About

Rheumatoid Arthritis (RA) is a chronic systemic disease in which immunologically mediated inflammation of synovia-lined joints can result in marked disruption of joint structure and function.The most common form of this disease is chronic inflammatory arthritis, which begins with inflammation of the synovial membrane of the affected joints and eventually leads to disability of the affected limb. Over time, it typically leads to the destruction of cartilage and bone, joint deformity, and organ failure, and eventually results in disability.

The number of affected joints and other organs usually increases with rapid disease progression. The treatment and the diagnostics of RA have been evolved through the years; the first non-specific medication was aspirin, followed by more appropriate drugs, such as cortisone, and methotrexate, and the revolution arrived within the last 20 years with biologics. Simultaneously diagnostics have been improved, starting from the detection of Rheumatoid Factor (RF) only to progressing to completing the diagnosis by the new ACPA (anti-citrullinated protein antibodies) tests, like citrulline peptide (anti-CCP) and citrullinated vimentin (MCV).

These improvements in the diagnostic tools are included in the ACR-EULAR classification criteria for RA, established in 2010 as a pillar for the correct management of patients affected by RA.

1%
RA worldwide prevalence.
3:1
is the women-men affected ratio.

Diagnosis

Autoantibodies against citrullinated peptides/proteins (ACPA), e.g. anti-MCV, anti-CCP, and RF are essential components of the ACR/EULAR criteria for classification of RA.

Anti-MCV

  • Measurement of autoantibodies against mutated citrullinated vimentin as a useful additional marker, particularly in patients who are anti-CCP negative
  • Highly specific and extremely sensitive for RA

 

Anti-CCP hs

  • Tailored antigen profile for enhanced autoantibody recognition
  • Numerous different epitopes for higher sensitivity

 

Rheumatoid Factor IgM, IgA, IgG

  • Quantitative measurement of individual RF isotypes
  • IgM + IgA RF double positive is highly specific for RA

Sebia’s Expertise

Sebia offers the largest portfolio for RA laboratory diagnostics with the Alegria Monotest random access solution, and ELISA testing for high throughput. A special proprietary antigen coating procedure ensures reliable test results, excellent accuracy, reproducibility, and consistency, minimizing the risk of misdiagnosis and inappropriate treatment. Sebia´s superior ELISA-based immunoassays comply with the latest ACR/EULAR RA 2010 classification criteria. The all-in-one Alegria Monotest is particularly suited for small series and offers unique flexibility for maximum workflow efficiency with the Alegria 2 system.