Evidence map›Paper›PMID 40033322›Full record

ArticleThrombosis journal2025

Exploration of the causal relationship and mechanisms between serum albumin and venous thrombosis: a bidirectional mendelian randomization analysis and bioinformatics study.

Xuemei Xia, Xin Tie, Maolin Hong, Wanhong Yin

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Article in Thrombosis journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers 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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5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xuemei XiaDepartment of Critical Care Medicine, West China Hospital, Sichuan University, No.37, Guoxue Alley, Wuhou District, Chengdu, Sichuan Province, China.
Xin TieDepartment of Critical Care Medicine, West China Hospital, Sichuan University, No.37, Guoxue Alley, Wuhou District, Chengdu, Sichuan Province, China.
Maolin HongDepartment of Critical Care Medicine, West China Hospital, Sichuan University, No.37, Guoxue Alley, Wuhou District, Chengdu, Sichuan Province, China.
Wanhong YinDepartment of Critical Care Medicine, West China Hospital, Sichuan University, No.37, Guoxue Alley, Wuhou District, Chengdu, Sichuan Province, China. yinwanhong@wchscu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo explore the causal relationship between serum albumin and venous thromboembolism (VTE) comprises deep vein thrombosis (DVT) and its consequential condition, pulmonary embolism (PE), through Mendelian randomization (MR) design, seeking to clarify the protective roles of albumin in the development of venous thrombosis.

methodsWe performed a bidirectional two-sample Mendelian randomization analysis utilizing albumin genome-wide association study (GWAS) data alongside VTE datasets from various sources. Additionally, to minimize heterogeneity across different datasets, a meta-analysis of the Mendelian randomization results was conducted. Furthermore, genes associated with such exposures were identified to unravel how exposure impacts outcomes. This was followed by applying bioinformatics techniques for gene enrichment analysis and employing the Cytoscape software to pinpoint the hub genes.

resultsThe findings from the meta-analysis of the Mendelian randomization indicate that reduced levels of albumin are associated with an elevated risk of VTE (OR = 0.739, 95% CI: 0.695 to 0.787, P = 1.82e-9), DVT (OR = 0.700, 95% CI: 0.646 to 0.772, P = 2.96e-15), and PE (OR = 0.717, 95% CI: 0.647 to 0.793, P = 1.74e-10). Bioinformatics analysis revealed that serum albumin primarily protects against VTE by influencing inflammation and cytokines.

conclusionsOur bidirectional MR analysis confirmed a substantial causal association linking serum albumin to VTE. Bioinformatics analysis revealed that this causal link is mediated by the immune response through inflammation and cytokines.

Indexed as

Bioinformatics analysisMendelian randomizationSerum albuminVenous thromboembolism

Identifiers

PMID40033322
PMCPMC11874119

What Socratic holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.