Spondyloarthropathies: Using Presentation to Make the Diagnosis
Key Points
Common features of the spondyloathropathies are enthesitis of the axial and
peripheral skeleton and variable involvement of the peripheral joints, gut,
skin, eye, or aorta.
Human leukocyte antigen B27 is strongly associated with spondyloarthropathy but is not a diagnostic test.
Serologic tests for rheumatoid factor and antinuclear antibody are usually negative in patients with a spondyloarthropathy. The erythrocyte sedimentation rate and the C-reactive protein concentration are often elevated, but elevations do not always correlate with disease activity.
Tumor necrosis factor inhibitors have recently been approved for the treatment of spondyloarthropathy and may have disease-modifying effects. Clinical experience with these drugs in patients with spondyloarthropathies has been limited, but quite positive.
Spondyloarthropathy is a family of arthritides that includes:
Ankylosing spondylitis
Reactive arthritis (including Reiter syndrome)
Psoriatic arthritis
Enteropathic spondyloarthropathy (ie, spondyloarthropathy associated with inflammatory bowel disease)
Undifferentiated spondyloarthropathy (forms that fail to meet the clinical criteria for the other categories).(1)
The spondyloarthropathies are linked by association with the class 1 human leukocyte antigen (HLA)-B27 and by a common clinicopathologic lesion-enthesitis.
There is no serologic test to aid in the diagnosis. Rather, the diagnosis is made by analyzing a constellation of factors, such as axial and peripheral joint and skeletal involvement, associated clinical features, and genetic predisposing factors.(2)
Treatment has been focused on the relief of symptoms with drugs such as nonsteroidal antiinflammatory drugs. The new tumor necrosis factor inhibitors may have a role in modifying the course of this family of conditions, but experience with these drugs is limited.
In this article, we review the clinical presentation of the spondyloarthropathies to help guide the clinician through diagnosis and treatment.
Epidemiology
An epidemiologic assessment of blood donors in Berlin, Germany,3 found that
1.9% had a spondyloarthropathy: 0.86% had ankylosing spondylitis, 0.67% had
undifferentiated spondyloarthropathy, and 0.29% had psoriatic arthritis. Reactive
arthritis and enteropathic spondylitis were much less common.(3)
The prevalence of spondyloarthropathy, particularly of ankylosing spondylitis, correlates most strongly with the prevalence of HLA-B27 in the general population. The percentage of spondyloarthropathy patients with this gene varies from about 90% in those with ankylosing spondylitis to 20% in those with psoriatic arthritis or undifferentiated spondyloarthropathy (Table 1).(4-9) Ankylosing spondylitis and reactive arthritis are more common in men, but are likely underdiagnosed in women. The mean age at diagnosis is generally in the 30s and 40s. Most people with the HLA-B27 gene do not develop ankylosing spondylitis. Table 1 (3-11) provides the key demographic characteristics of the spondyloarthropathies.
Table 1: Demographic Features of the Spondyloarthropathies
| General Prevalence | Relative Prevalence* | Precentage of Male Patients | Mean Age (Years) at Diagnosis | Positive for B27 Antigen | |
| Ankylosing Spondylitis | 0.86% | 42% | 75% | 41 | 86% |
| Reactive arthritis | 0.1% | 17% | 75% | 33 | 69% |
| Psoriatic arthritis | 0.29% | 10% | 43% | 47 | 20%-34% |
| Enteropathic | NA | 4% | 67% | 38 | 50%-75% |
| Undifferentiated | 0.67% | 27% | 31% | 53 | 18% |
*Based on the European Spondyloarthropathy Study Group data from seven rheumatology centers, including 403 patients diagnosed with spondyloarthropathy.
Cleveland Clinic Journal of Medicine
Volume 71, Number 3, March 2004
This paper discusses therapies that are experimental or are not approved by the U.S. Food and Drug Administration for use under discussion.









