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PLA2 receptor antibody
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Autoantibody test.
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PLA2 Receptor Antibody Test Information Guide
- Why is it done?
- Detects autoantibodies directed against the M-type phospholipase A2 receptor (PLA2R), a major antigen in membranous nephropathy
- Diagnose primary membranous nephropathy (PMN) and differentiate it from secondary causes of membranous glomerulonephritis
- Assess disease activity and prognosis in patients with established membranous nephropathy
- Monitor treatment response and disease progression over time
- Evaluate patients presenting with nephrotic syndrome, proteinuria, or glomerulonephritis
- Performed when kidney biopsy demonstrates membranous pattern or when clinical suspicion for membranous nephropathy exists
- Normal Range
- Negative/Not Detected: <0.5 RU/mL or negative result
- Equivocal/Borderline: 0.5-1.0 RU/mL (may require repeat testing)
- Positive: >1.0 RU/mL (indicates presence of anti-PLA2R antibodies)
- Units of Measurement: RU/mL (Relative Units per milliliter)
- Normal Result: Absence of anti-PLA2R antibodies indicates either healthy status or membranous nephropathy caused by secondary factors (lupus, hepatitis B, NSAIDs, malignancy) rather than primary membranous nephropathy
- Abnormal Result: Positive antibody test strongly suggests primary membranous nephropathy and correlates with disease activity
- Interpretation
- Positive Result (>1.0 RU/mL): Indicates primary membranous nephropathy; found in approximately 70-80% of primary PMN cases; higher antibody titers often correlate with worse prognosis and greater likelihood of progression; suggests active autoimmune response against glomerular basement membrane
- Negative Result (<0.5 RU/mL): May indicate secondary membranous nephropathy (10-20% of PMN is actually PLA2R-negative); suggests membranous changes due to systemic disease, malignancy, infection, or medications; requires investigation for alternative etiologies
- Borderline Result (0.5-1.0 RU/mL): Requires repeat testing; may represent emerging disease or falling titers after treatment; clinical correlation recommended
- Antibody Titer Correlation: Higher titers correlate with proteinuria severity, active disease, and higher risk of progression to renal failure; declining titers after treatment suggest therapeutic response; rising titers may indicate disease relapse or inadequate treatment response
- Factors Affecting Results:
- Stage of disease (early disease may have lower titers); immunosuppressive therapy (can reduce antibody levels); genetic predisposition; concurrent infections or malignancies; timing of sample collection relative to disease onset
- Clinical Significance: PLA2R antibodies have 98% specificity for primary membranous nephropathy; negative test in membranous pattern should prompt evaluation for secondary causes and THSD7A antibodies; serial monitoring helps predict renal outcome and guides treatment intensity
- Associated Organs
- Primary Organ System: Kidneys (specifically glomeruli within the renal filtration system)
- Primary Membranous Nephropathy: Autoimmune glomerulonephritis characterized by immune complex deposition along the glomerular basement membrane; leads to proteinuria and progressive renal dysfunction
- Associated Diseases and Conditions:
- Nephrotic syndrome (massive proteinuria >3.5g/day, hypoalbuminemia, edema, hyperlipidemia); chronic kidney disease (progressive loss of renal function); end-stage renal disease (ESRD) requiring dialysis or transplantation; hypertension secondary to renal disease
- Potential Complications:
- Acute kidney injury; rapid progression to renal failure; thrombosis (venous and arterial due to urinary loss of anticoagulant proteins); severe hypertension; cardiovascular complications from proteinuria and hypertension; infection from immunosuppressive therapy; malnutrition from protein wasting
- Secondary Organ Involvement: Cardiovascular system (hypertension, atherosclerosis, coronary artery disease); hematologic system (hypercoagulability, thromboembolism); metabolic system (dyslipidemia, malnutrition)
- Follow-up Tests
- Recommended Follow-up Testing:
- Repeat PLA2R antibody testing at 3-6 month intervals to monitor disease activity and treatment response; declining titers indicate therapeutic efficacy
- Serum creatinine and calculated glomerular filtration rate (GFR) to assess renal function; baseline and periodic monitoring monthly to quarterly depending on disease progression
- 24-hour urine protein quantification or urine protein-to-creatinine ratio to measure proteinuria severity; critical for prognosis and treatment decisions
- Serum albumin and total serum protein to assess nutritional status and disease severity
- Lipid panel (cholesterol, triglycerides) as nephrotic syndrome causes dyslipidemia and cardiovascular risk
- THSD7A (thrombospondin type 1 domain-containing protein 7A) antibody testing for PLA2R-negative cases to identify alternative causes of primary membranous nephropathy
- Kidney biopsy if diagnosis unclear or to confirm membranous pattern histologically; immunofluorescence microscopy shows IgG and C3 deposits along glomerular basement membrane
- Screening for Secondary Causes:
- Antinuclear antibody (ANA), anti-double stranded DNA (dsDNA), and complement levels (C3, C4) to screen for lupus
- Hepatitis B and C serologies to exclude hepatitis-associated membranous nephropathy
- Imaging studies (chest X-ray, abdominal ultrasound, CT imaging) to screen for underlying malignancy in older patients with new-onset membranous nephropathy
- Monitoring During Treatment:
- Immunosuppressive therapy monitoring (complete blood count, liver function tests, drug levels if applicable)
- Coagulation studies and D-dimer if thrombosis suspected due to hypercoagulability
- Blood pressure monitoring (periodic checks, home monitoring if hypertensive)
- Fasting Required?
- Fasting Requirement: No - fasting is not required for PLA2 receptor antibody testing
- Sample Collection: Standard blood draw can be performed at any time of day; food and fluid intake do not affect antibody detection or measurement
- Medications: Continue all current medications as prescribed; immunosuppressive therapy does not interfere with test accuracy (though it may lower antibody titers); notify laboratory of all medications being taken, especially immunosuppressants, corticosteroids, anticoagulants
- Patient Preparation:
- No special preparation required; arrive at collection time well-hydrated (normal fluid intake acceptable and helpful for phlebotomy)
- Wear loose or easily rolled-up sleeves to facilitate blood draw from the arm
- Inform phlebotomist of any bleeding disorders, anticoagulant use, or difficulty with blood draws
- Inform laboratory of recent infections or vaccinations (may theoretically affect immune response, though rarely clinically significant for this test)
- Note if sample is being collected at baseline for diagnostic purposes or as follow-up testing during disease monitoring/treatment response assessment
- Specimen Handling: Blood drawn into serum separator tube (SST); allow specimen to clot for 30-60 minutes at room temperature before centrifugation; ship at appropriate temperature according to laboratory protocols
How our test process works!

