What labs are recommended for diagnosing and managing IgA (Immunoglobulin A) nephritis?

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Laboratory Tests for IgA Nephropathy: Diagnosis and Management

For diagnosing and managing IgA nephropathy, a comprehensive panel of laboratory tests is essential, including urinalysis with microscopy, proteinuria quantification, kidney function tests, and serological markers to assess disease activity and exclude secondary causes. 1

Initial Diagnostic Evaluation

Essential Laboratory Tests

  • Urinalysis with microscopy

    • Assess for glomerular hematuria (dysmorphic red blood cells)
    • Look for red blood cell casts
    • Evaluate for proteinuria by dipstick
  • Quantification of Proteinuria

    • 24-hour urine collection for total protein excretion (gold standard) 1
    • First morning urine protein-to-creatinine ratio (PCR) (preferred in pediatric patients) 1
    • Note: Random "spot" urine collections are not ideal due to variation in protein and creatinine excretion 1
  • Kidney Function Assessment

    • Serum creatinine
    • Estimated glomerular filtration rate (eGFR)
    • Blood urea nitrogen (BUN)
  • Complement Studies

    • C3 and C4 levels (typically normal in primary IgA nephropathy)
    • Low C3 may indicate secondary forms or infection-related glomerulonephritis 1

Exclusion of Secondary Causes

  • Serological Tests

    • Hepatitis B surface antigen and core antibody
    • Hepatitis C antibody
    • HIV antibody
    • Antinuclear antibody (ANA)
    • Anti-neutrophil cytoplasmic antibody (ANCA)
    • Anti-glomerular basement membrane (anti-GBM) antibody 1
  • Immunological Tests

    • Serum immunoglobulin levels (IgA, IgG, IgM)
    • Rheumatoid factor
    • Cryoglobulins 1

Risk Assessment for Disease Progression

Prognostic Laboratory Markers

  • Persistent proteinuria (>1 g/day is a major risk factor) 1
  • eGFR at presentation and during follow-up 1
  • Time-averaged proteinuria (most important prognostic factor) 1

Monitoring Parameters

  • Regular monitoring of proteinuria
    • Target: reduction to <1 g/day 1
  • Blood pressure measurements
    • Target: <130/80 mmHg if proteinuria <1 g/day
    • Target: <125/75 mmHg if proteinuria >1 g/day 1
  • Serum creatinine and eGFR trends
    • Monitor for decline in kidney function 1

Special Considerations

Pediatric Patients

  • First morning PCR is preferred over 24-hour collections 1
  • More frequent monitoring may be required 1

Patients with Suspected IgA Vasculitis (Henoch-Schönlein Purpura)

  • Additional urinary biomarkers may be helpful:
    • Kidney injury molecule-1
    • Monocyte chemotactic protein-1
    • N-acetyl-β-glucosaminidase
    • Angiotensinogen 2

Monitoring During Treatment

  • For patients on immunosuppressive therapy:
    • Complete blood count
    • Liver function tests
    • Drug levels (if applicable)
    • Monitor for medication side effects 1

Kidney Biopsy Indications

While not a laboratory test per se, kidney biopsy is the gold standard for diagnosis and should be considered when:

  • Proteinuria >0.5-1 g/day
  • Persistent hematuria with any level of proteinuria
  • Declining kidney function
  • To assess histological features for prognosis (MEST-C score) 1, 3

Follow-up Laboratory Testing

  • Frequency: Every 3-6 months initially, then adjusted based on disease activity
  • Parameters:
    • Urinalysis with microscopy
    • Quantification of proteinuria (24-hour collection or PCR)
    • Serum creatinine and eGFR
    • Blood pressure monitoring 1

Common Pitfalls to Avoid

  • Don't rely solely on dipstick for proteinuria quantification - formal quantification is essential
  • Don't assume normal complement levels rule out all secondary causes
  • Don't overlook the need for long-term monitoring - even patients with minimal proteinuria at presentation can progress (44% develop adverse events within 7 years) 4
  • Don't miss the opportunity for early intervention - patients with hematuria and minimal proteinuria may have significant histological damage and risk of progression 5

By systematically applying these laboratory tests, clinicians can accurately diagnose IgA nephropathy, assess disease severity, monitor progression, and guide therapeutic decisions to improve patient outcomes.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

IgA vasculitis nephritis.

Current opinion in pediatrics, 2022

Research

IgA nephropathy in adults-treatment standard.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2023

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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