Evidence map›Paper›PMID 41160510›Full record

ArticlePloS one2025

Lower Firmicutes abundance in gut microbiota associated with amyloid-β positivity in older adults in Japan as assessed by positron emission tomography.

Narumi Kojima, Yosuke Osuka, Hiroyuki Sasai, Shoji Shinkai, Kenji Ishii, Noriyuki Kohda, Yodai Kobayashi, Hunkyung Kim

Abstract read
In one paragraph

Article in PloS one, 2025. 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

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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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.

Narumi KojimaTokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.ORCID https://orcid.org/0000-0001-5742-0389
Yosuke OsukaTokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.
Hiroyuki SasaiTokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.
Shoji ShinkaiTokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.
Kenji IshiiTokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.
Noriyuki KohdaOtsu Nutraceuticals Research Institute, Otsuka Pharmaceutical Co., Ltd., Shiga, Japan.
Yodai KobayashiOtsu Nutraceuticals Research Institute, Otsuka Pharmaceutical Co., Ltd., Shiga, Japan.
Hunkyung KimTokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlzheimer's disease, marked by amyloid-β accumulation, is a leading cause of dementia. Gut microbiota may influence its development by affecting inflammation or amyloid-β metabolism. However, this association is not well studied in older adults in Japan, whose characteristic diet may uniquely impact gut bacteria.

objectiveTo determine the association between the gut microbiota and positron emission tomography (PET)-determined brain amyloid-β positivity in community-dwelling older adults in Japan.

methodsThis cross-sectional study investigated 136 participants aged 68-86 years from Tokyo. Brain amyloid-β was assessed using PET imaging, and gut microbiota were analyzed from fecal samples using 16S rRNA gene sequencing processed with the QIIME2 pipeline. Taxonomic composition was evaluated at both the phylum and genus levels; participants were classified into above- and below-median groups based on the relative abundance of each taxon. Binomial logistic regression adjusted for age, sex, and antibiotic use was conducted to examine the association between bacterial abundance and PET positivity. For genus-level analyses, p-values were further corrected for multiple comparisons. In addition, α diversity (Shannon, Simpson, Observed OTUs) and β diversity (PCoA based on unweighted UniFrac distances, PERMANOVA) were compared between PET-positive and PET-negative groups.

resultsOf the 136 participants, 34.6% were PET-positive for amyloid-β. Firmicutes showed a significant difference: 26.4% PET-positive in the above-median group vs. 42.6% in the below-median group (p for χ² = 0.047). The binomial logistic regression analysis showed that lower Firmicutes abundance was significantly associated with an increased odds of PET positivity (odds ratio and confidence interval: 2.15 [1.03, 4.52]). At the genus level, no taxon remained significant after correction for multiple comparisons. No significant differences were observed in α or β diversity indices between groups.

conclusionA lower abundance of Firmicutes may be associated with amyloid-β accumulation in the brain, linking the gut microbiota to Alzheimer's disease.

Indexed as

Amyloid beta-PeptidesBacillotaGastrointestinal MicrobiomePositron-Emission TomographyAgedAged, 80 and overAlzheimer DiseaseBrainCross-Sectional StudiesFecesFemaleHumansJapanMaleRNA, Ribosomal, 16SAmyloid beta-PeptidesRNA, Ribosomal, 16S

Identifiers

PMID41160510
PMCPMC12571266

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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.