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

The aim of our study was the identification of genetic variants associated with postoperative complications after cardiac surgery. We conducted a prospective, double-blind, multicenter, randomized trial (RIPHeart). We performed a genome-wide association study (GWAS) in 1170 patients of both genders...

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Veröffentlicht in:BMC cardiovascular disorders 2019-01, Vol.19 (1), p.26-26, Article 26
Hauptverfasser: Westphal, Sabine, Stoppe, Christian, Gruenewald, Matthias, Bein, Berthold, Renner, Jochen, Cremer, Jochen, Coburn, Mark, Schaelte, Gereon, Boening, Andreas, Niemann, Bernd, Kletzin, Frank, Roesner, Jan, Strouhal, Ulrich, Reyher, Christian, Laufenberg-Feldmann, Rita, Ferner, Marion, Brandes, Ivo F, Bauer, Martin, Kortgen, Andreas, Stehr, Sebastian N, Wittmann, Maria, Baumgarten, Georg, Struck, Rafael, Meyer-Treschan, Tanja, Kienbaum, Peter, Heringlake, Matthias, Schoen, Julika, Sander, Michael, Treskatsch, Sascha, Smul, Thorsten, Wolwender, Ewa, Schilling, Thomas, Degenhardt, Frauke, Franke, Andre, Mucha, Soeren, Tittmann, Lukas, Kohlhaas, Madeline, Fuernau, Georg, Brosteanu, Oana, Hasenclever, Dirk, Zacharowski, Kai, Meybohm, Patrick
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Sprache:eng
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Zusammenfassung:The aim of our study was the identification of genetic variants associated with postoperative complications after cardiac surgery. 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. A total of 547,644 genotyped markers were available for analysis. Following quality control and adjustment for clinical covariate, one SNP reached genome-wide significance (PHLPP2, rs78064607, p = 3.77 × 10 ) and 139 (adjusted for all other outcomes) SNPs showed promising association with p 
ISSN:1471-2261
1471-2261
DOI:10.1186/s12872-019-1002-x