Method for identifying persons with increased genetic risk of decease after myocardial infarction

摘要

In the present invention, there is described a method for identifying persons with increased genetic risk of decease due to cardiovascular complications within 6 months from the moment of occurrence of acute myocardial infarction wherein the method is characterized in that there is determined in a biological sample taken from a patient body the intensity of gene expression and genetic loci ADORA3, (M97723), ERLIN1, CLYBL, TCEA3, (BC070337), HSD17B8, FLT3, AXIN2 and (CR596519). Subsequently logarithmic value of the expression intensity at the base of 2 is then compared with a reference value of the expression intensity, whereby a deviation from the reference value equal to at least a minimum deviation of all indicated genes and genetic loci represents an increased risk.