M. Tishler et al., Clinical and immunological characteristics of elderly onset Sjogren's syndrome: A comparison with younger onset disease, J RHEUMATOL, 28(4), 2001, pp. 795-797
Objective. To compare the clinical and laboratory characteristics of patien
ts with primary Sjogren's syndrome (SS) with an elderly onset to those with
a younger onset.
Methods. The study group comprised 85 consecutive patients (79 women and 6
men) attending the Sjogren's clinic. Primary SS was diagnosed according to
the San Diego criteria. Elderly onset disease (EOD) was determined as the a
ppearance of symptoms suggestive of SS after age 65. Clinical and laborator
y variables for EOD were compared to those of a younger onset disease (YOD)
. Salivary and serum samples of all patients were examined for concentratio
ns of interleukin 6 (IL-6) and hyaluronic acid (HA).
Results. Seventeen patients with SS (20%) matched the definition of EOD and
their median disease onset was 71 years(range 65-80). No significant diffe
rences were noted in the clinical disease manifestations between the 2 grou
ps of patients. Rheumatoid factor and anti-Ro(SSA) antibodies were more com
mon in the YOD group (p = 0.012 and p = 0.023. respectively). Significant e
levations of salivary IL-6 and HA levels were detected in the YOD group com
pared to the EOD group with SS (17.3 +/- 3.6 vs 8.8 +/- 2.1 pg/ml and 230.2
+/- 41.1 vs 128.8 +/- 33.3 ng/ml. respectively) (p < 0.0001).
Conclusion. EOD SS has somewhat milder clinical symptoms with fewer immunol
ogical manifestations than YOD. The elevations of salivary IL-6 and HA in t
he younger group of SS patients support in part the differences in the infl
ammatory process between the 2 groups.