Bonora E, Targher G, Zenere M B, Saggiani F, Cacciatori V, Tosi F, Travia D, Zenti M G, Branzi P, Santi L, Muggeo M
Division of Endocrinology and Metabolic Diseases, University of Verona Medical School, Italy.
Int J Obes Relat Metab Disord. 1996 Nov;20(11):975-80.
To examine the relationships of serum uric acid concentration with several risk factors of cardiovascular diseases (CVD).
957 men 18 y old participating in the Verona Young Men Atherosclerosis Risk Factors Study, a cross-sectional population-based study.
Body mass index (BMI), waist/hip ratio (WHR), serum uric acid, serum lipids, blood pressure, fasting insulin and behavioural variables.
Serum uric acid concentration showed positive associations with BMI (r = 0.24; P < 0.0001), WHR (r = 0.19; P < 0.0001) and serum triglyceride levels (r = 0.19; P < 0.0001); it was also significantly correlated to systolic (r = 0.08; P < 0.01) and diastolic (r = 0.11; P < 0.001) blood pressure, fasting insulin (r = 0.11; P < 0.001), total (r = 0.12; P < 0.001) and LDL cholesterol (r = 0.10; P < 0.01) plasma concentrations. Life-style characteristics, such as smoking and physical activity did not show any significant association, while daily alcohol intake was positively associated with uric acid concentration (r = 0.09; P < 0.01). While the adjustment for fasting insulin did not substantially change these results, the magnitude of the correlations between uric acid and CVD risk factors markedly decreased when allowance was made for BMI and WHR. Only triglycerides maintained an independent correlation with uric acid levels (r = 0.17; P < 0.0001). In multivariate regression analysis, serum triglycerides, BMI and WHR (at borderline significance) were independent positive predictors of uric acid (R2 of the model 0.122, P < 0.001), while fasting insulin concentration did not give any independent contribution to explain the variability uric acid levels.
These data indicate that, already in young, essentially health subjects, hyperuricaemia associates with several components of the so-called insulin resistance syndrome, thus suggesting that increased levels of uric acid might be another member of this syndrome. In addition, these data suggest that obesity and central body fat distribution, rather than hyperinsulinaemia/insulin resistance, play a major role in linking hyperuricaemia with CVD risk factors clustering in the insulin resistance syndrome. Nevertheless, hypertrigliceridemia is related to hyperuricemia independently of obesity and central body fat distribution.
研究血清尿酸浓度与心血管疾病(CVD)若干危险因素之间的关系。
957名18岁男性,参与维罗纳青年男性动脉粥样硬化危险因素研究,这是一项基于人群的横断面研究。
体重指数(BMI)、腰臀比(WHR)、血清尿酸、血脂、血压、空腹胰岛素及行为变量。
血清尿酸浓度与BMI(r = 0.24;P < 0.0001)、WHR(r = 0.19;P < 0.0001)及血清甘油三酯水平(r = 0.19;P < 0.0001)呈正相关;还与收缩压(r = 0.08;P < 0.01)和舒张压(r = 0.11;P < 0.001)、空腹胰岛素(r = 0.11;P < 0.001)、总血浆浓度(r = 0.12;P < 0.001)及低密度脂蛋白胆固醇(r = 0.10;P < 0.01)显著相关。生活方式特征,如吸烟和体育活动未显示出任何显著相关性,而每日酒精摄入量与尿酸浓度呈正相关(r = 0.09;P < 0.01)。虽然对空腹胰岛素进行校正并没有实质性改变这些结果,但在考虑BMI和WHR后,尿酸与CVD危险因素之间的相关性强度明显降低。只有甘油三酯与尿酸水平保持独立相关性(r = 0.17;P < 0.0001)。在多变量回归分析中,血清甘油三酯、BMI和WHR(具有临界显著性)是尿酸的独立正向预测因子(模型的R2为0.122,P < 0.001),而空腹胰岛素浓度对解释尿酸水平的变异性没有任何独立贡献。
这些数据表明,在年轻的基本健康的受试者中,高尿酸血症就与所谓胰岛素抵抗综合征的若干成分相关,因此提示尿酸水平升高可能是该综合征的另一个成员。此外,这些数据表明,肥胖和中心性体脂分布,而非高胰岛素血症/胰岛素抵抗,在将高尿酸血症与胰岛素抵抗综合征中聚集的CVD危险因素联系起来方面起主要作用。然而,高甘油三酯血症与高尿酸血症相关,独立于肥胖和中心性体脂分布。