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Ankylosing spondylitis

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Ankylosing spondylitis
SpecialtyRheumatology Edit this on Wikidata

Ankylosing spondylitis (AS; also known as Bechterew's disease; Bechterew syndrome; Marie Strümpell disease / Marie Struempell disease / Spondyloarthritis) is a chronic, painful, degenerative inflammatory arthritis primarily affecting spine and sacroiliac joints, causing eventual fusion of the spine; it is a member of the group of the autoimmune spondyloarthropathies with a probable genetic predisposition. Complete fusion results in a complete rigidity of the spine, a condition known as bamboo spine.[1]

Signs and symptoms

The typical patient is young, of 15 to 30 years of age with chronic pain and stiffness in the lower part of the spine. Men are affected more than women by a ratio in excess of 2:1.[2] In 40% of cases, ankylosing spondylitis is associated with iridocyclitis (anterior uveitis, also known as iritis) causing eye pain and photophobia (increased sensitivity to light). Other common symptoms are recurring mouth ulcers (aphthae) and fatigue. Pain can fluctuate from one side to the other.

Typical prodromes (early symptoms) may occur at a very young age (e.g. 3 years old), where the patient may experience recurring painful joints (e.g. knees, elbows), commonly misinterpreted as simple rheumatism.

AS is also associated with ulcerative colitis, Crohn's disease, psoriasis, and Reiter's disease.

Diagnosis

The ankylosis process.

There is no direct test to diagnose AS. A clinical examination and X-ray studies of the spine, which show characteristic spinal changes and sacroiliitis, are the major diagnostic tools. A drawback of X-ray diagnosis is that signs and symptoms of AS have usually been established as long as 8-10 years prior to X-ray evident changes occurring on a plain film X-ray, which means a delay of as long as 10 years before adequate therapies can be introduced. An option for more accurate (and much earlier) diagnosis are tomography and magnetic resonance imaging of the sacroiliac joints. The Schober's test is a useful clinical measure of flexion of the lumbar spine performed during examination.[3]

During acute inflammatory periods, AS patients will usually show an increase in the blood concentration of C-reactive protein (CRP) and an increase in the erythrocyte sedimentation rate (ESR).

Variations of the HLA-B gene increase the risk of developing ankylosing spondylitis, although it is not a diagnostic test. Those with the HLA-B27 variant are at high 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).

In 2007, a collaborative effort by an international team of researchers in the U.K., Australia and the United States led to the discovery of two genes, ARTS1 and IL23R, that also cause AS. The findings were published in the November 2007 edition of Nature Genetics, a journal that emphasizes research on the genetic basis for common and complex diseases.[4]

The Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), developed in Bath (UK), is an index designed to detect the inflammatory burden of active disease. The BASDA can help to establish a diagnosis of AS in the presence of other factors such as HLA-B27 positivity, persistent buttock pain which resolves with exercise, and X-ray or MRI evident involvement of the sacroiliac joints. (See: "Diagnostic Tools", below)[5] It can be easily calculated and accurately assesses a patient's need for additional therapy; a score of 4 out of a possible 10 points while on adequate NSAID therapy is usually considered a good candidate for biologic therapy.

The Bath Ankylosing Spondylitis Functional Index (BASFI) is a functional index which can accurately assess a patient's functional impairment due to the disease, as well as improvements following therapy. (See: "Diagnostic Tools", below)[6] The BASFI is not usually used as a diagnostic tool, but as a tool to establish a patient's current baseline and subsequent response to therapy.

Pathophysiology

AS is a systemic rheumatic disease, and is one of the seronegative spondyloarthropathies. About 90% of the patients express the HLA-B27 genotype. Tumor necrosis factor-alpha (TNF α) and IL-1 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).[7] 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.[8] Similarly, Toivanen (1999) found no support for the role of klebsiella in the etiology of primary AS.[9]

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 incidence (number of new cases) is fairly low.

History

Leonard Trask, the Wonderful Invalid.

AS was probably first recognized as a disease which was different from Rheumatoid Arthritis by Galen as early as the second century AD[10]; however, skeletal evidence of the disease (ossification of joints and entheses primarily of the axial skeleton, known as "bamboo spine") were first discovered in an archaeological dig that unearthed the skeletal remains of a 5000 year–old Egyptian mummy with evidence of "bamboo spine".[11]

The anatomist and surgeon Realdo Colombo described what could have been the disease in 1559,[12] and the first account of pathologic changes to the skeleton possibly associated with AS was published in 1691 by Bernard Connor.[13] In 1818, Benjamin Brodie became the first physician to document that iritis accompanied what is believed to have been a patient with active AS.[14] In 1858, David Tucker published a small booklet which clearly described a patient by the name of Leonard Trask who suffered from severe spinal deformity subsequent to AS.[15][16] In 1833 Trask fell from a horse, exacerbating the condition and resulting in severe deformity. Tucker reported that

It was not until he [Trask] had exercised for some time that he could perform any labor [..., and that] his neck and back have continued to curve drawing his head downward on his breast.

evidence of inflammatory disease characteristics of AS, and the hallmark of deforming injury in AS. This account became the first documented case of AS in the United States.

