BARTÁKOVÁ, Vendula, Katarína KURICOVÁ, Lukáš PÁCAL, Zuzana NOVÁ, Veronika DVOŘÁKOVÁ, Martina ŠVRČKOVÁ, Denisa MALÚŠKOVÁ, Ivana SVOBODOVÁ, Jitka ŘEHOŘOVÁ, Jan SVOJANOVSKÝ, Jindřich OLŠOVSKÝ, Jana BĚLOBRÁDKOVÁ and Kateřina KAŇKOVÁ. Hyperuricemia contributes to the faster progression of diabetic kidney disease in type 2 diabetes mellitus. Journal of Diabetes and its Complications. New York: Elsevier Science Inc., 2016, vol. 30, No 7, p. 1300-1307. ISSN 1056-8727. Available from: https://dx.doi.org/10.1016/j.jdiacomp.2016.06.002.
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Basic information
Original name Hyperuricemia contributes to the faster progression of diabetic kidney disease in type 2 diabetes mellitus
Authors BARTÁKOVÁ, Vendula (203 Czech Republic, guarantor, belonging to the institution), Katarína KURICOVÁ (703 Slovakia, belonging to the institution), Lukáš PÁCAL (203 Czech Republic, belonging to the institution), Zuzana NOVÁ (703 Slovakia, belonging to the institution), Veronika DVOŘÁKOVÁ (203 Czech Republic, belonging to the institution), Martina ŠVRČKOVÁ (203 Czech Republic, belonging to the institution), Denisa MALÚŠKOVÁ (203 Czech Republic, belonging to the institution), Ivana SVOBODOVÁ (203 Czech Republic, belonging to the institution), Jitka ŘEHOŘOVÁ (203 Czech Republic), Jan SVOJANOVSKÝ (203 Czech Republic), Jindřich OLŠOVSKÝ (203 Czech Republic), Jana BĚLOBRÁDKOVÁ (203 Czech Republic) and Kateřina KAŇKOVÁ (203 Czech Republic, belonging to the institution).
Edition Journal of Diabetes and its Complications, New York, Elsevier Science Inc. 2016, 1056-8727.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30202 Endocrinology and metabolism
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 2.734
RIV identification code RIV/00216224:14110/16:00088861
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1016/j.jdiacomp.2016.06.002
UT WoS 000382097600016
Keywords in English Diabetic kidney disease; uric acid; allopurinol; type 2 diabetes mellitus; mortality; single nucleotide polymorphism
Tags EL OK
Tags International impact, Reviewed
Changed by Changed by: Ing. Mgr. Věra Pospíšilíková, učo 9005. Changed: 24/10/2016 15:16.
Abstract
The aims of the study: (i) to ascertain prognostic value of serum uric acid (SUA) for diabetic kidney disease (DKD) progression and major adverse cardiovascular event (MACE) in a cohort of T2DM patients, (ii) to ascertain eventual protective effect of allopurinol treatment, (iii) to determine the effect of genetic variability in UA transporters on DKD progression, and (iv) to define optimal cut-off values for SUA in patients with DKD. Study comprised 422 subjects with diabetes duration at least 15 years. Participants were categorized into stable or progressors according to their change in albuminuria or chronic kidney disease (CKD) stage. At baseline, 68% patients had hyperuricemia (SUA above 420 umol/l for men and above 360 umol/l for women and/or allopurinol treatment). Five SNPs in the SLC2A9 and ABCG2 genes were determined by PCR. Time-to-event analysis with subgroups defined by the presence/absence of initial hyperuricemia revealed significant differences in all three end-points (P les than 0.0001 for DKD progression, P = 0.0022 for MACE and P = 0.0002 for death, log-rank test). Subjects with normal SUA not requiring allopurinol had median time to DKD progression 49 months compared with remaining subjects (32 months, P = 0.0002, log rank test). Multivariate Cox regression model revealed hyperuricemia (i.e. high SUA and/or allopurinol treatment) significant predictor of DKD progression independent of baseline CKD stage. Optimal cut-off values identified by ROC analysis for T2DM subjects were less than 377.5 umol/l for men and less than 309.0 umol/l for women. We found no differences in allele or genotype frequencies in selected SNPs between patients with and without hyperuricemia (all P more than 0.05). Initial hyperuricemia or need for allopurinol are independent risk factors for DKD progression and that SUA levels in diabetics subjects conferring protection against DKD progression might be lower than current cut-offs for general population.
Links
NT13198, research and development projectName: Pentózový cyklus jako potenciální nový terapeutický cíl v prevenci diabetických komplikací
Investor: Ministry of Health of the CR
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