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Effect of direct renin inhibitor monotherapy on proteinuria in overt diabetic nephropathy
Somrutat Silaratana1, Sangduen Sumransurp, Soodkate Duangchana
1Nephrology Unit, Department of Medicine, Faculty of Medicine, Thammasat University, Klong Nung, Klong Luang, Pathumtani, Thailand.
Background:
Diabetic nephropathy is one of the major causes of chronic kidney disease (CKD), consequently progression to end stage renal disease. The previous studies demonstrated that the inhibition on renin-angiotensin-aldosterone system (RAAS) such as by angiotensin converting enzyme inhibitor (ACEI) and angiotensin type I receptor blocker (ARB) reduced proteinuria and slow progression of CKD. Direct renin inhibitor (DRI) theoretical complete block RAAS by reducing plama renin activity angiotensin I and angiotensin II. The present study aimed to determine the efficacy of aliskiren (DRI) monotherapy on blood pressure control and proteinuria reduction.
Material And Method:
Diabetic mellitus patients with estimated glomerular filtration rate (eGFR) > or = 30 ml/min who had proteinuria > 300 mg/day were enrolled to receive aliskiren 150 mg/day for 2 weeks then 300 mg/day until 24 weeks.
Results:
The SBP were significantly decreased form 137.8 to 123.7 (p = 0.01) at 2 weeks, 137.8 to 126.26 (p = 0.04) at 4 weeks and 137.8 to 121 mmHg (p = 0.002) at 24 weeks after treatment, respectively. Similar to SBP, the DBP was significantly decreased from 84.08 to 73.66 (p = 0.04) at 4 weeks and 84.08 to 75.85 mmHg (p = 0.002) at the end of study. Reduction of UPCR showed significantly reduced for 32.65% (p = 0.007) and 45% (p = 0.004) from baseline at 2 weeks and 24 weeks after DRI treatment respectively. Serum creatinine, eGFR and serum potassium were no significant changed from the baseline. There were no harmful adverse reaction in patients who receiving aliskirin.
Conclusion:
Aliskiren monotherapy showed significantly reduced proteinuria, good blood pressure control without harmful side effect in overt diabetic nephropathy patients.
Insights
Aliskiren, a direct renin inhibitor, effectively reduced blood pressure and proteinuria in patients with diabetic nephropathy. This treatment demonstrated good tolerability and safety, offering a promising option for managing this condition.
Area of Science:
- Nephrology
- Endocrinology
- Pharmacology
Background:
- Diabetic nephropathy is a leading cause of chronic kidney disease (CKD) and end-stage renal disease.
- Inhibition of the renin-angiotensin-aldosterone system (RAAS) via ACE inhibitors and ARBs can slow CKD progression.
- Direct renin inhibitors (DRIs) offer theoretical complete RAAS blockade by reducing renin activity.
Purpose of the Study:
- To evaluate the efficacy of aliskiren, a direct renin inhibitor (DRI), as monotherapy.
- To assess aliskiren's impact on blood pressure control in patients with diabetic nephropathy.
- To determine the effect of aliskiren on proteinuria reduction in overt diabetic nephropathy.
Main Methods:
- Diabetic mellitus patients with eGFR ≥ 30 ml/min and proteinuria > 300 mg/day were enrolled.
- Participants received aliskiren 150 mg/day for 2 weeks, followed by 300 mg/day for 24 weeks.
- Blood pressure, proteinuria (UPCR), serum creatinine, eGFR, and serum potassium were monitored.
Main Results:
- Significant reductions in systolic blood pressure (SBP) and diastolic blood pressure (DBP) were observed throughout the 24-week treatment period.
- Aliskiren treatment led to a significant reduction in urine protein-to-creatinine ratio (UPCR) by 45% at 24 weeks.
- No significant changes in serum creatinine, eGFR, or serum potassium were noted; no harmful adverse reactions were reported.
Conclusions:
- Aliskiren monotherapy effectively controls blood pressure in patients with overt diabetic nephropathy.
- Aliskiren significantly reduces proteinuria in this patient population.
- The treatment demonstrated a favorable safety profile with no significant adverse effects.
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