Praxis Medical Insights

Est. 2024 • Clinical Guidelines Distilled

Made possible by volunteer editors from the University of Calgary & University of Alberta

Last Updated: 7/25/2025

Kidney Disease Diagnosis and Management

Diagnostic Considerations

  • Immunofluorescence is recommended in specific scenarios, such as when glomeruli are lacking in frozen tissue samples or in patients with monoclonal gammopathy with C3 glomerulonephritis or unclassified proliferative glomerulonephritis, with a moderate level of evidence, as suggested by the American Society of Nephrology 1
  • IgA nephropathy diagnosis requires a kidney biopsy, with clinical features including nephritic urinary sediment, proteinuria, impaired renal function, arterial hypertension, and intermittent painless macrohematuria 2
  • Key diagnostic findings on kidney biopsy include immunofluorescence/immunohistochemistry showing mesangial dominant or co-dominant IgA deposits, and light microscopy showing variable mesangial hypercellularity, segmental glomerulosclerosis, endocapillary hypercellularity, tubular atrophy/interstitial fibrosis, and crescents (MEST-C scoring system) 2, 3
  • Electron microscopy may also show electron-dense deposits in the mesangium 3

Laboratory Tests and Monitoring

  • The American College of Radiology recommends assessing kidney function through serum creatinine and estimated glomerular filtration rate (eGFR) for patients with IgA nephropathy 4
  • Blood urea nitrogen (BUN) is also a useful marker for kidney function assessment in IgA nephropathy patients 4
  • Serum electrolytes, including sodium, potassium, chloride, and bicarbonate, should be monitored in patients with IgA nephropathy 4
  • Serum calcium and phosphate levels are also important to monitor in IgA nephropathy patients, according to Nature Reviews Nephrology 1
  • A complete blood count (CBC) with differential and platelet counts is recommended for patients with IgA nephropathy, as suggested by the Journal of the American College of Radiology 4
  • Serum albumin levels should be monitored in patients with IgA nephropathy, particularly those with significant proteinuria, as recommended by the Journal of the American College of Radiology 4
  • Serum uric acid levels are also important to monitor in IgA nephropathy patients, according to Nature Reviews Nephrology 1
  • Serum and urine glucose levels should be assessed to evaluate for Fanconi syndrome in patients with IgA nephropathy 1
  • Lactate dehydrogenase (LDH) levels may be useful in monitoring disease activity in IgA nephropathy patients, as suggested by the Journal of the National Comprehensive Cancer Network 5

Treatment and Management

  • All patients with IgA nephropathy should receive optimized supportive care, including RAS blockade (ACE inhibitors or ARBs) for all patients with proteinuria >0.5 g/day, regardless of hypertension status (Grade 1B) 2, 6
  • Blood pressure control with targets of <130/80 mmHg if proteinuria <1 g/day and <125/75 mmHg if proteinuria ≥1 g/day is recommended 6
  • Sodium restriction (<2.0 g/day) is recommended to enhance antiproteinuric effects 2, 6
  • SGLT2 inhibitors may be considered as emerging therapy for renoprotection 2, 6
  • For patients with persistent proteinuria despite supportive care, a 6-month course of glucocorticoid therapy (Grade 2B) may be considered if proteinuria remains >0.75-1 g/day despite at least 90 days of optimized supportive care 2
  • Glucocorticoids should be avoided or used with extreme caution in patients with certain conditions, such as eGFR <30 ml/min per 1.73 m², diabetes, obesity, latent infections, secondary disease, active peptic ulceration, uncontrolled psychiatric disease, and severe osteoporosis 2

Follow-up and Prevention

  • Regular monitoring should include proteinuria levels, renal function (serum creatinine, eGFR), blood pressure, and hematuria 2, 6
  • A reduction in proteinuria to under 1 g/day is a surrogate marker of improved kidney outcome in IgAN and represents a reasonable treatment target 2
  • Infection prevention measures, such as pneumococcal and influenza vaccines, should be considered, especially if immunosuppression is planned 2
  • The MEST-C histologic scoring system is used to evaluate mesangial and endocapillary hypercellularity, segmental glomerulosclerosis, interstitial fibrosis/tubular atrophy, and crescents, and helps estimate disease progression risk 2
  • The International IgAN Prediction Tool is also used to estimate disease progression risk 2