<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Tang J</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The diagnosis of Myocardial Infarction (MI) requires the discovery of specific diagnostic biomarkers beyond high-sensitivity cardiac troponins. To identify causal MI-associated genes regulated by lactylation modification and elucidate their roles in metabolic-immune dysregulation.&lt;h4>Methods&lt;/h4>This multi-omics study combined bioinformatic analyses of human MI datasets (GSE60993/GSE61144/GSE66360) with experimental validation to investigate lactylation-related genes (LRGs). Differential expression analysis (limma, P &lt; 0.05, |log&lt;sub>2&lt;/sub>FC|>0.585) identified 571 Differentially Expressed Genes (DEGs), which intersected with 2,051 curated lactylation-related genes (LRGs) (PubMed/GeneCards) yielding 56 lactylation-associated DEGs. Mendelian randomization (MR) utilized g</pubmed_abstract><journal>Frontiers in cell and developmental biology</journal><pagination>1653551</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12554677</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Metabolic-immune crosstalk in myocardial infarction: RLF and SMCHD1 identified as causal therapeutic targets via integrated lactylation-MR analysis.</pubmed_title><pmcid>PMC12554677</pmcid><pubmed_authors>Tang J</pubmed_authors><pubmed_authors>Yuan L</pubmed_authors><pubmed_authors>Han YL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Metabolic-immune crosstalk in myocardial infarction: RLF and SMCHD1 identified as causal therapeutic targets via integrated lactylation-MR analysis.</name><description>&lt;h4>Background&lt;/h4>The diagnosis of Myocardial Infarction (MI) requires the discovery of specific diagnostic biomarkers beyond high-sensitivity cardiac troponins. To identify causal MI-associated genes regulated by lactylation modification and elucidate their roles in metabolic-immune dysregulation.&lt;h4>Methods&lt;/h4>This multi-omics study combined bioinformatic analyses of human MI datasets (GSE60993/GSE61144/GSE66360) with experimental validation to investigate lactylation-related genes (LRGs). Differential expression analysis (limma, P &lt; 0.05, |log&lt;sub>2&lt;/sub>FC|>0.585) identified 571 Differentially Expressed Genes (DEGs), which intersected with 2,051 curated lactylation-related genes (LRGs) (PubMed/GeneCards) yielding 56 lactylation-associated DEGs. Mendelian randomization (MR) utilized g</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2026-05-14T03:22:21.874Z</modification><creation>2026-05-14T03:12:55.485Z</creation></dates><accession>S-EPMC12554677</accession><cross_references><pubmed>41158309</pubmed><doi>10.3389/fcell.2025.1653551</doi></cross_references></HashMap>