Evidence map›Paper›PMID 38664490›Full record

ArticleMolecular psychiatry2024

Gut microbiome predicts cognitive function and depressive symptoms in late life.

A Kolobaric, C Andreescu, E Jašarević, C H Hong, H W Roh, J Y Cheong, Y K Kim, T S Shin, C S Kang, C O Kwon and 5 more

Abstract read
In one paragraph

Article in Molecular psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
–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

38 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
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  5. Article
  6. Review
  7. Article
  8. Article
  9. The gut as a central hub for multi-organ crosstalk in aging.Cellular and molecular life sciences : CMLS · 2026
    Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Regulating the crosstalk betweenFrontiers in immunology · 2026
    Review
  16. Article
  17. Article
  18. Supplementation with abioRxiv : the preprint server for biology · 2025
    Article
  19. Gut microbes · 2025
    Article
  20. The influence of depression onset timing after gastrointestinal diseases on dementia risk.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    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

15 authors.

A KolobaricCenter for Neuroscience, University of Pittsburgh, Pittsburgh, USA.
C AndreescuDepartment of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, USA.ORCID 0000-0003-3767-5127
E JašarevićDepartment of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, USA.
C H HongDepartment of Psychiatry, Ajou University School of Medicine, Suwon, Republic of Korea.
H W RohDepartment of Psychiatry, Ajou University School of Medicine, Suwon, Republic of Korea.
J Y CheongDepartment of Gastroenterology, Ajou University School of Medicine, Suwon, Republic of Korea.
Y K KimInstitute of MD Healthcare Inc, Seoul, Republic of Korea.
T S ShinInstitute of MD Healthcare Inc, Seoul, Republic of Korea.
C S KangInstitute of MD Healthcare Inc, Seoul, Republic of Korea.
C O KwonInstitute of MD Healthcare Inc, Seoul, Republic of Korea.
S Y YoonInstitute of MD Healthcare Inc, Seoul, Republic of Korea.
S W HongDepartment of Psychiatry, Ajou University School of Medicine, Suwon, Republic of Korea.
H J AizensteinDepartment of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, USA.
H T KarimDepartment of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, USA. hek26@pitt.edu.ORCID 0000-0002-9286-0694
S J SonDepartment of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, USA. sjsonpsy@ajou.ac.kr.ORCID 0000-0001-7434-7996

Funding

The RAW Brain - The Effect of Rumination, Anxiety and Worry on Aging and Dementia RiskR01MH108509 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Carmen Andreescu · 2016 to 2026
$10.6M
NIMH NIH HHS R01 MH108509
6 · The paper itself

Abstract

Depression in older adults with cognitive impairment increases progression to dementia. Microbiota is associated with current mood and cognition, but the extent to which it predicts future symptoms is unknown. In this work, we identified microbial features that reflect current and predict future cognitive and depressive symptoms. Clinical assessments and stool samples were collected from 268 participants with varying cognitive and depressive symptoms. Seventy participants underwent 2-year follow-up. Microbial community diversity, structure, and composition were assessed using high-resolution 16 S rRNA marker gene sequencing. We implemented linear regression to characterize the relationship between microbiome composition, current cognitive impairment, and depressive symptoms. We leveraged elastic net regression to discover features that reflect current or future cognitive function and depressive symptoms. Greater microbial community diversity associated with lower current cognition in the whole sample, and greater depression in participants not on antidepressants. Poor current cognitive function associated with lower relative abundance of Bifidobacterium, while greater GABA degradation associated with greater current depression severity. Future cognitive decline associated with lower cognitive function, lower relative abundance of Intestinibacter, lower glutamate degradation, and higher baseline histamine synthesis. Future increase in depressive symptoms associated with higher baseline depression and anxiety, lower cognitive function, diabetes, lower relative abundance of Bacteroidota, and lower glutamate degradation. Our results suggest cognitive dysfunction and depression are unique states with an overall biological effect detectable through gut microbiota. The microbiome may present a noninvasive readout and prognostic tool for cognitive and psychiatric states.

Indexed as

CognitionCognitive DysfunctionDepressionFecesGastrointestinal MicrobiomeAgedAged, 80 and overFemaleHumansMaleMiddle AgedRNA, Ribosomal, 16SRNA, Ribosomal, 16S

Identifiers

PMID38664490
PMCPMC11449789

What OpenQuestion holds

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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 OpenQuestion graph.