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Stapedius reflex and brainstem auditory evoked responses in multiple sclerosis patients
Scandinavian Audiology
|January 1, 1984
Summary
Multiple sclerosis patients showed abnormal auditory brainstem responses in 40% of cases. While stapedius reflex abnormalities were less common, they correlated with bilateral auditory brainstem response issues.
Area of Science:
- Neuroscience
- Audiology
- Clinical Neurology
Background:
- Multiple sclerosis (MS) is a demyelinating disease affecting the central nervous system.
- Auditory pathway involvement is common in MS, impacting hearing function.
- The stapedius reflex (SR) and brainstem auditory evoked potential (ABR) are sensitive electrophysiological measures of auditory pathway integrity.
Purpose of the Study:
- To investigate the prevalence and correlation of stapedius reflex (SR) and brainstem auditory evoked potential (ABR) abnormalities in multiple sclerosis patients.
- To assess the relationship between these electrophysiological findings and clinical disability.
- To explore the intercorrelation between SR and ABR abnormalities.
Main Methods:
- Recorded SR (including adaptation) and ABR in 53 definite multiple sclerosis patients (Hyllested grade 1-4).
- Assessed peripheral hearing using pure-tone audiogram and speech threshold.
- Analyzed correlations between SR, ABR, and clinical data.
Main Results:
- ABR was abnormal in 40% of patients; SR was abnormal in 11% and borderline in 21%.
- Peripheral hearing was normal in most cases (44/53).
- SR and ABR abnormalities showed limited correlation with clinical disability but a better, though not implicit, correlation with each other. Bilateral ABR abnormalities were associated with higher SR abnormality rates.
Conclusions:
- Electrophysiological auditory testing, particularly ABR, reveals significant abnormalities in a substantial proportion of MS patients.
- SR abnormalities are less frequent but may indicate more widespread auditory pathway dysfunction when present with bilateral ABR issues.
- Further research is needed to clarify the precise relationship between SR, ABR, and MS pathophysiology.