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Abstract Title:

N-Acetyl-cysteine against noise-induced temporary threshold shift in male workers.

Abstract Source:

Hear Res. 2010 Jul 16. Epub 2010 Jul 16. PMID: 20638463

Abstract Author(s):

Cheng-Yu Lin, Jiunn-Liang Wu, Tung-Sheng Shih, Perng-Jy Tsai, Yih-Min Sun, Mi-Chia Ma, Yueliang L Guo

Article Affiliation:

Department of Otolaryngology, Tainan Hospital, Department of Health, No.125, Zhong-Shan Road, West Central District, Tainan City 700, Taiwan; Institute of Environmental and Occupational Health Medicine, College of Medicine, National Cheng Kung University, No.138, Sheng-Li Road, North District, Tainan City 704, Taiwan.

Abstract:

Previous animal studies showed protective effects of antioxidant medicines against noise-induced hearing loss (NIHL). It is unclear whether antioxidants would protect humans from NIHL. We conducted a study to determine whether N-Acetyl-cysteine (NAC) protected men against noise-induced temporary threshold shift (TTS), and whether subgroups with genetic polymorphisms of glutathione S-transferase (GST) T1 and M1 responded to NAC differently. In this prospective, double-blind, crossover study, 53 male workers were randomly assigned to receive either NAC (1200 mg/day, 14 days) during the first period and placebo during the second period, or placebo during the first period and NAC during the second period. Dosing periods were separated by a washout period of 2 weeks. The hearing threshold changes were determined before and after each dosing period. Pre-shift hearing threshold for high frequencies was 19.1 dB. Daily exposure to noise ranged from 88.4 to 89.4 dB. The noise levels of different frequencies ranged from 80.0 to 89.4 dB with a peak-value at 4 kHz. NAC significantly reduced TTS (p = 0.03). When the participants were grouped by GST M1/T1 genotypes, the NAC effect was only significant among workers with null genotypes in both GSTM1 and GSTT1 (p = 0.004). NAC may prevent noise-induced TTS among occupationally noise-exposed men. The protective effect of NAC was more prominent in subjects with both GSTM1-null and GSTT1-null genotypes. (clinicaltrials.gov Identifier: NCT00552786).

Study Type : Human Study

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Sayer Ji
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