Serum uric acid is associated with increased risk of posttransplantation diabetes in kidney transplant recipients: a prospective cohort study

被引:5
|
作者
Sotomayor, Camilo G. [1 ]
Oskooei, Sara Sokooti [1 ]
Bustos, Nicolas I. [2 ]
Nolte, Ilja M. [3 ]
Gomes-Neto, Antonio W. [1 ]
Erazo, Marcia [2 ]
Gormaz, Juan G. [2 ]
Berger, Stefan P. [1 ]
Navis, Gerjan J. [1 ]
Rodrigo, Ramon [2 ]
Dullaart, Robin P. F. [4 ]
Bakker, Stephan J. L. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Internal Med, Div Nephrol, Groningen, Netherlands
[2] Univ Chile, Fac Med, Santiago, Chile
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Endocrinol, Groningen, Netherlands
来源
关键词
Uric acid; Posttransplantation diabetes; Kidney transplantation; Inflammation; Oxidative stress; Metabolic syndrome; ENDOTHELIAL DYSFUNCTION; RENAL-TRANSPLANTATION; COMPETING RISKS; GLUCOSE-UPTAKE; HYPERURICEMIA; MELLITUS; SURVIVAL; INFLAMMATION; RECOMMENDATIONS; METABOLISM;
D O I
10.1016/j.metabol.2020.154465
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Serum uric acid (SUA) is associated with fasting glucose in healthy subjects, and prospective epidemological studies have shown that elevated SUA is associated with increased risk of type 2 diabetes. Whether SUA is independently associated with higher risk of posttransplantation diabetes mellitus (PTDM) in kidney transplant recipients (KTR) remains unknown. Methods: We performed a longitudinal cohort study of 524 adult KTR with a functioning graft >= 1-year, recruited at a university setting (2008-2011). Multivariable-adjusted Cox proportional-hazards regression analyses were performed to assess the association between time-updated SUA and risk of PTDM (defined according the American Diabetes Association's diagnostic criteria). Results: Mean (SD) SUA was 0.43 (0.11) mmol/L at baseline. During 5.3 (IQR, 4.1-6.0) years of follow-up, 52 (10%) KTR developed PTDM. In univariate prospective analyses, SUA was associated with increased risk of PTDM (HR 1.75, 95% CI 1.36-2.26 per 1-SD increment; P < 0.001). This finding remained materially unchanged after adjustment for components of the metabolic syndrome, lifestyle, estimated glomerular filtration rate, immunosuppressive therapy, cytomegalovirus and hepatitis C virus infection (HR 1.89, 95% CI 1.32-2.70; P = 0.001). These findings were consistent in categorical analyses, and robust in sensitivity analyses without outliers. Conclusions: In KTR, higher SUA levels are strongly and independently associated with increased risk of PTDM. Our findings are in agreement with accumulating evidence supporting SUA as novel independent risk marker for type 2 diabetes, and extend the evidence, for the first time, to the clinical setting of outpatient KTR. (C) 2020 The Author(s). Published by Elsevier Inc.
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页数:7
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