It was not until the late nineteenth century (1893-1898), however, when the neurophysiologist Vladimir Bekhterev of Russia in 1893,[17] Adolph Strümpell of Germany in 1897,[18] and Pierre Marie of France in 1898,[19] were the first to give adequate descriptions which permitted an accurate diagnosis of AS prior to severe spinal deformity. For this reason, AS is also known as Bechterew Disease or Marie–Strümpel Disease.

Prognosis

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

Unattended cases of AS normally lead to knee pain, and may be accompanied by dactylitis or enthesitis, which may result in a misdiagnosis of normal rheumatism. In a long-term undiagnosed period, osteopenia or osteoporosis of AP spine may occur, causing eventual compression fractures and a back "hump" if untreated. Typical signs of progressed AS are the visible formation of syndesmophytes on X-rays, an abnormal bone outgrowth similar to osteophytes, affecting the spine. Due to the fusion of the vertrbrae paresthesia is a complication due to the inflammation of the tissue surrounding nerves.

Organs affected by AS, other than the axial spine and other joints, are commonly the heart, lungs, colon, and kidney. Other complications are aortic regurgitation, Achilles tendinitis, AV node block and amyloidosis.[20] Due to lung fibrosis, chest X-rays may show apical fibrosis while pulmonary function testing may reveal a restrictive lung defect. Very rare complications involve neurologic conditions such as the cauda equina syndrome.[21][20]

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 diminishing pain and stiffness, while exercises in an active inflammatory state will just make the pain worse.

Patients who are able to do so, lie flat on their face or back on the floor for a prescribed cumulative period of time each week, to prevent the chronic stooping which may otherwise result.[22]

Medication

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

TNFα blockers have been 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. A drawback is the fact that 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 treatment. In case of recurrent infections, 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.

In addition, AS can have some manifestations which make anaesthesia more complex.

Changes in the upper airway can lead to difficulties in intubating the airway, spinal and epidural anaesthesia may be difficult due to calicification of ligaments, and a small number have aortic regurgitation. The stiffness of the thoracic ribs results in ventilation being mainly diaphragm-driven, so there may be a decrease in pulmonary function.

Physical therapy

All physical therapies must be approved in advance by a rheumatologist, since movements that normally have great benefits on one's health, may harm a patient with AS: massages and physical manipulations should be practiced by therapists familiar with this disease.

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 treatments to the medicaments and physical exercises, like a starch free diet[23] (also known as the No Starch Diet or NSD).[24][25][26] Some patients may find relief under acupuncture treatments. This is administered at various points directly on the spine where the pain is located, although efficacy is uncertain. Herbal medicine, may also relieve pain.[27][dead link‍]

Famous patients

Well known sufferers of AS include:

Additional images

  • Morbus Bechterew
    Morbus Bechterew

See also

  • NASC, North American AS federation
  • NIAMS, the National Institute of Arthritis and Musculoskeletal and Skin Diseases
  • SAA, Spondylitis Association of America

