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A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness

机译:一种检测与氨基糖苷类诱导的耳聋相关的五种已知突变的快速方法

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摘要

Background: South Africa has one of the highest incidences of multidrug-resistant tuberculosis (MDR-TB) in the world. Concomitantly, aminoglycosides are commonly used in this country as a treatment against MDR-TB. To date, at least five mutations are known to confer susceptibility to aminoglycoside-induced hearing loss. The aim of the present study was to develop a rapid screening method to determine whether these mutations are present in the South African population. Methods: A multiplex method using the SNaPshot technique was used to screen for five mutations in the MT-RNR1 gene: A1555G, C1494T, T1095C, 961delT+C(n) and A827G. A total of 204 South African control samples, comprising 98 Mixed ancestry and 106 Black individuals were screened for the presence of the five mutations. Results: A robust, cost-effective method was developed that detected the presence of all five sequence variants simultaneously. In this pilot study, the A1555G mutation was identified at a frequency of 0.9% in the Black control samples. The 961delT+C(n) variant was present in 6.6% of the Black controls and 2% of the Mixed ancestry controls. The T1095C, C1494T and A827G variants were not identified in any of the study participants. Conclusion: The frequency of 0.9% for the A1555G mutation in the Black population in South Africa is of concern given the high incidence of MDR-TB in this particular ethnic group. Future larger studies are warranted to determine the true frequencies of the aminoglycoside deafness mutations in the general South African population. The high frequencies of the 961delT+C(n) variant observed in the controls suggest that this change is a common non-pathogenic polymorphism. This genetic method facilitates the identification of individuals at high risk of developing hearing loss prior to the start of aminoglycoside therapy. This is important in a low-resource country like South Africa where, despite their adverse side-effects, aminoglycosides will continue to be used routinely and are accompanied with very limited or no audiological monitoring.
机译:背景:南非是世界上耐多药结核病(MDR-TB)发病率最高的国家之一。同时,该国通常使用氨基糖苷类药物作为抗MDR-TB的治疗方法。迄今为止,已知至少有五个突变赋予氨基糖苷诱导的听力损失敏感性。本研究的目的是开发一种快速筛选方法,以确定南非人群中是否存在这些突变。方法:使用SNaPshot技术的多重方法筛选MT-RNR1基因的五个突变:A1555G,C1494T,T1095C,961delT + C(n)和A827G。筛选了总共204个南非对照样品,包括98个混合血统和106个黑人个体,以确定是否存在这五个突变。结果:开发了一种可靠,具有成本效益的方法,该方法可以同时检测所有五个序列变体的存在。在该初步研究中,在黑人对照样品中发现A1555G突变的频率为0.9%。 961delT + C(n)变体存在于6.6%的黑人对照和2%的混合祖先对照中。在任何研究参与者中均未鉴定出T1095C,C1494T和A827G变体。结论:鉴于该特定族群中耐多药结核病的发生率很高,南非黑人人口中A1555G突变发生率为0.9%,这令人关注。将来需要进行更大的研究以确定南非一般人群中氨基糖苷性耳聋突变的真实频率。在控件中观察到的961delT + C(n)变异的高频率表明,这种变化是常见的非致病性多态性。这种遗传方法有助于在氨基糖苷治疗开始之前鉴定具有发展为听力损失高风险的个体。这在南非这样资源匮乏的国家很重要,尽管该国有不良的副作用,但氨基糖苷类将继续常规使用,并且伴有非常有限的听力监测或没有听力监测。

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