E. Toubi et al., AUTOIMMUNE ABERRATION IN SUDDEN SENSORINEURAL HEARING-LOSS - ASSOCIATION WITH ANTICARDIOLIPIN ANTIBODIES, Lupus, 6(6), 1997, pp. 540-542
In view of the presence of autoantibodies against inner ear antigens,
the pathogenesis of sudden dearness (SD) and progressive sensorineural
hearing loss (PSNHL) is suggested to be of an autoimmune nature. Howe
ver, microthrombosis of the inner ear may result from pathogenic antic
ardiolipin antibody (aCL) activity. We studied 30 patients (17 females
and 13 males, age range 20-52 y), of whom 11 suffered from SD and 19
from PSNHL. All were clinically and serologically evaluated for associ
ation with autoimmune disorders (serological examination included: aCL
, ANA, ENA, ANCA, proteinelectrophoresis, and complement levels). Twen
ty healthy matched subjects served as controls. None of the control gr
oup were aCL positive, whereas 8 out of 30 (27%) patients demonstrated
low-moderate titers (P < 0.02), of whom 5 out of 8 suffered from SD.
In addition, 2 aCL negative patients with PSNHL demonstrated hypergamm
aglubolinemia accompanied by hypocomplementemia, whereas none with SD
had such abnormalities. Our data suggests that aCL is detected in pati
ents with sudden sensorineural hearing loss and therefore may play an
important role in the pathogenesis of this disability. If sustained by
additional studies, these findings would warrant the consideration of
anticoagulant therapy.