Dai Huajie, Hou Tianzhichao, Wang Qi, Zhu Zheng, Zhu Yijie, Zhao Zhiyun, Li Mian, Xu Yu, Lu Jieli, Wang Tiange, Ning Guang, Wang Weiqing, Bi Yufang, Zheng Jie, Xu Min
Department of Endocrine and Metabolic Diseases, Shanghai Institute of Endocrine and Metabolic Diseases, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Shanghai National Clinical Research Center for Metabolic Diseases, Key Laboratory for Endocrine and Metabolic Diseases of the National Health Commission of the PR China, Shanghai Key Laboratory for Endocrine Tumor, State Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Diabetes Obes Metab. 2024 Jan;26(1):242-250. doi: 10.1111/dom.15310. Epub 2023 Oct 9.
To evaluate the effect of metformin on urate metabolism.
Using the UK Biobank, we first performed association analyses of metformin use with urate levels, risk of hyperuricaemia and incident gout in patients with diabetes. To explore the causal effect of metformin on urate and gout, we identified genetic variants proxying the glycated haemoglobin (HbA1c)-lowering effect of metformin targets and conducted a two-sample Mendelian randomization (MR) utilizing the urate and gout genetic summary-level data from the CKDGen (n = 288 649) and the FinnGen cohort. We conducted two-step MR to explore the mediation effect of body mass index and systolic blood pressure. We also performed non-linear MR in the UK Biobank (n = 414 055) to show the results across HbA1c levels.
In 18 776 patients with type 2 diabetes in UK Biobank, metformin use was associated with decreased urate [β = -4.3 μmol/L, 95% confidence interval (CI) -7.0, -1.7, p = .001] and reduced hyperuricaemia risk (odds ratio = 0.87, 95% CI 0.79, 0.96, p = .004), but not gout. Genetically proxied averaged HbA1c-lowering effects of metformin targets, equivalent to a 0.62% reduction in HbA1c, was associated with reduced urate (β = -12.5 μmol/L, 95% CI -21.4, -4.2, p = .004). Body mass index significantly mediated this association (proportion mediated = 33.0%, p = .002). Non-linear MR results suggest a linear trend of the effect of metformin on urate reduction across various HbA1c levels.
The effect of metformin may reduce urate levels but not incident gout in the general population.
评估二甲双胍对尿酸代谢的影响。
利用英国生物银行,我们首先对糖尿病患者中二甲双胍的使用与尿酸水平、高尿酸血症风险及痛风发生率进行了关联分析。为探究二甲双胍对尿酸和痛风的因果效应,我们确定了代表二甲双胍靶点糖化血红蛋白(HbA1c)降低效应的基因变异,并利用慢性肾脏病基因(CKDGen,n = 288649)和芬兰基因队列的尿酸和痛风基因汇总水平数据进行了两样本孟德尔随机化(MR)分析。我们进行了两步MR以探究体重指数和收缩压的中介效应。我们还在英国生物银行(n = 414055)中进行了非线性MR以展示不同HbA1c水平下的结果。
在英国生物银行的18776例2型糖尿病患者中,使用二甲双胍与尿酸降低相关[β = -4.3 μmol/L,95%置信区间(CI)-7.0,-1.7,p = 0.001],高尿酸血症风险降低(优势比 = 0.87,95% CI 0.79,0.96,p = 0.004),但与痛风无关。二甲双胍靶点的遗传代理平均HbA1c降低效应,相当于HbA1c降低0.62%,与尿酸降低相关(β = -12.5 μmol/L,95% CI -21.4,-4.2,p = 0.004)。体重指数显著介导了这种关联(介导比例 = 33.0%,p = 0.002)。非线性MR结果表明,二甲双胍对不同HbA1c水平下尿酸降低的影响呈线性趋势。
在普通人群中,二甲双胍的作用可能是降低尿酸水平,但不会降低痛风发生率。