Kiortsis D N, Elisaf M S
Department of Internal Medicine, Medical School, University of Ioannina, Ioannina, Greece.
Fundam Clin Pharmacol. 2001 Dec;15(6):401-3. doi: 10.1046/j.1472-8206.2001.00049.x.
The purpose of our study was to investigate whether measurement of serum uric acid levels is a reliable method to assess adherence to fenofibrate treatment. This was a 21 week, open-label study conducted in our lipid clinic. After an 8 week dietary baseline phase, we implemented a treatment phase, during which patients received 200 mg/day micronized fenofibrate for 3 months. Serum lipid profiles, including levels of lipoprotein(a) and fibrinogen, serum uric acid, as well as muscle and liver enzymes, were measured after the dietary phase, and at the end of the 3 month treatment period. Compliance was assessed using a clinical interview. A significant decrease in serum uric acid levels was observed in the compliant, while no significant change was noticed in the non-compliant. The compliant had lower serum uric acid concentrations compared to the non-compliant (P < 0.01) after fenofibrate treatment. Furthermore, they demonstrated lower levels of triglycerides and higher high-density lipoprotein (HDL) cholesterol concentrations (P < 0.05 for both parameters). The results show that serum uric acid concentrations may be used as a useful tool to assess compliance with fenofibrate therapy.
我们研究的目的是调查测量血清尿酸水平是否是评估非诺贝特治疗依从性的可靠方法。这是一项在我们的血脂门诊进行的为期21周的开放标签研究。在为期8周的饮食基线期后,我们进入了治疗阶段,在此期间患者接受每日200毫克微粒化非诺贝特治疗3个月。在饮食期结束时以及3个月治疗期结束时,测量了血脂谱,包括脂蛋白(a)和纤维蛋白原水平、血清尿酸以及肌肉和肝脏酶。通过临床访谈评估依从性。在依从者中观察到血清尿酸水平显著下降,而在不依从者中未发现显著变化。非诺贝特治疗后,依从者的血清尿酸浓度低于不依从者(P < 0.01)。此外,他们的甘油三酯水平较低,高密度脂蛋白(HDL)胆固醇浓度较高(两个参数均P < 0.05)。结果表明,血清尿酸浓度可作为评估非诺贝特治疗依从性的有用工具。