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Definition !!navigator!!

AS is a chronic and progressive inflammatory disease of the axial skeleton with sacroiliitis (usually bilateral) as its hallmark. Peripheral joints and extra-articular structures may also be affected. Most frequently presents in second or third decade more commonly in men; strong association with histocompatibility antigen HLA-B27.

Clinical Manifestations !!navigator!!

  • Back pain and stiffness: not relieved by lying down, often present at night forcing pt to leave bed, worse in the morning, improves with activity, insidious onset, duration >3 months (often called symptoms of “inflammatory” back pain).
  • Extra-axial arthritis: hip and shoulders 25-35%, other peripheral joint involvement up to 30%, usually asymmetric.
  • Chest pain: from involvement of thoracic skeleton and muscular insertions.
  • Extra/juxta-articular pain: due to “enthesitis”: inflammation at insertion of tendons and ligaments into bone; frequently affects greater trochanter, iliac crests, ischial tuberosities, tibial tubercles, heels.
  • Extra-articular findings-include acute anterior uveitis in up to 40% of pts, aortitis, aortic insufficiency, GI inflammation, cardiac conduction defects, amyloidosis, bilateral upper lobe pulmonary fibrosis.
  • Constitutional symptoms: fever, fatigue, weight loss may occur.
  • Neurologic complications: related to spinal fracture/dislocation (can occur with even minor trauma), atlantoaxial subluxation (can lead to spinal cord compression), cauda equina syndrome.

Physical Examination !!navigator!!

  • Tenderness over involved joints
  • Diminished chest expansion
  • Diminished flexion and extension of spine (Schober test measures lumbar spine flexion)

Evaluation !!navigator!!

  • ESR and C-reactive protein often elevated.
  • Mild anemia.
  • Rheumatoid factor and ANA negative.
  • HLA-B27 may be helpful in pts with inflammatory back symptoms but negative x-rays.
  • Radiographs: early may be normal. Sacroiliac joints: usually symmetric; bony erosions with “pseudowidening” followed by fibrosis and ankylosis. Spine: squaring of vertebrae; syndesmophytes; ossification of annulus fibrosis and anterior longitudinal ligament causing “bamboo spine.” Sites of enthesitis may ossify and be visible on x-ray. MRI is procedure of choice when plain radiographs do not reveal sacroiliac abnormalities and can show early intra-articular inflammation, cartilage changes, and bone marrow edema.

Diagnosis !!navigator!!

(Table 163-1 ASAS Criteria for Classification of Axial Spondyloarthritis (To Be Applied for Pts with Back Pain 3 Months and Age of Onset 45 Years)a )

Differential Diagnosis

Osteoarthritis/spondylosis, degenerative disk disease, muscular strain, fibromyalgia; metabolic, infectious, or malignant causes of back pain; diffuse idiopathic skeletal hyperostosis.

TREATMENT

Ankylosing Spondylitis

  • Exercise program to maintain posture and mobility is important.
  • NSAIDs first-line treatment, useful in most pts.
  • TNF-modulatory agents (etanercept, infliximab, adalimumab, golimumab, certolizumab pegol) have been found to improve disease activity and function and reduce bone marrow edema on MRI. Generally used in active disease with failure of at least two NSAIDs.
  • Secukinumab, an IL-17A antagonist, has been found to reduce signs and symptoms of active disease.
  • Sulfasalazine 2-3 g/d is of modest benefit, primarily for peripheral arthritis.
  • No documented therapeutic role for systemic glucocorticoids.
  • Intra-articular glucocorticoids for persistent enthesitis or peripheral synovitis.
  • Uveitis managed with ocular or systemic glucocorticoids, other immunosuppressive agents, TNF-inhibitors.
  • Surgery done rarely for severe hip arthritis, extreme flexion deformities, atlantoaxial subluxation.

Outline

Section 12. Allergy, Clinical Immunology, and Rheumatology