Cardoso Claudia R L, da Silva Pereira Lucas, Leite Nathalie C, Salles Gil F
Department of Internal Medicine, University Hospital Clementino Fraga Filho, School of Medicine; Universidade Federal do Rio de Janeiro, Brazil.
Department of Internal Medicine, University Hospital Clementino Fraga Filho, School of Medicine; Universidade Federal do Rio de Janeiro, Brazil.
J Diabetes Complications. 2025 Jan;39(1):108921. doi: 10.1016/j.jdiacomp.2024.108921. Epub 2024 Nov 27.
To investigate the associations between baseline/changes in serum uric acid (sUA) and the risks for cardiovascular/microvascular outcomes and mortality in a type 2 diabetes cohort.
Baseline sUA was measured in 685 individuals, and 463 had a second sUA measurement during follow-up; sUA was analyzed as a continuous variable and categorized into sex-specific tertile subgroups and low/high levels (>4.5 mg/dl women; >5.5 mg/dl men). The risks associated with baseline sUA and its changes were examined by Cox analyses for all outcomes.
Median follow up was 10.7 years, there were 173 major cardiovascular events (MACEs), 268 all-cause deaths, 127 microalbuminuria, 104 renal failure, 160 retinopathy and 178 peripheral neuropathy outcomes. Baseline sUA was predictor of all outcomes, except all-cause mortality and retinopathy. In tertile and high/low sUA analyses, the hazard ratios (HRs) varied from 1.6 (microalbuminuria development) to 2.4 (MACEs; cardiovascular mortality). There was interaction with sex for MACEs, an increased risk was observed in women (HR: 2.6), but not in men (HR: 1.2). Changes in sUA were associated with the renal failure (HR: 2.4).
In a prospective cohort, high baseline sUA was a predictor of cardiovascular, renal and peripheral neuropathy. However, sUA changes were only predictor of renal failure.
在2型糖尿病队列中研究血清尿酸(sUA)的基线水平/变化与心血管/微血管结局及死亡率风险之间的关联。
对685名个体测量了基线sUA,463名在随访期间进行了第二次sUA测量;sUA作为连续变量进行分析,并分为按性别划分的三分位数亚组以及低/高尿酸水平组(女性>4.5mg/dl;男性>5.5mg/dl)。通过Cox分析检查与基线sUA及其变化相关的所有结局的风险。
中位随访时间为10.7年,发生了173例主要心血管事件(MACE)、268例全因死亡、127例微量白蛋白尿、104例肾衰竭、160例视网膜病变和178例周围神经病变结局。基线sUA是除全因死亡率和视网膜病变外所有结局的预测因素。在三分位数和高/低sUA分析中,风险比(HR)从1.6(微量白蛋白尿发生)到2.4(MACE;心血管死亡率)不等。MACE存在性别交互作用,女性风险增加(HR:2.6),而男性未增加(HR:1.2)。sUA的变化与肾衰竭相关(HR:2.4)。
在一个前瞻性队列中,高基线sUA是心血管、肾脏和周围神经病变的预测因素。然而,sUA变化仅是肾衰竭的预测因素。