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ANA Profile
Blood
8 parameters
Report in 12Hrs
At Home
No Fasting Required
Details
Extended panel of antinuclear antibodies.
₹8,499₹12,450
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Parameters
- List of Tests
- Anti Nuclear Antibodies (ANA)
- Anti Ds_DNA
- MPO-ANCA (P-ANCA)
- PR3 - ANCA (C-ANCA)
- Anti-ro SSA Antibodies by Immunoblot
- Anti-la SSB Antibodies by Immunoblot
- Anti-J0-1 Antibodies by Immunoblot
- Anti-SM Antibodies by Immunoblot
ANA Profile
- Why is it done?
- The ANA Profile is a comprehensive autoimmune screening panel designed to detect and identify autoantibodies associated with systemic autoimmune diseases
- Anti-Nuclear Antibodies (ANA): Primary screening test for systemic lupus erythematosus (SLE), scleroderma, and other connective tissue diseases; detects autoimmune activity targeting nuclear antigens
- Anti-Ds-DNA: Specific marker for SLE diagnosis and disease activity monitoring; highly specific for systemic lupus erythematosus
- MPO-ANCA (P-ANCA): Detects perinuclear Anti-Neutrophil Cytoplasmic Antibodies; aids in diagnosis of microscopic polyangiitis, granulomatosis with polyangiitis, and other vasculitides
- PR3-ANCA (C-ANCA): Detects cytoplasmic Anti-Neutrophil Cytoplasmic Antibodies; primarily associated with granulomatosis with polyangiitis (formerly Wegener's granulomatosis)
- Anti-Ro SSA Antibodies: Marker for Sjögren's syndrome, neonatal lupus, and SLE; associated with systemic manifestations and photosensitivity
- Anti-La SSB Antibodies: Specific marker for primary Sjögren's syndrome; almost always occurs with Anti-Ro SSA positivity
- Anti-Jo-1 Antibodies: Marker for idiopathic inflammatory myositis and myositis-associated autoimmune disease; associated with polymyositis and dermatomyositis
- Anti-SM Antibodies: Highly specific marker for SLE; rarely present in other autoimmune conditions; excellent diagnostic specificity with 99%
- Ordered when patients present with symptoms suggestive of autoimmune disease including arthritis, lupus-like rash, photosensitivity, dry mouth/eyes, muscle weakness, or unexplained systemic inflammation
- Tests work synergistically to provide pattern recognition allowing differentiation between various autoimmune diseases and establishing definitive diagnosis
- Normal Range
- Anti-Nuclear Antibodies (ANA): Negative or titer <1:80; Positive results require follow-up with reflex to specific antibody testing
- Anti-Ds-DNA: Negative (<0.9 IU/mL) or <5 IU/mL depending on laboratory; values below this threshold indicate normal immune response
- MPO-ANCA (P-ANCA): Negative (<1.0 unit/mL); Normal result indicates absence of perinuclear ANCA antibodies
- PR3-ANCA (C-ANCA): Negative (<1.0 unit/mL); Normal result indicates absence of cytoplasmic ANCA antibodies
- Anti-Ro SSA Antibodies: Negative (< 0.1 Index or <1.0 IU/mL); Normal results indicate no detectable anti-Ro autoimmunity
- Anti-La SSB Antibodies: Negative (< 0.1 Index or <1.0 IU/mL); Normal results indicate no detectable anti-La autoimmunity
- Anti-Jo-1 Antibodies: Negative (< 0.1 Index or <1.0 IU/mL); Normal results indicate no detectable anti-Jo-1 antibodies
- Anti-SM Antibodies: Negative (< 0.1 Index or <1.0 IU/mL); Normal results indicate no detectable anti-Smith autoimmunity
- Borderline results (typically 0.1-1.0 Index) may warrant repeat testing or clinical correlation; normality varies by specific laboratory reagents and methodology
- Interpretation
- Anti-Nuclear Antibodies (ANA) Positive: Suggests autoimmune disease but not diagnostic alone; requires clinical symptoms and additional specific antibody testing for definitive diagnosis; approximately 3-5% of healthy population shows low-titer positive results
- Anti-Ds-DNA Elevated (>0.9 IU/mL or >5 IU/mL): Highly specific for SLE diagnosis; levels often correlate with disease activity and lupus nephritis development; considered one of SLE classification criteria
- MPO-ANCA Positive (>1.0 unit/mL): Associated with microscopic polyangiitis, eosinophilic granulomatosis with polyangiitis, and other primary systemic vasculitides; pattern indicates possible pulmonary or renal involvement
- PR3-ANCA Positive (>1.0 unit/mL): Highly specific for granulomatosis with polyangiitis; associated with upper respiratory tract, lower respiratory tract, and glomerulonephritis manifestations
- Anti-Ro SSA Positive (>0.1 Index or >1.0 IU/mL): Consistent with Sjögren's syndrome, SLE, or neonatal lupus; indicates risk of photosensitive skin disease and cardiac conduction abnormalities if pregnant
- Anti-La SSB Positive (>0.1 Index or >1.0 IU/mL): Highly specific for primary Sjögren's syndrome; virtually always occurs concurrently with Anti-Ro SSA; rarely occurs in isolation; indicates significant risk of systemic manifestations
- Anti-Jo-1 Positive (>0.1 Index or >1.0 IU/mL): Indicates myositis-associated autoimmune disease; associated with polymyositis, dermatomyositis, and interstitial lung disease; frequently accompanied by other myositis antibodies
- Anti-SM Positive (>0.1 Index or >1.0 IU/mL): Highly specific for SLE with 99% specificity; present in only 20-30% of SLE patients but virtually diagnostic when detected; used as SLE classification criterion
- Multiple antibody positivity patterns help distinguish between autoimmune diseases; for example, Anti-Ro and Anti-La together strongly suggest Sjögren's while Anti-Ds-DNA and Anti-SM suggest SLE
