Rapidly progressive glomerulonephritis laboratory findings

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mohammed Abdelwahed M.D[2] Nazia Fuad M.D.

The most important step in managing rapidly progressive glomerulonephritis is rapid diagnosis. It is essential for organ preservation. Laboratory studies include, complete blood cell count (CBC) with differential, serum electrolytes, BUN, creatinine, lactate dehydrogenase (LDH), creatine phosphokinase (CPK), and liver function tests: The most common abnormality is an increased serum creatinine level. However, the level can be normal at presentation. Tissue enzyme (ie, LDH, CPK) levels may be elevated if there is significant muscle inflammation and myalgias. Urinalysis with microscopy usually show proteinuria but is rarely greater than 2-3 g in 24 hours. Microscopic hematuria may be present and may be the only clue to renal disease at presentation. The presence of red cell casts indicates glomerulonephritis and is a very helpful clue. Erythrocyte sedimentation rate is usually elevated with active disease. C-reactive protein levels are elevated and correspond with disease activity. High antinuclear antibody (ANA) titer rises the suspicion toward systemic lupus erythematosus. More than 80% of patients with microscopic polyangiitis are ANCA-positive. The symptoms of cryoglobulinemia are very similar to those of ANCA-related disease. However, in persons with ANCA-related diseases, the cryoglobulin titer result should be negative. Hepatitis profile should be performed as hepatitis B is associated with polyarteritis nodosa and hepatitis C is associated with mixed cryoglobulinemia. Urine and serum protein electrophoresis is done in any middle-aged or elderly person presenting with rapidly progressive glomerulonephritis to exclude the presence of light-chain disease or noticeable multiple myeloma as a cause of the clinical findings.

• Complete blood count (CBC)
  • Anemia
  • Eosinophilia

• Serum electrolytes

• Creatinine and blood urea nitrogen

• Lactate dehydrogenase (LDH)

• Creatine phosphokinase (CPK)

• Liver function tests

• Erythrocyte sedimentation rate and C-reactive protein (CRP)

• Antinuclear antibody (ANA)

• Anti-GBM antibodies

• ANCA

• Cryoglobulins

• HBV and HCV titers

• Complement C3 and C4 levels

• Serum protein electrophoresis

Laboratory findings

• Anemia , mostly due to impaired production of erythropoietin by kidneys. or GI bleeding.
• Eosinophilia is usually seen in patients with Churg-Strauss disease.
• Patients with RPGN may show formation of immune complexes and cryoglobulins.
• Complement C3 levels is usually low in immune-complex mediated RPGN.
• The presence of ANCA and anti-GBM is variable.
• ANCA-associated glomerulonephritis have high levels of ANCA, it is associated with disease activity.^[1][2][3]

• ESR and CRP may be elevated and indicate inflammation and activity of the disease.

• Urinalysis
• Urinary protein electrophoresis
• Patients with RPGN do not usually have a full-blown picture of nephrotic syndrome; Nephrotic syndrome only occurs in less than 30% of cases.^[4]
• Proteinuria, if present, is usually mild to moderate. Hematuria of glomerular type with dysmorphic red blood cells is usually present on urinalysis and associated with red cell casts.
• Mild to moderate leukocyturia may be seen and other casts, such as epithelial cell leukocyte, or fatty casts. Urinary findings in RPGN are important features that not only favor diagnostic work-up, but also follow-up and therapeutic effectiveness.

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