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Overweight modifies the longitudinal association between uric acid and some components of the metabolic syndrome: The Troms? Study

机译:超重改变了尿酸和代谢综合征某些成分之间的纵向联系:Troms?研究

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Background Elevated uric acid (UA) is associated with the presence of the metabolic syndrome (MetS). In a prospective cohort study, we assessed whether baseline and longitudinal change in UA were risk factors for development of MetS and its individual components. Methods We included 3087 women and 2996 men who had UA measured in the population based Troms? Study 1994–95. The participants were stratified according to body mass index (BMI). Endpoints were MetS and each component of the syndrome after 7 years, according to the revised National Cholesterol Education Program’s Adult Treatment Panel III (NCEP-ATP III) definition. Results Multiple logistic regression analyses showed that higher baseline UA was associated with higher odds of developing elevated blood pressure in overweight subjects (BMI?≥?25?kg/m2, odds ratio [OR] per 59?μmol/L UA increase 1.44, 95?% confidence interval [CI]?=?1.17–1.77, P =?0.001), but not in normal-weight subjects (BMI?2, P for interaction?=?0.04). Overweight also modified the association between baseline UA and the development of elevated fasting glucose (P for interaction?=?0.01). UA was a predictor of MetS in all subjects (OR per 59?μmol/L UA increase 1.29, 95?% CI 1.18–1.41, P Conclusion Increased levels of baseline UA independently predicted development of elevated blood pressure and higher fasting glycemia in the overweight, but not the normal-weight subjects. Baseline UA and longitudinal increase in UA over 7 years was associated with the development of MetS in all subjects. Whether increased UA should be treated differently in normal-weight and overweight persons needs further study.
机译:背景尿酸(UA)升高与代谢综合征(MetS)的存在有关。在一项前瞻性队列研究中,我们评估了UA的基线和纵向变化是否是MetS及其各个组成部分发展的危险因素。方法我们纳入了以人群为基础的Troms? 1994–95研究。根据体重指数(BMI)对参与者进行分层。根据修订后的国家胆固醇教育计划的成人治疗小组III(NCEP-ATP III)的定义,终点是MetS和7年后综合征的每个组成部分。结果多项逻辑回归分析显示,超重受试者中较高的基线UA与血压升高的可能性更高(BMI≥25?kg / m 2 ,比值比[OR] / 59? μmol/ L UA增加1.44,95%置信区间[CI]?=?1.17–1.77,P =?0.001),但在体重正常的受试者(BMI?2 ,交互作用P =? 0.04)。超重还改变了基线UA与空腹血糖升高之间的相关性(相互作用P = 0.01)。 UA是所有受试者中MetS的预测因子(或每59?μmol/ L UA升高1.29,95%CI 1.18-1.41,P结论结论基线UA水平升高独立预测超重患者血压升高和空腹血糖升高基线UA和7年内UA的纵向升高与所有受试者MetS的发展有关,在正常体重和超重人群中是否应区别对待UA升高,尚需进一步研究。

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