Antioxidant Therapies in the Treatment of Aminoglycoside-Induced Ototoxicity: A Meta-Analysis
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Published on: November 26, 2015
Patrick J Gaffney1, Kunal R Shetty1, Sancak Yuksel1
1Department of Otorhinolaryngology - Head and Neck Surgery, The University of Texas Health Science Center at Houston, Houston, Texas, USA.
Objective:
A feared complication of aminoglycoside treatment is ototoxicity, which is theorized to be attributed to the production of aminoglycoside-induced reactive oxygen species. Previous studies using animal models have suggested that numerous therapies targeting reducing oxidative stress may prevent ototoxicity from aminoglycosides. However, few clinical studies have been conducted on these antioxidants. This systematic review and meta-analysis examines the effectiveness of antioxidant therapies in the treatment of aminoglycoside-induced ototoxicity.
Data Sources:
PubMed, Embase, Web of Science, and ClinicalTrials.gov.
Review Method:
A literature search was conducted in August 2024. This review sought randomized controlled trials to be conducted on humans to examining otologic outcomes in aminoglycoside-induced ototoxicity following administration of medications intended to reduce oxidative stress.
Results:
A systematic review yielded 2037 results, of which seven studies met inclusion criteria. N-acetylcysteine (NAC) was investigated in four studies, aspirin in two studies, and vitamin E in one study. Six studies examined the benefit of antioxidant treatments for up to 8 weeks after administration while one study tested subjects' hearing after 1 year. In pooled analysis, two studies assessing NAC showed the greatest reduction in ototoxicity (RR 0.112, 95% CI, 0.032-0.395; p = 0.0007; I2 = 18%), followed by two studies examining aspirin (RR 0.229, 95% CI, 0.080-0.650; p = 0.0057; I2 = 0%). One study performed with vitamin E did not find a reduction in ototoxicity compared to the placebo (RR 0.841, 95% CI, 0.153-4.617; p = 0.8416).
Conclusions:
Multiple studies have shown that NAC and aspirin are effective in reducing ototoxicity from treatment with aminoglycosides. However, there is a lack of high-quality evidence. Additional studies should examine whether aspirin and N-acetylcysteine provide long-term benefit, and which of the other promising antioxidants translate from animal models.
Level Of Evidence:
NA Laryngoscope, 135:1278-1286, 2025.
Insights
N-acetylcysteine (NAC) and aspirin show promise in preventing aminoglycoside-induced ototoxicity. While effective in reducing hearing damage, more high-quality clinical trials are needed to confirm long-term benefits and explore other antioxidants.
Area of Science:
- Ototoxicity research
- Antioxidant therapies
- Clinical trial analysis
Background:
- Aminoglycoside treatment can cause ototoxicity, potentially due to reactive oxygen species.
- Animal studies suggest antioxidants may prevent this, but human clinical data is limited.
- This review focuses on antioxidant efficacy in preventing aminoglycoside-induced ototoxicity.
Purpose of the Study:
- To systematically review and meta-analyze the effectiveness of antioxidant therapies in preventing aminoglycoside-induced ototoxicity in humans.
- To evaluate clinical evidence for antioxidants like N-acetylcysteine, aspirin, and vitamin E.
Main Methods:
- Systematic literature search of PubMed, Embase, Web of Science, and ClinicalTrials.gov conducted in August 2024.
- Inclusion of randomized controlled trials (RCTs) examining otologic outcomes in humans.
- Meta-analysis of data from seven included studies.
Main Results:
- Seven studies met inclusion criteria, investigating N-acetylcysteine (NAC), aspirin, and vitamin E.
- Pooled analysis indicated NAC (RR 0.112) and aspirin (RR 0.229) significantly reduced ototoxicity.
- Vitamin E did not show a significant reduction in ototoxicity compared to placebo (RR 0.841).
Conclusions:
- N-acetylcysteine (NAC) and aspirin demonstrate effectiveness in mitigating aminoglycoside-induced ototoxicity.
- Current evidence lacks high-quality data, necessitating further research.
- Future studies should assess long-term benefits and investigate other promising antioxidants.
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