Kanbay Mehmet, Brinza Crischentian, Copur Sidar, Sekreter Ozge, Burlacu Alexandru, Tuttle Katherine R, Rossing Peter, Covic Adrian
Department of Medicine, Division of Nephrology, Koç University School of Medicine, Istanbul, Turkey.
Faculty of Medicine, Grigore T Popa University of Medicine and Pharmacy, Iasi, Romania.
Nephrol Dial Transplant. 2025 Apr 1;40(4):671-678. doi: 10.1093/ndt/gfae179.
Sodium-glucose co-transporter 2 (SGLT2) inhibitors are novel anti-diabetic medications with potential beneficial effects on cardiovascular and renal outcomes, metabolic parameters and body weight. In addition to the beneficial effects on renal function, including estimated glomerular filtration rate and reduction in proteinuria, recent studies have investigated the potential role of SGLT2 inhibitor (SGLT2i) therapy on nephrolithiasis development. Nephrolithiasis, a condition affecting almost 10% of the general population at least once during a lifetime, is a common disorder with considerable risk for acute and chronic kidney injury and relatively few effective therapeutic options.
We performed a literature search through multiple databases, including PubMed, Ovid MEDLINE, Web of Science, Scopus and Cochrane Library. We followed the systematic review and meta-analysis guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses. We included a total of 11 635 698 patients who experienced nephrolithiasis from six clinical trials in this meta-analysis study.
In the pooled analysis, nephrolithiasis occurred in 1.27% of patients in the SGLT2i group (n = 739 197), compared with 1.56% of patients (n = 10 896 501) in the control arm (active control, placebo or no therapy). SGLT-2 inhibitor therapy has been associated with a lower risk for nephrolithiasis compared with placebo {odds ratio [OR] 0.61 [95% confidence interval (CI) 0.53-0.70], P < .00001} or active therapy such as glucagon-like peptide 1 and dipeptidyl peptidase 4 inhibitors [OR 0.66 (95% CI 0.47-0.93), P = .02].
We demonstrated a lower risk of nephrolithiasis with SGLT2i therapy compared with placebo or active control. Potential underlying mechanisms include osmotic diuresis leading to a reduction in the concentration of lithogenic substances, anti-inflammatory and anti-fibrotic effects and an increase in urine pH. There is a clear need for future large-scale randomized clinical trials evaluating such associations for better understanding.
钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂是新型抗糖尿病药物,对心血管和肾脏结局、代谢参数及体重具有潜在有益作用。除了对肾功能有益,包括估算肾小球滤过率及降低蛋白尿外,近期研究还探讨了SGLT2抑制剂(SGLT2i)治疗在肾结石形成中的潜在作用。肾结石是一种在一生中至少影响近10%普通人群的疾病,是一种常见病症,有相当大的急性和慢性肾损伤风险,且有效治疗选择相对较少。
我们通过多个数据库进行文献检索,包括PubMed、Ovid MEDLINE、Web of Science、Scopus和Cochrane图书馆。我们遵循系统评价和Meta分析的首选报告项目(PRISMA)指南。在这项Meta分析研究中,我们纳入了来自六项临床试验的总共11635698例发生肾结石的患者。
在汇总分析中,SGLT2i组中1.27%的患者发生肾结石(n = 739197),而对照组(活性对照、安慰剂或未治疗)中为1.56%(n = 10896501)。与安慰剂相比,SGLT-2抑制剂治疗与较低的肾结石风险相关{比值比[OR] 0.61 [95%置信区间(CI)0.53 - 0.70],P <.00001},或与胰高血糖素样肽1和二肽基肽酶4抑制剂等活性治疗相比[OR 0.66(95% CI 0.47 - 0.93),P =.02]。
我们证明与安慰剂或活性对照相比,SGLT2i治疗降低了肾结石风险。潜在的潜在机制包括渗透性利尿导致致石物质浓度降低、抗炎和抗纤维化作用以及尿液pH值升高。显然需要未来进行大规模随机临床试验以更好地评估此类关联。