Banerjee Mainak, Pal Rimesh, Mukhopadhyay Satinath
Department of Endocrinology, Institute of Postgraduate Medical Education and Research, Kolkata, 700020, India.
Department of Endocrinology, Post Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Acta Diabetol. 2022 Jun;59(6):783-791. doi: 10.1007/s00592-022-01866-3. Epub 2022 Mar 6.
To collate the effect of SGLT2 inhibitors (SGLT2i) on adverse gout events in people with type 2 diabetes mellitus (T2DM).
PubMed/MEDLINE, Embase, and Web of Science databases were systematically searched using appropriate keywords/MeSH/Emtree terms till January 25, 2022, to identify observational studies, randomized controlled trials (RCTs) or post hoc analysis reporting incident gout events and/or commencement of anti-gout drug in people with T2DM receiving SGLT2i versus those not receiving SGLT2i. Subgroup analyses were performed using comparators as placebo/other antidiabetic drugs and presence/absence of baseline hyperuricemia (uric acid ≥ 7 or < 7 mg/dl). Hazard ratios (HR) with 95% confidence intervals (CI) were calculated.
We identified 5 studies (3 observational, 2 post hoc analysis of RCTs) pooling data retrieved from 568,010 people with T2DM. Pooled analysis showed that SGLT2i use was associated with 30% reduction in incident gout events/gout flares (HR 0.70, 95% CI: 0.59, 0.84, p < 0.001, I = 84%). Sensitivity analysis after excluding the retrospective observational study showed similar estimates (HR 0.65, 95% CI: 0.60, 0.70, p < 0.001, I = 0%). Subgroup analysis of data retrieved only from RCTs also showed significant benefits (HR 0.74, 95% CI: 0.55, 0.98, p = 0.03, I = 0%). Pooled analysis of data from 2 studies showed that SGLT2i use led to a significant reduction in the need for commencement of new anti-gout drug (pooled HR 0.58, 95% CI: 0.48, 0.71, p < 0.001, I = 0%). Consistent benefits were also observed for subgroup without baseline hyperuricemia (pooled HR 0.65, 95% CI: 0.47, 0.89, p < 0.01, I = 0%).
SGLT2i may potentially prevent gout-related adverse events in people with T2DM.
整理钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)对2型糖尿病(T2DM)患者痛风不良事件的影响。
使用适当的关键词/医学主题词/Emtree术语,对PubMed/MEDLINE、Embase和Web of Science数据库进行系统检索,直至2022年1月25日,以识别观察性研究、随机对照试验(RCT)或事后分析,报告接受SGLT2i的T2DM患者与未接受SGLT2i的患者发生痛风事件和/或开始使用抗痛风药物的情况。使用安慰剂/其他抗糖尿病药物作为对照,以及根据是否存在基线高尿酸血症(尿酸≥7或<7mg/dl)进行亚组分析。计算风险比(HR)及95%置信区间(CI)。
我们确定了5项研究(3项观察性研究、2项RCT的事后分析),汇总了从568,010名T2DM患者中检索到的数据。汇总分析表明,使用SGLT2i可使痛风事件/痛风发作减少30%(HR 0.70,95%CI:0.59,0.84,p<0.001,I=84%)。排除回顾性观察性研究后的敏感性分析显示了相似的估计值(HR 0.65,95%CI:0.60,0.70,p<0.001,I=0%)。仅从RCT中检索到的数据进行亚组分析也显示出显著益处(HR 0.74,95%CI:0.55,0.98,p=0.03,I=0%)。对2项研究的数据进行汇总分析表明,使用SGLT2i可显著减少开始使用新抗痛风药物的需求(汇总HR 0.58,95%CI:0.48,0.71,p<0.001,I=0%)。在无基线高尿酸血症的亚组中也观察到了一致的益处(汇总HR 0.65,95%CI:0.47,0.89,p<0.01,I=0%)。
SGLT2i可能有助于预防T2DM患者痛风相关不良事件。