BACKGROUND/
AIMS:
Immunoglobulin A nephropathy (IgAN) is a generally progressive
disease, even in
patients with favorable prognostic features. In this study, we aimed to investigate the antiproteinuric effect and tolerability of low-
dose valsartan (an
angiotensin II receptor blocker)
therapy in normotensive IgAN
patients with minimal
proteinuria of less than 0.5 to 1.0 g/day.
METHODS:
Normotensive IgAN
patients,
who had persistent
proteinuria with a spot
urine protein-to-
creatinine ratio of 0.3 to 1.0 mg/mg
creatinine, were recruited from five
hospitals and randomly assigned to either 40 mg of
valsartan as the low-
dose group or 80 mg of
valsartan as the regular-
dose group. Clinical and
laboratory data were collected at baseline, and at 4, 8, 12, and 24 weeks after
valsartan therapy.
RESULTS:
Forty-three
patients (low-
dose group, n = 23; regular-
dose group, n = 20) were enrolled in the study.
Proteinuria decreased significantly not only in the regular-
dose group but also in the low-
dose group. The change in
urine protein-to-
creatinine ratio at week 24 was -41.3% +/- 26.1% (p < 0.001) in the regular-
dose group and -21.1% +/- 45.1% (p = 0.005) in the low-
dose group. In the low-
dose group, blood pressure was constant throughout the study period, and there was no symptomatic
hypotension. In the regular-
dose group, blood pressure decreased at weeks 8 and 12. No significant change in
glomerular filtration rate,
serum creatinine level, or
serum potassium level was observed during the study period.
CONCLUSIONS:
Our results suggest that low-
dose valsartan can significantly reduce
proteinuria without causing any intolerability in normotensive IgAN
patients with minimal
proteinuria.