| Literature DB >> 32193173 |
Dermot F Reilly1, Matthew D Breyer2.
Abstract
As opposed to diseases such as cancer, autoimmune disease, and diabetes, identifying drugs to treat CKD has proven significantly more challenging. Over the past 2 decades, new potential therapeutic targets have been identified as genetically altered proteins involved in rare monogenetic kidney diseases. Other possible target genes have been implicated through common genetic polymorphisms associated with CKD in the general population. Significant challenges remain before translating these genetic insights into clinical therapies for CKD. This paper will discuss how genetic variants may be leveraged to develop drugs and will especially focus on those genes associated with CKD to exemplify the value and challenges in including genetic information in the drug development pipeline.Entities:
Keywords: autoimmune diseases; chronic; diabetes mellitus; diabetic nephropathy; drug development; drug discovery; drug transporter; genetic; genetic renal disease; genomics; kidney; neoplasms; polymorphism; renal insufficiency
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Year: 2020 PMID: 32193173 PMCID: PMC7480559 DOI: 10.2215/CJN.11070919
Source DB: PubMed Journal: Clin J Am Soc Nephrol ISSN: 1555-9041 Impact factor: 8.237