldInstitute of Biomedicine, Department of Infectious Diseases, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0001-9196-5040
Carl BruniusFood and Nutrition Science, Department of Life Sciences, Chalmers University of Technology, Göteborg, Sweden.ORCID 0000-0003-3957-870X
Ann-Sofie SandbergFood and Nutrition Science, Department of Life Sciences, Chalmers University of Technology, Göteborg, Sweden.ORCID 0000-0002-9681-3342
Chalmers University of Technology · SEUniversity of Gothenburg · SEUmeå University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAllergies and other immune-mediated diseases are thought to result from incomplete maturation of the immune system early in life. We previously showed that infants' metabolites at birth were associated with immune cell subtypes during infancy. The placenta supplies the fetus with nutrients, but may also provide immune maturation signals.

objectivesTo examine the relationship between metabolites in placental villous tissue and immune maturation during the first year of life and infant and maternal characteristics (gestational length, birth weight, sex, parity, maternal age, and BMI).

methodsUntargeted metabolomics was measured using Liquid Chromatography-Mass Spectrometry. Subpopulations of T and B cells were measured using flow cytometry at birth, 48 h, one, four, and 12 months. Random forest analysis was used to link the metabolomics data with the T and B cell sub populations as well as infant and maternal characteristics.

resultsModest associations (Q2 = 0.2-0.3) were found between the placental metabolome and kappa-deleting recombination excision circles (KREC) at birth and naïve B cells and memory T cells at 12 months. Weak associations were observed between the placental metabolome and sex and parity. Still, most metabolite features of interest were of low intensity compared to associations previously found in cord blood, suggesting that underlying metabolites were not of placental origin.

conclusionOur results indicate that metabolomic measurements of the placenta may not effectively recognize metabolites important for immune maturation.

Indexed as

MetabolomicsPlacentaFemaleFetal BloodHumansInfantInfant, NewbornMetabolomePregnancySwedenB cellsBirth cohortImmune maturationParityPlacental metabolomeT cellsUntargeted metabolomics

Identifiers

PMID38407648
PMCPMC10896773
OpenAlexW4392162555

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