Concise reports
Late onset spondylarthropathy: clinical and biological comparison
with early onset patients
Department of Rheumatology, Hôpital
Ambroise Pare, Boulogne, France
Correspondence to: Professor J M Le Parc, Department of Rheumatology, Hopital Ambroise Pare, 9 Avenue Charles de Gaulle, 92104 Boulogne Cedex, France.
Accepted for publication 17 December 1996.
OBJECTIVE
To compare the clinical, radiological,
and biological profile of patients presenting late onset
spondylarthropathy (LOSPA) with patients with early onset
spondylarthropathy (EOSPA).
METHODS
During the period April 1987 to April
1995 a retrospective chart review of inpatients and outpatients
identified eight patients with LOSPA. They were matched with 32 patients with EOSPA examined during the same period of time. Clinical,
radiological, and biological signs were compared. All patients
fulfilled Amor criteria for spondylarthropathy.
RESULTS
Mean age of patients with LOSPA was 65.1 years (range 58-72), and 26.6 years (range 11-40) in patients with
EOSPA. The sex ratio (female/male) was 5/3 in LOSPA and 9/23 in EOSPA
(p = 0.007). Patients with LOSPA had more significantly cervical and
dorsal pain (p = 0.002, p = 0.02 respectively), anterior chest wall
involvement (p = 0.04), number of peripheral arthritis (p = 0.04),
aseptic osteitis (p = 0.004), and systemic symptoms : fever, fatigue, weight loss (p = 0.04). Mean (SD) erythrocyte sedimentation rate was 87 (24) in LOSPA and 24 (35) in EOSPA patients (p = 0.001). Inflammatory
bowel disease was diagnosed in three patients with EOSPA. A definite
family history of SPA was found in 50% of patients with LOSPA and in
31% of patients with EOSPA. A clear response to NSAID was obtained in
62% of LOSPA patients and in 90.6% of EOSPA patients (p = 0.05).
Three LOSPA patients (two with Crohn's disease) not responding to
NSAID were successfully treated with prednisone.
CONCLUSION
The onset of spondylarthropathy is
uncommon after 55 years. Patients with LOSPA, according to accepted
international criteria present a different clinical and biological
profile when compared with younger patients. These results suggests
that age may influence the presentation of SPA at onset.
© 1997 by Annals of the Rheumatic Diseases
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