Ankylosing Spondylitis in Orthopedic Surgery
- Author: S Craig Humphreys, MD; Chief Editor: Mary Ann E Keenan, MD more...
Background
Ankylosing spondylitis (AS) is a chronic, multisystem inflammatory disorder of the sacroiliac (SI) joints and the axial skeleton.[1, 2, 3, 4] AS is characterized as a seronegative spondyloarthropathy. The disorder is often found in association with other seronegative spondyloarthropathies, including reactive arthritis, psoriasis, juvenile chronic arthritis, ulcerative colitis, and Crohn disease.
The etiology of this condition is not understood completely; however, a strong genetic predisposition exists.[5, 6] A direct relationship between AS and the major histocompatibility human leukocyte antigen (HLA)-B27 has been determined.[7] The precise role of HLA-B27 in precipitating AS remains unknown; however, it is believed that HLA-B27 may resemble or act as a receptor for an inciting antigen such as bacteria.
A genetic predisposition exists among persons with the HLA-B27 major histocompatibility antigen. The prevalence increases from 0.1-0.2% in the general population to 1-2% in persons with the HLA-B27 antigen. Additionally, 10-20% of those who have a first-degree relative with AS and who inherit the HLA-B27 antigen eventually develop AS.
Patients often have a family history of either AS or another seronegative spondyloarthropathy.
An image depicting ankylosing spondylitis can be seen below.
Patient with ankylosing spondylitis affecting the cervical and upper thoracic spine. The patient's spine has been fused in a flexed position. Pathophysiology
AS most commonly affects the SI joints and the axial skeleton. Involvement of the SI joints is required to establish the diagnosis. Hip and shoulder joints are affected less frequently. Peripheral joint involvement is least common.
The initial presentation generally occurs in the SI joints and is followed by involvement of the discovertebral, apophyseal, costovertebral, and costotransverse joints and the paravertebral ligaments.
Early lesions include subchondral granulation tissue that erodes the joint and is replaced gradually by fibrocartilage and then ossification. This occurs in ligamentous and capsular attachment sites to bone and is called enthesitis.[8]
In the spine, this initial process occurs at the junction of the vertebrae and the anulus fibrosus of the intervertebral discs. The outer fibers of the discs eventually undergo ossification to form a syndesmophyte. The condition progresses to the characteristic bamboo spine appearance.
The inflammatory response includes CD4+ and CD8+ T lymphocytes and macrophages as well as cytokines, including tumor necrosis factor-alpha (TNF-α) and transforming growth factor-beta (TGF-β).[9, 10]
Extra-articular involvement can include acute iritis, aortitis, aortic fibrosis, pulmonary fibrosis, and neurologic deficits.
Acute iritis occurs in 25-30% of patients and generally is unilateral. Symptoms include pain, lacrimation, photophobia, and blurred vision.
Cardiac involvement is generally a late finding. Severe cases can lead to complete heart block.[11]
Pulmonary involvement is secondary to inflammation of the costovertebral and costotransverse joints, which limits chest-wall range of motion (ROM). Pulmonary fibrosis is generally an asymptomatic incidental radiographic finding.
Neurologic deficits are secondary to spinal fracture or cauda equina syndrome resulting from spinal stenosis. Spinal fracture is most common in the cervical spine.
Epidemiology
Frequency
United States
AS affects 0.1-0.2% of the US population.
International
AS affects 0.1-1.0% of the world population.
Mortality/Morbidity
Chronic pain and stiffness are the most common complaints of patients with AS. More than 70% of patients report daily pain and stiffness.[12]
Fatigue is another common complaint of patients with AS, occurring in approximately 65% of patients. Most patients report their fatigue to be moderately severe. Increased levels of fatigue are associated with increased pain and stiffness and decreased functional capacity.[13, 14]
Severe physical disability is not common among patients with AS. Problems with mobility occur in approximately 47% of patients. Disability is related to the duration of the disease, peripheral arthritis, cervical spine involvement, younger age at onset of symptoms, and coexisting illnesses. Disability has been demonstrated to improve with prolonged periods of exercise or surgical correction of peripheral joint and cervical spine involvement.
Most patients are able to continue to work after onset of symptoms.[15, 16, 17, 18, 19] Vocational counseling has been demonstrated to decrease the risk of employment disability by greater than 60%. Although most patients are able to continue to work, up to 37% change occupations to less physically demanding jobs as symptoms progress.
Emotional problems related to the disease are reported in 20% of patients. Depression is more common among women, and contributing factors include the level of pain and functional disability involved.
Increased rates of mortality related to AS are rare. Death is generally the result of long-standing disease with either extra-articular manifestations, such as heart block, or from coexisting diseases, such as inflammatory bowel disease.
Race
- The disease is most prevalent in persons of northern European heritage and least prevalent in sub-Saharan Africa.
- The less common juvenile-onset version of AS is more common among Native Americans, Mexicans, and persons in developing countries.
Sex
- The male-to-female incidence for AS is 3:1.
Age
- Symptoms generally develop in late adolescence or early adulthood. Onset of symptoms in an individual older than 45 years is uncommon.
- If symptoms develop when an individual is younger than 16 years, the disease is termed juvenile-onset spondylitis.
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