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dc.contributor.authorCasanova, Alfredo G. 
dc.contributor.authorMorales Martín, Ana Isabel 
dc.contributor.authorVicente Vicente, Rosa Laura 
dc.contributor.authorLópez Hernández, Francisco José 
dc.date.accessioned2025-10-31T11:06:53Z
dc.date.available2025-10-31T11:06:53Z
dc.date.issued2024-03-26
dc.identifier.citationCasanova, A. G., Morales, A. I., Vicente-Vicente, L., y López-Hernández, F. J. (2024). Effect of uric acid reduction on chronic kidney disease. Systematic review and meta-analysis. Frontiers in Pharmacology, 15, 1373258. https://doi.org/10.3389/fphar.2024.1373258es_ES
dc.identifier.issn1663-9812
dc.identifier.urihttp://hdl.handle.net/10366/167575
dc.description.abstract[EN]Accumulating evidence suggests that hyperuricemia is a pathological factor in the development and progression of chronic kidney disease. However, the potential benefit afforded by the control of uric acid (UA) is controversial. Individual studies show discrepant results, and most existing meta-analysis, especially those including the larger number of studies, lack a placebo or control group as they aim to compare efficacy between drugs. On these grounds, we performed a me-ta-analysis restricted to studies including the action of any anti-gout therapies referenced to a control or placebo arm. This approach allows for a clearer association between UA reduction and renal effect. Of the twenty-nine papers included, most used allopurinol and febuxostat and, therefore, solid conclusions could only be obtained for these drugs. Both were very effective in reducing UA, but only allopurinol was able to significantly improve glomerular filtration rate (GFR), although not in a dose-dependent manner. These results raised doubts as to whether it is the hypouricemic effect of anti-gout drugs, or a pleiotropic effect, what provides protection of kidney function. Accordingly, in a correlation study that we next performed between UA reduction and GFR improvement, no association was found, which suggests that additional mechanisms may be involved. Of note, most trials show large inter-individual response variability, probably because they included patients with heterogeneous phenotypes and pathological characteristics, including different stages of CKD and comorbidities. This highlights the need to sub classify the effect of UA-lowering therapies according to the pathological scenario, in order to identify those CKD patients that may benefit most from them. Systematic Review Registration: CRD42022306646 https://www.crd.york.ac.uk/prospero/.es_ES
dc.language.isoenges_ES
dc.publisherFrontiers Mediaes_ES
dc.rightsAttribution-4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectallopurinoles_ES
dc.subjectchronic kidney diseasees_ES
dc.subjectpreventiones_ES
dc.subjectprotectiones_ES
dc.subjecturic acid-lowering therapyes_ES
dc.subject.meshUric Acid *
dc.subject.meshAllopurinol *
dc.subject.meshKidney Diseases *
dc.titleEffect of uric acid reduction on chronic kidney disease. Systematic review and meta-analysises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.3389/fphar.2024.1373258es_ES
dc.subject.unesco3209 Farmacologíaes_ES
dc.identifier.doi10.3389/fphar.2024.1373258
dc.relation.projectIDPI20/01351es_ES
dc.relation.projectIDRD21/0005/0004es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.pmid38601468
dc.journal.titleFrontiers in pharmacologyes_ES
dc.volume.number15es_ES
dc.page.initial1373258es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decsácido úrico *
dc.subject.decsalopurinol *
dc.subject.decsenfermedades renales *


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