highly significantp = 0.0004
In contrast, subjects carrying either of the other two genotypes did not derive any benefit from this treatment, resulting in a highly significant SNP x fenofibrate interaction ( p = 0.0004).
In contrast, subjects carrying either of the other two genotypes did not derive any benefit from this treatment, resulting in a highly significant SNP x fenofibrate interaction ( p = 0.0004).
It should be noted that the CAD-PGRS used in these studies were different (based on 27 SNPs associated with CAD in FOURIER and based on six million variants in the ODYSSEY), yet they were both characterized by a clear trend for interaction with PCSK9i treatment (reported as significant in FOURIER and estimated to be significant in ODYSSEY).