Abstract
Overt clinical features of IgA nephropathy0 frequently resolve spontaneously and the disease may remain quiescent clinically for months or years. As such, episodes of macroscopic hematuria and evanescent decline in renal function are probably not reliable indices of long-term disease activity whereby the effects of treatment may be gauged. Urinary abnormalities, particularly microscopic hematuria, persist in the majority of patients, however, and many develop gradually increasing proteinuria and hypertension. It is the policy of our unit to monitor these features and serial measurements of renal function to assess progress. It has become clear, however, from study of repeat renal biopsies, that such monitoring does not reflect accurately the changes occurring in kidney morphology. Although there is a loose association between disease progression as assessed by decline of renal function, proteinuria and hypertension with glomerular sclerosis, interstitial scarring and vascular changes, these features are often present in biopsies from patients with no symptoms. By contrast, it is not unusual to discover rather bland changes of mesangial proliferative glomerulonephritis in patients with overt symptoms.
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© 1987 Martinus Nijhoff Publishing, Boston
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Clarkson, A.R. (1987). The Treatment of IgA Nephropathy. In: Clarkson, A.R. (eds) IgA Nephropathy. Topics in Renal Medicine, vol 2. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-2039-5_15
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DOI: https://doi.org/10.1007/978-1-4613-2039-5_15
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