<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yoon BW</submitter><funding>National Research Foundation of Korea</funding><funding>Chung-Ang University Research Grant</funding><pagination>807</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11047998</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(4)</volume><pubmed_abstract>Researchers have proposed a possible correlation between age-related macular degeneration (AMD) and inflammation or C-reactive protein (CRP) levels. We investigated the potential causal relationship between CRP levels and AMD. Single-nucleotide polymorphisms (SNPs) associated with CRP exposure were selected as the instrumental variables (IVs) with significance (&lt;i>p&lt;/i> &lt; 5 × 10&lt;sup>-8&lt;/sup>) from the genome-wide association study (GWAS) meta-analysis data of Biobank Japan and the UK Biobank. GWAS data for AMD were obtained from 11 International AMD Genomics Consortium studies. An evaluation of causal estimates, utilizing the inverse-variance-weighted (IVW), weighted-median, MR-Egger, MR-Pleiotropy-Residual-Sum, and Outlier tests, was conducted in a two-sample Mendelian randomization (MR) </pubmed_abstract><journal>Biomedicines</journal><pubmed_title>Potential Causal Association between C-Reactive Protein Levels in Age-Related Macular Degeneration: A Two-Sample Mendelian Randomization Study.</pubmed_title><pmcid>PMC11047998</pmcid><funding_grant_id>2022</funding_grant_id><funding_grant_id>2022R1C1C1002929</funding_grant_id><pubmed_authors>Yoon BW</pubmed_authors><pubmed_authors>Seo JH</pubmed_authors><pubmed_authors>Lee Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Potential Causal Association between C-Reactive Protein Levels in Age-Related Macular Degeneration: A Two-Sample Mendelian Randomization Study.</name><description>Researchers have proposed a possible correlation between age-related macular degeneration (AMD) and inflammation or C-reactive protein (CRP) levels. We investigated the potential causal relationship between CRP levels and AMD. Single-nucleotide polymorphisms (SNPs) associated with CRP exposure were selected as the instrumental variables (IVs) with significance (&lt;i>p&lt;/i> &lt; 5 × 10&lt;sup>-8&lt;/sup>) from the genome-wide association study (GWAS) meta-analysis data of Biobank Japan and the UK Biobank. GWAS data for AMD were obtained from 11 International AMD Genomics Consortium studies. An evaluation of causal estimates, utilizing the inverse-variance-weighted (IVW), weighted-median, MR-Egger, MR-Pleiotropy-Residual-Sum, and Outlier tests, was conducted in a two-sample Mendelian randomization (MR) </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-04-15T03:21:33.087Z</modification><creation>2026-04-15T03:15:14.747Z</creation></dates><accession>S-EPMC11047998</accession><cross_references><pubmed>38672162</pubmed><doi>10.3390/biomedicines12040807</doi></cross_references></HashMap>