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Lookup NU author(s): Professor John LoughlinORCiD
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND).
The ultimate goal of molecular genetic studies of human diseases is to translate the discoveries for patient benefit. For diseases that lack licensed disease modifying therapeutics, such as osteoarthritis (OA), the need is acute. OA is polygenic and affects older individuals, with a recent genome-wide study of over 800,000 individuals adding 52 novel association signals to those already reported on for this common arthritis. Many of the predicted effector genes of these signals encode proteins that are targets of drugs for other indications, highlighting re-purposing opportunities. Here, the potential for OA genetic data to translate is discussed, including whether the developmental origin of OA will limit the application of genetic risk data for disease modification purposes.
Author(s): Loughlin J
Publication type: Article
Publication status: Published
Journal: Trends in Molecular Medicine
Year: 2022
Volume: 28
Issue: 3
Pages: 176-182
Print publication date: 01/03/2022
Online publication date: 12/01/2022
Acceptance date: 03/01/2022
Date deposited: 17/01/2022
ISSN (print): 1471-4914
ISSN (electronic): 1471-499X
Publisher: Elsevier Ltd. * Trends Journals
URL: https://doi.org/10.1016/j.molmed.2021.12.007
DOI: 10.1016/j.molmed.2021.12.007
ePrints DOI: 10.57711/j897-hy20
PubMed id: 35033441
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