Evidence map›Paper›PMID 36856720›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2023

Mitigating the detrimental developmental impact of early fetal alcohol exposure using a maternal methyl donor-enriched diet.

Mélanie Breton-Larrivée, Elizabeth Elder, Lisa-Marie Legault, Alexandra Langford-Avelar, Amanda J MacFarlane, Serge McGraw

Open access · hybridAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2023. 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
12.8field-weighted citation impact, top 1% 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.

  1. Folic acid prevention of neural tube defects requires retinoic acid produced by ALDH1L1.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  9. Mitigating the detrimental developmental impact of early fetal alcohol exposure using a maternal methyl donor-enriched diet.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
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 at 2 institutions in 2 countries.

Mélanie Breton-LarrivéeCentre Hospitalier Universitaire Sainte-Justine Research Center, Montreal, Canada.
Elizabeth ElderCentre Hospitalier Universitaire Sainte-Justine Research Center, Montreal, Canada.
Lisa-Marie LegaultCentre Hospitalier Universitaire Sainte-Justine Research Center, Montreal, Canada.
Alexandra Langford-AvelarCentre Hospitalier Universitaire Sainte-Justine Research Center, Montreal, Canada.
Amanda J MacFarlaneAgriculture, Food, and Nutrition Evidence Center, Texas A&M University, Texas, Fort Worth, USA.
Serge McGrawCentre Hospitalier Universitaire Sainte-Justine Research Center, Montreal, Canada.ORCID https://orcid.org/0000-0002-3504-8253
Centre Hospitalier Universitaire Sainte-Justine · CATexas A&M University School of Law · US

Funding

CIHR
6 · The paper itself

Abstract

Fetal alcohol exposure at any stage of pregnancy can lead to fetal alcohol spectrum disorder (FASD), a group of life-long conditions characterized by congenital malformations, as well as cognitive, behavioral, and emotional impairments. The teratogenic effects of alcohol have long been publicized; yet fetal alcohol exposure is one of the most common preventable causes of birth defects. Currently, alcohol abstinence during pregnancy is the best and only way to prevent FASD. However, alcohol consumption remains astoundingly prevalent among pregnant women; therefore, additional measures need to be made available to help protect the developing embryo before irreparable damage is done. Maternal nutritional interventions using methyl donors have been investigated as potential preventative measures to mitigate the adverse effects of fetal alcohol exposure. Here, we show that a single acute preimplantation (E2.5; 8-cell stage) fetal alcohol exposure (2 × 2.5 g/kg ethanol with a 2h interval) in mice leads to long-term FASD-like morphological phenotypes (e.g. growth restriction, brain malformations, skeletal delays) in late-gestation embryos (E18.5) and demonstrate that supplementing the maternal diet with a combination of four methyl donor nutrients, folic acid, choline, betaine, and vitamin B12, prior to conception and throughout gestation effectively reduces the incidence and severity of alcohol-induced morphological defects without altering DNA methylation status of imprinting control regions and regulation of associated imprinted genes. This study clearly supports that preimplantation embryos are vulnerable to the teratogenic effects of alcohol, emphasizes the dangers of maternal alcohol consumption during early gestation, and provides a potential proactive maternal nutritional intervention to minimize FASD progression, reinforcing the importance of adequate preconception and prenatal nutrition.

Indexed as

Fetal Alcohol Spectrum DisordersAnimalsBetaineDietEthanolFemaleHumansMicePregnancyTissue DonorsBetaineEthanolDNA methylationDOHaDembryonic developmentenvironmental exposureFASDfetal alcohol exposurematernal nutritionmethyl donors

Identifiers

PMID36856720
PMCPMC11977608
OpenAlexW4322719064

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.