<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>55</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>12(4)</volume><submitter>Viazzi F</submitter><pubmed_abstract>&lt;h4>Background and aims&lt;/h4>Metabolic Syndrome (Mets) and increased serum uric acid (SUA), are well known renal risk predictors and often coexist in patients with type 2 diabetes (T2D). Whether they independently contribute to the onset of CKD is at present unclear.&lt;h4>Methods and results&lt;/h4>Within the AMD Annals database we identified patients with T2D and normal renal function and urine albumin excretion at baseline and regular follow-up visits during a 4-year period. Blood pressure, BMI, HDL, triglycerides, and SUA were available in 14,267 patients. The association between Mets and/or hyperuricemia (HU, top fifth gender specific quintile) and the occurrence of renal outcomes were evaluated.&lt;h4>Results&lt;/h4>At baseline 59% of patients (n = 8,408) showed Mets and 18% (n = 2,584) HU. Over the 4-year follow-up, 14% (n = 1,990) developed low eGFR (i.e. below 60 mL/min/1.73 m2), and 26% (n = 3,740) albuminuria. After adjustment for confounders, BP≥130/85, low HDL, triglycerides ≥150 and HU were independently related to the development of low eGFR (1.57, P&lt;0.001; 1.13, P = 0.056; 1.18, P = 0.008; 1.26, P = 0.001) and of albuminuria (1.35, P&lt;0.001; 1.18, P = 0.001; 1.15, P = 0.002; 1.24, P = 0.001), respectively. The incidence of low eGFR was higher in patients with HU independent of the presence or absence of Mets (21%, OR 1.30, p = 0.009 and 20%, 1.57, p&lt;0.000 respectively), while albuminuria occurred more frequently in those with Mets and HU (32%, OR 1.25, p = 0.005) as compared to the reference group.&lt;h4>Conclusions&lt;/h4>HU and Mets are independent predictors of CKD and its individual components in patients with T2D.</pubmed_abstract><journal>PloS one</journal><pagination>e0176058</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5396926</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Metabolic syndrome, serum uric acid and renal risk in patients with T2D.</pubmed_title><pmcid>PMC5396926</pmcid><pubmed_authors>AMD-Annals Study Group</pubmed_authors><pubmed_authors>Fioretto P</pubmed_authors><pubmed_authors>Pontremoli R</pubmed_authors><pubmed_authors>Russo G</pubmed_authors><pubmed_authors>Giorda C</pubmed_authors><pubmed_authors>Genovese S</pubmed_authors><pubmed_authors>De Cosmo S</pubmed_authors><pubmed_authors>Viazzi F</pubmed_authors><pubmed_authors>Piscitelli P</pubmed_authors><pubmed_authors>Ceriello A</pubmed_authors><pubmed_authors>Guida P</pubmed_authors><view_count>55</view_count></additional><is_claimable>false</is_claimable><name>Metabolic syndrome, serum uric acid and renal risk in patients with T2D.</name><description>&lt;h4>Background and aims&lt;/h4>Metabolic Syndrome (Mets) and increased serum uric acid (SUA), are well known renal risk predictors and often coexist in patients with type 2 diabetes (T2D). Whether they independently contribute to the onset of CKD is at present unclear.&lt;h4>Methods and results&lt;/h4>Within the AMD Annals database we identified patients with T2D and normal renal function and urine albumin excretion at baseline and regular follow-up visits during a 4-year period. Blood pressure, BMI, HDL, triglycerides, and SUA were available in 14,267 patients. The association between Mets and/or hyperuricemia (HU, top fifth gender specific quintile) and the occurrence of renal outcomes were evaluated.&lt;h4>Results&lt;/h4>At baseline 59% of patients (n = 8,408) showed Mets and 18% (n = 2,584) HU. Over the 4-year follow-up, 14% (n = 1,990) developed low eGFR (i.e. below 60 mL/min/1.73 m2), and 26% (n = 3,740) albuminuria. After adjustment for confounders, BP≥130/85, low HDL, triglycerides ≥150 and HU were independently related to the development of low eGFR (1.57, P&lt;0.001; 1.13, P = 0.056; 1.18, P = 0.008; 1.26, P = 0.001) and of albuminuria (1.35, P&lt;0.001; 1.18, P = 0.001; 1.15, P = 0.002; 1.24, P = 0.001), respectively. The incidence of low eGFR was higher in patients with HU independent of the presence or absence of Mets (21%, OR 1.30, p = 0.009 and 20%, 1.57, p&lt;0.000 respectively), while albuminuria occurred more frequently in those with Mets and HU (32%, OR 1.25, p = 0.005) as compared to the reference group.&lt;h4>Conclusions&lt;/h4>HU and Mets are independent predictors of CKD and its individual components in patients with T2D.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017</publication><modification>2024-02-15T22:15:41.298Z</modification><creation>2019-03-27T02:41:36Z</creation></dates><accession>S-EPMC5396926</accession><cross_references><pubmed>28423036</pubmed><doi>10.1371/journal.pone.0176058</doi></cross_references></HashMap>