We have previously reported our experience with the use of alternate-d
ay prednisone in the treatment of 6 patients with IgA nephropathy who
have clinical or pathological risk factors for disease progression. We
have now treated a total of 13 patients and followed them from 4 to 1
0 years. Patients received an alternate-morning dose of prednisone for
2-4 years. Dosage began at 60 mg/m2 for 3 month, was reduced to 30 mg
/m2 by 1 year and 15 mg/m2 by 2 years. At last observation, urinary pr
otein excretion was normal in 12 patients and no patient had hematuria
. Twelve patients had normal estimated glomerular filtration rate (GFR
) and one had renal insufficiency (GFR = 38 ml/min per 1.73 m2). A ren
al biopsy was performed in 11 patients after 2 years of treatment. Act
ivity score decreased from 5.2 to 4.3 (P = 0.03) and chronicity score
increased from 2.2 to 2.8 (P = 0.12). There were no complications of t
reatment. When compared with a historical group, the treated patients
had a significant improvement in urinalysis (P <0.00001) and preservat
ion of normal GFR (P = 0.03). We conclude that alternate-day prednison
e therapy may benefit patients with IgA nephropathy. A large prospecti
ve controlled trial is needed.