<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>20(10)</volume><submitter>Li J</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Diabetic cardiomyopathy (DCM) represents a distinct myocardial pathology arising from chronic diabetic metabolic disturbances, characterized by progressive structural and functional abnormalities that frequently culminate in heart failure. Cuproptosis, a novel form of cell death, is highly linked to mitochondrial metabolism and mediated by protein lipoylation. However, studies are limited on the clinical significance of cuproptosis-related genes (CRGs) in DCM. Therefore, it is helpful to identify CRGs involved in DCM and explore their expression and molecular mechanisms.&lt;h4>Methods&lt;/h4>We downloaded three datasets of DCM from the GEO database and a set of cuproptosis-related genes with 176 genes. Following the identification of the differentially expressed cuproptosis-re</pubmed_abstract><journal>PloS one</journal><pagination>e0328512</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12558461</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Comprehensive analysis of cuproptosis-related genes in diabetic cardiomyopathy.</pubmed_title><pmcid>PMC12558461</pmcid><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Zhang M</pubmed_authors><pubmed_authors>Hao C</pubmed_authors><pubmed_authors>Duan X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comprehensive analysis of cuproptosis-related genes in diabetic cardiomyopathy.</name><description>&lt;h4>Background&lt;/h4>Diabetic cardiomyopathy (DCM) represents a distinct myocardial pathology arising from chronic diabetic metabolic disturbances, characterized by progressive structural and functional abnormalities that frequently culminate in heart failure. Cuproptosis, a novel form of cell death, is highly linked to mitochondrial metabolism and mediated by protein lipoylation. However, studies are limited on the clinical significance of cuproptosis-related genes (CRGs) in DCM. Therefore, it is helpful to identify CRGs involved in DCM and explore their expression and molecular mechanisms.&lt;h4>Methods&lt;/h4>We downloaded three datasets of DCM from the GEO database and a set of cuproptosis-related genes with 176 genes. Following the identification of the differentially expressed cuproptosis-re</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2026-06-05T05:30:57.369Z</modification><creation>2026-05-13T14:29:22.539Z</creation></dates><accession>S-EPMC12558461</accession><cross_references><pubmed>41144543</pubmed><doi>10.1371/journal.pone.0328512</doi></cross_references></HashMap>