Abstract

BackgroundAlthough urinary angiotensinogen (AGT) and renin reflect intrarenal renin-angiotensin system activity and are enhanced in proteinuric chronic kidney disease, the clinical value of urinary AGT and renin levels during antiproteinuric treatment has yet to be determined. We investigated the clinical usefulness of initial urinary AGT or renin to determine the antiproteinuric effects of angiotensin receptor blockers (ARBs).MethodsThis multicenter, prospective, single-arm study included 205 patients with overt proteinuria (urinary protein/creatinine ratio [uPCR] ≥ 1 mg/mg) enrolled between April 2009 and December 2011. All patients were treated with valsartan. The urinary AGT/creatinine ratio (uAGT/Cr) was measured at the baseline and 24 weeks, and the renin/creatinine ratio (uR/Cr) was measured at the baseline. Fifty-six patients were followed-up for 5 years.ResultsThe mean age was 47.6 years and 51.2% were male. The mean uPCR was 2.32 mg/mg and the mean eGFR was 63.2 mL/min/1.73m2. Natural logarithms (ln) (uAGT/Cr), ln(uR/Cr), and diabetes mellitus were associated with proteinuria decrement (decrease in uPCR ≥1 mg/mg). Ln(uAGT/Cr) was an independent predictor for proteinuria decrement (OR 1.372, 95% CI, 1.068–1.762, P = 0.013). Among the 56 patients followed-up for 5 years, Δln(uAGT/Cr) at 24 weeks was an independent predictor for uPCR < 1 mg/mg at 5 years (OR 0.379, 95% CI, 0.20–0.715, P = 0.003).ConclusionsOur study demonstrates the potential role of both baseline urinary AGT and changes in urinary AGT during the initial 24 weeks as surrogate markers predicting the antiproteinuric effects of ARBs in patients with overt proteinuria.

Highlights

  • Urinary angiotensinogen (AGT) and renin reflect intrarenal renin-angiotensin system activity and are enhanced in proteinuric chronic kidney disease, the clinical value of urinary AGT and renin levels during antiproteinuric treatment has yet to be determined

  • Previous studies have shown that angiotensin-converting enzyme inhibitors (ACEi) or angiotensin II receptor blockers (ARBs) that inhibit renin-angiotensin system (RAS) mitigate the progression of chronic kidney disease (CKD) by reducing proteinuria beyond their blood pressure-lowering effects [1, 2]

  • We aimed to investigate the clinical relevance of urinary AGT or renin in the treatment of proteinuria by analyzing the association between urinary AGT or renin excretion and the antiproteinuric effects of RAS inhibitors

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Summary

Introduction

Urinary angiotensinogen (AGT) and renin reflect intrarenal renin-angiotensin system activity and are enhanced in proteinuric chronic kidney disease, the clinical value of urinary AGT and renin levels during antiproteinuric treatment has yet to be determined. We investigated the clinical usefulness of initial urinary AGT or renin to determine the antiproteinuric effects of angiotensin receptor blockers (ARBs). Inhibition of the renin-angiotensin system (RAS) is a cornerstone of managing chronic kidney disease (CKD) patients with proteinuria including diabetic nephropathy and glomerulonephritis. Previous studies have shown that angiotensin-converting enzyme inhibitors (ACEi) or angiotensin II receptor blockers (ARBs) that inhibit RAS mitigate the progression of CKD by reducing proteinuria beyond their blood pressure-lowering effects [1, 2]. Since the enzyme-linked immunosorbent assay (ELISA) system measuring AGT was developed, several clinical studies have demonstrated that urinary AGT excretion increases in patients with hypertension [9], CKD [7, 10], or diabetes mellitus (DM) [11] regardless of plasma AGT levels

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