Ankylosing spondylitis

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(Redirected from Bamboo spine)

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}} Ankylosing spondylitis (AS) is a chronic, painful, progressive inflammatory arthritis primarily affecting spine and sacroiliac joints, causing eventual fusion of the spine; it is a member of the group of the autoimmune spondylarthropathies with a probable genetic predisposition. Complete fusion results in a complete rigidity of the spine, a condition known as bamboo spine.

Contents

Signs and symptoms

The typical patient is a young man of 15-30 years old with chronic pain and stiffness in the lower part of the spine. Males are affected by ankylosing spondylitis three times more than women. Younger patients may experience knee pain even at very young ages (3 years old), commonly misinterpreted as simple rheumatisms. Recurring aphtae may also be experienced and are part of typical AS symptoms. Fatigue is also a widely spread symptom.

In 40% of cases, ankylosing spondylitis it is associated with iridocyclitis (anterior uveitis) causing eye pain and photophobia (increased sensitivity to light). Other less common complications are ulcerative colitis, psoriasis and Reiter's disease.

Osteopenia or osteoporosis of AP spine, causing eventual compression fractures and a back "hump" if untreated.

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

Diagnosis

The diagnosis of AS is done by X-ray studies of the spine, which show characteristic spinal changes and sacroiliitis. Other options for effective diagnosis are tomography and magnetic resonance of the sacroiliac joints.

During acute inflammation periods, AS patients will usually show an increased values of C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR).

Variations of the HLA-B gene increase the risk of developing ankylosing spondylitis. Those with the HLA-B27 variant are at highest risk of developing the disorder. HLA-B27, demonstrated in a blood test, is occasionally used as a diagnostic, but does not distinguish AS from other diseases and is therefore not of real diagnostic value. Over 95% of people with AS are HLA-B27 positive, although this ratio varies from population to population (only 50% of African American patients with AS possess HLA-B27, and it is close to 80% among AS patients from Mediterranean countries).

Unattended cases normally lead to knee pain, resulting in a fair assumption of normal rheumatism.

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. Although specific autoantibodies cannot be detected, its response to immunosuppresive medication has prompted its classification as an autoimmune disease.

Hypotheses on its pathogenesis include a cross-reaction with antigens of the Klebsiella bacterial strain (Tiwana et al. 2001). Particular authorities argue that elimination of the prime nutrients of Klebsiella (starches) would decrease antigenemia and improve the musculoskeletal symptoms. On the other hand, Khan (2002) argues that the evidence for a correlation between Klebsiella and AS is circumstantial so far, and that the efficacy of low-starch diets has not yet been scientifically evaluated. Similarly, Toivanen (1999) found no support for the role of klebsiella in the etiology of primary AS.

Epidemiology

The sex ratio is 3:1 for men:women. In the USA, the prevalence is 0.25%, but as it is a chronic condition, the number of new cases (incidence) is fairly low.

Therapy

No cure is known for AS, although treatments and medications are available to reduce symptoms and pain.

Physical therapy and exercise, along with medication, are at the heart of therapy for ankylosing spondylitis. Physiotherapy and physical exercises are clearly preceded by medical treatment in order to reduce the inflammation and pain, and commonly followed by a physician. This way the movements will help in diminish pain and stiffness, while exercises in an active inflammatory state will just make the pain worse.

Medication

There are three major types of medications used to treat ankylosing spondylitis.

TNFα blockers have been shown shown to be the best promising treatment, slowing the progress of AS in the majority of clinical cases. They have also been shown to be highly effective in treating not only the arthritis of the joints but the spinal arthritis associated with AS.

Note on TNFα blockers: TNFα blockers are constituted by proteins that are effective immunosuppressants. This means that treatments with these drugs increase the risk of infections. For this reason, the protocol for any of the TNF-α blockers include a test for tubercolosis (like Mantoux or Heaf) before starting taking any drug. In case of recurrent infections, like even recurrent sore throats, the therapy may be suspended due to the involved immunosuppression.

Surgery

In severe cases of AS, surgery can be an option in the form of joint replacements, particularly in the knees and hips. Surgical correction is also possible for those with severe flexion deformities (severe downward curvature) of the spine, particularly in the neck, although this procedure is considered risky.

Physical therapy

Alternative medicine

Although the effectiveness of alternative medicines has not been proved by any clinical trial, some patients find some relief in adding these alternative treatements to the medicaments and physical exercises:

Prognosis

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

Famous patients

Well known sufferers of AS include:

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See also

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

References

External links

National organizations

Support groups

de:Spondylitis ankylosans fr:Spondylarthrite ankylosante it:Spondilite anchilosante nl:Ziekte van Bechterew no:Bekhterevs sykdom pl:Zesztywniające zapalenie stawów kręgosłupa tr:Ankilozan spondilit