Evidence map›Paper›PMID 28487553›Full record

ArticleInternational journal of obesity (2005)2017

Maternal cytokine status may prime the metabolic profile and increase risk of obesity in children.

B Englich, G Herberth, U Rolle-Kampczyk, S Trump, S Röder, M Borte, G I Stangl, M von Bergen, I Lehmann, K M Junge

Abstract read
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In one paragraph

Article in International journal of obesity (2005), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.7field-weighted citation impact, top 5% of its field
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

17 citing papers in PubMed, 22 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

B EnglichHelmholtz Centre for Environmental Research (UFZ), Department of Environmental Immunology, Leipzig, Germany.
G HerberthHelmholtz Centre for Environmental Research (UFZ), Department of Environmental Immunology, Leipzig, Germany.
U Rolle-KampczykHelmholtz Centre for Environmental Research (UFZ), Department of Systems Biology, Leipzig, Germany.
S TrumpHelmholtz Centre for Environmental Research (UFZ), Department of Environmental Immunology, Leipzig, Germany.
S RöderHelmholtz Centre for Environmental Research (UFZ), Department of Environmental Immunology, Leipzig, Germany.
M BorteChildren's Hospital, Municipal Hospital 'St Georg', Leipzig, Germany.
G I StanglMartin Luther University Halle-Wittenberg, Institute of Agricultural and Nutritional Sciences, Halle (Saale), Germany.
M von BergenHelmholtz Centre for Environmental Research (UFZ), Department of Systems Biology, Leipzig, Germany.
I LehmannHelmholtz Centre for Environmental Research (UFZ), Department of Environmental Immunology, Leipzig, Germany.
K M JungeHelmholtz Centre for Environmental Research (UFZ), Department of Environmental Immunology, Leipzig, Germany.
Helmholtz Centre for Environmental Research · DEKlinikum St. Georg · DEMartin Luther University Halle-Wittenberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe maternal inflammation status during pregnancy has been associated with metabolic imprinting and obesity development in the child. However, the influence of the maternal Th2 cytokines, interleukin-4 (IL4), IL5 and IL13, has not been studied so far.

methodsWe investigated the relationship between maternal innate (IL6, IL8, IL10 and tumor necrosis factor-α (TNFa)) and adaptive (interferon-γ, IL4, IL5 and IL13) blood cytokine levels at 34 weeks of gestation and children's overweight development until the age of 3 years in 407 children of the German longitudinal LINA (Lifestyle and Environmental Factors and their Influence on Newborns Allergy risk) cohort. Children's body weight and height were measured during the annual clinical visits or acquired from questionnaires. Body mass index (BMI) Z-scores were calculated according to the WHO reference data to adjust for child's age and gender. Cytokine secretion was stimulated with phytohemagglutinin or lipopolysaccharide and measured by cytometric bead assay. Furthermore, we assessed metabolic parameter in blood of 318 children at age 1 using the AbsoluteIDQ p180 Kit (Biocrates LIFE Science AG).

resultsApplying logistic regression models, we found that an increase of maternal IL4 and IL13 was associated with a decreased risk for overweight development in 1- and 2-year-old children. This effect was consistent up to the age of 3 years for IL13 and mainly concerns children without maternal history of atopy. Children's acylcarnitine concentrations at 1 year were positively correlated with maternal IL13 levels and inversely associated with the BMI Z-score at age 1.

conclusionsWe were able to show for the first time that the maternal Th2 status may be linked inversely to early childhood overweight development accompanied by an altered metabolic profile of the fetus. However, our data do not support a direct mediating role of acylcarnitines on maternal IL13-induced weight development.

Indexed as

Adaptive ImmunityAdultBody Mass IndexChild, PreschoolFemaleGenetic Predisposition to DiseaseGermanyHumansImmunity, InnateInfantInfant, NewbornInflammationInterleukin-13Interleukin-4Interleukin-5Longitudinal StudiesIL13 protein, humanIL4 protein, humanIL5 protein, humanInterleukin-13Interleukin-4Interleukin-5Tumor Necrosis Factor-alpha

Identifiers

PMID28487553
OpenAlexW2612720127

What OpenQuestion holds

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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.