Extended report
A longitudinal cohort study of Finnish patients with primary
Sjögren's syndrome: clinical, immunological, and epidemiological
aspects
M Pertovaaraa, E Pukkalab, P Laippalac, A Miettinend, A Pasternacke
a Department of
Internal Medicine, Tampere University Hospital, Tampere, Finland, b Finnish Cancer Registry,
Helsinki, Finland, c Department
of Public Health, University of Tampere, d Department
of Clinical Microbiology, Tampere University Hospital, e Medical School, University of Tampere
Correspondence to: Dr M Pertovaara, Department of Internal Medicine, Section of Rheumatology, Tampere University Hospital, PO Box 2000, FIN-33521 Tampere, Finland marja.pertovaara{at}tays.fi
Accepted for publication 11 October
2000
OBJECTIVE
To evaluate
outcome in a cohort of Finnish patients with primary Sjögren's
syndrome (pSS).
METHODS
Clinical and
laboratory data from the time of diagnosis and follow up were collected
from 110 patients with pSS (107 women, three men) diagnosed in
1977-1992 in central Finland. The standardised incidence ratio for
cancers was determined as the ratio of the observed number of cases to
the expected number based on regional population rates. Eighty one of
the 93 patients still alive were interviewed, and clinical and
laboratory examinations performed in 1994-1997.
RESULTS
The mean (SD)
erythrocyte sedimentation rate (33 (22) v 45 (28) mm/1st h), serum IgG (18.8 (7.4) v 22.5 (8.5) g/l), and serum IgM (1.6 (1.1) v 2.0 (1.2) g/l) at the control visit were significantly (p<0.0001) lower
than those at baseline. A similar change was observed in a subgroup of
patients never treated with glucocorticosteroids or disease modifying
antirheumatic drugs. Three non-Hodgkin's lymphomas were diagnosed
(standardised incidence ratio 13; 95% confidence interval 2.7 to 38).
In a logistic regression model, the patients with pSS with subsequent
lymphoma were found to have higher baseline levels of serum
2 microglobulin than the others (odds ratio 1.9; 95%
confidence interval 1.1 to 3.4).
CONCLUSION
The results
suggest that mean concentrations of serum IgG and IgM in patients with
pSS decline with time, possibly reflecting diminishing inflammatory
activity. As in previous studies, the incidence of non-Hodgkin's
lymphomas in this cohort of patients with pSS was significantly higher
than in the reference population.
© 2001 by Annals of the Rheumatic Diseases
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