Hubbard, Demetria
Colantonio, Lisandro D.
Rosenson, Robert S.
Brown, Todd M.
Jackson, Elizabeth A.
Huang, Lei
Orroth, Kate K.
Reading, Stephanie
Woodward, Mark
Bittner, Vera
Gutierrez, Orlando M.
Safford, Monika M.
Farkouh, Michael E.
Muntner, Paul
Funding for this research was provided by:
Amgen
Article History
Received: 23 November 2020
Accepted: 15 February 2021
First Online: 1 March 2021
Ethics approval and consent to participate
: The Institutional Review Board at the University of Alabama at Birmingham approved the study and waived the requirement to obtain informed consent.
: Not applicable.
: KO and SR: Amgen employees and have stock in Amgen. OG: research support and consulting fees from Amgen and Akebia; consulting fees from QED; research support from GSK. TMB: research support from Amgen. PM: research support and consulting fees from Amgen. MW: consulting fees from Kirin and Amgen. RSR: research support from Amgen, Astra Zeneca, Novartis and Regeneron; consulting fees from Amgen, Amyrt, C5, CVS Caremark, Novartis and Regeneron; honoraria from Amgen, Kowa and Regeneron; royalties from Wolters Kluwer (UpToDate); has stock in MediMergent, LLC., EAJ: receives research support from Amgen and NIH; consulting fees from the American College of Cardiology, UpToDate, and McKesson; expert witness for DeBlase Brown Everly, LLP, and editor for American Heart Association. MEF: receives research support from Amgen, Novartis and Novo Nordisk. VB: Executive Steering Committee: ODYSSEY OUTCOMES trial (Sanofi); National Coordinator: STRENGTH (Astra Zeneca), DalGene (Dalcor), and CLEAR (Esperion); Local site investigator: ORION IV; Research support: Amgen; Consultant: Sanofi (2018). LDC: receives research support from Amgen, Inc. DH and LH: no disclosures.