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Sunday, August 10, 2025

Rheumatoid arthritis


Definition
Rheumatoid arthritis is a chronic, systemic, autoimmune inflammatory disease that primarily targets synovial joints, leading to progressive joint damage, deformity, and disability. It may also cause extra-articular manifestations affecting skin, eyes, lungs, cardiovascular system, and other organs.


Causes & Pathophysiology

  • Autoimmune mechanism: Immune system attacks synovial membrane, causing synovitis

  • Genetic factors: HLA-DR4 and HLA-DR1 association

  • Environmental triggers: Smoking, infections, periodontal disease

  • Pathogenesis: Inflammatory cytokines (TNF-α, IL-1, IL-6) drive pannus formation → cartilage destruction and bone erosion


Risk Factors

  • Female sex (3× more common than in men)

  • Age 30–50 years

  • Family history of RA

  • Smoking

  • Obesity


Clinical Features

Joint Symptoms

  • Symmetrical pain, swelling, and stiffness (especially small joints of hands and feet)

  • Morning stiffness >1 hour

  • Warmth and tenderness over joints

  • Progressive joint deformities (ulnar deviation, swan-neck, boutonnière)

Extra-Articular Manifestations

  • Rheumatoid nodules

  • Interstitial lung disease

  • Pericarditis, vasculitis

  • Scleritis, episcleritis

  • Anaemia of chronic disease


Diagnosis

Laboratory Tests

  • Rheumatoid factor (RF) — positive in ~70–80%

  • Anti-cyclic citrullinated peptide antibodies (anti-CCP) — high specificity

  • ESR and CRP — elevated in active disease

  • Normocytic, normochromic anaemia

Imaging

  • X-rays: Joint space narrowing, marginal erosions, osteopenia

  • Ultrasound/MRI: Synovitis and early erosions

Classification Criteria (ACR/EULAR 2010)

  • Joint involvement

  • Serology (RF, anti-CCP)

  • Acute phase reactants (ESR, CRP)

  • Duration of symptoms


Treatment

General Measures

  • Patient education, exercise, joint protection, smoking cessation

  • Multidisciplinary care (rheumatologist, physiotherapist, occupational therapist)

Pharmacological

  1. Disease-Modifying Antirheumatic Drugs (DMARDs) — start early (“treat to target” strategy)

    • Methotrexate: 7.5–25 mg orally/weekly, with folic acid supplementation

    • Sulfasalazine: 500 mg–1 g twice daily

    • Leflunomide: 10–20 mg daily

    • Hydroxychloroquine: 200–400 mg daily

  2. Biologic DMARDs (for inadequate response to conventional DMARDs)

    • TNF-α inhibitors: etanercept, adalimumab, infliximab

    • IL-6 inhibitors: tocilizumab

    • B-cell depletion: rituximab

    • T-cell costimulation blocker: abatacept

  3. Janus Kinase (JAK) Inhibitors

    • Tofacitinib, baricitinib, upadacitinib

  4. Glucocorticoids

    • Low-dose prednisolone (≤10 mg/day) for short-term symptom control or flares

  5. NSAIDs

    • For pain relief and stiffness (not disease-modifying)


Complications

  • Joint destruction and deformity

  • Cervical spine instability (atlantoaxial subluxation)

  • Cardiovascular disease

  • Lung involvement

  • Osteoporosis from inflammation and corticosteroid use


Quick-Reference Clinical Chart — Rheumatoid Arthritis

FeatureDetails
DefinitionChronic autoimmune inflammatory arthritis affecting synovial joints
Key SymptomsSymmetrical joint pain/swelling, morning stiffness >1 hr
Extra-Articular SignsNodules, lung disease, vasculitis, ocular inflammation
LabsRF+, anti-CCP+, ↑ESR/CRP
ImagingErosions, joint space narrowing
First-Line DMARDMethotrexate (weekly) + folic acid
BiologicsTNF-α inhibitors, IL-6 inhibitors, rituximab, abatacept
Other DrugsSulfasalazine, hydroxychloroquine, leflunomide, JAK inhibitors
AdjunctsNSAIDs, glucocorticoids for flares
PreventionEarly aggressive treatment to achieve remission
PrognosisVariable; early treatment improves outcomes



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