Druggability of coronary artery disease risk loci

Vinicius Tragante*, Daiane Hemerich, Mohammad Alshabeeb, Ingrid Brænne, Harri Lempiäinen, Riyaz S. Patel, Hester M. Den Ruijter, Michael R. Barnes, Jason H. Moore, Heribert Schunkert, Jeanette Erdmann, Folkert W. Asselbergs

*Korrespondierende/r Autor/-in für diese Arbeit
2 Zitate (Scopus)


BACKGROUND: Genome-wide association studies have identified multiple loci associated with coronary artery disease and myocardial infarction, but only a few of these loci are current targets for on-market medications. To identify drugs suitable for repurposing and their targets, we created 2 unique pipelines integrating public data on 49 coronary artery disease/myocardial infarction-genome-wide association studies loci, drug-gene interactions, side effects, and chemical interactions. METHODS: We first used publicly available genome-wide association studies results on all phenotypes to predict relevant side effects, identified drug-gene interactions, and prioritized candidates for repurposing among existing drugs. Second, we prioritized gene product targets by calculating a druggability score to estimate how accessible pockets of coronary artery disease/myocardial infarction-associated gene products are, then used again the genome-wide association studies results to predict side effects, excluded loci with widespread cross-tissue expression to avoid housekeeping and genes involved in vital processes and accordingly ranked the remaining gene products. RESULTS: These pipelines ultimately led to 3 suggestions for drug repurposing: pentolinium, adenosine triphosphate, and riociguat (to target CHRNB4, ACSS2, and GUCY1A3, respectively); and 3 proteins for drug development: LMOD1 (leiomodin 1), HIP1 (huntingtin-interacting protein 1), and PPP2R3A (protein phosphatase 2, regulatory subunit b-double prime, α). Most current therapies for coronary artery disease/ myocardial infarction treatment were also rediscovered. CONCLUSIONS: Integration of genomic and pharmacological data may prove beneficial for drug repurposing and development, as evidence from our pipelines suggests.

ZeitschriftCirculation: Genomic and Precision Medicine
PublikationsstatusVeröffentlicht - 2018

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  • Querschnittsbereich: Medizinische Genetik


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