SENSORINEURAL HEARING DISORDERS IN SYSTEMIC LUPUS-ERYTHEMATOSUS - A CONTROLLED-STUDY

Citation
Ap. Andonopoulos et al., SENSORINEURAL HEARING DISORDERS IN SYSTEMIC LUPUS-ERYTHEMATOSUS - A CONTROLLED-STUDY, Clinical and experimental rheumatology, 13(2), 1995, pp. 137-141
Citations number
29
Categorie Soggetti
Rheumatology
ISSN journal
0392856X
Volume
13
Issue
2
Year of publication
1995
Pages
137 - 141
Database
ISI
SICI code
0392-856X(1995)13:2<137:SHDISL>2.0.ZU;2-H
Abstract
Objective. Hearing abnormalities have been described in several connec tive tissue diseases, but. relevant data in systemic lupus erythematos us (SLE) is very insufficient. We therefore prospectively evaluated fo rty unselected consecutive female SLE patients for evidence of audiove stibular dysfunction and compared the results with those of 65 age-mat ched healthy women. Methods. Patients and controls were separated into five age groups, Le. 16-29 years, 30-39, 40-49, 50-59 and 60-69 years . Evaluation included pure tone audiometry thresholds at octave freque ncies from 125Hz to 8000Hz, tympanometry and the stapedial reflex test in both ears. In particular, SLE activity, the presence of vasculitis and severe kidney and nervous system involvement, and serum levels of anti-ds-DNA antibodies and C3 and C4 were recorded. Results. A statis tically significant decrease in hearing acuity at low frequencies (125 -500Hz) was found in the patients aged 16-59 compared with the control s, whereas in the first group of young patients (16-29) a similar decr ease was observed in the high frequencies as well. No correlation was found between these abnormalities and any parameter of the underlying disease. Conclusion. With regard to the high frequencies, our results suggest that young SLE patients exhibit a ''premature aging'' of the i nner ear which eventually stabilizes. On the contrary, at low frequenc ies there is a regular decrease in acuity in all groups (except for th e elderly patients: 60-69), which may indicate a subclinical vestibula r hydrops. This could be accounted for by an autoimmune process in the inner ear, quite possible in SLE.