Association between serum uric acid and renal outcome in patients with biopsy-confirmed diabetic nephropathy

Author:

Zou Yutong12,Zhao Lijun12,Zhang Junlin12,Wang Yiting12,Wu Yucheng12,Ren Honghong12,Wang Tingli12,Zhang Rui12,Wang Jiali12,Zhao Yuancheng12,Qin Chunmei12,Xu Huan3,Li Lin3,Chai Zhonglin4,Cooper Mark E4,Tong Nanwei56,Liu Fang12ORCID

Affiliation:

1. 1Division of Nephrology, West China Hospital of Sichuan University, Chengdu, Sichuan, China

2. 2Laboratory of Diabetic Kidney Disease, Centre of Diabetes and Metabolism Research, West China Hospital of Sichuan University, Chengdu, Sichuan, China

3. 3Division of Pathology, West China Hospital of Sichuan University, Chengdu, Sichuan, China

4. 4Department of Diabetes, Central Clinical School, Monash University, Melbourne, Australia

5. 5Division of Endocrinology, West China Hospital of Sichuan University, Chengdu, Sichuan, China

6. 6Centre of Diabetes and Metabolism Research, West China Hospital of Sichuan University, Chengdu, Sichuan, China

Abstract

Objective To investigate the relationship between serum uric acid (SUA) level and renal outcome in patients with type 2 diabetes mellitus (T2DM) and diabetic nephropathy (DN). Methods A total of 393 Chinese patients with T2DM and biopsy-proven DN and followed at least 1 year were enrolled in this study. Patients were stratified by the quartiles of baseline level of SUA: Q1 group: 286.02 ± 46.66 μmol/L (n = 98); Q2 group: 358.23 ± 14.03 μmol/L (n = 99); Q3 group: 405.50 ± 14.59 μmol/L (n = 98) and Q4 group: 499.14 ± 56.97μmol/L (n = 98). Renal outcome was defined by progression to end-stage renal disease (ESRD). Kaplan–Meier survival analysis and Cox proportional hazards model were used to analyze the association between SUA quartiles and the renal outcomes. Results During the median 3-year follow-up period, there were 173 ESRD outcome events (44.02%). No significant difference between SUA level and the risk of progression of DN (P = 0.747) was shown in the Kaplan–Meier survival analysis. In multivariable-adjusted model, hazard ratios for developing ESRD were 1.364 (0.621–2.992; P = 0.439), 1.518 (0.768–3.002; P = 0.230) and 1.411 (0.706–2.821; P = 0.330) for the Q2, Q3 and Q4, respectively, in comparison with the Q1 (P = 0.652). Conclusions No significant association between SUA level and renal outcome of ESRD in Chinese patients with T2DM and DN was found in our study. Besides, the role of uric acid-lowering therapy in delaying DN progression and improving ESRD outcome had not yet been proven. Further study was needed to clarify the renal benefit of the uric acid-lowering therapy in the treatment of DN.

Publisher

Bioscientifica

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

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