Evidence map›Paper›PMID 41329541›Full record

ArticlePhysiological research2025

The Linkage Among Gut Microbiota, Inflammatory Cytokines, and Immune Cell Dynamics in Osteoporosis: A Mendelian Randomization Study.

Y Guo, J Du, H Chen

Abstract read
In one paragraph

Article in Physiological research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Y GuoDepartment of Medical Laboratory, Northern Jiangsu People's Hospital Affiliated to Yangzhou University, Yangzhou City, Jiangsu Province, China; Department of Science and Technology, Northern Jiangsu People's Hospital Affiliated to Yangzhou University, Yangzhou City, Jiangsu Province, China. 18051061691@yzu.edu.cn.
J Du
H Chen

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This investigation attempted to discern the causal link of gut microbiota with osteoporosis, examining potential mediating factors, involving inflammatory markers and immune cell activity. Bidirectional two-sample univariable Mendelian randomization (UVMR) was used to decipher the causal link of gut microbiota with osteoporosis, verifying three core assumptions. External datasets were utilized to validate UVMR outcomes and implemented reverse analyses to identify potential reverse causality. Additionally, mediation effects were figured out through UVMR, estimating effect sizes and proportions for every qualifying mediator. It was attempted to precisely select instrumental variables (IVs), ensuring that those influenced by linkage disequilibrium (LD) or demonstrating weak correlations were excluded. The inverse-variance weighted (IVW) analysis unveiled 12 gut microbiota species that were remarkably linked with osteoporosis risk. Specifically, five families, involving Pasteurellaceae, could elevate the risk of osteoporosis, while another five, such as Oxalobacteraceae, were protective. Additionally, two inflammatory markers exhibited a remarkable linkage with osteoporosis following heterogeneity testing, and 37 distinct immune cell types were recognized as being relevant to the disease after adjusting for heterogeneity and pleiotropy. Reverse MR analysis confirmed the absence of reverse causality among gut microbiota, inflammatory factors, immune cells, and osteoporosis. Notably, mediation analysis unveiled that Cyanobacteria influenced HLA DR++ monocytes' percentage in leukocytes, contributing to osteoporosis's pathogenesis. The outcomes highlighted specific gut microbiota, inflammatory factors, and immune cells, noticeably contributing to osteoporosis's pathogenesis. The identified mediating pathways provided innovative insights into disease mechanisms and potential therapeutic targets. Key words Gut Microbiota " Inflammatory cytokines " Immune cell dynamics " Osteoporosis " Mendelian randomization.

Indexed as

CytokinesGastrointestinal MicrobiomeInflammation MediatorsOsteoporosisHumansMendelian Randomization AnalysisCytokinesInflammation Mediators

Identifiers

PMID41329541
PMCPMC12746856

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