Cited by 56Alzheimer's disease research and treatmentsGut microbiota and healthNeuroinflammation and Neurodegeneration Mechanisms

The microbiome: A target for Alzheimer disease?

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Seo, Dong-oh, Boros, Benjamin D., Holtzman, David M.·2019·Cell Research

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Crossref · 10.1038/s41422-019-0227-7

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10 of 10 references verified0 citation errors · 0 not checkable

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  • The AppNL-F and AppNL-G-F alleles impact the gut microbiome in ways that link to cognitive performance.

    “Collectively, these results suggest that the AppNL-F and AppNL-G-F alleles impact the gut microbiome in ways that link to cognitive performance, and support the hypothesis that AD risk alleles may elicit their impact on cognition at least in part by altering the microbiome’s contribution to neurophysiology49–52.”

    From Integrated analysis of behavioral, epigenetic, and gut microbiome analyses in AppNL-G-F, AppNL-F, and wild type mice (2021) · cites this paper as [49]

    The main text (pp. 779–780) links gut-microbiome changes with cognitive impairment in 5xFAD and APP/PS1 mouse models. It does not discuss the AppNL-F or AppNL-G-F alleles, so it does not support the allele-specific claim. (LLM, conf=0.86)

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  • AD risk alleles may elicit their impact on cognition at least in part by altering the microbiome's contribution to neurophysiology.

    “Collectively, these results suggest that the AppNL-F and AppNL-G-F alleles impact the gut microbiome in ways that link to cognitive performance, and support the hypothesis that AD risk alleles may elicit their impact on cognition at least in part by altering the microbiome’s contribution to neurophysiology49–52.”

    From Integrated analysis of behavioral, epigenetic, and gut microbiome analyses in AppNL-G-F, AppNL-F, and wild type mice (2021) · cites this paper as [49]

    The main text (pp. 779–780) reports microbiome changes and cognitive impairment in 5xFAD mice, and says that modulating the gut microbiota partly improved cognition in APP/PS1 mice. This supports a possible microbiome–cognition link, but the paper does not test the AppNL-F or AppNL-G-F alleles or establish that AD risk alleles generally affect cognition through the microbiome. (LLM, conf=0.84)

    Experimental — accuracy not yet measured

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Cites

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Research works printed but not linked: 5

  1. Marsh, S. E. et al. Proc. Natl Acad. Sci. USA 113, E1316-E1325 (2016).
  2. Baruch, K. et al. Nat. Commun. 6, 916 (2015).
  3. Vogt, N. M. et al. Sci. Rep. 7, 13537 (2017).
  4. Harach, T. et al. Sci. Rep. 7, 41802 (2017).
  5. Minter, M. R. et al. Sci. Rep. 7, 10411 (2017).

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Authors
Seo, D.-O., Boros, B. D., & Holtzman, D. M.
Affiliations
Washington University in St. Louis (US)
Corresponding author
Holtzman, David M.
Venue
Cell Research
Published
2019-09-06
Volume
29
Issue
10
Pages
779-780
ISSN
  • 1001-0602 (ISSN-L)
  • 1748-7838
OpenAlex
W2971579341
Cited by
56
References
10
Citations by year
2026: 5 · 2025: 7 · 2024: 9 · 2023: 8 · 2022: 9 · 2021: 11 · 2020: 5 · 2019: 2
FWCI
4.63
Type
journal article
Language
en
Open access
Locations
  • Cell Research (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
Keywords
Alzheimer's disease, gut microbiota, microbiome, peripheral immune cells, amyloidosis, mouse model, behavior change, neuroinflammation, gut-brain axis
MeSH terms
Gastrointestinal Microbiome, Alzheimer Disease, Amino Acids, Humans, Sodium, Disease Progression, Microbiota

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