Department of Applied Statistics and Information Science, Ming Chuan University, Taoyuan City, Taiwan.
Artificial Intelligence Development Center, Fu Jen Catholic University, Taipei, Taiwan.
Diabetes Obes Metab. 2024 Sep;26(9):3868-3879. doi: 10.1111/dom.15734. Epub 2024 Jul 1.
To assess if early change in albuminuria was linked to an initial change in estimated glomerular filtration rate (eGFR) and long-term kidney outcomes in people with type 2 diabetes (T2D) receiving sodium-glucose cotransporter-2 (SGLT2) inhibitors.
Using a medical database from a multicentre healthcare institute in Taiwan, we retrospectively enrolled 8310 people receiving SGLT2 inhibitors from 1 June 2016 to 31 December 2021. We compared the risks of initial eGFR decline, major adverse renal events (MARE; >50% eGFR reduction or development of end-stage kidney disease), major adverse cardiovascular events (MACE), or hospitalization for heart failure (HHF) using a Cox proportional hazards model.
In all, 36.8% (n = 3062) experienced a >30% decrease, 21.0% (n = 1743) experienced a 0%-30% decrease, 14.4% (n = 1199) experienced a 0%-30% increase, and 27.7% (n = 2306) experienced a >30% increase in urine albumin-to-creatine ratio (UACR) after 3 months of SGLT2 inhibitor treatment. Greater acute eGFR decline at 3 months correlated with greater UACR reduction: -3.6 ± 10.9, -2.0 ± 9.5, -1.1 ± 8.6, and -0.3 ± 9.7 mL/min/1.73 m for the respective UACR change groups (p < 0.001). Over a median of 29.0 months, >30% UACR decline was associated with a higher risk of >30% initial eGFR decline (hazard ratio [HR] 2.68, 95% confidence interval [CI] 1.61-4.47]), a lower risk of MARE (HR 0.66, 95% CI 0.48-0.89), and a comparable risk of MACE or HHF after multivariate adjustment (p < 0.05). The nonlinear analysis showed early UACR decline was linked to a lower risk of MARE but a higher risk of initial steep eGFR decline of >30%.
Physicians should be vigilant for the potential adverse effects of abrupt eGFR dipping associated with a profound reduction in UACR, despite the favourable long-term kidney outcomes in the population with T2D receiving SGLT2 inhibitor treatment.
评估 2 型糖尿病(T2D)患者接受钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂治疗后,早期白蛋白尿变化与估算肾小球滤过率(eGFR)的初始变化及长期肾脏结局之间的关系。
我们使用来自台湾一家多中心医疗机构的医疗数据库,回顾性纳入了 2016 年 6 月 1 日至 2021 年 12 月 31 日期间接受 SGLT2 抑制剂治疗的 8310 名患者。我们使用 Cox 比例风险模型比较了初始 eGFR 下降、主要不良肾脏事件(MARE;eGFR 下降超过 50%或发展为终末期肾病)、主要不良心血管事件(MACE)或因心力衰竭住院(HHF)的风险。
在所有患者中,36.8%(n=3062)的患者 UACR 下降超过 30%,21.0%(n=1743)的患者 UACR 下降 0%30%,14.4%(n=1199)的患者 UACR 升高 0%30%,27.7%(n=2306)的患者 UACR 升高超过 30%。SGLT2 抑制剂治疗 3 个月后,急性 eGFR 下降越大,UACR 下降幅度越大:分别为-3.6±10.9、-2.0±9.5、-1.1±8.6 和-0.3±9.7 mL/min/1.73 m(p<0.001)。在中位随访 29.0 个月期间,UACR 下降超过 30%与初始 eGFR 下降超过 30%的风险增加相关(风险比[HR]2.68,95%置信区间[CI]1.61-4.47]),MARE 的风险降低(HR 0.66,95% CI 0.48-0.89),且多变量调整后 MACE 或 HHF 的风险无差异(p<0.05)。非线性分析显示,早期 UACR 下降与 MARE 风险降低相关,但与 eGFR 急剧下降超过 30%的风险增加相关。
尽管 T2D 患者接受 SGLT2 抑制剂治疗后具有长期肾脏获益,但医生仍应警惕与 UACR 显著下降相关的 eGFR 急性下降带来的潜在不良影响。