“…Without proteinuria, the majority of the patients have early IgAN, with the remainder having thin basement membrane disease, Alport's syndrome, interstitial diseases, papillary necrosis, hypercalciuria, hyperuricosuria, or sickle cell trait/disease. [23][24][25] However, in most centers, a renal biopsy is not warranted unless the result would be useful for screening potential living related kidney donors for genetically determined diseases such as Alport's syndrome, for life insurance and employment purposes, or for providing reassurance to the patient. Although the study by Gutiérrez et al gives clinical reassurance that the long-term prognosis of IgAN with minimal proteinuria is favorable, the true prognosis of patients with isolated microhematuria is not completely elucidated, and the findings that isolated microhematuria is an independent risk factor for ESRD is concerning.…”