Evidence map›Paper›PMID 42029761›Full record

ArticleMetabolic brain disease2026

A perspective for alzheimer disease from gut microbiota-associated NMR-based fecal metabolomics: a study with 5XFAD mice.

Nazlıhan Tekin, Furkan Şahin, Betül Şahin, Zelal Zuhal Kaya, Ali Yılmaz, Stewart F Graham, Mustafa Serteser, Ahmet Tarık Baykal

Abstract read
In one paragraph

Article in Metabolic brain disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Nazlıhan TekinAcibadem Labmed Clinical Laboratories, Istanbul, Turkey. nazlihanyildirim@hotmail.com.ORCID 0000-0003-1922-594X
Furkan ŞahinAcibadem Labmed Clinical Laboratories, Istanbul, Turkey.ORCID 0000-0002-1296-9711
Betül ŞahinDepartment of Medical Biology, Faculty of Medicine, Bahcesehir University, Istanbul, Turkey.ORCID 0000-0001-8663-5741
Zelal Zuhal KayaDepartment of Medical Biochemistry, Faculty of Medicine, Nisantasi University, Istanbul, 34398, Turkey.ORCID 0000-0002-1415-3708
Ali YılmazMetabolomics Department, Corewell Health Research Institute, Royal Oak, MI 48073, USA.ORCID 0000-0001-9991-0554
Stewart F GrahamMetabolomics Department, Corewell Health Research Institute, Royal Oak, MI 48073, USA.ORCID 0000-0003-1001-0002
Mustafa SerteserAcibadem Labmed Clinical Laboratories, Istanbul, Turkey.ORCID 0000-0001-7868-7613
Ahmet Tarık BaykalAcibadem Labmed Clinical Laboratories, Istanbul, Turkey. ahmet.baykal@acibadem.edu.tr.ORCID 0000-0002-8814-7351

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer’s disease (AD), a neurodegenerative, irreversible, and progressive brain disorder, is characterized by memory loss and cognitive dysfunction. In neurodegeneration, gut microbiota and their metabolites have an impact on behavior and brain function. This study aimed to identify fecal candidate discriminant metabolites in 5XFAD mice assosciated with AD as compared to an age-matched wild-type (WT) healthy mice groups at three different time points (3, 6, and 9 month) using Proton Nuclear Magnetic Resonance (1H NMR) spectroscopy. A total of 18 male mice (n = 9 for 5XFAD mice and n = 9 for WT, with three animals per age group) were used to determine the fecal candidate discriminant metabolites. As a result of the study, it was identified a total of 67 metabolites in fecal samples. Among these, 19 metabolites were found significantly up-regulated or down-regulated in 5XFAD mice compared to WT mice during the disease progress. According to the volcano plot analysis (FC ≥ 1.2 and p-value ≤ 0.05), the potential candidate discriminant metabolites were fumarate and malate in 3-month-old 5XFAD mice, 3-methylxanthine, glucose, cholate, phenylacetate, and trimethylamine N-oxide (TMAO) in 6-month-old 5XFAD mice and cholate and succinate in 9-month-old 5XFAD mice. These findings highlight the potential of fecal metabolomics as a non-invasive exploratory approach for understanding AD disease mechanisms and progression. Furthermore, to the best of our knowledge, this pilot study is the first to utilize NMR spectroscopy to investigate age-stratified cross-sectional changes in fecal metabolites in 5xFAD mice, thereby advancing our understanding of disease progression and potentially informing future therapeutic strategies.

Indexed as

Alzheimer DiseaseFecesGastrointestinal MicrobiomeMetabolomicsAnimalsDisease Models, AnimalMagnetic Resonance SpectroscopyMaleMiceMice, Transgenic5XFAD miceAlzheimer's diseaseFecal metabolitesNuclear magnetic resonance spectroscopy

Identifiers

PMID42029761
PMCPMC13109219

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.