- Clinical correlation essential: Antibody positivity alone is insufficient for diagnosis; patient symptoms, physical examination findings, and laboratory results must support diagnosis
- False positives may occur with infections (particularly viral), medications, malignancy, or other inflammatory conditions; repeat testing may be warranted for confirmation
- Associated Organs
- Anti-Nuclear Antibodies (ANA): Associated with multiple organ systems including kidneys (lupus nephritis), heart (pericarditis, myocarditis), lungs (pleuritis, pulmonary hemorrhage), skin (photosensitive rash, discoid lesions), and central nervous system
- Anti-Ds-DNA: Primarily associated with kidney involvement; strong correlation with lupus nephritis development and renal disease progression; also associated with CNS lupus manifestations
- MPO-ANCA: Associated with lung involvement (alveolar hemorrhage, pulmonary infiltrates), kidneys (glomerulonephritis, crescentic GN), and skin vasculitis; primary concern is end-stage renal disease development
- PR3-ANCA: Associated with triad of upper respiratory tract (sinusitis, nasal crusting), lower respiratory tract (pulmonary infiltrates, hemoptysis), and kidneys (rapidly progressive glomerulonephritis); can affect heart with myocarditis
- Anti-Ro SSA: Associated with exocrine glands (salivary gland dysfunction), eyes (dry eye syndrome), lungs (interstitial lung disease), heart (congenital heart block), and skin (photosensitivity, rash)
- Anti-La SSB: Associated primarily with exocrine glands (salivary, lacrimal), skin (xerosis), lungs (interstitial fibrosis), kidneys (interstitial nephritis, glomerulonephritis), and nervous system (peripheral neuropathy)
- Anti-Jo-1: Associated with skeletal muscle (myositis, muscle weakness), lungs (interstitial lung disease, pulmonary fibrosis), hands (Raynaud's phenomenon, mechanic's hands), and heart (cardiomyopathy, arrhythmias)
- Anti-SM: Associated with kidneys (lupus nephritis), heart (pericarditis, endocarditis), lungs (pleuritis, pulmonary hemorrhage), and joints (arthritis); helps define systemic lupus erythematosus organ involvement
- Potential complications from abnormal results include renal failure (from nephritis or GN), pulmonary hypertension, organ fibrosis, vasculitic crisis, neurological complications, and cardiac arrhythmias
- Follow-up Tests
- For positive ANA results: Consider ANA reflex panel with specific antibodies (already included in this comprehensive profile); additional imaging such as chest X-ray, high-resolution CT chest if pulmonary involvement suspected
- For elevated Anti-Ds-DNA: Order urinalysis with microscopy, urine protein quantification, and serum creatinine to assess for lupus nephritis; assess C3 and C4 complement levels; baseline renal function essential
- For positive ANCA results (MPO or PR3): Obtain baseline serum creatinine, urinalysis, and urine protein; consider chest imaging; renal biopsy may be indicated if rapidly progressive GN suspected
- For positive Anti-Ro SSA: Evaluate for systemic involvement with chest imaging, pulmonary function tests if indicated; assess for cardiac arrhythmias with ECG; consider ophthalmology referral for Sjögren's evaluation
- For positive Anti-La SSB: Refer to rheumatology and ENT; perform Schirmer's test and Rose Bengal staining for keratoconjunctivitis sicca confirmation; assess renal function with creatinine and urinalysis
- For positive Anti-Jo-1: Order muscle enzyme testing (CK, aldolase, LDH, transaminases); perform EMG/NCS if myositis suspected; obtain pulmonary function tests and high-resolution CT chest to assess for ILD
- For positive Anti-SM: Strongly suggests SLE requiring complete SLE workup including CBC, comprehensive metabolic panel, urinalysis, chest X-ray; assess for lupus nephritis with renal function tests
- General follow-up monitoring frequency: Repeat ANA panel every 6-12 months for stable disease; more frequently (every 3 months) if disease activity suspected; correlate antibody titers with clinical symptoms
- Complementary tests to consider: ESR and CRP for inflammation assessment; CBC for cytopenias; comprehensive metabolic panel for organ function; LFTs for hepatic involvement; coagulation studies if thrombosis risk
- Consider comprehensive metabolic panel and CBC in all positive cases to assess overall systemic involvement and organ dysfunction
- Fasting Required?
- Fasting is NOT required for the ANA Profile or any of its individual component tests
- Patients may eat and drink normally before specimen collection; no dietary restrictions apply to this serological panel
- No specific medications need to be withheld; immunosuppressive therapy should continue as prescribed and does not interfere with accurate antibody detection
- Specimen collection: Blood draw via venipuncture using standard serum separator or EDTA tube depending on laboratory protocol; typically 5-7 mL of blood required
- Patient preparation: Arrive for blood draw during regular business hours; inform phlebotomist of any bleeding disorders or medications affecting coagulation
- No need for special preparation or timing; specimen processing time typically 24-48 hours depending on laboratory; stat processing may be available if clinically urgent
- Recommend scheduling appointment at patient convenience; multiple tests not recommended on same day unless medically necessary to avoid unnecessary blood draws
How our test process works!

