Liu Zhengtao, Que Shuping, Zhou Lin, Zheng Shusen
Key Laboratory of Combined Multi-Organ Transplantation, Ministry of Public Health and Key Laboratory of Organ Transplantation of Zhejiang Province, Hangzhou, 310003, Zhejiang province, China.
Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Hangzhou, 310003, China.
Sci Rep. 2015 Sep 23;5:14325. doi: 10.1038/srep14325.
Emerging evidence has shown that serum uric acid (SUA) elevation might cause metabolic derangements, including metabolic syndrome (MetS) and non-alcoholic fatty liver disease (NAFLD); however, magnitude of the risk has not been quantified. We searched PubMed, EMBASE, and ISI databases for relevant studies through 10 May 2015. Prospective studies reporting the risk of SUA elevation on the incidence of MetS/NAFLD were enrolled. Pooled HR of MetS was 1.55 (95%CI: 1.40-1.70) for the highest versus lowest SUA categories, and 1.05 (95%CI: 1.04-1.07) per incremental increased in SUA of 1 mg/dl. The pooled HR of MetS in younger women was higher than age-matched men and older women (1.17 vs. 1.05 and 1.04, respectively, P < 0.05). Individuals in the highest SUA category had a 40% greater risk of disease NAFLD occurrence. Dose-response increment of NAFLD events was 1.03 (95%CI: 1.02-1.05). A positive relationship with a linear trend for SUA elevation with MetS and NAFLD in different genders was examined by a dose-response meta-analysis (P < 0.001).SUA assay is useful in screening metabolic disorders for linear trend between its elevation and MetS/NAFLD incidence. SUA-lowering therapy is a potential strategy for preventing systemic/hepatic metabolic abnormalities.
新出现的证据表明,血清尿酸(SUA)升高可能会导致代谢紊乱,包括代谢综合征(MetS)和非酒精性脂肪性肝病(NAFLD);然而,这种风险的程度尚未量化。我们检索了PubMed、EMBASE和ISI数据库,以查找截至2015年5月10日的相关研究。纳入了报告SUA升高对MetS/NAFLD发病率风险的前瞻性研究。SUA最高类别与最低类别相比,MetS的合并风险比(HR)为1.55(95%置信区间:1.40 - 1.70),SUA每增加1mg/dl,合并HR为1.05(95%置信区间:1.04 - 1.07)。年轻女性中MetS的合并HR高于年龄匹配的男性和老年女性(分别为1.17 vs. 1.05和1.04,P < 0.05)。SUA最高类别的个体发生NAFLD疾病的风险高40%。NAFLD事件的剂量反应增量为1.03(95%置信区间:1.02 - 1.05)。通过剂量反应荟萃分析检验了不同性别中SUA升高与MetS和NAFLD之间呈线性趋势的正相关关系(P < 0.001)。SUA检测对于筛查代谢紊乱很有用,因为其升高与MetS/NAFLD发病率之间存在线性趋势。降低SUA治疗是预防全身/肝脏代谢异常的一种潜在策略。