Evidence map›Paper›PMID 41060947›Full record

ArticleClinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis

Exploring the Causal Relationship Between Circulating miRNAs and Sepsis Through Mendelian Randomization Analysis.

Yan Jin, Yuan Zhang

Abstract read
In one paragraph

Article in Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis. 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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Yan JinDepartment of Intensive Care Medicine, Hangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Yuan ZhangDepartment of Intensive Care Medicine, Hangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.ORCID 0009-0003-8874-3318

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundMicroRNAs (miRNAs) play a crucial role in the pathophysiology of sepsis, with aberrant expression documented in peripheral blood samples from sepsis patients. This study aims to investigate the causal relationship between circulating miRNAs and sepsis using Mendelian Randomization (MR) approaches.MethodsWe utilized miRNA expression quantitative trait loci (eQTL) data and genome-wide association study (GWAS) data on sepsis. MR analysis was conducted using Inverse Variance Weighted (IVW) and MR-Egger regression methods to identify miRNAs significantly associated with sepsis risk. Potential targets and related pathways of these miRNAs were also analyzed.ResultsIVW and MR-Egger regression analyses revealed that three circulating miRNAs (hsa-miR-125a-5p, hsa-miR-494-3p, and hsa-miR-885-5p) exhibited significant associations with reduced sepsis risk, indicating protective effects. Conversely, hsa-miR-196b-5p, hsa-miR-27b-3p, and hsa-miR-598-3p were linked to increased sepsis risk. The association between hsa-miR-27b-3p and increased sepsis risk was further validated in an independent cohort. Target identification and enrichment analysis indicated that the targets of these miRNAs are closely related to biological processes such as bacterial infection, apoptosis, and the FoxO signaling pathway.ConclusionOur study provides novel insights into the causal relationships between circulating miRNAs and sepsis through MR analysis, offering new perspectives for early prevention and treatment strategies for sepsis. These findings provide a foundation for further investigation into the potential application of miRNAs in the diagnosis and treatment of sepsis.

Indexed as

Circulating MicroRNAMendelian Randomization AnalysisMicroRNAsSepsisFemaleGenome-Wide Association StudyHumansMaleQuantitative Trait LociCirculating MicroRNAMicroRNAseQTLGWASMendelian randomizationmiRNAssepsis

Identifiers

PMID41060947
PMCPMC12511739

What Socratic holds

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