Evidence map›Paper›PMID 39302361›Full record

ArticleJournal of Alzheimer's disease : JAD2024

Effects of Menopause and High Fat Diet on Metabolic Outcomes in a Mouse Model of Alzheimer's Disease.

Charly Abi-Ghanem, Abigail E Salinero, Rachel M Smith, Richard D Kelly, Kasey M Belanger, Riane N Richard, Aaron S Paul, Ava A Herzog, Christina A Thrasher, Krystyna A Rybka and 11 more

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. High-Fat Diet Disrupt Nerve Function by Targeting Schwann Cells.Journal of the peripheral nervous system : JPNS · 2025
    Article
  7. 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

21 authors.

Charly Abi-GhanemDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
Abigail E SalineroDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
Rachel M SmithDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
Richard D KellyDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
Kasey M BelangerDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
Riane N RichardDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
Aaron S PaulDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
Ava A HerzogDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
Christina A ThrasherDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
Krystyna A RybkaDepartment of Psychology and Center for Neuroscience Research, State University of New York at Albany, Albany, NY, USA.
David RiccioDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
Olivia J GannonDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
David KorditDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
Nyi-Rein KyawDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
Febronia M MansourDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
Emily GroomDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.
Heddwen L BrooksDepartment of Physiology, Tulane University School of Medicine, New Orleans, LA, USA.
Lisa S RobisonDepartment of Psychology and Neuroscience, Nova Southeastern University, Fort Lauderdale, FL, USA.
Kevin PumigliaDepartment of Regenerative and Cancer Cell Biology, Albany Medical College, Albany, NY, USA.
Damian G ZuloagaDepartment of Psychology and Center for Neuroscience Research, State University of New York at Albany, Albany, NY, USA.
Kristen L ZuloagaDepartment of Neuroscience & Experimental Therapeutics, Albany Medical College, Albany, NY, USA.

Funding

Investigating the Functional Impact of AD Risk Genes on Neuro-Vascular InteractionsU01AG072464 · NIA · REGENERATIVE RESEARCH FOUNDATION · PI HARARI, OSCAR, KAMPMANN, MARTIN · 2021 to 2025
$8.7M
Metabolic and Hormonal Mechanisms of VCIDR01NS110749 · NINDS · ALBANY MEDICAL COLLEGE · PI Kristen Leanne Zuloaga · 2019 to 2026
$4.3M
NIA NIH HHS U01 AG072464NINDS NIH HHS R01 NS110749
6 · The paper itself

Abstract

Background: About two-thirds of those with Alzheimer's disease (AD) are women, most of whom are post-menopausal. Menopause accelerates dementia risk by increasing the risk for metabolic, cardiovascular, and cerebrovascular diseases. Mid-life metabolic disease (obesity, diabetes/prediabetes) is a well-known risk factor for dementia. A high fat diet can lead to poor metabolic health in both humans and rodents. Objective: Our goal was to determine the effects of a high fat diet on metabolic outcomes in the AppNL-F knock-in mouse model of AD and assess the effects of menopause. Methods: First, 3-month-old AppNL-F and WT female mice were placed on either a control or a high fat diet until 10 months of age then assessed for metabolic outcomes. Next, we did a more extensive assessment in AppNL-F mice that were administered VCD (4-vinylcyclohexene diepoxide) or vehicle (oil) and placed on a control or high fat diet for 7 months. VCD was used to model menopause by causing accelerated ovarian failure. Results: Compared to WT controls, AD female mice had worse glucose intolerance. Menopause led to metabolic impairment (weight gain and glucose intolerance) and further exacerbated obesity in response to a high fat diet. There were interactions between diet and menopause on some metabolic health serum biomarkers and the expression of hypothalamic markers related to energy balance. Conclusions: This work highlights the need to model endocrine aging in animal models of dementia and will contribute to further understanding the interaction between menopause and metabolic health in the context of AD.

Indexed as

Alzheimer DiseaseDiet, High-FatDisease Models, AnimalMenopauseMice, TransgenicAmyloid beta-Protein PrecursorAnimalsCyclohexenesFemaleMiceMice, Inbred C57BLObesityVinyl Compounds4-vinyl-1-cyclohexene dioxideAmyloid beta-Protein PrecursorCyclohexenesVinyl CompoundsAlzheimer’s diseaseglucose metabolismhypothalamusmenopausemetabolic diseaseobesity

Identifiers

PMID39302361
PMCPMC12045035

What OpenQuestion holds

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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.