Evidence map›Paper›PMID 39201308›Full record

ArticleInternational journal of molecular sciences2024

Maternal Exposure to Low-Dose BDE-47 Induced Weight Gain and Impaired Insulin Sensitivity in the Offspring.

Sandra Strunz, Rebecca Strachan, Mario Bauer, Ana C Zenclussen, Beate Leppert, Kristin M Junge, Tobias Polte

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

7 authors.

Sandra StrunzHelmholtz Centre for Environmental Research-UFZ, Department of Environmental Immunology, 04318 Leipzig, Germany.
Rebecca StrachanHelmholtz Centre for Environmental Research-UFZ, Department of Environmental Immunology, 04318 Leipzig, Germany.
Mario BauerHelmholtz Centre for Environmental Research-UFZ, Department of Environmental Immunology, 04318 Leipzig, Germany.ORCID 0000-0001-5752-038X
Ana C ZenclussenHelmholtz Centre for Environmental Research-UFZ, Department of Environmental Immunology, 04318 Leipzig, Germany.ORCID 0000-0003-3544-4552
Beate LeppertHelmholtz Centre for Environmental Research-UFZ, Department of Environmental Immunology, 04318 Leipzig, Germany.
Kristin M JungeHelmholtz Centre for Environmental Research-UFZ, Department of Environmental Immunology, 04318 Leipzig, Germany.
Tobias PolteHelmholtz Centre for Environmental Research-UFZ, Department of Environmental Immunology, 04318 Leipzig, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polybrominated diphenyl ethers (PBDEs), commonly used as synthetic flame retardants, are present in a variety of consumer products, including electronics, polyurethane foams, textiles, and building materials. Initial evidence from epidemiological and experimental studies suggests that maternal PBDE exposure may be associated with a higher BMI in children, with disturbance of energy metabolism and an increased risk of Type 2 diabetes. However, the causality between early exposure to real-life PBDE concentrations and increased weight as well as mechanisms underlying impaired metabolic pathways in the offspring remain elusive. Here, using a mouse model we examined the effect of maternal exposure to 2,2',4,4'-tetrabrominated diphenyl ether (BDE-47), the most abundant congener in human samples, on offspring weight gain and energy homeostasis using a mouse model. Maternal exposure to BDE-47 at low dose resulted in weight gain in female offspring together with an impaired glucose and insulin tolerance in both female and male mice. In vitro and in vivo data suggest increased adipogenesis induced by BDE-47, possibly mediated by DNA hypermethylation. Furthermore, mRNA data suggest that neuronal dysregulation of energy homeostasis, driven via a disturbed leptin signaling may contribute to the observed weight gain as well as impaired insulin and glucose tolerance.

Indexed as

Halogenated Diphenyl EthersInsulin ResistanceMaternal ExposurePrenatal Exposure Delayed EffectsWeight GainAdipogenesisAnimalsDNA MethylationEnergy MetabolismFemaleFlame RetardantsLeptinMaleMicePregnancy2,2',4,4'-tetrabromodiphenyl etherFlame RetardantsHalogenated Diphenyl EthersLeptinBDE-47epigeneticsleptinmetabolismoverweightpregnancysex-specific effect

Identifiers

PMID39201308
PMCPMC11354368

What Socratic 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 Socratic graph.