References

  1. ^ Jiménez-Balderas FJ, Mintz G. (1993). "Ankylosing spondylitis: clinical course in women and men". J Rheumatol. 20 (12): 2069–72. PMID 7516975.
  2. ^ http://www.spondylitis.org/patient_resources/women.aspx
  3. ^ Thomas E, Silman AJ, Papageorgiou AC, Macfarlane GJ, Croft PR. (1998). "Association between measures of spinal mobility and low back pain. An analysis of new attenders in primary care". Spine. 23 (2): 343–7. PMID 9507623.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^ Spondylitis Association of America (October 21, 2007), "Spondylitis Association of America Participates in Study That Uncovers Two Genes Related to Disabling Form of Arthritis"
  5. ^ Garrett S, Jenkinson T, Kennedy L, Whitelock H, Gaisford P, Calin A (1994). "A new approach to defining disease status in ankylosing spondylitis: the Bath Ankylosing Spondylitis Disease Activity Index". J Rheumatol. 21 (12): 2286–91. PMID 7699630.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  6. ^ Calin A, Garrett S, Whitelock H, Kennedy L, O'Hea J, Mallorie P, Jenkinson T (1994). "A new approach to defining functional ability in ankylosing spondylitis: the development of the Bath Ankylosing Spondylitis Functional Index". J Rheumatol. 21 (12): 2281–5. PMID 7699629.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  7. ^ Tiwana H, Natt R, Benitez-Brito R, Shah S, Wilson C, Bridger S, Harbord M, Sarner M, Ebringer A (2001). "Correlation between the immune responses to collagens type I, III, IV and V and Klebsiella pneumoniae in patients with Crohn's disease and ankylosing spondylitis". Rheumatology (Oxford). 40 (1): 15–23. PMID 11157137.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  8. ^ Khan MA. (2002). Ankylosing spondylitis: The facts. Oxford University Press. ISBN 0-19-263282-5.
  9. ^ Toivanen P, Hansen D, Mestre F, Lehtonen L, Vaahtovuo J, Vehma M, Möttönen T, Saario R, Luukkainen R, Nissilä M (1999). "Somatic serogroups, capsular types, and species of fecal Klebsiella in patients with ankylosing spondylitis". J Clin Microbiol. 37 (9): 2808–12. PMID 10449457.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  10. ^ Dieppe P (1988). "Did Galen describe rheumatoid arthritis?". Annals of the Rheumatic Diseases. 47: 84–87.
  11. ^ Calin A. (1985). "Ankylosing spondilitis". Clinics in Rheumatic Diseases. 11: 41–60.
  12. ^ Pierre Marie (1995). "Benoist M. - Historical Perspective". Spine. 20: 849–852.
  13. ^ Blumberg BS (1958). "?". Arch Rheum. 1: 553.
  14. ^ Leden I (1994). "Did Bechterew describe the disease which is named after him? A question raised due to the centennial of his primary report". Scand J Rheumatol. 23 (1): 42–5. PMID 8108667.
  15. ^ "Life and sufferings of Leonard Trask" (PDF for registered members)). Ankylosing Spondylitis Information Matrix.
  16. ^ "Life and sufferings of Leonard Trask".
  17. ^ Bechterew W. (1893). "Steifigkeit der Wirbelsaule und ihre Verkrummung als besondere Erkrankungsform". Neurol Centralbl. 12: 426–434.
  18. ^ Strumpell A. (1897). "Bemerkung uber die chronische ankylosirende Entzundung der Wirbelsaule und der Huftgelenke". Dtsch Z Nervenheilkd. 11: 338–342.
  19. ^ Marie P. (1898). "Sur la spondylose rhizomelique". Rev Med. 18: 285–315.
  20. ^ a b Alpert, Joseph S. (2006). The AHA Clinical Cardiac Consult. Lippincott Williams & Wilkins. ISBN 0781764904.
  21. ^ Nicholas U. Ahn, Uri M. Ahn, Elizabeth S. Garrett; et al. (2001). "Cauda Equina Syndrome in AS (The CES-AS Syndrome): Meta-analysis of outcomes after medical and surgical treatments". J of Spinal Disorders. 14 (5): 427–433. PMID 11586143. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
  22. ^ "Remicade.com". Living with Ankylosing Spondylitis. Retrieved 2007-12-30.
  23. ^ Ebringer A, Wilson C (1996). "The use of a low starch diet in the treatment of patients suffering from ankylosing spondylitis". Clin Rheumatol. 15 Suppl 1: 62–66. PMID 8835506. {{cite journal}}: Unknown parameter |month= ignored (help)
  24. ^ 'No Starch Diet' Post List
  25. ^ Ebringer, Alan (1996). "The London AS Diet". Kick AS. Retrieved 2008-01-18. Low starch/high protein diet for ankylosing spondylitis patients.
  26. ^ Sinclair, Carol. The IBS Low-Starch Diet. UK: London: Vermilion. pp. pp. 23-35. ISBN 9780091912864. {{cite book}}: |pages= has extra text (help); Unknown parameter |accessyear= ignored (|access-date= suggested) (help)
  27. ^ National Institute of Health
  28. ^ Cousins wrote a bestselling book about his illness,Anatomy of an Illness. But since he was "cured" of the disease, which is incurable, he may have been misdiagnosed.
  29. ^ Trnavsky K., Sabova L. (1992). "Karel Capek-Czech writer, sufferer from ankylosing spondylitis". Clin Rheumatol. 11 (3): 337–40. PMID 1458780.

National organizations

Diagnostic tools

Current research

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