T he clinical importance of ABO blood groups extends beyond the direct implications on transfusion and organ-transplantation compatibility. It is increasingly being recognized that individuals with non-O blood groups may be at elevated risk of venous thromboembolic events (VTEs), myocardial infarction, cerebrovascular ischemic events, and peripheral vascular disease compared with individuals with blood group O.1-4 This risk increase has been attributed to higher concentrations of factor VIII and von Willebrand factor. 5,6 Approximately 70% of the variation in the levels of these factors is genetically determined, and 30% of the explained variation is attributable to ABO blood groups. 7 In addition, Sode and colleagues 8 have shown that ABO blood type has an additive effect on the risk of VTE when combined with factor V Leiden R506Q and prothrombin G20210A mutations. A recent genome-wide association study has identified variants in the ABO locus that are associated with VTE, 9 providing additional clues to the genetic influence on thromboembolic risk. Available epidemiological data, however, fail to provide a coherent picture of the association between ABO blood group and thromboembolic risk. First, there is a Background-ABO blood groups have been shown to be associated with increased risks of venous thromboembolic and arterial disease. However, the reported magnitude of this association is inconsistent and is based on evidence from smallscale studies. Methods and Results-We used the SCANDAT2 (Scandinavian Donations and Transfusions) database of blood donors linked with other nationwide health data registers to investigate the association between ABO blood groups and the incidence of first and recurrent venous thromboembolic and arterial events. Blood donors in Denmark and Sweden between 1987 and 2012 were followed up for diagnosis of thromboembolism and arterial events. Poisson regression models were used to estimate incidence rate ratios as measures of relative risk. A total of 9170 venous and 24 653 arterial events occurred in 1 112 072 individuals during 13.6 million person-years of follow-up. Compared with blood group O, non-O blood groups were associated with higher incidence of both venous and arterial thromboembolic events. The highest rate ratios were observed for pregnancy-related venous thromboembolism (incidence rate ratio, 2.22; 95% confidence interval, 1.77-2.79), deep vein thrombosis (incidence rate ratio, 1.92; 95% confidence interval, 1.80-2.05), and pulmonary embolism (incidence rate ratio, 1.80; 95% confidence interval, 1.71-1.88).
Conclusions-In