Department of Internal Medicine, Divisions of Mineral Metabolism and Endocrinology, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas, USA.
Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, and Division of Mineral Metabolism, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
J Investig Med. 2018 Oct;66(7):1031-1036. doi: 10.1136/jim-2018-000728. Epub 2018 Apr 4.
Hyperuricemia has been associated in epidemiological studies with the development of obesity, hypertension, insulin resistance and type 2 diabetes. Nevertheless, it remains unclear whether lowering of serum uric acid (UA) alters any of the features of the metabolic syndrome. In this prospective study (ClinicalTrials.gov identifier: NCT01654276), 24 patients with gouty arthritis and hyperuricemia were treated for 6 months with the xanthine oxidase inhibitor febuxostat to lower serum UA to <6 mg/dL. Measurements of 24 hours ambulatory blood pressure (ABP) and serum and urine markers of the metabolic syndrome were measured at baseline and at the end of 6 months of febuxostat. The study population consisted of 18 men and 6 women, 18 of which completed the baseline and 6 months visits. Serum UA decreased significantly from 8.7±1.5 mg/dL at baseline to 4.4±1.1 mg/dL at 6 months (P<0.0001). During that time frame, there was no significant change in body mass index, systolic or diastolic blood pressure measured by 24 hours ABP monitor, serum glucose, insulin or homeostatic model assessment for insulin resistance, serum total and high-density lipoprotein-cholesterol, serum triglycerides or urine pH (P>0.05 for all). There was no correlation between parameters of the metabolic syndrome and the decline in serum UA or serum UA achieved at study end. In conclusion, in patients with gouty arthritis, UA lowering with febuxostat below 6 mg/dL had no significant impact on features of the metabolic syndrome.
高尿酸血症与肥胖症、高血压、胰岛素抵抗和 2 型糖尿病的发生在流行病学研究中相关。然而,降低血清尿酸(UA)是否会改变代谢综合征的任何特征仍不清楚。在这项前瞻性研究(ClinicalTrials.gov 标识符:NCT01654276)中,24 例痛风性关节炎和高尿酸血症患者接受黄嘌呤氧化酶抑制剂非布司他治疗 6 个月,将血清 UA 降低至<6mg/dL。在基线和非布司他治疗 6 个月时测量 24 小时动态血压(ABP)和代谢综合征的血清和尿液标志物。研究人群包括 18 名男性和 6 名女性,其中 18 名完成了基线和 6 个月的访视。血清 UA 从基线时的 8.7±1.5mg/dL 显著下降至 6 个月时的 4.4±1.1mg/dL(P<0.0001)。在此期间,24 小时 ABP 监测仪测量的体重指数、收缩压或舒张压、血清葡萄糖、胰岛素或胰岛素抵抗的稳态模型评估、血清总胆固醇和高密度脂蛋白胆固醇、血清甘油三酯或尿 pH 均无显著变化(所有 P>0.05)。代谢综合征的参数与血清 UA 的下降或研究结束时的血清 UA 水平之间没有相关性。总之,在痛风性关节炎患者中,非布司他将 UA 降低至<6mg/dL 对代谢综合征的特征没有显著影响。