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Review
. 2023 Nov;11(11):822-835.
doi: 10.1016/S2213-8587(23)00165-1. Epub 2023 Oct 4.

Precision medicine for cardiometabolic disease: a framework for clinical translation

Affiliations
Review

Precision medicine for cardiometabolic disease: a framework for clinical translation

Paul W Franks et al. Lancet Diabetes Endocrinol. 2023 Nov.

Abstract

Cardiometabolic disease is a major threat to global health. Precision medicine has great potential to help to reduce the burden of this common and complex disease cluster, and to enhance contemporary evidence-based medicine. Its key pillars are diagnostics; prediction (of the primary disease); prevention (of the primary disease); prognosis (prediction of complications of the primary disease); treatment (of the primary disease or its complications); and monitoring (of risk exposure, treatment response, and disease progression or remission). To contextualise precision medicine in both research and clinical settings, and to encourage the successful translation of discovery science into clinical practice, in this Series paper we outline a model (the EPPOS model) that builds on contemporary evidence-based approaches; includes precision medicine that improves disease-related predictions by stratifying a cohort into subgroups of similar characteristics, or using participants' characteristics to model treatment outcomes directly; includes personalised medicine with the use of a person's data to objectively gauge the efficacy, safety, and tolerability of therapeutics; and subjectively tailors medical decisions to the individual's preferences, circumstances, and capabilities. Precision medicine requires a well functioning system comprised of multiple stakeholders, including health-care recipients, health-care providers, scientists, health economists, funders, innovators of medicines and technologies, regulators, and policy makers. Powerful computing infrastructures supporting appropriate analysis of large-scale, well curated, and accessible health databases that contain high-quality, multidimensional, time-series data will be required; so too will prospective cohort studies in diverse populations designed to generate novel hypotheses, and clinical trials designed to test them. Here, we carefully consider these topics and describe a framework for the integration of precision medicine in cardiometabolic disease.

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Conflict of interest statement

Declaration of interests CM serves or has served on the advisory panel for Novo Nordisk, Sanofi, Merck Sharp and Dohme, Eli Lilly, Novartis, AstraZeneca, Boehringer Ingelheim, Roche, Medtronic, ActoBio Therapeutics, Pfizer, Insulet, Imcyse, and Zealand Pharma, and reports that financial compensation for these activities has been received by KU Leuven; and serves or has served on the speakers' bureau for Novo Nordisk, Sanofi, Eli Lilly, Boehringer Ingelheim, Novartis, and AstraZeneca, and reports that financial compensation for these activities has been received by KU Leuven. JCF has received consulting fees or speaking honoraria from Goldfinch Bio, AstraZeneca, Novo Nordisk, and Merck Sharp and Dohme. HHS has received consulting fees from Bayer, Novo Nordisk, and Philips Ultrasound; and has stock in Novo Nordisk, Lundbeck, Bavarian Nordic, Zealand Pharma, AstraZeneca, Arrowhead, Pfizer, Agilent, Eli Lilly, and Airfinity. MR holds stock in Novo Nordisk. PWF has received consulting fees from Zoe. WTC, RWM, and CDAS declare no competing interests related to this work. PWF, RWM, MR, and HHS are employees of the Novo Nordisk Foundation. The views expressed in this Series paper do not necessarily reflect those of the institutions to which the authors are affiliated.

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