Evidence map›Paper›PMID 42233835›Full record

ArticleArquivos brasileiros de cardiologia2026

The Causal Association between Plasma Metabolites-Mediated Immune Cells and Myocardial Infarction: A Mendelian Randomization Study.

Yue Liu, Xing Chen, Yingzhi Liu, Yvwen Lu, Yun Zhu, Lingli Chen, Jie Li

Abstract read
In one paragraph

Article in Arquivos brasileiros de cardiologia, 2026. 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

7 authors.

Yue LiuHunan University of Chinese Medicin, Changsha, Hunan - China.ORCID http://orcid.org/0009-0006-4741-435X
Xing ChenHunan University of Chinese Medicin, Changsha, Hunan - China.
Yingzhi LiuHunan University of Chinese Medicin, Changsha, Hunan - China.
Yvwen LuHunan University of Chinese Medicin, Changsha, Hunan - China.
Yun ZhuHunan University of Chinese Medicin, Changsha, Hunan - China.
Lingli ChenHunan University of Chinese Medicin, Changsha, Hunan - China.
Jie LiHunan University of Chinese Medicin, Changsha, Hunan - China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundblaMyocardial infarction (MI), as an acute cardiovascular event, has been shown in previous studies to be associated with immune responses and metabolites. However, the causal relationship between immune cells and MI, as well as the mediating role of plasma metabolites, has not been clearly confirmed.

objectivesSystematic analysis of the causal association between 731 immune cells and MI, as well as the mediating roles of 1400 plasma metabolites.

methodsBidirectional Mendelian randomization (MR) analysis was used to explore the causal relationship between immune cells and MI, and one-step and two-step mediation analyses were performed to identify plasma metabolites. The analysis methods included inverse variance weighted (p<0.05), weighted median (p<0.05), simple mode (p<0.05), weighted mode (p<0.05), MR-Egger regression (p<0.05), MR-Egger intercept (p>0.05) and MR-PRESSO (p>0.05) to assess the reliability of the results. SNPs associated with immune cells and metabolites were subjected to gene selection using the STRING database, followed by enrichment analysis.

resultsA total of 44 immune cells were identified to have a causal association with MI (p<0.05), among which HLA DR on Dendritic Cell (ebi-a-GCST90002106) showed the strongest significance (p<0.001). A total of 19 SNPs were identified (OR=1.038, 95% CI 1.018-1.059). Reverse analysis showed no statistical significance (p>0.05). Plasma metabolites, including Deoxycholic acid glucuronide levels, Phosphate to N-acetylneuraminate ratio, and Glycosyl ceramide, played a mediating role in immune cells and MI, with mediation effects of 7.0%, 4.6%, and 6.6%, respectively. STRING database analysis identified eight key genes and one signaling pathway that potentially link the immune phenotypes and the three metabolites (p< 0.05).

conclusionsThis study identified a causal relationship between immune cells and MI. The metabolites Deoxycholic acid glucuronide levels, Phosphate to N-acetylneuraminate ratio, and Glycosyl ceramide played a partial mediating role in this causal relationship.

Indexed as

Mendelian Randomization AnalysisMyocardial InfarctionHumansPolymorphism, Single NucleotideReproducibility of ResultsRisk Factors

Identifiers

PMID42233835
PMCPMC13155783

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