Publication
Title
The effect of naltrexone on the perception and distress in tinnitus : an open-label pilot study
Author
Abstract
Objective. Tinnitus is a perceived sensation of sound without actual acoustic stimulation. Currently there are no standardized drug therapies for the treatment of tinnitus patients. A potential novel treatment for chronic tinnitus is naltrexone. Tinnitus can be considered an auditory phantom phenomenon similar to phantom pain. Naltrexone acts predominantly on mu-opioid receptors which are present in multiple areas of the brain, including the thalamus, dorsal part of the anterior cingulate, insula, amygdala, nucleus accumbens, and ventromedial to orbitofrontal cortex. These areas overlap with the areas involved in tinnitus-related distress. The aim of the present study is to investigate three doses of naltrexone, namely 5, 12.5, and 50 mg and determine their influence on tinnitus complaints. We conducted a 4-week single-center, open-label treatment study. Subjects and methods: 86 patients received the drug treatment, while 30 patients received no treatment. Results: Overall tinnitus distress was significantly reduced for the drug treatment group, while for the waiting control group this was not the case. No significant effect could be obtained for tinnitus intensity. A closer look at the data indicates that this effect is mainly generated due to a significant difference in the 50 mg drug treatment group for tinnitus distress. Conclusion: our results indicate that naltrexone might have an effect on tinnitus distress and more particularly higher doses of naltrexone.
Language
English
Source (journal)
International journal of clinical pharmacology and therapeutics. - München
Publication
München : 2013
ISSN
0946-1965
Volume/pages
51:1(2013), p. 5-11
ISI
000320839200002
Full text (Publishers DOI)
UAntwerpen
Faculty/Department
Research group
Publication type
Subject
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identification
Creation 10.09.2013
Last edited 04.04.2017
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