<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Westphal S</submitter><funding>Deutsche Forschungsgemeinschaft</funding><pagination>26</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6345037</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The aim of our study was the identification of genetic variants associated with postoperative complications after cardiac surgery.&lt;h4>Methods&lt;/h4>We conducted a prospective, double-blind, multicenter, randomized trial (RIPHeart). We performed a genome-wide association study (GWAS) in 1170 patients of both genders (871 males, 299 females) from the RIPHeart-Study cohort. Patients undergoing non-emergent cardiac surgery were included. Primary endpoint comprises a binary composite complication rate covering atrial fibrillation, delirium, non-fatal myocardial infarction, acute renal failure and/or any new stroke until hospital discharge with a maximum of fourteen days after surgery.&lt;h4>Results&lt;/h4>A total of 547,644 genotyped markers were available for analysis. Following qua</pubmed_abstract><journal>BMC cardiovascular disorders</journal><pubmed_title>Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study.</pubmed_title><pmcid>PMC6345037</pmcid><funding_grant_id>ME 3559/1-1</funding_grant_id><pubmed_authors>Renner J</pubmed_authors><pubmed_authors>Alms A</pubmed_authors><pubmed_authors>Tittmann L</pubmed_authors><pubmed_authors>Meybohm P</pubmed_authors><pubmed_authors>Hachenberg T</pubmed_authors><pubmed_authors>Knuefermann P</pubmed_authors><pubmed_authors>Heinze H</pubmed_authors><pubmed_authors>Boehm O</pubmed_authors><pubmed_authors>Paxian M</pubmed_authors><pubmed_authors>Bein B</pubmed_authors><pubmed_authors>Hasenclever D</pubmed_authors><pubmed_authors>Mucha S</pubmed_authors><pubmed_authors>Goerlach G</pubmed_authors><pubmed_authors>Bauer M</pubmed_authors><pubmed_authors>Zacharowski K</pubmed_authors><pubmed_authors>Stevanovic A</pubmed_authors><pubmed_authors>Schilling T</pubmed_authors><pubmed_authors>Goetzenich A</pubmed_authors><pubmed_authors>Rossaint R</pubmed_authors><pubmed_authors>Moormann T</pubmed_authors><pubmed_authors>Werner C</pubmed_authors><pubmed_authors>Gruenewald M</pubmed_authors><pubmed_authors>Sander M</pubmed_authors><pubmed_authors>Wittmann M</pubmed_authors><pubmed_authors>Boening A</pubmed_authors><pubmed_authors>Meyer-Treschan T</pubmed_authors><pubmed_authors>Chalk K</pubmed_authors><pubmed_authors>Heringlake M</pubmed_authors><pubmed_authors>Kohlhaas M</pubmed_authors><pubmed_authors>Kuhr B</pubmed_authors><pubmed_authors>Kletzin F</pubmed_authors><pubmed_authors>Schwarzmann G</pubmed_authors><pubmed_authors>Stehr SN</pubmed_authors><pubmed_authors>Paarmann H</pubmed_authors><pubmed_authors>Strauchmann J</pubmed_authors><pubmed_authors>August K</pubmed_authors><pubmed_authors>Roesner J</pubmed_authors><pubmed_authors>Schoen J</pubmed_authors><pubmed_authors>Fichtlscherer AZS</pubmed_authors><pubmed_authors>Brosteanu O</pubmed_authors><pubmed_authors>Strouhal U</pubmed_authors><pubmed_authors>Albrecht M</pubmed_authors><pubmed_authors>Franke A</pubmed_authors><pubmed_authors>Sievers HH</pubmed_authors><pubmed_authors>Kienbaum P</pubmed_authors><pubmed_authors>Boening U</pubmed_authors><pubmed_authors>Morsbach KU</pubmed_authors><pubmed_authors>Westphal S</pubmed_authors><pubmed_authors>Treskatsch S</pubmed_authors><pubmed_authors>Mauff S</pubmed_authors><pubmed_authors>Fuernau G</pubmed_authors><pubmed_authors>Schaelte G</pubmed_authors><pubmed_authors>RIPHeart-Study Collaborators</pubmed_authors><pubmed_authors>Wiedenbeck C</pubmed_authors><pubmed_authors>Klotz S</pubmed_authors><pubmed_authors>Ferner M</pubmed_authors><pubmed_authors>Brandes IF</pubmed_authors><pubmed_authors>Felzen M</pubmed_authors><pubmed_authors>Winterhalter M</pubmed_authors><pubmed_authors>Degenhardt F</pubmed_authors><pubmed_authors>Smul T</pubmed_authors><pubmed_authors>Wolwender E</pubmed_authors><pubmed_authors>Laufenberg-Feldmann R</pubmed_authors><pubmed_authors>Reinhard K</pubmed_authors><pubmed_authors>Roewer N</pubmed_authors><pubmed_authors>Struck R</pubmed_authors><pubmed_authors>Hoeft A</pubmed_authors><pubmed_authors>Bergt S</pubmed_authors><pubmed_authors>Stoppe C</pubmed_authors><pubmed_authors>Weber C</pubmed_authors><pubmed_authors>Kortgen A</pubmed_authors><pubmed_authors>Coburn M</pubmed_authors><pubmed_authors>Reyher C</pubmed_authors><pubmed_authors>Wollbrueck M</pubmed_authors><pubmed_authors>Weigand M</pubmed_authors><pubmed_authors>Cremer J</pubmed_authors><pubmed_authors>Francksen H</pubmed_authors><pubmed_authors>Niemann B</pubmed_authors><pubmed_authors>Pense K</pubmed_authors><pubmed_authors>Baumgarten G</pubmed_authors><pubmed_authors>Iken S</pubmed_authors><pubmed_authors>Broch O</pubmed_authors><pubmed_authors>Scholz J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study.</name><description>&lt;h4>Background&lt;/h4>The aim of our study was the identification of genetic variants associated with postoperative complications after cardiac surgery.&lt;h4>Methods&lt;/h4>We conducted a prospective, double-blind, multicenter, randomized trial (RIPHeart). We performed a genome-wide association study (GWAS) in 1170 patients of both genders (871 males, 299 females) from the RIPHeart-Study cohort. Patients undergoing non-emergent cardiac surgery were included. Primary endpoint comprises a binary composite complication rate covering atrial fibrillation, delirium, non-fatal myocardial infarction, acute renal failure and/or any new stroke until hospital discharge with a maximum of fourteen days after surgery.&lt;h4>Results&lt;/h4>A total of 547,644 genotyped markers were available for analysis. Following qua</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2026-05-04T08:18:34.541Z</modification><creation>2019-03-26T22:43:48Z</creation></dates><accession>S-EPMC6345037</accession><cross_references><pubmed>30678657</pubmed><doi>10.1186/s12872-019-1002-x</doi></cross_references></HashMap>