Extended reports
Clinical follow up study of 87 patients with sicca symptoms
(dryness of eyes or mouth, or both)
Marja Pertovaaraa, Markku Korpelaa, Hannu Uusitalob, Juhani Pukanderc, Ari Miettinend, Heikki Heline, Amos Pasternackc
a Department of
Internal Medicine, Tampere University Hospital, Finland, b Department of
Ophthalmology, Tampere University Hospital, Finland, c Medical School, University of Tampere, Finland, d Clinical
Microbiology Unit, Tampere University Hospital, Finland, e Pathology Unit, Tampere University
Hospital, Finland
Correspondence to: Dr M Pertovaara, Department of Internal Medicine, Section of Rheumatology, Tampere University Hospital, PO Box 2000, FIN-33521 Tampere, Finland.
Accepted for publication 18 March 1999
OBJECTIVE
To assess
the prognosis of patients with sicca symptoms and to identify the
clinical and immunological factors that most sensitively predict the
later development of primary Sjögren's syndrome (SS) or other
connective tissue diseases.
METHODS
Eighty seven
patients (72 female, 15 male) with sicca symptoms were re-evaluated
after a median follow up time of 11 years (range 8-17). The clinical
examination included ophthalmological examination (Schirmer's test,
break up time and Rose-Bengal staining). Labial salivary gland biopsy
was performed and histological findings graded according to the
Chisholm-Mason scale. The immunoserological tests included
determination of rheumatoid factor (RF), antinuclear antibodies (ANA),
anti-extractable nuclear antigen-antibodies (ENA), serum
immunoglobulins IgA, IgG, and IgM, and serum
2-microglobulin (
2m).
RESULTS
At follow up
31 patients (36%) fulfilled modified Californian criteria (salivary
flow measurements were not performed and Chisholm-Mason grades 3-4
were regarded as diagnostic histological findings) for possible or
definite SS. Likewise, a significant progression of the histological
findings was observed. Labial salivary gland re-biopsy was performed in
42 patients with grade 0-2 findings at baseline, progression to grades
3-4 being observed in 21 (50%) at follow up. The patients who later
developed SS were at baseline significantly older (mean (SD) 52 (9)
v 44 (14) years, p
0.005) compared with
those not fulfilling the SS criteria at follow up; they also had
significantly higher serum
2m (p
0.0005) and IgG
concentrations (p
0.005), and they had positive ANA more frequently
(p
0.01).
CONCLUSION
These
results suggest that high age, increased values of serum
2m, ANA positivity and increased concentrations of serum
IgG, might be useful indicators for the subsequent development of SS in
patients with sicca symptoms. The prognosis of patients with these
symptoms was favourable, and the clinical course was benign even in the
36% of patients who developed SS. No cases of lymphoma were observed.
© 1999 by Annals of the Rheumatic Diseases
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