<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>69</volume><submitter>Chang KJ</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>The clinical presentations of dry eye disease (DED) and depression (DEP) often comanifest. However, the robustness and the mechanisms underlying this association were undetermined.&lt;h4>Objectives&lt;/h4>To this end, we set up a three-segment study that employed multimodality results (meta-analysis, genome-wide association study [GWAS] and Mendelian randomization [MR]) to elucidate the association, common pathways and causality between DED and DEP.&lt;h4>Methods&lt;/h4>A meta-analysis comprising 26 case-control studies was first conducted to confirm the DED-DEP association. Next, we performed a linkage disequilibrium (LD)-adjusted GWAS and targeted phenotype association study (PheWAS) in East Asian TW Biobank (TWB) and European UK Biobank (UKB) populations. Single-nucleotide poly</pubmed_abstract><journal>Journal of advanced research</journal><pagination>197-213</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11954816</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Decoding and reconstructing disease relations between dry eye and depression: a multimodal investigation comprising meta-analysis, genetic pathways and Mendelian randomization.</pubmed_title><pmcid>PMC11954816</pmcid><pubmed_authors>Yu TH</pubmed_authors><pubmed_authors>Wu YR</pubmed_authors><pubmed_authors>Tsai HY</pubmed_authors><pubmed_authors>Li CY</pubmed_authors><pubmed_authors>Dai HJ</pubmed_authors><pubmed_authors>Chang YJ</pubmed_authors><pubmed_authors>Chen YC</pubmed_authors><pubmed_authors>Li CT</pubmed_authors><pubmed_authors>Wu HY</pubmed_authors><pubmed_authors>Chang KJ</pubmed_authors><pubmed_authors>Cheng CY</pubmed_authors><pubmed_authors>Hsu CC</pubmed_authors><pubmed_authors>Chen SJ</pubmed_authors><pubmed_authors>Hsu YT</pubmed_authors><pubmed_authors>Chiang PH</pubmed_authors><pubmed_authors>Weng PY</pubmed_authors><pubmed_authors>Yang YP</pubmed_authors><pubmed_authors>Chen YH</pubmed_authors><pubmed_authors>Hsieh AR</pubmed_authors><pubmed_authors>Chiou SH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Decoding and reconstructing disease relations between dry eye and depression: a multimodal investigation comprising meta-analysis, genetic pathways and Mendelian randomization.</name><description>&lt;h4>Introduction&lt;/h4>The clinical presentations of dry eye disease (DED) and depression (DEP) often comanifest. However, the robustness and the mechanisms underlying this association were undetermined.&lt;h4>Objectives&lt;/h4>To this end, we set up a three-segment study that employed multimodality results (meta-analysis, genome-wide association study [GWAS] and Mendelian randomization [MR]) to elucidate the association, common pathways and causality between DED and DEP.&lt;h4>Methods&lt;/h4>A meta-analysis comprising 26 case-control studies was first conducted to confirm the DED-DEP association. Next, we performed a linkage disequilibrium (LD)-adjusted GWAS and targeted phenotype association study (PheWAS) in East Asian TW Biobank (TWB) and European UK Biobank (UKB) populations. Single-nucleotide poly</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-06-02T12:02:02.035Z</modification><creation>2026-04-18T03:11:02.948Z</creation></dates><accession>S-EPMC11954816</accession><cross_references><pubmed>38548265</pubmed><doi>10.1016/j.jare.2024.03.015</doi></cross_references></HashMap>