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Discussion on the relationship between gut microbiota and glioma through Mendelian randomization test based on the brain gut axis.
Cui, Chenzhi; Yang, Tianke; Wang, ShengYu; Jia, Zhuqiang; Zhao, Lin; Han, Xin; Sun, Xiaohong; Zong, Junwei; Wang, Shouyu; Chen, Dong.
Affiliation
  • Cui C; Graduate school, Dalian Medical University, Dalian, Dalian, China.
  • Yang T; Department of Neurosurgery, Dalian Municipal Central Hospital, Dalian, China.
  • Wang S; Department of Orthopaedic Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, China.
  • Jia Z; College of Integrative Medicine, Dalian Medical University, Dalian, China.
  • Zhao L; Medical Laboratory Technology, College of Medical Laboratory, Dalian Medical University, Dalian, China.
  • Han X; The First Affiliated Hospital of Dalian Medical University, Dalian, China.
  • Sun X; Naqu People's Hospital, Tibet, China.
  • Zong J; Department of Quality Management, Dalian Municipal Central Hospital, Dalian, China.
  • Wang S; Naqu People's Hospital, Tibet, China.
  • Chen D; Department of Orthopaedic Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
PLoS One ; 19(5): e0304403, 2024.
Article in En | MEDLINE | ID: mdl-38809931
ABSTRACT

BACKGROUND:

In the realm of Gut-Brain axis research, existing evidence points to a complex bidirectional regulatory mechanism between gut microbiota and the brain. However, the question of whether a causal relationship exists between gut microbiota and specific types of brain tumors, such as gliomas, remains unresolved. To address this gap, we employed publicly available Genome-Wide Association Study (GWAS) and MIOBEN databases, conducting an in-depth analysis using Two-Sample Mendelian Randomization (MR).

METHOD:

We carried out two sets of MR analyses. The preliminary analysis included fewer instrumental variables due to a high genome-wide statistical significance threshold (5×10-8). To enable a more comprehensive and detailed analysis, we adjusted the significance threshold to 1×10-5. We performed linkage disequilibrium analysis (R2 <0.001, clumping distance = 10,000kb) and detailed screening of palindromic SNPs, followed by MR analysis and validation through sensitivity analysis.

RESULTS:

Our findings reveal a causal relationship between gut microbiota and gliomas. Further confirmation via Inverse Variance Weighting (IVW) identified eight specific microbial communities related to gliomas. Notably, the Peptostreptococcaceae and Olsenella communities appear to have a protective effect, reducing glioma risk.

CONCLUSION:

This study not only confirms the causal link between gut microbiota and gliomas but also suggests a new avenue for future glioma treatment.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / Polymorphism, Single Nucleotide / Genome-Wide Association Study / Mendelian Randomization Analysis / Gastrointestinal Microbiome / Glioma Limits: Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / Polymorphism, Single Nucleotide / Genome-Wide Association Study / Mendelian Randomization Analysis / Gastrointestinal Microbiome / Glioma Limits: Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2024 Document type: Article Affiliation country: China