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A study on the causal relationship between the gut microbiome and herpes zoster using Mendelian randomization
Zenan Meng1, Tingting Wang2, Yue Liao1
1Hubei Key Laboratory of Tumor Microenvironment and Immunotherapy, College of Basic Medical Sciences, China Three Gorges University, Yichang, China.
Frontiers in Medicine
|September 16, 2024
Summary
This study reveals a two-way causal link between the gut microbiome and herpes zoster (HZ). Specific gut bacteria like Tyzzerella3 and Cyanobacteria may increase HZ risk, while others might offer protection, opening new treatment avenues.
Area of Science:
- Microbiome research
- Infectious disease epidemiology
- Genetic association studies
Background:
- Herpes zoster (HZ) has high global incidence, often linked to aging and immune status.
- Increased HZ incidence in inflammatory bowel diseases suggests a gut-related etiology.
- Previous research did not explore the gut microbiome's role in HZ recurrence.
Purpose of the Study:
- To investigate the potential causal relationship between the gut microbiome and herpes zoster (HZ).
- To explore the bidirectional nature of this interaction using genetic data.
- To identify specific gut microbial taxa associated with HZ onset and recurrence.
Main Methods:
- Utilized large-scale Genome-Wide Association Study (GWAS) databases (FinnGen, Mibiogen).
- Employed two-sample Mendelian randomization (MR) analysis to assess causality.
- Conducted bidirectional MR analyses to determine the direction of the relationship.
Main Results:
- Identified genus Tyzzerella3 and phylum Cyanobacteria as potential risk factors for HZ reactivation.
- Found that HZ onset may inhibit the Eubacterium hallii group.
- Observed potential protective effects from genus Escherichia/Shigella, genus Veillonella, and phylum Proteobacteria.
Conclusions:
- Established the gut microbiome as a novel factor influencing HZ reactivation.
- Demonstrated a potential bidirectional relationship where HZ may also affect gut flora composition.
- Highlighted specific bacterial taxa as potential therapeutic targets for HZ management.
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