jamunjar-logo
whatsapp
cartmembermenu
Search for
"test & packages"
"physiotherapy"
"heart"
"lungs"
"diabetes"
"kidney"
"liver"
"cancer"
"thyroid"
"bones"
"fever"
"vitamin"
"iron"
"HTN"

Rheumatoid Factor (RF)

Immunity
image

Report in 4Hrs

image

At Home

nofastingrequire

No Fasting Required

Details

Rheumatoid factor test used in diagnosis of rheumatoid arthritis and other autoimmune conditions.

299495

40% OFF

Rheumatoid Factor (RF) - Comprehensive Medical Test Guide

  • Why is it done?
    • Test measures antibodies (specifically IgM, IgG, or IgA) produced by the immune system that attack the body's own tissues, particularly affecting joints and connective tissue
    • Primary indication: Diagnose or confirm rheumatoid arthritis (RA) when joint pain, swelling, and stiffness are present
    • Evaluate other autoimmune conditions such as systemic lupus erythematosus (SLE), Sjögren's syndrome, and mixed connective tissue disease
    • Assess disease activity and severity in patients already diagnosed with RA
    • Monitor treatment response and prognosis in autoimmune disease management
    • Typical timing: Performed during initial diagnostic workup when symptoms suggest autoimmune disease, or periodically during disease monitoring
  • Normal Range
    • Normal/Negative Result: Less than 14 IU/mL (International Units per milliliter) or negative on qualitative testing
    • Borderline/Weakly Positive: 14-20 IU/mL - may warrant repeat testing or additional evaluation
    • Positive Result: Greater than 20 IU/mL - indicates presence of rheumatoid factor antibodies
    • Highly Positive: Greater than 60 IU/mL - suggests higher likelihood of RA or other autoimmune disease
    • Units of measurement: IU/mL (International Units per milliliter) or may be reported as positive/negative or as a titer
    • Note: Reference ranges may vary slightly between laboratories; consult your specific lab's reference interval
    • Normal result indicates absence of detectable rheumatoid factor, suggesting lower likelihood of RA; however, seronegative RA exists in 20-30% of patients
  • Interpretation
    • Positive RF Result (>20 IU/mL): Suggests autoimmune activity; when combined with clinical symptoms (joint pain, swelling, morning stiffness), strongly supports RA diagnosis
    • Negative RF Result (<14 IU/mL): Does not exclude RA diagnosis; seronegative RA occurs in approximately 20-30% of RA patients; further testing with anti-CCP antibodies recommended
    • High Titers (>60 IU/mL): Associated with more severe disease, increased risk of extra-articular manifestations (nodules, vasculitis), and worse prognosis
    • Borderline Results (14-20 IU/mL): Warrant repeat testing in 4-6 weeks; trending upward increases diagnostic likelihood
    • Factors affecting results:
    • Age: RF positivity increases with age; may be positive in 5-10% of healthy elderly individuals
    • Gender: More common in women; female-to-male ratio approximately 2.5:1 for RA
    • Infections: Certain infections (hepatitis C, tuberculosis, EBV) can elevate RF transiently
    • Disease activity: RF levels may fluctuate with disease activity in established RA; poor correlation with symptom severity
    • Early disease: RF may not appear until several months after symptom onset
    • Clinical significance:
    • RF-positive patients have worse long-term outcomes compared to RF-negative patients
    • Used in combination with anti-CCP antibodies for improved diagnostic accuracy (RF+/anti-CCP+ has highest specificity)
    • Helps stratify risk for severe disease and need for aggressive treatment
  • Associated Organs
    • Primary organ systems involved:
    • Musculoskeletal system: Primarily affects synovial joints; inflammatory cascade leads to cartilage and bone destruction
    • Immune system: B and T lymphocyte dysfunction; immune complex formation and deposition
    • Connective tissue: Systemic inflammation affecting multiple tissue types
    • Conditions commonly associated with abnormal RF results:
    • Rheumatoid Arthritis (RA): Most common autoimmune condition associated with elevated RF; positive in 70-80% of RA patients
    • Systemic Lupus Erythematosus (SLE): Positive RF in 40-60% of SLE patients; indicates more severe disease
