Aliskiren Combined With Losartan in Proteinuric, Non-diabetic Chronic Kidney Disease

Aliskiren is a direct renin inhibitor that has been shown to reduce proteinuria and retard renal deterioration in type 2 diabetic patients with overt nephropathy. However, it is not known if these therapeutic effects can be extended to nondiabetic chronic renal disease. The current study aims to explore this research question by randomly assigning patients with various stages of chronic renal disease to receive either aliskiren on top of losartan, or continuation of losartan.

Inclusion criteria

• Male or female 18 - 80 years of age
• Presence of nondiabetic CKD stages 3 to 4 as defined by estimated glomerular filtration rate (eGFR by 4-variable MDRD equation) as follows:

• Stage 3: Moderate decrease in GFR 30-59 mL/min/1.73 sq.m
• Stage 4: Severe decrease in GFR 15-29 mL/min/1.73 sq.m
• CKD is defined as either kidney damage or GFR <60 mL/min/1.73 m2 for > 3 months with variations of less than 30% in the 3 months before screening
• Early-morning urinary protein-to-creatinine ratio of >500 mg/g or 57 mg/mmol on at least 2 occasions four weeks apart
• Patients who are willing to give written, informed consent

Exclusion criteria

• eGFR < 15 or > 60 ml/min/1.73m2
• Early-morning urinary protein-to-creatinine ratio of >5000 mg/g or 570 mg/mmol, or urinary protein-to-creatinine ratio of <500 mg/g or 57 mg/mmol
• Serum K+ > 5.2 mmol/L
• Presence of bilateral renal artery stenosis
• Known allergy to losartan or aliskiren
• Patients who are receiving angiotensin II receptor blocker / angiotensin converting enzyme inhibitor combination within 12 weeks of randomization
• Concurrent treatment with corticosteroids, nonsteroidal antiinflammatory drugs, or immunosuppressive agent
• Patients with connective tissue disease or obstructive uropathy
• Patients with concomitant malignancy or any such conditions that will severely limit life expectancy
• Female who are pregnant or intending to conceive
• Female of child-bearing age who are unwilling to practice effective contraception
• Patients who are unable to give informed consent
• Patients simultaneously participating in another study or who have participated in another study within the last 30 days of entry into this study