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A Genomic Approach to Characterize the Vulnerable Patient – a Clinical Update Cover

A Genomic Approach to Characterize the Vulnerable Patient – a Clinical Update

Open Access
|Nov 2019

Abstract

Atherosclerosis is the elemental precondition for any cardiovascular disease and the predominant cause of ischemic heart disease that often leads to myocardial infarction. Systemic risk factors play an important role in the starting and progression of atherosclerosis. The complexity of the disease is caused by its multifactorial origin. Besides the traditional risk factors, genetic predisposition is also a strong risk factor. Many studies have intensively researched cardioprotective drugs, which can relieve myocardial ischemia and reperfusion injury, thereby reducing infarct size. A better understanding of abnormal epigenetic pathways in the myocardial pathology may result in new treatment options. Individualized therapy based on genome sequencing is important for an effective future medical treatment. Studies based on multiomics help to better understand the pathophysiological mechanism of several diseases at a molecular level. Epigenomic, transcriptomic, proteomic, and metabolomic research may be essential in detecting the pathological phenotype of myocardial ischemia and ischemic heart failure.

DOI: https://doi.org/10.2478/jim-2019-0023 | Journal eISSN: 2501-8132 | Journal ISSN: 2501-5974
Language: English
Page range: 141 - 144
Submitted on: Jul 29, 2019
Accepted on: Sep 5, 2019
Published on: Nov 12, 2019
Published by: Asociatia Transilvana de Terapie Transvasculara si Transplant KARDIOMED
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2019 Evelin Szabó, Zsolt Parajkó, Diana Opincariu, Monica Chițu, Nóra Raț, Imre Benedek, published by Asociatia Transilvana de Terapie Transvasculara si Transplant KARDIOMED
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.