Evidence map›Paper›PMID 41074266›Full record

ArticleAlcohol, clinical & experimental research2025

Postnatal choline supplementation improves sleep in a rat model of developmental alcohol exposure.

Jaclyn B Hanson, Jessica A Baker, Daniel S Whittaker, Jennifer D Thomas

Abstract read
In one paragraph

Article in Alcohol, clinical & experimental research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

4 authors.

Jaclyn B HansonCenter for Behavioral Teratology, San Diego State University, San Diego, California, USA.
Jessica A BakerCenter for Behavioral Teratology, San Diego State University, San Diego, California, USA.ORCID https://orcid.org/0000-0002-4527-0640
Daniel S WhittakerDepartment of Neurosciences, University of California, San Diego, La Jolla, California, USA.ORCID https://orcid.org/0000-0002-4293-5192
Jennifer D ThomasCenter for Behavioral Teratology, San Diego State University, San Diego, California, USA.

Funding

Alcohol Research in the Science/Practitioner ModelT32AA013525 · NIAAA · SAN DIEGO STATE UNIVERSITY · PI EDWARD P RILEY, ANDREA SPADONI TOWNSEND · 2002 to 2026
$8.4M
Fetal Alcohol Effects and Choline InterventionR01AA012446 · NIAAA · SAN DIEGO STATE UNIVERSITY · PI THOMAS, JENNIFER D · 2001 to 2015
$3.8M
Fetal Alcohol Effects and Choline InterventionR37AA012446 · NIAAA · SAN DIEGO STATE UNIVERSITY · PI JENNIFER D THOMAS · 2018 to 2026
$3.1M
NIAAA NIH HHS R01 AA012446NIAAA NIH HHS R37 AA012446NIAAA NIH HHS R37AA012446NIAAA NIH HHS T32 AA013525NIAAA NIH HHS T32AA013525
6 · The paper itself

Abstract

backgroundFetal alcohol spectrum disorders (FASD) is an umbrella term used to describe physical, neuropathological, and behavioral alterations caused by prenatal alcohol exposure. Caretakers often report that children with FASD experience sleep problems. However, interventions to improve sleep have not been well-studied in this population. Interestingly, supplementation with the essential nutrient choline can attenuate many behavioral alterations associated with prenatal alcohol exposure. Moreover, choline is a precursor to acetylcholine, a neurochemical that is also involved in sleep-wake modulation. Using an animal model, this study investigated the effects of developmental alcohol exposure on sleep and examined whether postnatal choline supplementation can modulate sleep alterations associated with FASD.

methodsSprague-Dawley rat pups received ethanol (5.25 g/kg/day, 11.9% v/v) or sham intubations from postnatal days (PD) 4-9, a period of development equivalent to the human third-trimester brain growth spurt. Subjects then received subcutaneous injections with choline chloride (100 mg/kg/day) or saline from PD 10-30. On PD 32-37, subjects were individually housed to measure sleep-wake behaviors using the PiezoSleep Adapt-A-Base System. Sleep parameters, including sleep time, bout length, and number, were recorded.

resultsEthanol-exposed subjects, particularly females, slept less during the dark cycle. In addition, females exposed to developmental alcohol exhibited more night-to-night variability in sleep duration, consistent with findings from clinical populations. In contrast, choline supplementation increased sleep duration, particularly among males exposed to developmental alcohol. Choline specifically increased sleep bout duration in ethanol-exposed subjects during the dark cycle, suggesting that choline can modify sleep patterns among subjects exposed to prenatal alcohol.

conclusionsThese results illustrate that alcohol exposure during late gestation may lead to sleep disturbances and suggest that postnatal choline supplementation affects sleep quality. Importantly, this nutritional intervention was administered after the alcohol insult, suggesting that nutritional supplements in children with FASD may impact sleep problems.

Indexed as

CholineDietary SupplementsEthanolFetal Alcohol Spectrum DisordersSleepAnimalsAnimals, NewbornDisease Models, AnimalFemaleMalePregnancyPrenatal Exposure Delayed EffectsRatsRats, Sprague-DawleyCholineEthanoladolescencealcoholcholinedevelopmentsex differencessleepteratologytreatment

Identifiers

PMID41074266
PMCPMC12638278

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.