Objective, Evaluation of the course and the prognosis of juvenile chronic a
rthritis (JCA) and juvenile spondyloarthropathy (JSpA).
Methods. The entire medical histories of 171 patients with JCA or JSpA were
reviewed, The study cohort comprised 102 patients with oligoarticular, 17
with systemic, and 24 with polyarticular onset of JCA; 28 patients had a Sp
A; 91 patients with JCA from a population based cohort were included in tha
t study cohort. The mean period of followup was 7.4 years. The probability
of remission was estimated by survival analysis methods (Kaplan-Meier metho
d).
Results. After a disease duration of 10 years the highest probability of co
mplete remission was estimated for patients with oligoarticular or systemic
onset of JCA (54% and 38%, respectively). In the oligoarthritis group with
late onset of JCA, a lower probability of remission was found fur the HLA-
B27+ patients compared with HLA-B27- patients. Patients with polyarticular
onset of JCA had the poorest prognosis, with a significantly lower probabil
ity of complete remission (15%) within 10 years, more secondary injuries, a
nd a lower functional capacity at followup, Patients with JSpA showed a 17%
probability of remission after a disease duration of 5 years and ranged be
tween the remission rates for oligoarticular and polyarticular JCA. The est
imated remission rates for the patients with JCA in the population based co
hort and in the whole cohort were quite similar.
Conclusion, Our data suggest a favorable prognosis for JCA and JSpA in gene
ral, but with differences among the subtypes, It seems that more than 50% o
f the patients with JCA and JSpA reach adulthood with active arthritis and
need further rheumatological care.