Precision Medicine and cardiac channelopathies: when dreams meet reality

Author:

Gnecchi Massimiliano123ORCID,Sala Luca4ORCID,Schwartz Peter J4ORCID

Affiliation:

1. Department of Cardiothoracic and Vascular Sciences—Coronary Care Unit and Laboratory of Clinical and Experimental Cardiology, Fondazione IRCCS Policlinico San Matteo, Viale Golgi 19, 27100 Pavia, Italy

2. Department of Molecular Medicine, Unit of Cardiology, University of Pavia, Viale Golgi 19, 27100 Pavia, Italy

3. Department of Medicine, University of Cape Town, J-Floor, Old Main Building, Groote Schuur Hospital, Observatory, 7925 Cape Town, South Africa

4. Istituto Auxologico Italiano IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Via Pier Lombardo 22 - 20135 Milan, Italy

Abstract

Abstract Precision Medicine (PM) is an innovative approach that, by relying on large populations’ datasets, patients’ genetics and characteristics, and advanced technologies, aims at improving risk stratification and at identifying patient-specific management through targeted diagnostic and therapeutic strategies. Cardiac channelopathies are being progressively involved in the evolution brought by PM and some of them are benefiting from these novel approaches, especially the long QT syndrome. Here, we have explored the main layers that should be considered when developing a PM approach for cardiac channelopathies, with a focus on modern in vitro strategies based on patient-specific human-induced pluripotent stem cells and on in silico models. PM is where scientists and clinicians must meet and integrate their expertise to improve medical care in an innovative way but without losing common sense. We have indeed tried to provide the cardiologist’s point of view by comparing state-of-the-art techniques and approaches, including revolutionary discoveries, to current practice. This point matters because the new approaches may, or may not, exceed the efficacy and safety of established therapies. Thus, our own eagerness to implement the most recent translational strategies for cardiac channelopathies must be tempered by an objective assessment to verify whether the PM approaches are indeed making a difference for the patients. We believe that PM may shape the diagnosis and treatment of cardiac channelopathies for years to come. Nonetheless, its potential superiority over standard therapies should be constantly monitored and assessed before translating intellectually rewarding new discoveries into clinical practice.

Funder

Leducq Foundation for Cardiovascular Research

Towards Precision Medicine with Human iPSCs for Cardiac Channelopathies

Marie Skłodowska-Curie Individual Fellowship

Biomedical Research Conducted by Young Researchers

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

Reference149 articles.

1. Inherited cardiac arrhythmias;Schwartz;Nat Rev Dis Primers,2020

2. Long QT syndrome modelling with cardiomyocytes derived from human-induced pluripotent stem cells;Sala;Arrhythm Electrophysiol Rev,2019

3. 1970-2020: 50 years of research on the long QT syndrome-from almost zero knowledge to precision medicine;Schwartz;Eur Heart J,2020

4. A new initiative on precision medicine;Collins;N Engl J Med,2015

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