在肾小球滤过率低于25 mL/min/1.73 m2的情况下,finerenone对糖尿病肾病结局的影响

Akira Mima, Rina Lee, Ami Murakami, Hidemasa Gotoda, Ryosuke Akai, Sayumi Kidooka, Takahiro Nakamoto, Suguru Kido, Shinji Lee
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引用次数: 1

摘要

背景在芬瑞酮降低糖尿病肾病心血管死亡率和发病率的试验中,芬瑞酮减少了慢性肾病(CKD)和2型糖尿病患者心血管事件的风险,而在芬瑞诺降低糖尿病肾病肾衰竭和疾病进展的试验中,它改善了晚期CKD患者的肾脏和心血管结果。然而,以前没有研究评估肾小球滤过率(eGFR)低于25 mL/min/1.73 m2的CKD和2型糖尿病患者。研究了从给药前1年到给药后6个月eGFR、尿蛋白和血清钾水平的变化。结果平均基线eGFR斜率为−7.63±9.84(mL/min/1.73m2/年)。芬瑞酮治疗后,平均eGFR坡度显著改善−1.44±3.17(mL/mn/1.73m2/6个月,P=0.038)。然而,芬瑞酮处理并没有显著减少蛋白尿。此外,芬瑞酮不会增加血清钾水平。结论芬瑞酮治疗的患者肾小球滤过率下降速度明显减慢。此外,除了本研究外,没有报告表明芬瑞酮对eGFR低于25 mL/min/1.73 m2的晚期CKD患者的有效性。正如我们的临床试验所证实的那样,芬瑞酮对广泛的肾功能有效的发现可以推广到临床实践中。然而,这项研究的样本量很小。因此,将需要进一步的大规模调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of finerenone on diabetic kidney disease outcomes with estimated glomerular filtration rate below 25 mL/min/1.73 m2

Background

In the Finerenone in Reducing Cardiovascular Mortality and Morbidity in Diabetic Kidney Disease trial, finerenone reduced the risk of cardiovascular events in patients with chronic kidney disease (CKD) and type 2 diabetes, while in the Finerenone in Reducing Kidney Failure and Disease Progression in Diabetic Kidney Disease trial, it improved renal and cardiovascular outcomes in patients with advanced CKD. However, no previous studies have assessed patients with CKD and type 2 diabetes with an estimated glomerular filtration rate (eGFR) below 25 mL/min/1.73 m2

Methods

Nine patients with CKD and type 2 diabetes who received finerenone 10 mg/day were analyzed retrospectively. Changes in eGFR, urinary protein, and serum potassium levels were studied from 1 year before administration of finerenone until 6 months after administration.

Results

The mean baseline eGFR slope was −7.63 ± 9.84 (mL/min/1.73 m2/year). After finerenone treatment, the mean eGFR slope significantly improved −1.44 ± 3.17 (mL/min/1.73 m2/6 months, P=0.038). However, finerenone treatment did not significantly reduce proteinuria. Furthermore, finerenone did not increase serum potassium levels.

Conclusions

Patients treated with finerenone showed a significantly slower decline in eGFR. Furthermore, aside from the present study, no reports have indicated the effectiveness of finerenone in patients with advanced CKD with an eGFR below 25 mL/min/1.73 m2. As confirmed in our clinical trials, the finding that finerenone is effective in a wide range of renal functions can be generalized to clinical practice. However, sample size in this study was small. Thus, further large-scale investigations will be needed.

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来源期刊
Metabolism open
Metabolism open Agricultural and Biological Sciences (General), Endocrinology, Endocrinology, Diabetes and Metabolism
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