Efficacy and Safety of Low-Dose Spironolactone in Management of Diabetic Kidney Disease in a Real-World Setting

IF 2.6 Q3 ENDOCRINOLOGY & METABOLISM
Manochehr Amini, Davood Dalil, Fatemeh Yaghoubi, Zoleykha Valizadeh, Farnaz Tavakoli, Zohreh Koohpayezadeh
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Abstract

Background

Adding spironolactone to renin-angiotensin-aldosterone system (RAAS) blockers has been shown to reduce albuminuria in patients with diabetic kidney disease (DKD). However, the increased risk of hyperkalaemia is a major concern. This study aimed to evaluate the efficacy and safety of low-dose (12.5 mg/day) spironolactone in reducing albuminuria and improving renal function in Iranian adults with DKD.

Methods

This was a pre-post-treatment study of 60 patients with type 2 diabetes, age > 18 years, albuminuria ≥ 30 mg, estimated glomerular filtration rate (eGFR) ≥ 30 mL/min/1.73 m2, and serum potassium level ≤ 5 mEq/L, who were referred to the diabetes clinic of Shariati Hospital, Tehran, Iran. The patients were prescribed spironolactone (12.5 mg) once daily. Changes in urinary albumin excretion (U.Alb), urine albumin-to-creatinine ratio (uACR), blood pressure, serum creatinine (Cr) levels, and serum potassium levels from the baseline over the 12-week intervention period were measured. Statistical significance was set at p < 0.05.

Results

After 12 weeks of taking 12.5 mg/day spironolactone, there was a statistically significant but modest increase in eGFR (p = 0.042), and a statistically significant decrease was observed in both the U.Alb and uACR (p < 0.001). There was a significant reduction in the mean Cr level (p = 0.003). Systolic blood pressure did not decrease significantly (p = 0.079), but diastolic blood pressure decreased significantly (p = 0.007). Changes in serum potassium levels over time were not significant (p = 0.302). The reduction in albuminuria in patients taking only spironolactone and those taking spironolactone with SGLT2i was not significantly different (p = 0.916 and p = 0.948, respectively).

Conclusions

This study found that adding spironolactone to RAAS blockers effectively reduced albuminuria, mildly increased eGFR, and improved renal outcomes in patients with DKD. Additionally, spironolactone significantly reduced albuminuria, regardless of the concurrent use of SGLT2i.

Abstract Image

低剂量螺内酯治疗糖尿病肾病的有效性和安全性
在肾素-血管紧张素-醛固酮系统(RAAS)阻滞剂中加入螺内酯已被证明可以减少糖尿病肾病(DKD)患者的蛋白尿。然而,高钾血症风险的增加是一个主要问题。本研究旨在评估低剂量(12.5 mg/天)螺内酯在减少伊朗成人DKD患者蛋白尿和改善肾功能方面的有效性和安全性。方法对60例就诊于伊朗德黑兰Shariati医院糖尿病门诊、年龄18岁、蛋白尿≥30 mg、估计肾小球滤过率(eGFR)≥30 mL/min/1.73 m2、血清钾水平≤5 mEq/L的2型糖尿病患者进行治疗前后研究。患者给予螺内酯12.5 mg,每日1次。在12周的干预期内测量尿白蛋白排泄(ualb)、尿白蛋白与肌酐比值(uACR)、血压、血清肌酐(Cr)水平和血清钾水平的变化。p <; 0.05为统计学意义。结果服用12.5 mg/d螺内酯12周后,eGFR升高有统计学意义但幅度不大(p = 0.042), ualb和uACR降低有统计学意义(p < 0.001)。平均Cr水平显著降低(p = 0.003)。收缩压无明显降低(p = 0.079),舒张压明显降低(p = 0.007)。血清钾水平随时间的变化不显著(p = 0.302)。单用螺内酯组与单用螺内酯组合并SGLT2i组蛋白尿减少量差异无统计学意义(p = 0.916, p = 0.948)。本研究发现,在RAAS阻滞剂中加入螺内酯可有效降低DKD患者的蛋白尿,轻度增加eGFR,并改善肾脏预后。此外,无论是否同时使用SGLT2i,螺内酯均可显著降低蛋白尿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Endocrinology, Diabetes and Metabolism
Endocrinology, Diabetes and Metabolism Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
5.00
自引率
0.00%
发文量
66
审稿时长
6 weeks
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