4.6 Article

Evidence for Clinical Implementation of Pharmacogenomics in Cardiac Drugs

Journal

MAYO CLINIC PROCEEDINGS
Volume 90, Issue 6, Pages 716-729

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.mayocp.2015.03.016

Keywords

-

Funding

  1. University of Chicago
  2. National Institutes of Health (NIH) [K12 CA139160, K23 GM100288-01A1]
  3. NIH/National Heart, Lung, and Blood Institute [5 U01 HL105198-09]
  4. Conquer Cancer Foundation of the American Society for Clinical Oncology
  5. William F. O'Connor Foundation

Ask authors/readers for more resources

Objective: To comprehensively assess the pharmacogenomic evidence of routinely used drugs for clinical utility. Methods: Between January 2, 2011, and May 31, 2013, we assessed 71 drugs by identifying all drug/genetic variant combinations with published clinical pharmacogenomic evidence. Literature supporting each drug/variant pair was assessed for study design and methods, outcomes, statistical significance, and clinical relevance. Proposed clinical summaries were formally scored using a modified AGREE (Appraisal of Guidelines for Research and Evaluation) II instrument, including recommendation for or against guideline implementation. Results: Positive pharmacogenomic findings were identified for 51 of 71 cardiovascular drugs (71.8%), representing 884 unique drug/variant pairs from 597 publications. After analysis for quality and clinical relevance, 92 drug/variant pairs were proposed for translation into clinical summaries, encompassing 23 drugs (32.4% of drugs reviewed). All were recommended for clinical implementation using AGREE II, with mean +/- SD overall quality scores of 5.18 +/- 0.91 (of 7.0; range, 3.67-7.0). Drug guidelines had highest mean +/- SD scores in AGREE II domain 1 (Scope) (91.9 +/- 6.1 of 100) and moderate but still robust mean +/- SD scores in domain 3 (Rigor) (73.1 +/- 11.1), domain 4 (Clarity) (67.8 +/- 12.5), and domain 5 (Applicability) (65.8 +/- 10.0). Clopidogrel (CYP2C19), metoprolol (CYP2D6), simvastatin (rs4149056), dabigatran (rs2244613), hydralazine (rs1799983, rs1799998), and warfarin (CYP2C9/VKORC1) were distinguished by the highest scores. Seven of the 9 most commonly prescribed drugs warranted translation guidelines summarizing clinical pharmacogenomic information. Conclusion: Considerable clinically actionable pharmacogenomic information for cardiovascular drugs exists, supporting the idea that consideration of such information when prescribing is warranted. (C) 2015 Mayo Foundation for Medical Education and Research

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available