H. Mielants et al., THE EVOLUTION OF SPONDYLOARTHROPATHIES IN RELATION TO GUT HISTOLOGY .1. CLINICAL ASPECTS, Journal of rheumatology, 22(12), 1995, pp. 2266-2272
Objective. To study prospectively the clinical evolution of different
forms of spondyloarthropathy (SpA) (excluding inflammatory bowel disea
se, IBD): reactive arthritis, undifferentiated SpA, and ankylosing spo
ndylitis (AS). Methods. Ileocolonoscopy was performed on 217 patients
with SpA (149 men, 68 women), They also underwent clinical, laboratory
, and radiological examinations. Two to 9 years later, 123 patients (8
4 men, 39 women) who had been regularly monitored were reviewed and gi
ven the same examinations. For the remaining 94 patients clinical data
were obtained by telephone. Results. At the time of clinical review,
53 (43%) of the regularly monitored patients were in clinical remissio
n, The remission rate was higher in patients with non-ankylosing spond
ylitis SpA (non-AS-SpA) than in patients with AS (19%), Fourteen patie
nts with non-AS-SpA had developed AS; 4 of them also had IBD. IBD was
also found in 4 patients with AS and in 3 patients from the telephone
group. The prevalence of HLA-B27 was significantly higher in all SpA s
ubgroups, while HLA-BW62 was elevated in the undifferentiated SpA. At
review, HLA-B27 was significantly more prevalent in patients with pers
istent locomotor inflammation compared to patients in clinical remissi
on, while HLA-BW62 was predominant in the latter group. Conclusion. Pa
tients with SpA, especially those with non-AS-SpA, have a good longter
m prognosis. However, patients with non-AS-SpA may develop AS, Six per
cent of the patients with SpA in whom manifestations of IBD are absent
will develop this disease. This confirms the hypothesis that some of
these patients with SpA initially have a form of subclinical Crohn's d
isease, of which locomotor inflammation is the only clinical expressio
n. HLA-B27 positivity predisposes to a more severe course of locomotor
inflammation, while HLA-BW62 has a protective effect but is associate
d with gut inflammation.