Evidence map›Paper›PMID 39323879›Full record

ArticleFrontiers in microbiology2024

Causality investigation among gut microbiota, immune cells, and prostate diseases: a Mendelian randomization study.

Shao-Yu Yue, Wei-Yi Li, Shun Xu, Xiao-Xin Bai, Wen-Long Xu, Xu Wang, He-Kang Ding, Jia Chen, He-Xi Du, Ling-Fan Xu and 2 more

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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  5. Article
  6. Review
  7. Microbiota and urinary tumor immunity: Mechanisms, therapeutic implications, and future perspectives.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2024
    Article
  8. 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

12 authors.

Shao-Yu Yue *Department of Urology, The First Affiliated Hospital of Anhui Medical University, Anhui Medical University, Hefei, China.
Wei-Yi Li *Department of Urology, The First Affiliated Hospital of Anhui Medical University, Anhui Medical University, Hefei, China.
Shun Xu *Department of Urology, The First Affiliated Hospital of Anhui Medical University, Anhui Medical University, Hefei, China.
Xiao-Xin BaiDepartment of Infectious Disease, The Second People's Hospital of Fuyang City, Fuyang, China.
Wen-Long XuDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Anhui Medical University, Hefei, China.
Xu WangDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Anhui Medical University, Hefei, China.
He-Kang DingDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Anhui Medical University, Hefei, China.
Jia ChenDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Anhui Medical University, Hefei, China.
He-Xi DuDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Anhui Medical University, Hefei, China.
Ling-Fan XuDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Anhui Medical University, Hefei, China.
Di NiuDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Anhui Medical University, Hefei, China.
Chao-Zhao LiangDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Anhui Medical University, Hefei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The gut microbiota has been demonstrated to have a significant role in the pathogenesis and progression of a variety of diseases, including prostate cancer, prostatitis, and benign prostatic hyperplasia. Potential links between prostate diseases, immune cells and the gut microbiota have not been adequately investigated. Methods: MR studies were conducted to estimate the effects of instrumental variables obtained from genome-wide association studies (GWASs) of 196 gut microbial taxa and 731 immune cells on the risk of prostate diseases. The primary method for analysing causal relationships was inverse variance-weighted (IVW) analysis, and the MR results were validated through various sensitivity analyses. Results: MR analysis revealed that 28 gut microbiome taxa and 75 immune cell types were significantly associated with prostate diseases. Furthermore, reverse MR analysis did not support a causal relationship between prostate diseases and the intestinal microbiota or immune cells. Finally, the results of the mediation analysis indicated that Secreting Treg % CD4 Treg, Activated & resting Treg % CD4 Treg, and Mo MDSC AC inhibited the role of the class Mollicutes in reducing the risk of PCa. In prostatitis, CD8+ T cells on EM CD8br hinder the increased risk associated with the genus Conclusion: This study highlights the complex relationships among the gut microbiota, immune cells and prostate diseases. The involvement of the gut microbiota in regulating immune cells to impact prostate diseases could provide novel methods and concepts for its therapy and management.

Indexed as

benign prostatic hyperplasiaimmune cellsmediating effectMendelian randomization analysisprostate cancerprostate diseasesprostatitis

Identifiers

PMID39323879
PMCPMC11422081

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Registered trials

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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.