Causal pathways in lymphoid leukemia: the gut microbiota, immune cells, and serum metabolites.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2024
Historique:
received: 24 05 2024
accepted: 23 08 2024
medline: 1 10 2024
pubmed: 1 10 2024
entrez: 1 10 2024
Statut: epublish

Résumé

We employed Mendelian randomization (MR) to investigate the causal relationship between the gut microbiota and lymphoid leukemia, further exploring the causal relationships among immune cells, lymphoid leukemia, and potential metabolic mediators. We utilized data from the largest genome-wide association studies to date, encompassing 418 species of gut microbiota, 713 types of immune cells, and 1,400 serum metabolites as exposures. Summary statistics for lymphoid leukemia, acute lymphocytic leukemia (ALL), and chronic lymphocytic leukemia (CLL) were obtained from the FinnGen database. We performed bidirectional Mendelian analyses to explore the causal relationships among the gut microbiota, immune cells, serum metabolites, and lymphoid leukemia. Additionally, we conducted a two-step mediation analysis to identify potential intermediary metabolites between immune cells and lymphoid leukemia. Several gut microbiota were found to have causal relationships with lymphoid leukemia, ALL, and CLL, particularly within the This MR study provides evidence supporting specific causal relationships between the gut microbiota and lymphoid leukemia, as well as between certain immune cells and lymphoid leukemia with potential intermediary metabolites.

Sections du résumé

Background UNASSIGNED
We employed Mendelian randomization (MR) to investigate the causal relationship between the gut microbiota and lymphoid leukemia, further exploring the causal relationships among immune cells, lymphoid leukemia, and potential metabolic mediators.
Methods UNASSIGNED
We utilized data from the largest genome-wide association studies to date, encompassing 418 species of gut microbiota, 713 types of immune cells, and 1,400 serum metabolites as exposures. Summary statistics for lymphoid leukemia, acute lymphocytic leukemia (ALL), and chronic lymphocytic leukemia (CLL) were obtained from the FinnGen database. We performed bidirectional Mendelian analyses to explore the causal relationships among the gut microbiota, immune cells, serum metabolites, and lymphoid leukemia. Additionally, we conducted a two-step mediation analysis to identify potential intermediary metabolites between immune cells and lymphoid leukemia.
Results UNASSIGNED
Several gut microbiota were found to have causal relationships with lymphoid leukemia, ALL, and CLL, particularly within the
Conclusion UNASSIGNED
This MR study provides evidence supporting specific causal relationships between the gut microbiota and lymphoid leukemia, as well as between certain immune cells and lymphoid leukemia with potential intermediary metabolites.

Identifiants

pubmed: 39351228
doi: 10.3389/fimmu.2024.1437869
pmc: PMC11439652
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1437869

Informations de copyright

Copyright © 2024 Zhuang, Yin, Yang, Man, Wang, Geng and Shi.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Xin Zhuang (X)

Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

Qingning Yin (Q)

Department of Vice President, Qinghai Province Women and Children's Hospital, Xining, Qinghai, China.

Rong Yang (R)

Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

Xiaoying Man (X)

Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

Ruochen Wang (R)

Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

Hui Geng (H)

Department of Vice President, Qinghai Province Women and Children's Hospital, Xining, Qinghai, China.

Yifen Shi (Y)

Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Department of Vice President, Qinghai Province Women and Children's Hospital, Xining, Qinghai, China.
Zhejiang Provincial Clinical Research Center For Hematological Disorders, Wenzhou, China.

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