<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(4)</volume><submitter>Park S</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Selenium is a trace mineral that is commonly included in micronutrient supplements. The effect of selenium on kidney function remains unclear. A genetically predicted micronutrient and its association with estimated glomerular filtration rate (eGFR) can be used to assess the causal estimates by Mendelian randomization (MR).&lt;h4>Methods&lt;/h4>In this MR study, we instrumented 11 genetic variants associated with blood or total selenium levels from a previous genome-wide association study (GWAS). The association between genetically predicted selenium concentration and eGFR was first assessed by summary-level MR in the chronic kidney disease(CKDGen) GWAS meta-analysis summary statistics, including 567,460 European samples. Inverse-variance weighted and pleiotropy-robust MR an</pubmed_abstract><journal>Kidney international reports</journal><pagination>851-859</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10105058</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genetically Predicted Body Selenium Concentration and estimated GFR: A Mendelian Randomization Study.</pubmed_title><pmcid>PMC10105058</pmcid><pubmed_authors>Lee S</pubmed_authors><pubmed_authors>Kim K</pubmed_authors><pubmed_authors>Lee H</pubmed_authors><pubmed_authors>Lim CS</pubmed_authors><pubmed_authors>Park S</pubmed_authors><pubmed_authors>Han SS</pubmed_authors><pubmed_authors>Kim DK</pubmed_authors><pubmed_authors>Kim YC</pubmed_authors><pubmed_authors>Kim SG</pubmed_authors><pubmed_authors>Lee JP</pubmed_authors><pubmed_authors>Joo KW</pubmed_authors><pubmed_authors>Kim Y</pubmed_authors><pubmed_authors>Cho S</pubmed_authors><pubmed_authors>Kim YS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genetically Predicted Body Selenium Concentration and estimated GFR: A Mendelian Randomization Study.</name><description>&lt;h4>Introduction&lt;/h4>Selenium is a trace mineral that is commonly included in micronutrient supplements. The effect of selenium on kidney function remains unclear. A genetically predicted micronutrient and its association with estimated glomerular filtration rate (eGFR) can be used to assess the causal estimates by Mendelian randomization (MR).&lt;h4>Methods&lt;/h4>In this MR study, we instrumented 11 genetic variants associated with blood or total selenium levels from a previous genome-wide association study (GWAS). The association between genetically predicted selenium concentration and eGFR was first assessed by summary-level MR in the chronic kidney disease(CKDGen) GWAS meta-analysis summary statistics, including 567,460 European samples. Inverse-variance weighted and pleiotropy-robust MR an</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2025-04-18T15:00:51.649Z</modification><creation>2025-04-07T01:27:17.721Z</creation></dates><accession>S-EPMC10105058</accession><cross_references><pubmed>37069993</pubmed><doi>10.1016/j.ekir.2023.01.009</doi></cross_references></HashMap>