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. Author manuscript; available in PMC: 2016 Jun 1.
Published in final edited form as: Mayo Clin Proc. 2015 Jun;90(6):716–729. doi: 10.1016/j.mayocp.2015.03.016

Table 1.

Comprehensive evaluation of the scope, depth, and quality of pharmacogenomic evidence for cardiovascular drugs.

Cardiovascular drugs, N=71
 Positive PGxa 51 (71.8%)
 Clinical summary warranted 23 (32.4%)

Drug/variant pairs, N=884

Classification
Clinical summaries warranted
N N Level 1 Level 2 Level 3
 3+ Studies & PharmGKB 33 25 (75.8%) 4 6 15
 PharmGKB only 43 10 (23.3%) 0 5 5
 3+ Studies only 37 9 (24.3%) 0 4 5
 Other (None of above) 771 48 (6.2%) 0 32 16


884 92 (10.4%) 4 47 41

71 cardiovascular drugs with pharmacogenomic information were identified and critically reviewed, encompassing analysis of 884 unique drug/variant pairs; of the 71 drugs, 51 had positive pharmacogenomic findings in the literature (“Positive PGx”). The existence of 3 or more positive supporting publications for any given drug/variant pair (“3+ Studies”) and/or existence of a PharmGKB clinical annotation (“PharmGKB”) were the criteria used to stratify drug/variant pairs into one of four groups.