Evidence map›Paper›PMID 39683562›Full record

ArticleNutrients2024

Assessing the Benefit of Dietary Choline Supplementation Throughout Adulthood in the Ts65Dn Mouse Model of Down Syndrome.

Savannah Tallino, Rachel Etebari, Ian McDonough, Hector Leon, Isabella Sepulveda, Wendy Winslow, Samantha K Bartholomew, Sylvia E Perez, Elliott J Mufson, Ramon Velazquez

Abstract read
In one paragraph

Article in Nutrients, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

10 authors.

Savannah TallinoBanner Neurodegenerative Disease Research Center, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Rachel EtebariBanner Neurodegenerative Disease Research Center, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.ORCID 0009-0004-5752-7900
Ian McDonoughBanner Neurodegenerative Disease Research Center, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.ORCID 0000-0003-4023-7961
Hector LeonBanner Neurodegenerative Disease Research Center, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Isabella SepulvedaBanner Neurodegenerative Disease Research Center, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Wendy WinslowBanner Neurodegenerative Disease Research Center, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Samantha K BartholomewBanner Neurodegenerative Disease Research Center, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.ORCID 0009-0009-4495-5187
Sylvia E PerezBarrow Neurological Institute, Phoenix, AZ 85013, USA.
Elliott J MufsonBarrow Neurological Institute, Phoenix, AZ 85013, USA.
Ramon VelazquezBanner Neurodegenerative Disease Research Center, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.ORCID 0000-0003-2514-6818

Funding

Identify common mechanisms of neurodegeneration between Alzheimer's disease and Down syndromeR01AG059627 · NIA · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI VELAZQUEZ, RAMON · 2018 to 2022
$3.1M
Intergenerational Community Driven Training in Alzheimer's Disease Research: An AI+X ApproachT32AG082658 · NIA · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI JUDITH KLEIN, Baoxin Li · 2024 to 2026
$1.0M
NIA NIH HHS R01 AG059627NIA NIH HHS R01AG059627NIA NIH HHS T32 AG082658
6 · The paper itself

Abstract

BACKGROUND/

objectivesDown syndrome (DS) is the most common cause of early-onset Alzheimer's disease (AD). Dietary choline has been proposed as a modifiable factor to improve the cognitive and pathological outcomes of AD and DS, especially as many do not reach adequate daily intake levels of choline. While lower circulating choline levels correlate with worse pathological measures in AD patients, choline status and intake in DS is widely understudied. Perinatal choline supplementation (Ch+) in the Ts65Dn mouse model of DS protects offspring against AD-relevant pathology and improves cognition. Further, dietary Ch+ in adult AD models also ameliorates pathology and improves cognition. However, dietary Ch+ in adult Ts65Dn mice has not yet been explored; thus, this study aimed to supply Ch+ throughout adulthood to determine the effects on cognition and DS co-morbidities.

methodsWe fed trisomic Ts65Dn mice and disomic littermate controls either a choline normal (ChN; 1.1 g/kg) or a Ch+ (5 g/kg) diet from 4.5 to 14 months of age.

resultsWe found that Ch+ in adulthood failed to improve genotype-specific deficits in spatial learning. However, in both genotypes of female mice, Ch+ significantly improved cognitive flexibility in a reverse place preference task in the IntelliCage behavioral phenotyping system. Further, Ch+ significantly reduced weight gain and peripheral inflammation in female mice of both genotypes, and significantly improved glucose metabolism in male mice of both genotypes.

conclusionsOur findings suggest that adulthood choline supplementation benefits behavioral and biological factors important for general well-being in DS and related to AD risk.

Indexed as

CholineCognitionDietary SupplementsDisease Models, AnimalDown SyndromeAlzheimer DiseaseAnimalsFemaleMaleMiceSpatial LearningCholinecholinecognitiondiet supplementationdown syndromeinflammation

Identifiers

PMID39683562
PMCPMC11644426

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Registered trials

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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.