Ankylosing spondylitis

Ankylosing spondylitis (AS) is a chronic, progressive inflammatory arthritis primarily affecting spine and sacroiliac joints, causing eventual fusion of the spine. Complete fusion results in a complete rigidity of the spine, a condition known as bamboo spine.

AS is characterised as a spondyloarthropathy (SpA).

Table of contents
1 Signs and symptoms
2 Diagnosis
3 Epidemiology
4 Therapy
5 Prognosis
6 Pathophysiology
7 See also
8 External links

Signs and symptoms

The typical patient is a young man of 15-30 years old (although women are also affected) with pain and stiffness in the spine. It is also associated with iridocyclitis (anterior uveitis), ulcerative colitis, psoriasis and Reiter's disease, through HLA-B27 (see below).

Organs affected by AS, other than the axial spine, are the hips, heart, heels, and other areas (peripheral).

Diagnosis

The diagnosis is by X-ray studies of the spine, which show characteristic spinal changes and sacroiliitis. A normal X-ray does not exclude the disease.

HLA-B27 is occasionally used, but does not distinguish AS from other diseases and is therefore not of real diagnostic value.

Epidemiology

In the USA, the prevalence is 0.25%, but as it is a chronic condition, the number of new cases (incidence) is fairly low.

The sex ratio is 3:1 for men:women.

Therapy

Physical therapy and exercise, along with medication, are at the heart of therapy for ankylosating spondylitis.

Medications used are:

  • NSAIDs (anti-inflammatory and pain-reducing)
  • Steroids
  • DMARDs (immunosuppressants)

Prognosis

AS can range from mild to progressively debilitating, and from medically controlled to refractive.

Pathophysiology

AS is a systemic rheumatic disease, and about 90% of the patients are HLA-B27 positive. HLA-DR and IL1ra are also implicated in Ankylosing Spondylitis.

See also

  • NASC, the AS patients' federation
  • NIAMS, the National Institute of Arthritis and Musculoskeletal and Skin Diseases

External links






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