Evidence map›Paper›PMID 32690098›Full record

ArticleBiology of sex differences2020

An interaction between fetal sex and placental weight and efficiency predicts intrauterine growth in response to maternal protein insufficiency and gestational exposure window in a mouse model of FASD.

Sze Ting Cecilia Kwan, Brandon H Presswood, Kaylee K Helfrich, Joshua W Baulch, Sandra M Mooney, Susan M Smith

Abstract read
In one paragraph

Article in Biology of sex differences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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  6. Behavioral changes inFrontiers in neuroscience · 2023
    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

6 authors.

Sze Ting Cecilia KwanNutrition Research Institute, University of North Carolina at Chapel Hill, Room #3111, 500 Laureate Way, Kannapolis, NC, 28081, USA. cecilia_kwan@unc.edu.
Brandon H PresswoodNutrition Research Institute, University of North Carolina at Chapel Hill, Room #3111, 500 Laureate Way, Kannapolis, NC, 28081, USA.
Kaylee K HelfrichNutrition Research Institute, Department of Nutrition, University of North Carolina at Chapel Hill, Room #3104, 500 Laureate Way, Kannapolis, NC, 28081, USA.
Joshua W BaulchNutrition Research Institute, University of North Carolina at Chapel Hill, Room #3111, 500 Laureate Way, Kannapolis, NC, 28081, USA.
Sandra M MooneyNutrition Research Institute, Department of Nutrition, University of North Carolina at Chapel Hill, Room #3104, 500 Laureate Way, Kannapolis, NC, 28081, USA.
Susan M SmithNutrition Research Institute, Department of Nutrition, University of North Carolina at Chapel Hill, Room #3104, 500 Laureate Way, Kannapolis, NC, 28081, USA. susan_smith@unc.edu.ORCID 0000-0003-4782-6857

Funding

Craniofacial Morphogenesis in Prenatal Alcohol ExposureR01AA011085 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SMITH, SUSAN M. · 2001 to 2025
$6.3M
NUTRITION TRAINING PROGRAMT32DK007686 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BECK, MELINDA A., MAYER-DAVIS, ELIZABETH J · 1992 to 2022
$4.3M
Prenatal alcohol exposure disrupts maternal-fetal iron metabolism in FASDR01AA022999 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KLING, PAMELA J, SMITH, SUSAN M. · 2014 to 2018
$1.6M
Maternal-fetal amino acid transfer across placenta in a mouse model of prenatal alcohol exposureF32AA027121 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KWAN, SZE TING · 2018 to 2021
$212k
NIAAA NIH HHS F32 AA027121NIAAA NIH HHS R01 AA011085NIAAA NIH HHS R01 AA022999NIDDK NIH HHS T32 DK007686
6 · The paper itself

Abstract

backgroundIndividuals exposed to gestational stressors such as alcohol exhibit a spectrum of growth patterns, suggesting individualized responses to the stressors. We hypothesized that intrauterine growth responses to gestational alcohol are modified not only by the stressor's severity but by fetal sex and the placenta's adaptive capacity.

methodsPregnant C57BL/6J mice were assigned to one of three groups. Group 1 consumed a normal protein diet (18% protein by weight) and received 4.5 g alcohol/kg body weight (NP-Alc-8) or isocaloric maltodextrin (NP-MD-8) daily from embryonic day (E) 8.5-E17.5. Group 2 consumed the same diet but received alcohol (NP-Alc-13) or maltodextrin (NP-MD-13) daily from E13.5-E17.5. Group 3 consumed the same diet but containing a lower protein content (12% protein by weight) from E0.5 and also received alcohol (LP-Alc-8) or maltodextrin (LP-MD-8) daily from E8.5-E17.5. Maternal, placental, and fetal outcomes were assessed on E17.5 using 2-way ANOVA or mixed linear model.

resultsWe found that intrauterine growth differed in the alcohol-exposed fetuses depending on sex and insult severity. Both NP-Alc-8 (vs. NP-MD-8) males and females had lower body weight and asymmetrical growth, but only NP-Alc-8 females had lower placental weight (P < 0.05). NP-Alc-13 (vs. NP-MD-13) females, but not their male littermates, had lower body weight (P = 0.019). Alcohol exposure beginning from E8.5 (vs. E13.5) decreased the ratio of fetal liver-to-body weight and increased the ratio of fetal brain-to-liver weight in both sexes (P < 0.05). LP-Alc-8 (vs. NP-MD-8) group had smaller litter size (P = 0.048), but the survivors had normal placental and body weight at E17.5. Nevertheless, LP-Alc-8 fetuses still showed asymmetrical growth. Correlation analyses reveal a relationship between litter size and placental outcomes, which were related to fetal outcomes in a sex-dependent manner, suggesting that the placenta may mediate the consequence of LP-Alc-altered litter size on fetal development.

conclusionsOur data indicate that the placenta is strongly involved in the fetal stress response and adapts in a sex-dependent fashion to support fetal development under the alcohol stressor. These variables may further influence the spectrum of intrauterine growth outcomes observed in those diagnosed with fetal alcohol spectrum disorder.

Indexed as

AnimalsDietary ProteinsDrug Administration ScheduleEthanolFemaleFetal Alcohol Spectrum DisordersFetal DevelopmentGenotypeMaleMiceMice, Inbred C57BLOrgan SizePlacentaPregnancyPrenatal Nutritional Physiological PhenomenaSex FactorsDietary ProteinsEthanolFetal alcohol spectrum disorderFetal sexFetal stress responseIntrauterine growthLitter sizeMaternal protein insufficiencyPlacental developmentPrenatal alcohol exposure

Identifiers

PMID32690098
PMCPMC7372829

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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.