Hermínio Ometo University, Brazil.
Braz J Otorhinolaryngol. 2010 May-Jun;76(3):306-9. doi: 10.1590/S1808-86942010000300006.
The process of hair cell damage and death as a result of exposure to noise and ototoxins seems to be mediated by reactive oxygen species.
To investigate the relationship between genetic polymorphisms in the Glutathione S-transferase and the susceptibility to hearing loss induced by aminoglycosides.
Null genotypes were analyzed by multiplex-PCR in the DNA samples from 50 patients and 72 controls. The patients were divided into 3 groups, 10 with hearing loss using aminoglycosides (group A), 20 with hearing loss without exposure to the drug (group B) and 20 hearing individuals who used the antibiotic (group C).
Experimental.
Polymorphisms in the GSTM1 and GSTT1 genes were found in 16% and 42% of patients and in 18% and 53% of the control group, respectively. After statistical analysis no significant difference was observed between the control groups and A (p=0.86) and (p=0.41), controls and B (p=0.27) and (p=0.24), controls and C (p=0.07) and (p=0.47), controls and A + C (p=0.09) and (p=0.47), C and A (p=0.32) and (p=0.75), GSTT1 and GSTM1, respectively.
Our data show that polymorphisms in GSTM1 and GSTT1 genes have no influence on the ototoxicity of aminoglycosides.
由于暴露于噪声和耳毒性物质而导致的毛细胞损伤和死亡的过程似乎是由活性氧物质介导的。
研究谷胱甘肽 S-转移酶的遗传多态性与氨基糖苷类诱导的听力损失易感性之间的关系。
在来自 50 名患者和 72 名对照者的 DNA 样本中,通过多重 PCR 分析空基因型。将患者分为 3 组,10 名使用氨基糖苷类药物引起听力损失的患者(组 A),20 名无药物暴露引起听力损失的患者(组 B)和 20 名使用抗生素但听力正常的患者(组 C)。
实验性。
在患者中发现 GSTM1 和 GSTT1 基因的多态性分别为 16%和 42%,在对照组中分别为 18%和 53%。经统计学分析,对照组与 A 组(p=0.86)和(p=0.41)、对照组与 B 组(p=0.27)和(p=0.24)、对照组与 C 组(p=0.07)和(p=0.47)、对照组与 A+C 组(p=0.09)和(p=0.47)、C 组与 A 组(p=0.32)和(p=0.75)之间均无显著差异。GSTM1 和 GSTT1 分别与 C 和 A 之间也无显著差异。
我们的数据表明,GSTM1 和 GSTT1 基因的多态性对氨基糖苷类的耳毒性没有影响。