REUMATOID ARTHRITIS: DIAGNOSIS AND TREATMENT

24 November 2025, Monday
REUMATOID ARTHRITIS: DIAGNOSIS AND TREATMENT

Rheumatoid arthritis (RA) is a chronic autoimmune inflammatory disease of connective tissue, primarily affecting joints in a symmetrical pattern, leading to their progressive destruction, deformation, and functional impairment. It is classified as a systemic disease since extra-articular organs can also be involved.

 

Epidemiology

  • Prevalence in the general population: approximately 0.5–1%.
  • Women are affected 2–3 times more often than men.
  • Peak incidence: 30–50 years, but the disease can occur at any age, including childhood (juvenile idiopathic arthritis).

 

Etiology and Pathogenesis

The exact cause is unknown, but the disease is multifactorial:

  • Genetic predisposition (HLA-DR4, HLA-DR1).
  • Immune mechanisms: activation of T- and B-lymphocytes, production of rheumatoid factor (IgM against Fc fragment of IgG), anti-CCP antibodies.
  • Environmental factors: infections, smoking, hormonal influences.

The key link is chronic autoimmune inflammation with the formation of granulation tissue (pannus), which destroys cartilage and bone.

 

Clinical Manifestations

Articular

  • Symmetrical polyarthritis of small joints of hands and feet.
  • Morning stiffness lasting more than 30 minutes.
  • Pain, swelling, restricted mobility.
  • Progressive deformities (“swan neck,” “buttonhole,” ulnar deviation).

Extra-articular

  • Subcutaneous rheumatoid nodules.
  • Pulmonary involvement (interstitial fibrosis, pleuritis).
  • Vascular manifestations (vasculitis).
  • Cardiac involvement (pericarditis, increased risk of atherosclerosis).
  • Sjögren’s syndrome (dry eyes and mouth).

 

 

Diagnosis

Diagnosis is based on clinical, laboratory, and imaging data.

  • Clinical: symmetrical polyarthritis, morning stiffness > 6 weeks.
  • Laboratory: rheumatoid factor, anti-CCP antibodies, elevated ESR, CRP.
  • Imaging: X-ray (erosions, osteoporosis, joint space narrowing), US/MRI (synovitis, early erosive changes).

Diagnostic criteria: ACR/EULAR 2010.

 

Treatment

Goal: achieve remission or low disease activity.
1.    Pharmacological 
2.    Non-pharmacological measures 

  • physiotherapy, exercise, occupational therapy, 
  • psychological support, smoking cessation, 
  • surgical interventions (joint replacement) for severe deformities.

Prognosis

  • Without treatment — progressive disability.
  • Modern “treat-to-target” strategies significantly improve outcomes.
  • Early initiation of methotrexate or biologics can lead to sustained remission.

 

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