4.7 Review

Diagnosis and Risk Prediction of Dilated Cardiomyopathy in the Era of Big Data and Genomics

Journal

JOURNAL OF CLINICAL MEDICINE
Volume 10, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/jcm10050921

Keywords

dilated cardiomyopathy; diagnosis; prognosis; big data; artificial intelligence; deep learning; genetic

Funding

  1. Alexandre Suerman Stipendium
  2. Dutch Heart Foundation [2015T058, CVON 2015-12 eDETECT]
  3. UMC Utrecht
  4. Netherlands Heart Foundation [Dekker 2015T041]
  5. UCL Hospitals NIHR Biomedical Research Centre
  6. Netherlands Cardiovasular Research Initiative [CVON 2015-12 eDETECT]

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DCM is a leading cause of heart failure and LTVA, with great heterogeneity in phenotype and genotype making risk stratification challenging. Improved genetic testing has identified genotype-phenotype associations, allowing for better personalized risk assessments. Utilizing multivariable risk models, genetic risk scores, and advanced imaging techniques, as well as big data infrastructures and artificial intelligence, hold promise in enhancing predictive performance and prognosis of DCM.
Dilated cardiomyopathy (DCM) is a leading cause of heart failure and life-threatening ventricular arrhythmias (LTVA). Work-up and risk stratification of DCM is clinically challenging, as there is great heterogeneity in phenotype and genotype. Throughout the last decade, improved genetic testing of patients has identified genotype-phenotype associations and enhanced evaluation of at-risk relatives leading to better patient prognosis. The field is now ripe to explore opportunities to improve personalised risk assessments. Multivariable risk models presented as risk calculators can incorporate a multitude of clinical variables and predict outcome (such as heart failure hospitalisations or LTVA). In addition, genetic risk scores derived from genome/exome-wide association studies can estimate an individual's lifetime genetic risk of developing DCM. The use of clinically granular investigations, such as late gadolinium enhancement on cardiac magnetic resonance imaging, is warranted in order to increase predictive performance. To this end, constructing big data infrastructures improves accessibility of data by using electronic health records, existing research databases, and disease registries. By applying methods such as machine and deep learning, we can model complex interactions, identify new phenotype clusters, and perform prognostic modelling. This review aims to provide an overview of the evolution of DCM definitions as well as its clinical work-up and considerations in the era of genomics. In addition, we present exciting examples in the field of big data infrastructures, personalised prognostic assessment, and artificial intelligence.

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