Department of Medicine, Division of Rheumatology Immunology and Allergy Research, Brigham and Women's Hospital, Boston, Massachusetts, USA
Department of Medicine, Division of Rheumatology, University of Sherbrooke and Centre Intégré Universitaire de Santé et de Services Sociaux de l'Estrie-CIUSSSE-CHUS, Sherbrooke, QC, Canada.
Ann Rheum Dis. 2024 Sep 30;83(10):1368-1374. doi: 10.1136/ard-2024-225652.
Despite the strong association between gout and pre-diabetes, the role of metformin in gout among individuals with pre-diabetes remains uncertain. We compared the incidence rates of gout in adults with pre-diabetes starting metformin with those not using antidiabetic treatments.
We conducted a new-user, propensity score-matched cohort study using electronic health records from an academic health system (2007-2022). Pre-diabetes was defined based on haemoglobin A1c levels. Metformin users were identified and followed from the first metformin prescription date. Non-users of antidiabetic medications were matched to metformin users based on propensity score and the start of follow-up. The primary outcome was incident gout. Cox proportional hazards models estimated the HR for metformin. Linear regression analyses assessed the association between metformin use and changes in serum urate (SU) or C-reactive protein (CRP).
We identified 25 064 individuals with pre-diabetes and propensity score-matched 1154 metformin initiators to 13 877 non-users. Baseline characteristics were well balanced (all standardised mean differences <0.1). The median follow-up was 3.9 years. The incidence rate of gout per 1000 person-years was lower in metformin users 7.1 (95% CI 5.1 to 10) compared with non-users 9.5 (95% CI 8.8 to 10.2). Metformin initiation was associated with a reduced relative risk of gout (HR 0.68, 95% CI 0.48 to 0.96). No relationship was found between metformin and changes in SU or CRP.
Metformin use was associated with a reduced risk of gout among adults with pre-diabetes, suggesting that metformin may be important in lowering gout risk in individuals with pre-diabetes.
尽管痛风与糖尿病前期之间存在密切关联,但二甲双胍在糖尿病前期患者中对痛风的作用仍不确定。我们比较了起始使用二甲双胍与未使用抗糖尿病治疗的糖尿病前期成人的痛风发病率。
我们使用学术医疗系统的电子健康记录进行了一项新用户、倾向评分匹配的队列研究(2007-2022 年)。糖尿病前期基于糖化血红蛋白水平定义。从首次开具二甲双胍处方之日起确定二甲双胍使用者并进行随访。根据倾向评分和随访开始时间,将未使用抗糖尿病药物的患者与二甲双胍使用者匹配。主要结局是痛风发病。Cox 比例风险模型估计了二甲双胍的 HR。线性回归分析评估了二甲双胍使用与血清尿酸(SU)或 C 反应蛋白(CRP)变化之间的关联。
我们确定了 25064 名糖尿病前期患者,并对 1154 名起始使用二甲双胍的患者和 13877 名未使用者进行了倾向评分匹配。基线特征均衡(所有标准化均差 <0.1)。中位随访时间为 3.9 年。痛风的发病率为每 1000 人年 7.1 例(95%CI 5.1 至 10),低于未使用者的 9.5 例(95%CI 8.8 至 10.2)。二甲双胍起始与痛风的相对风险降低相关(HR 0.68,95%CI 0.48 至 0.96)。未发现二甲双胍与 SU 或 CRP 变化之间存在关系。
在糖尿病前期成人中,使用二甲双胍与痛风风险降低相关,这表明二甲双胍可能在降低糖尿病前期患者的痛风风险方面具有重要作用。