Asymptomatic Hyperuricemia and the Kidney: Lessons from the URRAH Study

Chronic kidney disease (CKD) is a prevalent global health concern affecting approximately 850 million people worldwide, with a significant and rising mortality rate. CKD often coexists with hyperuricemia (HSUA), which is also increasingly common due to its association with hypertension, obesity, and...

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Main Authors: Cecilia Barnini, Elisa Russo, Giovanna Leoncini, Maria Carla Ghinatti, Lucia Macciò, Michela Piaggio, Francesca Viazzi, Roberto Pontremoli
Format: Article
Language:English
Published: MDPI AG 2025-01-01
Series:Metabolites
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Online Access:https://www.mdpi.com/2218-1989/15/1/11
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author Cecilia Barnini
Elisa Russo
Giovanna Leoncini
Maria Carla Ghinatti
Lucia Macciò
Michela Piaggio
Francesca Viazzi
Roberto Pontremoli
author_facet Cecilia Barnini
Elisa Russo
Giovanna Leoncini
Maria Carla Ghinatti
Lucia Macciò
Michela Piaggio
Francesca Viazzi
Roberto Pontremoli
author_sort Cecilia Barnini
collection DOAJ
description Chronic kidney disease (CKD) is a prevalent global health concern affecting approximately 850 million people worldwide, with a significant and rising mortality rate. CKD often coexists with hyperuricemia (HSUA), which is also increasingly common due to its association with hypertension, obesity, and diabetes. The interplay between hyperuricemia and CKD is complex; while in vitro studies and animal models support a role for uric acid mediating glomerular and tubule-interstitial damage, and HSUA has been shown to predict the onset and progression of CKD, the expectations of renal protection by the use of urate lowering treatment (ULT) are inconsistent. A significant challenge in managing asymptomatic HSUA in CKD patients lies in determining the appropriate SUA threshold values. Recent research, including the URRAH project, has sought to identify SUA cut-offs predictive of cardiovascular mortality, but these thresholds may vary depending on the severity of CKD. This variability complicates the establishment of universal guidelines for treating asymptomatic HSUA, leading to a lack of specific recommendations in clinical practice. In conclusion, while hyperuricemia is recognized as a prognostic factor for CKD and cardiovascular risk, more research is needed to refine the threshold values for SUA and to identify which patients may benefit from ULT. Stratification based on glomerular filtration rate may be necessary to tailor the treatments and improve outcomes in this population.
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spelling doaj-art-e4a79198cd544f2d99a7ec7b8537fda82025-01-24T13:41:09ZengMDPI AGMetabolites2218-19892025-01-011511110.3390/metabo15010011Asymptomatic Hyperuricemia and the Kidney: Lessons from the URRAH StudyCecilia Barnini0Elisa Russo1Giovanna Leoncini2Maria Carla Ghinatti3Lucia Macciò4Michela Piaggio5Francesca Viazzi6Roberto Pontremoli7Department of Internal Medicine IV, Nephrology and Hypertension, Medical University Innsbruck, 6020 Innsbruck, Tirol, AustriaDepartment of Internal Medicine and Medical Specialties (DiMI), University of Genoa, 16132 Genoa, ItalyDepartment of Internal Medicine and Medical Specialties (DiMI), University of Genoa, 16132 Genoa, ItalyInternal Medicine Unit, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, ItalyDepartment of Internal Medicine and Medical Specialties (DiMI), University of Genoa, 16132 Genoa, ItalyUnit of Nephrology, Dialysis and Transplantation, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, ItalyDepartment of Internal Medicine and Medical Specialties (DiMI), University of Genoa, 16132 Genoa, ItalyDepartment of Internal Medicine and Medical Specialties (DiMI), University of Genoa, 16132 Genoa, ItalyChronic kidney disease (CKD) is a prevalent global health concern affecting approximately 850 million people worldwide, with a significant and rising mortality rate. CKD often coexists with hyperuricemia (HSUA), which is also increasingly common due to its association with hypertension, obesity, and diabetes. The interplay between hyperuricemia and CKD is complex; while in vitro studies and animal models support a role for uric acid mediating glomerular and tubule-interstitial damage, and HSUA has been shown to predict the onset and progression of CKD, the expectations of renal protection by the use of urate lowering treatment (ULT) are inconsistent. A significant challenge in managing asymptomatic HSUA in CKD patients lies in determining the appropriate SUA threshold values. Recent research, including the URRAH project, has sought to identify SUA cut-offs predictive of cardiovascular mortality, but these thresholds may vary depending on the severity of CKD. This variability complicates the establishment of universal guidelines for treating asymptomatic HSUA, leading to a lack of specific recommendations in clinical practice. In conclusion, while hyperuricemia is recognized as a prognostic factor for CKD and cardiovascular risk, more research is needed to refine the threshold values for SUA and to identify which patients may benefit from ULT. Stratification based on glomerular filtration rate may be necessary to tailor the treatments and improve outcomes in this population.https://www.mdpi.com/2218-1989/15/1/11uric acidkidney diseasecut-offscardiovascular risk
spellingShingle Cecilia Barnini
Elisa Russo
Giovanna Leoncini
Maria Carla Ghinatti
Lucia Macciò
Michela Piaggio
Francesca Viazzi
Roberto Pontremoli
Asymptomatic Hyperuricemia and the Kidney: Lessons from the URRAH Study
Metabolites
uric acid
kidney disease
cut-offs
cardiovascular risk
title Asymptomatic Hyperuricemia and the Kidney: Lessons from the URRAH Study
title_full Asymptomatic Hyperuricemia and the Kidney: Lessons from the URRAH Study
title_fullStr Asymptomatic Hyperuricemia and the Kidney: Lessons from the URRAH Study
title_full_unstemmed Asymptomatic Hyperuricemia and the Kidney: Lessons from the URRAH Study
title_short Asymptomatic Hyperuricemia and the Kidney: Lessons from the URRAH Study
title_sort asymptomatic hyperuricemia and the kidney lessons from the urrah study
topic uric acid
kidney disease
cut-offs
cardiovascular risk
url https://www.mdpi.com/2218-1989/15/1/11
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