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Xanthine Oxidase Inhibitors for Improving Renal Function in Chronic Kidney Disease Patients: An Updated Systematic Review and Meta-Analysis.
Pisano, Anna; Cernaro, Valeria; Gembillo, Guido; D'Arrigo, Graziella; Buemi, Michele; Bolignano, Davide.
Afiliação
  • Pisano A; CNR-Institute of Clinical Physiology, 89124 Reggio Calabria, Italy. pisanoanna@hotmail.it.
  • Cernaro V; Chair of Nephrology, Department of Clinical and Experimental Medicine, University of Messina, 98122 Messina, Italy. valecern82@virgilio.it.
  • Gembillo G; Chair of Nephrology, Department of Clinical and Experimental Medicine, University of Messina, 98122 Messina, Italy. guidogembillo@live.it.
  • D'Arrigo G; CNR-Institute of Clinical Physiology, 89124 Reggio Calabria, Italy. g.darrigostat@tin.it.
  • Buemi M; Chair of Nephrology, Department of Clinical and Experimental Medicine, University of Messina, 98122 Messina, Italy. buemim@unime.it.
  • Bolignano D; CNR-Institute of Clinical Physiology, 89124 Reggio Calabria, Italy. davide.bolignano@gmail.com.
Int J Mol Sci ; 18(11)2017 Oct 31.
Article em En | MEDLINE | ID: mdl-29088122
ABSTRACT

BACKGROUND:

Accruing evidence suggests that Xanthine Oxidase inhibitors (XOis) may bring direct renal benefits, besides those related to their hypo-uricemic effect. We hence aimed at performing a systematic review of randomized controlled trials (RCTs) to verify if treatment with XOis may improve renal outcomes in individuals with chronic kidney disease (CKD).

METHODS:

Ovid-MEDLINE, PubMed and CENTRAL databases were searched for RCTs comparing any XOi to standard therapy or placebo. The primary endpoint of interest was progression to End-Stage Kidney Disease (ESKD); secondary endpoints were changes in serum creatinine, glomerular filtration rate (eGFR), proteinuria and albuminuria.

RESULTS:

XOis treatment significantly reduced the risk of ESKD compared to the control (3 studies, 204 pts; RR = 0.42; 95% CI, 0.22, 0.80) and also improved eGFR in data pooled from RCTs with long follow-up times (>3 mo.) (4 studies, 357 pts; mean difference (MD) 6.82 mL/min/1.73 m²; 95% CI, 3.50, 10.15) and high methodological quality (blind design) (3 studies, 400 pts; MD 2.61 mL/min/1.73 m²; 95% CI, 0.23, 4.99). Conversely, no definite effects were apparently noticed on serum creatinine, proteinuria and albuminuria.

CONCLUSIONS:

XOis may represent a promising tool for retarding disease progression in CKD patients. Future trials are awaited to confirm the generalizability of these findings to the whole CKD population.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Piridinas / Xantina Oxidase / Alopurinol / Inibidores Enzimáticos / Insuficiência Renal Crônica / Febuxostat / Nitrilas Tipo de estudo: Clinical_trials / Systematic_reviews Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Mol Sci Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Piridinas / Xantina Oxidase / Alopurinol / Inibidores Enzimáticos / Insuficiência Renal Crônica / Febuxostat / Nitrilas Tipo de estudo: Clinical_trials / Systematic_reviews Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Mol Sci Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Itália