Yang Hao, Yang Lili, Jardine Meg J, Arnott Clare, Neuen Brendon L, Xu Kexi, Zhao Xiaohui, Qian Dehui, Cui Bin, Qiu Youzhu, Huang Yuli, Yu Jie, Wang Jiang, Yu Shiyong, Tan Hu, Huang Lan, Li Jing-Wei, Jin Jun
Department of Cardiology, Xinqiao Hospital, Army Military Medical University, No. 83 Xinqiao Street, Shapingba District, Chongqing, 400037, China.
Department of Information, Xinqiao Hospital, Army Medical University, Chongqing, China.
Eur J Med Res. 2024 Dec 24;29(1):621. doi: 10.1186/s40001-024-02214-7.
Sodium-glucose cotransporter-2 inhibitors (SGLT2i) have been proven to prevent decline in kidney function and failure. Whether SGLT2i affect the risk of contrast-associated acute kidney injury (CA-AKI) remains uncertain.
Use of SGLT2i was assessed in consecutive diabetics undergoing coronary angiography (CA) or percutaneous coronary intervention (PCI) from January 2020 to May 2023 at a tertiary hospital in Chongqing, China. Propensity-matched analysis was used to adjust for baseline variables. CA-AKI was defined by the Acute Kidney Injury Network (AKIN) as creatinine increase ≥ 0.3 mg/dl (26.4 μmol/l), or a percentage increase in the serum creatinine level of ≥ 50%.
A total of 604 new users of SGLT2i, and 298 chronic users of SGLT2i were matched with non-users. New use of SGLT2i was not associated with an increased incidence of AKIN-defined CA-AKI (OR 1.60; 95% CI 0.97-2.63; p = 0.065), in-hospital new-onset dialysis (OR 0.50; 95% CI 0.09-2.73; p = 0.422), or death (OR 0.55; 95% CI 0.18-1.66; p = 0.289). However, it was associated with a minor (> 25%) creatinine elevation (OR 1.55; 95% CI 1.04-2.30; p = 0.030), a 0.3 mg/dl increase in creatinine (OR 1.66; 95% CI 1.01-2.75; p = 0.048), and CMSC-defined CA-AKI (OR 1.51; 95% CI 1.02-2.24; p = 0.039). By 90 days, there was no evidence creatinine elevation differed between the two groups (p = 0.590). Chronic use of SGLT2i was not associated with AKIN-defined CA-AKI (OR, 0.92; 95% CI 0.41-2.05; p = 0.838).
New use of SGLT2i during CA or PCI was not associated with an AKIN-defined CA-AKI, and it did not translate into new-onset dialysis or death during hospital stay. Chronic usage of SGLT2i did not affect creatinine. Further randomized clinical trials are warranted to confirm this finding.
钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)已被证实可预防肾功能下降和肾衰竭。SGLT2i是否会影响造影剂相关急性肾损伤(CA-AKI)的风险仍不确定。
对2020年1月至2023年5月在中国重庆一家三级医院接受冠状动脉造影(CA)或经皮冠状动脉介入治疗(PCI)的连续性糖尿病患者使用SGLT2i的情况进行评估。采用倾向评分匹配分析来调整基线变量。急性肾损伤网络(AKIN)将CA-AKI定义为肌酐升高≥0.3mg/dl(26.4μmol/l),或血清肌酐水平升高≥50%。
共有604名SGLT2i新使用者和298名SGLT2i长期使用者与未使用者进行了匹配。SGLT2i的新使用与AKIN定义的CA-AKI发病率增加无关(比值比[OR]1.60;95%置信区间[CI]0.97-2.63;p=0.065)、住院期间新发透析(OR 0.50;95%CI 0.09-2.73;p=0.422)或死亡(OR 0.55;95%CI 0.18-1.66;p=0.289)。然而,它与肌酐轻度升高(>25%)(OR 1.55;95%CI 1.04-2.30;p=0.030)、肌酐升高0.3mg/dl(OR 1.66;95%CI 1.01-2.75;p=0.048)以及心血管和肾脏医学学会(CMSC)定义的CA-AKI(OR 1.51;95%CI 1.02-2.24;p=0.039)相关。到90天时,没有证据表明两组之间肌酐升高存在差异(p=0.590)。SGLT2i的长期使用与AKIN定义的CA-AKI无关(OR 0.92;95%CI 0.41-2.05;p=0.838)。
在CA或PCI期间新使用SGLT2i与AKIN定义的CA-AKI无关,且不会导致住院期间新发透析或死亡。SGLT2i的长期使用不影响肌酐水平。需要进一步的随机临床试验来证实这一发现。