Related Experiment Video
Updated: Jun 22, 2026

Dioscin Mediated IgA Nephropathy Alleviation by Inhibiting B Cell Activation In Vivo and Decreasing Galactose-Deficient IgA1 Production In Vitro
Published on: October 13, 2023
Beneficial effects of high-dose losartan in IgA nephritis
1Department of Renal Medicine, Singapore General Hospital, Singapore. woo.keng.thye@sgh.com.sg
Insights
High-dose angiotensin II receptor blockers (ARBs) significantly reduced proteinuria and preserved kidney function in IgA nephritis patients over six years. This therapy may even allow for renal function recovery, unlike standard doses.
Area of Science:
- Nephrology
- Pharmacology
- Immunology
Background:
- Short-term studies indicate high-dose Angiotensin II Receptor Blockers (ARBs) reduce proteinuria in diabetic nephropathy.
- Long-term efficacy of high-dose ARBs, specifically losartan, in IgA nephritis remains unexplored.
Purpose of the Study:
- To investigate the long-term effects of high-dose ARB losartan on renal function and proteinuria in patients with IgA nephritis.
- To compare high-dose ARB therapy with normal-dose ARB and ACEI (Angiotensin-Converting Enzyme Inhibitor) treatments.
Main Methods:
- A 6-year randomized trial involving 207 IgA nephritis patients.
- Comparison of four treatment groups: high-dose ARB (losartan 200 mg/day), normal-dose ARB (losartan 100 mg/day), normal-dose ACEI (20 mg/day), and low-dose ACEI (10 mg/day).
- Multivariate ANOVA used to analyze the impact of treatments on estimated Glomerular Filtration Rate (eGFR) and Total Urinary Protein (TUP).
Main Results:
- High-dose ARB group (n=63) showed significantly higher eGFR (p < 0.0005) and lower proteinuria (p < 0.005) compared to normal-dose ARB (n=43), normal-dose ACEI (n=61), and low-dose ACEI (n=40) groups.
- Annual eGFR loss was 0.7 ml/min/year for high-dose ARB versus 3.2-3.5 ml/min/year for other groups (p = 0.0005).
- More patients in the high-dose ARB group experienced eGFR improvement (p < 0.001).
Conclusions:
- High-dose ARB therapy demonstrates superior efficacy in reducing proteinuria and preserving renal function in IgA nephritis compared to standard ARB and ACEI doses.
- A notable gain in eGFR observed in Year 5 for high-dose ARB patients suggests potential for renal function recovery with long-term treatment.
Aim:
Several short-term studies have reported the efficacy of high-dose ARB in reducing proteinuria in patients with diabetic nephropathy. The benefits of long-term high-dose ARB losartan in IgA nephritis have not been explored.
Method:
This was a 6-year randomized trial in 207 patients with IgA nephritis comparing high-dose ARB (losartan 200 mg/day) with normal dose ARB (losartan 100 mg/day), normal dose ACEI (20 mg/day) and low-dose ACEI (10 mg/day). Multivariate ANOVA was used to test the effect of drug treatment on both eGFR and total urinary protein (TUP).
Results:
Comparing patients on high-dose ARB (n = 63) with those on normal dose ARB (n = 43), normal dose ACEI (n = 61) and low-dose ACEI (n = 40), patients on high Dose ARB had significantly higher eGFR (p < 0.0005) and lower proteinuria (p < 0.005) at the end of the study. The loss in eGFR was 0.7 ml/min/year for high-dose ARB compared to 3.2 - 3.5 ml/ min/year for the other 3 groups (p = 0.0005). There were more patients on high-dose ARB with improvement in eGFR compared to other 3 groups (p < 0.001).
Conclusion:
Data from this study suggest that high-dose ARB therapy is more efficacious in reducing proteinuria and preserving renal function when compared with normal dose ARB and ACEI. In Year 5, patients on high-dose ARB had a gain in eGFR suggesting that there is possibility of recovery of renal function in these patients on long-term high-dose therapy.
Related Concept Videos
Antihypertensive Drugs: Angiotensin II Receptor Blockers
Antihypertensive Drugs: Direct Renin Inhibitors
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors
Acute Kidney Injury IV: Diagnostic Studies and Prevention
Antihypertensive Drugs: Action of Diuretics
