Evidence map›Paper›PMID 27817987›Full record

ArticleAlcohol (Fayetteville, N.Y.)2017

Adolescent binge-pattern alcohol exposure alters genome-wide DNA methylation patterns in the hypothalamus of alcohol-naïve male offspring.

AnnaDorothea Asimes, Audrey Torcaso, Elena Pinceti, Chun K Kim, Nancy J Zeleznik-Le, Toni R Pak

Abstract readComparative Study
In one paragraph

Article in Alcohol (Fayetteville, N.Y.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 40 citations in OpenAlex.

  1. The mechanism of the JNK signaling pathway in drug addiction : Author list.Journal of molecular medicine (Berlin, Germany) · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. DNA Methylation in Alcohol Use Disorder.International journal of molecular sciences · 2023
    Review
  7. Review
  8. Article
  9. 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 at 1 institution in 1 country.

AnnaDorothea AsimesDepartment of Cell and Molecular Physiology, Loyola University Chicago, Maywood, IL, USA.
Audrey TorcasoDepartment of Cell and Molecular Physiology, Loyola University Chicago, Maywood, IL, USA.
Elena PincetiDepartment of Cell and Molecular Physiology, Loyola University Chicago, Maywood, IL, USA.
Chun K KimDepartment of Cell and Molecular Physiology, Loyola University Chicago, Maywood, IL, USA.
Nancy J Zeleznik-LeDepartment of Medicine, Loyola University Chicago, Maywood, IL, USA.
Toni R PakDepartment of Cell and Molecular Physiology, Loyola University Chicago, Maywood, IL, USA. Electronic address: tpak@luc.edu.
Loyola University Chicago · US

Funding

Training in Neuroimmunoendocrine Effects of AlcoholT32AA013527 · NIAAA · LOYOLA UNIVERSITY CHICAGO · PI CHOUDHRY, MASHKOOR A · 2002 to 2021
$4.4M
NeuroMolecular consequences of adolescent binge drinkingR01AA021517 · NIAAA · LOYOLA UNIVERSITY CHICAGO · PI Toni R. Pak · 2013 to 2026
$3.6M
NIAAA NIH HHS R01 AA021517NIAAA NIH HHS T32 AA013527
6 · The paper itself

Abstract

Teenage binge drinking is a major health concern in the United States, with 21% of teenagers reporting binge-pattern drinking behavior in the previous 30 days. Recently, our lab showed that alcohol-naïve offspring of rats exposed to alcohol during adolescence exhibited altered gene expression profiles in the hypothalamus, a brain region involved in stress regulation. We employed Enhanced Reduced Representation Bisulfite Sequencing as an unbiased approach to test the hypothesis that parental exposure to binge-pattern alcohol during adolescence alters DNA methylation profiles in their alcohol-naïve offspring. Wistar rats were administered a repeated binge-ethanol exposure paradigm during early (postnatal day (PND) 37-44) and late (PND 67-74) adolescent development. Animals were mated 24 h after the last ethanol dose and subsequent offspring were produced. Analysis of male PND7 offspring revealed that offspring of alcohol-exposed parents exhibited differential DNA methylation patterns in the hypothalamus. The differentially methylated cytosines (DMCs) were distinct between offspring depending on which parent was exposed to ethanol. Moreover, novel DMCs were observed when both parents were exposed to ethanol and many DMCs from single parent ethanol exposure were not recapitulated with dual parent exposure. We also measured mRNA expression of several differentially methylated genes and some, but not all, showed correlative changes in expression. Importantly, methylation was not a direct predictor of expression levels, underscoring the complexity of transcriptional regulation. Overall, we demonstrate that adolescent binge ethanol exposure causes altered genome-wide DNA methylation patterns in the hypothalamus of alcohol-naïve offspring.

Indexed as

Inheritance PatternsUnderage DrinkingAge FactorsAnimalsBinge DrinkingDNA MethylationEpigenesis, GeneticEthanolFemaleGene Expression RegulationHeredityHypothalamusMaleModels, AnimalPedigreePregnancyEthanolRNA, MessengerAdolescenceAlcoholDNA methylationEpigeneticsInheritance

Identifiers

PMID27817987
PMCPMC5403620
OpenAlexW2532640523

What OpenQuestion holds

Textmetadata
LicenceTDM
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.