Evidence map›Paper›PMID 28816587›Full record

ArticleEpigenetics2017

DNA methylation-independent growth restriction and altered developmental programming in a mouse model of preconception male alcohol exposure.

Richard C Chang, William M Skiles, Sarah S Chronister, Haiqing Wang, Gabrielle I Sutton, Yudhishtar S Bedi, Matthew Snyder, Charles R Long, Michael C Golding

Open access · bronzeAbstract read
In one paragraph

Article in Epigenetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
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  6. Functional Consequences Paternal Preconceptual Alcohol Consumption.Current topics in behavioral neurosciences · 2025
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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

9 authors at 1 institution in 1 country.

Richard C Changa Department of Veterinary Physiology & Pharmacology, College of Veterinary Medicine and Biomedical Sciences , Texas A&M University , College Station , Texas , USA.
William M Skilesa Department of Veterinary Physiology & Pharmacology, College of Veterinary Medicine and Biomedical Sciences , Texas A&M University , College Station , Texas , USA.
Sarah S Chronistera Department of Veterinary Physiology & Pharmacology, College of Veterinary Medicine and Biomedical Sciences , Texas A&M University , College Station , Texas , USA.
Haiqing Wanga Department of Veterinary Physiology & Pharmacology, College of Veterinary Medicine and Biomedical Sciences , Texas A&M University , College Station , Texas , USA.
Gabrielle I Suttona Department of Veterinary Physiology & Pharmacology, College of Veterinary Medicine and Biomedical Sciences , Texas A&M University , College Station , Texas , USA.
Yudhishtar S Bedia Department of Veterinary Physiology & Pharmacology, College of Veterinary Medicine and Biomedical Sciences , Texas A&M University , College Station , Texas , USA.
Matthew Snydera Department of Veterinary Physiology & Pharmacology, College of Veterinary Medicine and Biomedical Sciences , Texas A&M University , College Station , Texas , USA.
Charles R Longa Department of Veterinary Physiology & Pharmacology, College of Veterinary Medicine and Biomedical Sciences , Texas A&M University , College Station , Texas , USA.
Michael C Goldinga Department of Veterinary Physiology & Pharmacology, College of Veterinary Medicine and Biomedical Sciences , Texas A&M University , College Station , Texas , USA.ORCID 0000-0003-1631-2175
Texas A&M University · US

Funding

Altered genomic imprinting as a basis for FASD placental growth defectsR21AA022484 · NIAAA · TEXAS A&M AGRILIFE RESEARCH · PI GOLDING, MICHAEL C. · 2014 to 2015
$371k
NIAAA NIH HHS R21 AA022484
6 · The paper itself

Abstract

The preconception environment is a significant modifier of dysgenesis and the development of environmentally-induced disease. To date, fetal alcohol spectrum disorders (FASDs) have been exclusively associated with maternal exposures, yet emerging evidence suggests male-inherited alterations in the developmental program of sperm may be relevant to the growth-restriction phenotypes of this condition. Using a mouse model of voluntary consumption, we find chronic preconception male ethanol exposure associates with fetal growth restriction, decreased placental efficiency, abnormalities in cholesterol trafficking, sex-specific alterations in the genetic pathways regulating hepatic fibrosis, and disruptions in the regulation of imprinted genes. Alterations in the DNA methylation profiles of imprinted loci have been identified in clinical studies of alcoholic sperm, suggesting the legacy of paternal drinking may transmit via heritable disruptions in the regulation of imprinted genes. However, the capacity of sperm-inherited changes in DNA methylation to broadly transmit environmentally-induced phenotypes remains unconfirmed. Using bisulphite mutagenesis and second-generation deep sequencing, we find no evidence to suggest that these phenotypes or any of the associated transcriptional changes are linked to alterations in the sperm-inherited DNA methylation profile. These observations are consistent with recent studies examining the male transmission of diet-induced phenotypes and emphasize the importance of epigenetic mechanisms of paternal inheritance beyond DNA methylation. This study challenges the singular importance of maternal alcohol exposures and suggests paternal alcohol abuse is a significant, yet overlooked epidemiological factor complicit in the genesis of alcohol-induced growth defects, and may provide mechanistic insight into the failure of FASD children to thrive postnatally.

Indexed as

Alcohol DrinkingAnimalsChildDisease Models, AnimalDNA MethylationEpigenesis, GeneticEthanolFemaleFetal Alcohol Spectrum DisordersFetal Growth RetardationHumansMaleMicePhenotypePregnancyPrenatal Exposure Delayed EffectsEthanolbirth defectdevelopmental programmingDNA methylationDOHADepigeneticsfetal alcohol spectrum disorderfetal growth restrictionhepatic fibrosispreconceptionsperm

Identifiers

PMID28816587
PMCPMC5788439
OpenAlexW2747465281

What OpenQuestion holds

Textmetadata
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.