Personalized Medicine of Coronary Artery Disease
A special issue of Journal of Personalized Medicine (ISSN 2075-4426). This special issue belongs to the section "Methodology, Drug and Device Discovery".
Deadline for manuscript submissions: closed (28 February 2022) | Viewed by 20625
Special Issue Editor
Interests: ubiquitin proteasome; oncology; stents; apoptosis; cardiology; ubiquitination; coronary artery disease; vascular medicine; PCI
Special Issues, Collections and Topics in MDPI journals
Special Issue Information
As far as coronary artery disease is concerned, traditional risk factors fail to explain up to 50% of morbidity and mortality, and most traditional as well as novel risk factors have a genetic influence. Many studies have shown that treatment algorithms supported by consensus guidelines may lead to a situation in which a significant percentage of patients (such as patients with no Apo E genotype) are treated sub-optimally. Limiting disease management to the “one diet and standard drug therapy regimen fits all” approach is not the best option.
Recent studies suggest that the transformation of medicine in the 21st century can be called “P4 Medicine”, i.e., Predictive, Personalized, Preemptive, and Participatory. Moreover, the genome record might allow physicians to make treatment decisions based on patient genotypes. This might allow individuals to make appropriate lifestyle choices as well as to use appropriate drugs.
Personalized medicine is developing fast, and new data are emerging in huge amounts. This might enable the right risk assessment, diagnosis, prevention, and therapy specifically tailored to the unique characteristics of the individual, thus enhancing the quality of life as well as public health. Therefore, the aim of this Special Issue is to present recent developments in personalized medicine and coronary artery disease.
We invite authors to submit original clinical studies, reviews, meta-analyses, as well as case reports focused on the individualization of the prevention, diagnosis, and treatment of coronary artery disease, including myocardial infarction. We are soliciting not only genetic studies, but all papers on the broadly understood personalized medicine, including papers on novel drugs, medical devices, or approaches dedicated to special subsets of patients.
Dr. Jacek Bil
Guest Editor
Manuscript Submission Information
Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.
Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Journal of Personalized Medicine is an international peer-reviewed open access monthly journal published by MDPI.
Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2600 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.
Keywords
- pharmacogenetics
- pharmacogenomics
- response to drugs
- targeted treatment
- gene polymorphism
- gene–environment interaction
- CVD prevention
- residual cardiovascular risk
- e-Health
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