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dc.creatorTziastoudi M., Cholevas C., Stefanidis I., Theoharides T.C.en
dc.date.accessioned2023-01-31T10:21:32Z
dc.date.available2023-01-31T10:21:32Z
dc.date.issued2021
dc.identifier10.1016/j.clinthera.2021.09.020
dc.identifier.issn01492918
dc.identifier.urihttp://hdl.handle.net/11615/80239
dc.description.abstractA large subgroup of patients with chronic kidney disease still encounter serious adverse effects and lack of responsiveness to medications, possibly because of the interindividual genetic variability in genes involved in the metabolism and transport of the treatments used. As a consequence, several pharmacogenetic studies have been conducted in nephrology patients that examine the effect of genetic variants in response to treatment in kidney diseases. The present commentary focuses on immune-related genes (TNF [tumor necrosis factor], MIF [macrophage migration inhibitory factor], and IL-10 [interleukin 10]) or those genes that may regulate the response to immunosuppressive medications (ABCB1 [ATP binding cassette subfamily B member 1] and ITPA [inosine triphosphatase]) used in kidney diseases. These genes were selected from those showing significant results in a recent meta-analysis of pharmacogenetic studies of patients with chronic kidney disease. This commentary highlights that certain polymorphisms should be investigated in patients with kidney diseases, especially if they are to be administered immunosuppressive agents. In certain cases, flavonoids such as quercetin may be beneficial. © 2021 Elsevier Inc.en
dc.language.isoenen
dc.sourceClinical Therapeuticsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85120718720&doi=10.1016%2fj.clinthera.2021.09.020&partnerID=40&md5=7a2dbafb1fef7694e5a18bb54795a02a
dc.subjectgenisteinen
dc.subjectimmunosuppressive agenten
dc.subjectinosine triphosphateen
dc.subjectinterleukin 10en
dc.subjectkaempferolen
dc.subjectmacrophage migration inhibition factoren
dc.subjectmultidrug resistance protein 1en
dc.subjectmyricetinen
dc.subjectquercetinen
dc.subjectrutosideen
dc.subjecttumor necrosis factoren
dc.subjectArticleen
dc.subjectchronic kidney failureen
dc.subjectDNA polymorphismen
dc.subjectdrug metabolismen
dc.subjecthumanen
dc.subjectimmune-related geneen
dc.subjectimmunoregulationen
dc.subjectkidney diseaseen
dc.subjectmeta analysis (topic)en
dc.subjectnephrologyen
dc.subjectnonhumanen
dc.subjectpharmacogenetic testingen
dc.subjectrenal protectionen
dc.subjectsystematic review (topic)en
dc.subjectgenetic polymorphismen
dc.subjectgenotypeen
dc.subjectpharmacogeneticsen
dc.subjectsingle nucleotide polymorphismen
dc.subjectATP Binding Cassette Transporter, Subfamily B, Member 1en
dc.subjectGenotypeen
dc.subjectHumansen
dc.subjectNephrologyen
dc.subjectPharmacogeneticsen
dc.subjectPharmacogenomic Testingen
dc.subjectPolymorphism, Geneticen
dc.subjectPolymorphism, Single Nucleotideen
dc.subjectElsevier Inc.en
dc.titleImmune-Related Gene Polymorphisms and Pharmacogenetic Studies in Nephrologyen
dc.typejournalArticleen


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