    • Sjögren's Syndrome: Positive in 50-70% of patients with primary Sjögren's
    • Mixed Connective Tissue Disease (MCTD): Frequently RF-positive
    • Cryoglobulinemia: Often RF-positive, particularly associated with hepatitis C
    • Chronic infections: Tuberculosis, hepatitis C, endocarditis may cause transient RF elevation
    • Malignancies: Lymphoma and other cancers occasionally associated with RF positivity
    • Extra-articular complications (in RF-positive RA):
    • Rheumatoid nodules: Subcutaneous nodules over pressure points (elbows, fingers)
    • Pulmonary involvement: Interstitial lung disease, pleural effusion, increased infection risk
    • Cardiovascular disease: Increased risk of atherosclerosis, myocardial infarction, pericarditis
    • Ocular manifestations: Scleritis, episcleritis, keratitis
    • Vasculitis: Systemic vasculitis affecting medium and small vessels
    • Felty syndrome: Splenomegaly, leukopenia, thrombocytopenia in RF+ RA patients
  • Follow-up Tests
    • Recommended additional tests based on RF results:
    • Anti-CCP antibodies (anti-cyclic citrullinated peptide): Increased specificity for RA; positive in 65-75% of RA patients; more specific than RF alone; helps diagnose seronegative RA
    • Antinuclear antibody (ANA): Screen for systemic autoimmune diseases like SLE and Sjögren's when RF positive
    • Erythrocyte sedimentation rate (ESR): Marker of systemic inflammation; correlates with disease activity
    • C-reactive protein (CRP): Acute phase reactant; better correlation with clinical activity than ESR in some patients
    • Complete blood count (CBC): Assess for anemia, leukopenia, thrombocytopenia; check for Felty syndrome
    • Comprehensive metabolic panel: Baseline assessment before starting immunosuppressive therapy
    • Liver function tests: Important before initiating DMARDs (disease-modifying antirheumatic drugs)
    • Anti-tissue transglutaminase (anti-tTG): Screen for celiac disease (associated with increased RA risk)
    • Imaging studies: X-rays of affected joints to assess for structural damage; MRI for early erosive changes
    • Monitoring frequency:
    • Initial diagnosis: RF testing combined with clinical assessment and imaging; repeat if borderline
    • Ongoing disease monitoring: Typically every 3-6 months initially; frequency may decrease with disease remission
    • Treatment response assessment: RF levels correlate variably with clinical response; ESR and CRP more reliable for short-term monitoring
    • During remission: May monitor annually or less frequently if clinically stable
    • Complementary tests for differential diagnosis:
    • Anti-double stranded DNA (anti-dsDNA): Specific for SLE when RF positive
    • Anti-Ro/SSA and Anti-La/SSB: Differentiates Sjögren's syndrome from other autoimmune diseases
    • Anti-mitochondrial antibodies (AMA): Screen for primary biliary cholangitis when RF positive
    • Hepatitis C antibody: If RF positive and risk factors present, screen for hepatitis C-associated cryoglobulinemia
  • Fasting Required?
    • Fasting requirement: NO - Fasting is not required for the rheumatoid factor test
    • The RF test measures antibodies in serum and is not affected by food or fluid intake
    • Patients may eat and drink normally before the blood draw
    • Medications:
    • No specific medications need to be discontinued for RF testing
    • Continue all current medications including DMARDs, corticosteroids, and biologics as prescribed
    • Immunosuppressive medications may affect RF levels but should not be discontinued without physician approval
    • Patient preparation requirements:
    • Arrive well-hydrated (improves venipuncture success)
    • Wear loose-fitting sleeves to facilitate blood draw from the arm
    • Inform phlebotomist of any history of difficult venipuncture or bleeding disorders
    • No special positioning required; can be drawn while seated or lying down
    • Specimen collection: 3-5 mL of serum in standard SST (serum separator tube) or gold-top tube
    • Results typically available within 24-48 hours
    • No restrictions on activity after blood draw; normal daily activities can be resumed immediately

How our test process works!

customers
customers