Department of Rheumatology and Internal Diseases, Poznan University of Medical Sciences, Poznan, Poland.
Department of Computer Science and Statistics, Poznan University of Medical Sciences, Poznan, Poland.
Mol Cell Biochem. 2018 Jun;443(1-2):111-119. doi: 10.1007/s11010-017-3215-6. Epub 2017 Oct 26.
The aim of this study was to find the genetic, metabolic, and nutritional risk factors, which can be associated with uric acid (UA) level. The risk factors related to uricemia were assessed among 271 postmenopausal women without cardiometabolic disorders and hypolipidemic/hypoglycemic treatment selected from a cohort of 1423 obese postmenopausal women. The bioimpedance analysis and biochemical and genetic analyses were performed in two groups characterized by serum UA ≥ 4 mg/dL (238 μmol/L) and < 4 mg/dL. The TaqMan-based real-time PCR method was applied to assess the role of Pro12Ala of peroxisome proliferation-activated receptor (PPAR)gamma-2 and Trp64Arg of beta-3-adrenergic receptor (ADRB) polymorphisms. Women with UA level ≥ 4 mg/dL were characterized by larger body mass, triceps skinfold, waist circumference, body fat amount, and serum insulin, glucose, and triglyceride levels. There was no difference in dietary habits between the analyzed groups. Body mass, waist circumference, body fat amount, diastolic blood pressure, and serum insulin, glucose, high-density lipoprotein, and triglyceride levels, Homeostasis Model Assessment-Insulin Resistance, and energy from the dietary fat influence the UA level ≥ 4 mg/dL; however, the serum UA was not determined by Pro12Ala and Trp64Arg polymorphism analyses. The model of linear regression revealed that the group characterized by body mass index ≥ 25 kg/m and glucose ≥ 100 mg/dL has 4 times increased risk of UA level (p = 0.0009); after adding triglycerides ≥ 150 mg/dL, the risk of UA increased 7 times (p = 0.0216). Increasing the level of UA ≥ 4 mg/dL is associated with overweight, hyperglycemia, and hypertriglyceridemia in women without a history of cardiometabolic disorders. A better management of metabolic factors could help prevent further increase in UA levels.
本研究旨在寻找与尿酸(UA)水平相关的遗传、代谢和营养风险因素。在 1423 名肥胖绝经后妇女队列中选择无心血管代谢疾病和降脂/降糖治疗的 271 名绝经后妇女中,评估了与血尿酸相关的危险因素。在血清 UA≥4mg/dL(238μmol/L)和<4mg/dL 的两组中进行生物电阻抗分析和生化及基因分析。应用 TaqMan 实时 PCR 方法评估过氧化物酶体增殖物激活受体(PPAR)γ-2 Pro12Ala 和β-3 肾上腺素能受体(ADRB)Trp64Arg 多态性的作用。UA 水平≥4mg/dL 的女性具有更大的体重、三头肌皮褶、腰围、体脂肪量和血清胰岛素、葡萄糖和甘油三酯水平。两组的饮食习惯无差异。体重、腰围、体脂肪量、舒张压和血清胰岛素、葡萄糖、高密度脂蛋白和甘油三酯水平、稳态模型评估胰岛素抵抗和膳食脂肪的能量影响 UA 水平≥4mg/dL;然而,血清 UA 不受 Pro12Ala 和 Trp64Arg 多态性分析的影响。线性回归模型显示,体质指数≥25kg/m2 和葡萄糖≥100mg/dL 的组 UA 水平增加 4 倍的风险(p=0.0009);在加入甘油三酯≥150mg/dL 后,UA 风险增加 7 倍(p=0.0216)。UA 水平≥4mg/dL 的升高与无心血管代谢疾病史的女性超重、高血糖和高三酰甘油血症有关。更好地控制代谢因素可能有助于防止 UA 水平进一步升高。