Over the last 10 to 15 years, animal and human observational studies have identified elevated levels of both proinflammatory secretory phospholipase A2-IIA and lipoprotein-associated phospholipase A2 as potential risk factors for coronary heart disease. However, Mendelian randomization, a genetic tool to test causality of a biomarker, and phase III randomized controlled trials of inhibitors of theses enzymes (varespladib and darapladib) converged to indicate that elevated levels are unlikely to be themselves causal of coronary heart disease and that inhibition had little or no clinical utility. The concordance of findings from Mendelian randomization and clinical trials suggests that for these 2 drugs, and for other novel biomarkers in future, validation of potential therapeutic targets by genetic studies (such as Mendelian randomization) before embarking on costly phase III randomized controlled trials could increase efficiency and offset the high risk of drug development, thereby facilitating discovery of new therapeutics and mitigating against the exuberant costs of drug development.

Original publication

DOI

10.1161/ATVBAHA.115.305234

Type

Journal article

Journal

Arterioscler Thromb Vasc Biol

Publication Date

11/2015

Volume

35

Pages

2281 - 2289

Keywords

Mendelian randomization, darapladib, secretory phospholipase-IIA, varespladib, 1-Alkyl-2-acetylglycerophosphocholine Esterase, Acetates, Animals, Benzaldehydes, Biomarkers, Coronary Disease, Humans, Indoles, Molecular Targeted Therapy, Oximes, Phospholipase A2 Inhibitors, Phospholipases A2, Secretory, Signal Transduction, Treatment Outcome