Evidence map›Paper›PMID 38979211›Full record

ArticlebioRxiv : the preprint server for biology2024

Dynamic Human Gut Microbiome and Immune Shifts During an Immersive Psychosocial Therapeutic Program.

Xin Zhou, Ariel B Ganz, Andre Rayner, Tess Yan Cheng, Haley Oba, Benjamin Rolnik, Samuel Lancaster, Xinrui Lu, Yizhou Li, Jethro S Johnson and 4 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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

5 · Who and what money

Authors and funding

14 authors.

Xin ZhouDepartment of Genetics, Stanford University School of Medicine, CA, USA.ORCID 0000-0001-8089-4507
Ariel B GanzDepartment of Genetics, Stanford University School of Medicine, CA, USA.
Andre RaynerDepartment of Genetics, Stanford University School of Medicine, CA, USA.
Tess Yan ChengDepartment of Genetics, Stanford University School of Medicine, CA, USA.
Haley ObaDepartment of Genetics, Stanford University School of Medicine, CA, USA.
Benjamin RolnikDepartment of Genetics, Stanford University School of Medicine, CA, USA.
Samuel LancasterDepartment of Genetics, Stanford University School of Medicine, CA, USA.
Xinrui LuWest China Biomedical Big Data Center, West China Hospital, Sichuan University, Sichuan, China.
Yizhou LiWest China Biomedical Big Data Center, West China Hospital, Sichuan University, Sichuan, China.
Jethro S JohnsonOxford Centre for Microbiome Studies, Kennedy Institute of Rheumatology, University of Oxford, Oxford, UK.
Rebecca HoydThe Ohio State University Comprehensive Cancer Center, OH, USA.
Daniel J SpakowiczThe Ohio State University Comprehensive Cancer Center, OH, USA.
George M SlavichDepartment of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, CA, USA.
Michael P SnyderDepartment of Genetics, Stanford University School of Medicine, CA, USA.

Funding

Stanford Medicine Center for Longevity and Healthy Aging Research Education CoreP30AG059307 · NIA · STANFORD UNIVERSITY · PI PERIYAKOIL, VYJEYANTHI S, YESAVAGE, JEROME A · 2018 to 2025
$4.9M
Integrated, cell type specific functional genomics analyses of regulatory sequence elements and their dynamic interaction networks in neuropsychiatric brain tissuesR01MH116529 · NIMH · STANFORD UNIVERSITY · PI HALLMAYER, JOACHIM F, SNYDER, MICHAEL P. · 2023 to 2023
$1.6M
Genomics Diversity Summer Program (GDSP) at StanfordR25HG010857 · NHGRI · STANFORD UNIVERSITY · PI SNYDER, MICHAEL P. · 2019 to 2023
$1.3M
The microbiome in older adults with lung cancer: association of treatment regimens and diet with protective microbial profilesK01AG070310 · NIA · OHIO STATE UNIVERSITY · PI SPAKOWICZ, DANIEL J. · 2021 to 2025
$583k
NHGRI NIH HHS R25 HG010857NIA NIH HHS K01 AG070310NIA NIH HHS P30 AG059307NIMH NIH HHS R01 MH116529
6 · The paper itself

Abstract

Background: Depression is a leading cause of disability worldwide yet its underlying factors, particularly microbial associations, are poorly understood. Methods: We examined the longitudinal interplay between the microbiome and immune system in the context of depression during an immersive psychosocial intervention. 142 multi-omics samples were collected from 52 well-characterized participants before, during, and three months after a nine-day inquiry-based stress reduction program. Results: We found that depression was associated with both an increased presence of putatively pathogenic bacteria and reduced microbial beta-diversity. Following the intervention, we observed reductions in neuroinflammatory cytokines and improvements in several mental health indicators. Interestingly, participants with a Conclusions: Our findings reveal a protective link between the Prevotella-dominant microbiome and depression, associated with a less inflammatory environment and moderated symptoms. These insights, coupled with observed improvements in neuroinflammatory markers and mental health from the intervention, highlight potential avenues for microbiome-targeted therapies in depression management.

Indexed as

CXCL-1gut microbiomeneuro-inflammationpsychosocial intervention

Identifiers

PMID38979211
PMCPMC11230355

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.