<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE318nnn/GSE318387/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Methylation profiling</omics_type><species>Homo sapiens</species><gds_type>Methylation profiling by array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE318387</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Promoter hypomethylation of cadherin-7: a novel epigenetic marker associated with cerebral small vessel disease</name><description>Introduction: Cerebral small vessel disease (SVD), manifesting as white matter hyperintensities (WMH), lacunar infarctions, and cerebral microbleeds on MRI, has been linked to epigenetic alterations. Methods: Genome-wide promoter methylation was profiled using the Infinium MethylationEPIC v2.0 array in peripheral inflammatory cells from 16 patients without SVD and 16 patients with all three imaging features. Results: EPIC profiling identified 17 promoter regions with significant differences between groups, and CDH7 hypomethylation emerged as an independent predictor of SVD imaging features. Conclusion: CDH7 hypomethylation was identified and validated as an epigenetic marker predictive of MRI-defined SVD imaging features.</description><dates><publication>2026/04/01</publication></dates><accession>GSE318387</accession><cross_references><GSM>GSM9493614</GSM><GSM>GSM9493613</GSM><GSM>GSM9493612</GSM><GSM>GSM9493611</GSM><GSM>GSM9493618</GSM><GSM>GSM9493617</GSM><GSM>GSM9493616</GSM><GSM>GSM9493615</GSM><GSM>GSM9493619</GSM><GSM>GSM9493620</GSM><GSM>GSM9493603</GSM><GSM>GSM9493602</GSM><GSM>GSM9493601</GSM><GSM>GSM9493589</GSM><GSM>GSM9493600</GSM><GSM>GSM9493607</GSM><GSM>GSM9493606</GSM><GSM>GSM9493605</GSM><GSM>GSM9493604</GSM><GSM>GSM9493609</GSM><GSM>GSM9493608</GSM><GSM>GSM9493591</GSM><GSM>GSM9493590</GSM><GSM>GSM9493595</GSM><GSM>GSM9493594</GSM><GSM>GSM9493593</GSM><GSM>GSM9493592</GSM><GSM>GSM9493610</GSM><GSM>GSM9493599</GSM><GSM>GSM9493598</GSM><GSM>GSM9493597</GSM><GSM>GSM9493596</GSM><GPL>33022</GPL><GSE>318387</GSE><taxon>Homo sapiens</taxon><PMID>[41890232]</PMID></cross_references></HashMap>