Undifferentiated spondylarthropathy is one of the common disease subsets in
the group of so-called seronegative spondarthritides. It is not exactly kn
own how often it differentiates into ankylosing spondylitis or other well-d
efined disease subsets over time. The present study was designed to find ou
t the long-term outcome in this subset. Thirty-five patients diagnosed with
undifferentiated spondylarthropathy between January 1987 and December 1988
were recruited. Twenty-two (63%) of them were available for detailed asses
sment I I years after the original diagnosis. Their baseline characteristic
s did not differ from those of the original cohort of 35 patients and were
as follows: male:female ratio 19:3, median age of onset 17 years (range 8-3
9), and median duration of disease 8 months (range 4-24). Clinical features
were enthesitis (45%) and inflammatory pain in the back (100%), buttock (7
7%), hip (64%), shoulder (18%), knee (82%), ankle (77%), and hand and wrist
s (50%). There was no restriction in spinal movement. Family history was po
sitive in two cases. Radiologically, the only finding was grade I sacroilii
tis in 17 patients (77%). Human leukocyte antigen (HLA)-B27 was positive in
all. Functionally, all were in class 1. During follow-up, one patient deve
loped psoriatic skin lesions after 9 years. Uveitis developed in four patie
nts (18%). After a median follow-up of I I years, 15 (68%) had ankylosing s
pondylitis, one developed psoriatic arthritis, four remained undifferentiat
ed, and two had natural remission. Functionally, 19 patients (86%) were in
class I and three (14%) were in class III. No patient had bamboo spine, but
three underwent total hip replacement. Thus, a majority of patients (68%)
with undifferentiated spondylarthropathy gradually developed ankylosing spo
ndylitis of mild severity.