WARE: Wet AMD Risk-Evaluation Tool as a Clinical Decision-Support System Integrating Genetic and Non-Genetic Factors.
Détails
ID Serval
serval:BIB_54231F853CCB
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
WARE: Wet AMD Risk-Evaluation Tool as a Clinical Decision-Support System Integrating Genetic and Non-Genetic Factors.
Périodique
Journal of personalized medicine
ISSN
2075-4426 (Print)
ISSN-L
2075-4426
Statut éditorial
Publié
Date de publication
24/06/2022
Peer-reviewed
Oui
Volume
12
Numéro
7
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: epublish
Publication Status: epublish
Résumé
Given the multifactorial features characterizing age-related macular degeneration (AMD), the availability of a tool able to provide the individual risk profile is extremely helpful for personalizing the follow-up and treatment protocols of patients. To this purpose, we developed an open-source computational tool named WARE (Wet AMD Risk Evaluation), able to assess the individual risk profile for wet AMD based on genetic and non-genetic factors. In particular, the tool uses genetic risk measures normalized for their relative frequencies in the general population and disease prevalence. WARE is characterized by a user-friendly web page interface that is intended to assist clinicians in reporting risk assessment upon patient evaluation. When using the tool, plots of population risk distribution highlight a "low-risk zone" and a "high-risk zone" into which subjects can fall depending on their risk-assessment result. WARE represents a reliable population-specific computational system for wet AMD risk evaluation that can be exploited to promote preventive actions and personalized medicine approach for affected patients or at-risk individuals. This tool can be suitable to compute the disease risk adjusted to different populations considering their specific genetic factors and related frequencies, non-genetic factors, and the disease prevalence.
Mots-clé
AMD, aging, genetic and non-genetic factors, personalized approach, risk evaluation, tool
Pubmed
Web of science
Open Access
Oui
Création de la notice
01/02/2023 10:06
Dernière modification de la notice
16/02/2023 11:02