Our primary hypothesis is that a risk score comprised of approximately 10 single nucleotide polymorphisms (SNPs) that are associated with atrial fibrillation at the Genome Wide Association Study (GWAS) level is associated with the development of atrial fibrillation among previously undiagnosed patients at high risk for atrial fibrillation. A current example of these SNPs is shown in Table 1. As a secondary hypothesis, we will test the association between atrial fibrillation diagnosed in this study with a subset of SNPs reported to be associated with atrial fibrillation and with fine-mapping SNPs. We will also test the association between atrial fibrillation of less than and greater than 30 seconds and a panel of approximately 10 SNPs.
Study Type
OBSERVATIONAL
Enrollment
928
Scripps Clinic
La Jolla, California, United States
Association between events of Atrial Fibrillation and 4-SNP risk score
SNP effect sizes and frequencies were determined from the literature and the International HapMap Project database as indicated in Table 1. Expected occurrences of atrial fibrillation in the two groups were calculated using reference to previous studies as outlined above \[7, 8, 33\]. We expect 80 atrial fibrillation events in a 650 high-risk patients \[48, 49\]. Using these event rates and an alpha error of 5%, the power to detect an association between a 10-SNPs risk score and atrial fibrillation is \>90%. The power to detect association between a 4-SNP risk score and atrial fibrillation is \>80%.
Time frame: One time
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