Evidence map›Paper›PMID 30174229›Full record

ArticleMolecular metabolism2018

Sex dependent impact of gestational stress on predisposition to eating disorders and metabolic disease.

Mariana Schroeder, Mira Jakovcevski, Tamar Polacheck, Yonat Drori, Shifra Ben-Dor, Simone Röh, Alon Chen

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

9 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

7 authors at 3 institutions in 2 countries.

Mariana SchroederDepartment of Neurobiology, Weizmann Institute of Science, Rehovot, 76100, Israel; Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich, 80804, Germany. Electronic address: marianaschroeder.mail@gmail.com.
Mira JakovcevskiDepartment of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich, 80804, Germany.
Tamar PolacheckDepartment of Neurobiology, Weizmann Institute of Science, Rehovot, 76100, Israel.
Yonat DroriDepartment of Neurobiology, Weizmann Institute of Science, Rehovot, 76100, Israel.
Shifra Ben-DorBioinformatics and Biological Computing Unit, Biological Services, Weizmann Institute of Science, Rehovot, 76100, Israel.
Simone RöhDepartment of Translational Research in Psychiatry, Max Planck Institute of Psychiatry, Munich, 80804, Germany.
Alon ChenDepartment of Neurobiology, Weizmann Institute of Science, Rehovot, 76100, Israel; Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich, 80804, Germany. Electronic address: alon_chen@psych.mpg.de.
Weizmann Institute of Science · ILMax Planck Institute of Neurobiology · DEMax Planck Institute of Psychiatry · DE

Funding

Organ Design and Engineering Training Program (ODET Program)T32EB016652 · NIBIB · BRIGHAM AND WOMEN'S HOSPITAL · PI BONVENTRE, JOSEPH VINCENT · 2014 to 2023
$3.5M
NIBIB NIH HHS T32 EB016652
6 · The paper itself

Abstract

objectiveVulnerability to eating disorders (EDs) is broadly assumed to be associated with early life stress. However, a careful examination of the literature shows that susceptibility to EDs may depend on the type, severity and timing of the stressor and the sex of the individual. We aimed at exploring the link between chronic prenatal stress and predisposition to EDs and metabolic disease.

methodsWe used a chronic variable stress protocol during gestation to explore the metabolic response of male and female offspring to food restriction (FR), activity-based anorexia (ABA), binge eating (BE) and exposure to high fat (HF) diet.

resultsContrary to controls, prenatally stressed (PNS) female offspring showed resistance to ABA and BE and displayed a lower metabolic rate leading to hyperadiposity and obesity on HF diet. Male PNS offspring showed healthy responses to FR and ABA, increased propensity to binge and improved coping with HF compared to controls. We found that long-lasting abnormal responses to metabolic challenge are linked to fetal programming and adult hypothalamic dysregulation in PNS females, resulting from sexually dimorphic adaptations in placental methylation and gene expression.

conclusionsOur results show that maternal stress may have variable and even opposing effects on ED risk, depending on the ED and the sex of the offspring.

Indexed as

AnimalsBinge-Eating DisorderBody WeightDiet, High-FatFeeding and Eating DisordersFemaleHypothalamusInsulinMaleMetabolic DiseasesMiceMice, Inbred ICRObesityPregnancyPrenatal Exposure Delayed EffectsSex FactorsInsulinActivity based anorexiaBinge eatingEarly life programmingMetabolic syndromeObesityStress

Identifiers

PMID30174229
PMCPMC6197785
OpenAlexW2888244508

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.