Evidence map›Paper›PMID 27788773›Full record

ArticleAlcohol (Fayetteville, N.Y.)2016

Maternal choline supplementation in a sheep model of first trimester binge alcohol fails to protect against brain volume reductions in peripubertal lambs.

Sharla M Birch, Mark W Lenox, Joe N Kornegay, Beatriz Paniagua, Martin A Styner, Charles R Goodlett, Tim A Cudd, Shannon E Washburn

Abstract read
In one paragraph

Article in Alcohol (Fayetteville, N.Y.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 3 pooled it
3.9field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 3 syntheses or guidelines pooled it, 17 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Sharla M BirchDepartment of Veterinary Pathobiology, Texas A&M University College of Veterinary Medicine & Biomedical Sciences, College Station, TX 77843, USA.
Mark W LenoxTexas A&M Institute for Preclinical Studies (TIPS), Texas A&M University College of Veterinary Medicine & Biomedical Sciences, College Station, TX 77843, USA.
Joe N KornegayDepartment of Veterinary Pathobiology, Texas A&M University College of Veterinary Medicine & Biomedical Sciences, College Station, TX 77843, USA; Texas A&M Institute for Preclinical Studies (TIPS), Texas A&M University College of Veterinary Medicine & Biomedical Sciences, College Station, TX 77843, USA; Department of Veterinary Integrative Biosciences, Texas A&M University College of Veterinary Medicine & Biomedical Sciences, College Station, TX 77843, USA.
Beatriz PaniaguaDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Martin A StynerDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; Department of Computer Science, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Charles R GoodlettStark Neurosciences Research Institute, IU School of Medicine, Indianapolis, IN 46202, USA; Department of Psychology, Indiana University Purdue University Indianapolis (IUPUI), Indianapolis, IN 46202, USA.
Tim A CuddDepartment of Physiology and Pharmacology, Texas A&M University College of Veterinary Medicine & Biomedical Sciences, College Station, TX 77843, USA.
Shannon E WashburnDepartment of Physiology and Pharmacology, Texas A&M University College of Veterinary Medicine & Biomedical Sciences, College Station, TX 77843, USA. Electronic address: swashburn@cvm.tamu.edu.
Texas A&M University · USUniversity of North Carolina at Chapel Hill · USIndiana University – Purdue University Indianapolis · US

Funding

Comparative Biomedical Research Training for VeterinariansT32OD011083 · OD · TEXAS A&M AGRILIFE RESEARCH · PI ALBERT MULENGA · 2012 to 2026
$4.8M
Translational Studies of FASD Using a Sheep Model-U01U01AA017120 · NIAAA · TEXAS A&M AGRILIFE RESEARCH · PI WASHBURN, SHANNON E. · 2007 to 2011
$1.3M
Mechanisms and Nutritional Intervention for Fetal Alcohol Spectrum DisordersK08AA018166 · NIAAA · TEXAS A&M AGRILIFE RESEARCH · PI WASHBURN, SHANNON E. · 2010 to 2012
$264k
NIAAA NIH HHS K08 AA018166NIAAA NIH HHS U01 AA017120NIH HHS T32 OD011083
6 · The paper itself

Abstract

Fetal alcohol spectrum disorder (FASD) is a leading potentially preventable birth defect. Poor nutrition may contribute to adverse developmental outcomes of prenatal alcohol exposure, and supplementation of essential micronutrients such as choline has shown benefit in rodent models. The sheep model of first-trimester binge alcohol exposure was used in this study to model the dose of maternal choline supplementation used in an ongoing prospective clinical trial involving pregnancies at risk for FASD. Primary outcome measures including volumetrics of the whole brain, cerebellum, and pituitary derived from magnetic resonance imaging (MRI) in 6-month-old lambs, testing the hypothesis that alcohol-exposed lambs would have brain volume reductions that would be ameliorated by maternal choline supplementation. Pregnant sheep were randomly assigned to one of five groups - heavy binge alcohol (HBA; 2.5 g/kg/treatment ethanol), heavy binge alcohol plus choline supplementation (HBC; 2.5 g/kg/treatment ethanol and 10 mg/kg/day choline), saline control (SC), saline control plus choline supplementation (SCC; 10 mg/kg/day choline), and normal control (NC). Ewes were given intravenous alcohol (HBA, HBC; mean peak BACs of ∼280 mg/dL) or saline (SC, SCC) on three consecutive days per week from gestation day (GD) 4-41; choline was administered on GD 4-148. MRI scans of lamb brains were performed postnatally on day 182. Lambs from both alcohol groups (with or without choline) showed significant reductions in total brain volume; cerebellar and pituitary volumes were not significantly affected. This is the first report of MRI-derived volumetric brain reductions in a sheep model of FASD following binge-like alcohol exposure during the first trimester. These results also indicate that maternal choline supplementation comparable to doses in human studies fails to prevent brain volume reductions typically induced by first-trimester binge alcohol exposure. Future analyses will assess behavioral outcomes along with regional brain and neurohistological measures.

Indexed as

Disease Models, AnimalPregnancy Trimester, FirstAge FactorsAnimalsBinge DrinkingBrainCholineFemaleMaleNeuroprotective AgentsOrgan SizePregnancyPrenatal Exposure Delayed EffectsRandom AllocationSheepCholineNeuroprotective AgentsCholineDiagnosisFASDMagnetic resonance imagingPrenatal alcoholVolumetrics

Identifiers

PMID27788773
PMCPMC5098470
OpenAlexW2482828582

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.