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Ankylosing Spondylitis

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Our mission is to provide information on ankylosing spondylitis (abbreviated as AS) to patients and their families as well as to the health care providers.
ASIM also happens to be the middle (given) name of the chief consultant for this website, Professor Muhammad Asim Khan, MD, who has himself suffered from severe form of AS for 55 years.
 
Ankylosing Spondylitis
The name ankylosing spondylitis (or AS for short) is derived from Greek roots angkylos = ”bent” (although the word ankylosis now means joint stiffening or fusion) and spondylos = ”spinal vertebra”.

It is a chronic, inflammatory rheumatic disease with a prevalence of about 0.5% in epidemiologic studies in Europe, but the prevalence can vary in other populations.

It is the prototype of a group of diseases that share clinical and pathogenetic features and are grouped under the term "Spondyloarthropathies" (SpA) that include, in addition to AS, reactive SpA, psoriatic SpA, enteropathic SpA (associated with Crohn's disease and ulcerative colitis) and undifferentiated SpA.

These diseases can occur within families because of a strong genetic predisposition highlighted by its strong association with HLA-B27, a normal gene that is also present in a small percentage of the general population.

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Ankylosing Spondylitis

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Salient Features of Ankylosing Spondylitis

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· A chronic, systemic inflammatory rheumatic disorder with the predilection for inflammation at sites where the tendons and ligaments attach to the bones (enthesitis), especially in the sacroiliac joints and the spinal column.

· The symptoms usually start during late teens or early twenties (rarely after age 45), and is 2 to 3 times more common in males. The most common presenting symptoms is chronic back pain and stiffness resulting from inflammation affecting the sacroiliac joints (sacroilitis) and spine (spondylitis).

. There is generally good symptomatic relief from back pain with adequate (anti-inflammatory) dose of non steroidal anti-inflammatory drugs (NSAIDs), such as naprosyn, ibuprofen and diclofenac.

. The other clinical features of AS and related SpA may include asymmetric arthritis (that more often affects lower extremities) orinflammation of some of the extra-articular structures such as the eye (iritis), the skin (psoriasis) and the gut (Crohn's disease and ulcerative colitis). 

. The presenting clinical manifestations of these diseases can be very wide-ranging, and thus a variety of health care professionals (from primary care physicians, ophthalmologists and dermatologists to rheumatologists and other medical and surgical specialists) see such patients.

. Unfortunately, most patients with AS are either diagnosed late or are inadequately treated (and some are never diagnosed). The current mean delay in the diagnosis of AS ranges from 5 to 10 years.

. Earlier diagnosis and treatment can better mitigate the severity of the disease, and make a meaningful difference for patient care and quality of life.

. With the availability of newer, highly effective treatments (with TNF-blockers, such as Enbrel, Humira, Remicade), and better methods of musculoskeletal imaging (such as MRI), there is an urgent need to improve early diagnosis and reduce any inappropriate delay in obtaining effective treatment.



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The information posted on this website is not meant to take the place of medical advice from your personal physician or health care professional. We encourage users of our website to discuss all medical questions with their personal physician or specialist, and prior to initiating any change of treatment, medication, or therapy. We also encourage the viewers to discuss these questions with a rheumatologist if they have not done so in the past. We have provided a link to assist you in finding a rheumatologist in your area if your primary care physician is unable to recommend one.