J. Coll et al., HIGH PREVALENCE OF SUBCLINICAL SJOGRENS-SYNDROME FEATURES IN PATIENTSWITH AUTOIMMUNE THYROID-DISEASE, Journal of rheumatology, 24(9), 1997, pp. 1719-1724
Objective. To determine the prevalence of keratoconjunctivitis sicca a
nd xerostomia related to Sjogren's syndrome (SS) in asymptomatic patie
nts with diagnosed autoimmune thyroid diseases (AITD); and to investig
ate whether the immunopathologies of sialadenitis observed in AITD ass
ociated SS and primary SS are similar. Methods. One hundred seventy-si
x patients diagnosed with AITD (88 with Graves' disease, 40 Hashimoto'
s thyroiditis, 48 primary myxedema) were tested for keratoconjunctivit
is sicca (Schirmer's test and rose bengal staining) and for xerostomia
(salivary scintigraphy and labial salivary gland biopsy). Immunohisto
pathological studies were performed on cryostat sections of bucal muco
sa biopsies using antibodies to CD3, CD4, CD8, CD20, CD14, CD25, LFA-1
, ICAM-3, HLA class II, tumor necrosis factor-alpha, interleukin 1, an
d interferon-gamma. Results. Nineteen of 52 (37%) patients with AITD f
ulfilled the criteria for xerostomia and 39/170 (23%) for keratoconjun
ctivitis sicca. Features of SS were diagnosed in 43 of 176 (24%) patie
nts with AITD, with similar prevalence in Graves' (20%), Hashimoto's t
hyroiditis (27%), and primary myxedema (29%). In AITD associated SS, i
nfiltrating lymphocytes were mainly CD3+ T lymphocytes, with a CD4/CD8
ratio of 2:1. In most patients infiltrating lymphocytes expressed act
ivation markers, HLA class IT molecules, and interleukin 2 receptor (C
D25). In some patients HLA class II was inappropriately expressed in t
he epithelial gland cells. Conclusion. The finding that a third of pat
ients with AITD have SS features confirms that AITD and SS are mutuall
y associated. Together with the similarity of immunopathology of siala
denitis in AITD associated SS in primary SS, this supports the theory
that SS and AITD are 2 autoimmune diseases closely related pathogeneti
cally.