Literature DB >> 33657976

The effect of amiloride in decreasing albuminuria in patients with diabetic kidney diseases: a prospective, crossover, open-label study.

Ruizhao Li1, Zhiyong Xie1,2, Li Zhang1, Ying Huang2, Jianchao Ma1, Wei Dong1, Zhilian Li1, Yuanhan Chen1, Huaban Liang1, Yanhua Wu1, Xingchen Zhao1, Wenjian Wang1, Zhiming Ye1, Shuangxin Liu1, Wei Shi1, Xinling Liang1,2.   

Abstract

BACKGROUND: Diabetic kidney diseases (DKD) were the leading cause of End-stage renal diseases worldwide. Albuminuria was a target for treatment in DKD and decreasing albuminuria was particularly important for improving its prognosis. However, there is still a lack of specific treatment for DKD.
METHODS: We conducted a prospective, crossover, open-label study to investigate the effect of amiloride in patients with DKD. Safety and efficacy were assessed by monitoring urine protein creatinine ratio(uPCR), urinary albumin creatinine ratio (uACR), blood pressure, weight, serum sodium, serum potassium, cholesterol, triglyceride, uric acid, serum soluble urokinase-type plasminogen activator receptor (suPAR) and urinary suPAR. Ten subjects were enrolled in the trial.
RESULTS: In this prospective, crossover, open-label design, amiloride could induce a significant decrease of uACR in DKD. The decrease of serum and urinary suPAR in the amiloride/hydrochlorothiazide (HCTZ) group was also significant compared with those patients using HCTZ as the control group. Correlation analysis showed that the levels of urinary suPAR were positively associated with uPCR and uACR. No significant difference in blood pressure, weight, serum sodium, serum potassium, cholesterol, triglyceride, uric acid was seen between the amiloride/HCTZ group and the control group.
CONCLUSION: In summary, among patients with DKD, amiloride could decrease albuminuria without severe side effects, which was accompanied by the significant decline of urinary suPAR.

Entities:  

Keywords:  Diabetic kidney disease; albuminuria; amiloride; soluble urokinase-type plasminogen activator receptor

Mesh:

Substances:

Year:  2021        PMID: 33657976      PMCID: PMC7935116          DOI: 10.1080/0886022X.2021.1892759

Source DB:  PubMed          Journal:  Ren Fail        ISSN: 0886-022X            Impact factor:   2.606


  32 in total

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