Cc. Szeto et al., The natural history of immunoglobulin A nephropathy among patients with hematuria and minimal proteinuria, AM J MED, 110(6), 2001, pp. 434-437
Citations number
20
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
PURPOSE: To determine the natural history of immunoglobulin (Ig) A nephropa
thy among patients who presented with hematuria and minimal proteinuria, an
d factors associated with the development of adverse clinical events, such
as proteinuria.
SUBJECTS AND METHODS: In Hong Kong, all patients who present with isolated
hematuria are referred for renal biopsy after urologic diseases are ruled o
ut. We reviewed the clinical course of 72 consecutive patients with histolo
gically confirmed IgA nephropathy who presented with hematuria and minimal
proteinuria (0.4 g/day or less). All patients were normotensive and had nor
mal renal function at presentation. Adverse events were defined as proteinu
ria greater than 1 g per day, hypertension, or impaired renal function (ser
um creatinine level 120 mu mol/L or estimated creatinine clearance <70 mt p
er minute).
RESULTS: The mean (<plus/minus> SD) age at presentation was 27 +/- 8 years;
56 (78%) were female. Nine patients (13%) had grade 2 histologic lesions.
During a median follow-up of 7 years, 32 patients (44%) developed adverse e
vents: 24 (33%) developed proteinuria of 1 g per day or more, 19 (26%) beca
me hypertensive, and 5 (7%) developed impaired renal function. Another 30 p
atients (42%) had persistently abnormal urinalysis examinations. Only 10 pa
tients (14%) had complete resolution of hematuria. The median time for prog
ression from proteinuria (>1 g/day) to renal impairment was 84 months (rang
e 56 to 132). In a multivariate analysis, age at presentation (relative ris
k [RR] per 10 years of age = 2.0; 95% confidence interval [Ci], 1.2 to 3.4)
and histologic grade (grade 2 versus grade 1, RR = 4.5; 95% CI, 1.7 to 12)
were independent predictors of developing an adverse event.
CONCLUSIONS: IgA nephropathy that presents with hematuria and minimal prote
inuria is usually a progressive disease. Life-long follow-up with regular m
onitoring of blood pressure and proteinuria is recommended. Am (C) 2001 by
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