Obesity and Diabetes Clinical Research Section, Phoenix Epidemiology and Clinical Research Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health , Department of Health and Human Services, Phoenix, AZ 85016, USA.
Metab Syndr Relat Disord. 2013 Jun;11(3):157-62. doi: 10.1089/met.2012.0151. Epub 2013 Jan 29.
Uric acid (UA) is known to be associated with excess adiposity and insulin resistance. Our aim was to investigate the relationship between UA and the factors associated with the metabolic syndrome and type 2 diabetes mellitus (T2DM), both initially and longitudinally.
Serum UA was assessed as a potential determinant of concurrent blood pressure, serum lipids, glucose regulation measured via an oral glucose tolerance test (OGTT), acute insulin response (AIR), and insulin action (M) measured with hyperinsulinemic-euglycemic clamps in 245 participants (72% Native American, 56% male). UA was also assessed as a predictor of the above variables in 60 participants with follow-up data available (median follow-up time=11.2 years [interquartile range (IQR)=8.1, 13.6 years]. The impact of UA on the risk of T2DM was determined as 36 of the 245 participants developed T2DM after the baseline visit.
UA was negatively associated with both concurrent and future M, such that for every 1 mg/dL increase in serum UA, M decreased 7.6% (P<0.001) and future M decreased 6.3% (P=0.02). However, UA was not associated with AIR (P=0.7). UA concentrations were a predictor of T2DM [hazard risk ratio (HRR)=1.5; P=0.02]. UA was positively associated with both concurrent blood pressure and lipids and also predicted future increases in blood pressure and total cholesterol.
Not only did UA associate with concomitant insulin action, blood pressure, and lipids, it also predicted future declines in insulin action and T2DM. UA is a potential target for preventing decreases in insulin sensitivity and rises in blood pressure and cholesterol.
尿酸(UA)已知与超重和胰岛素抵抗有关。我们的目的是研究 UA 与代谢综合征和 2 型糖尿病(T2DM)相关因素之间的关系,包括初始和纵向关系。
在 245 名参与者(72%为美洲原住民,56%为男性)中,评估血清 UA 是否为同时存在的血压、血清脂质、口服葡萄糖耐量试验(OGTT)测量的血糖调节、急性胰岛素反应(AIR)和高胰岛素正葡萄糖钳夹测量的胰岛素作用(M)的潜在决定因素。在有随访数据的 60 名参与者中(中位随访时间=11.2 年[四分位距(IQR)=8.1,13.6 年]),UA 也被评估为上述变量的预测指标。在基线检查后,245 名参与者中有 36 名发展为 T2DM,确定 UA 对 T2DM 风险的影响。
UA 与同时存在的和未来的 M 呈负相关,即血清 UA 每增加 1mg/dL,M 降低 7.6%(P<0.001),未来的 M 降低 6.3%(P=0.02)。然而,UA 与 AIR 无关(P=0.7)。UA 浓度是 T2DM 的预测指标[风险比(HRR)=1.5;P=0.02]。UA 与同时存在的血压和血脂呈正相关,也预测了未来血压和总胆固醇的升高。
UA 不仅与同时存在的胰岛素作用、血压和血脂相关,还预测了未来胰岛素作用的下降和 T2DM。UA 是预防胰岛素敏感性下降、血压和胆固醇升高的潜在靶点。