Mitochondrial Deafness

线粒体DNA 遗传学 听力损失 老年性聋 生物 人类线粒体遗传学 线粒体 基因 突变 粒线体疾病 核基因 医学 听力学
作者
Nathan Fischel‐Ghodsian
出处
期刊:Ear and Hearing [Lippincott Williams & Wilkins]
卷期号:24 (4): 303-313 被引量:97
标识
DOI:10.1097/01.aud.0000079802.82344.b5
摘要

In Brief The last decade has led to the identification of several mitochondrial DNA mutations associated with hearing loss. Since the only known function of the human mitochondrial chromosome is to participate in the production of chemical energy through oxidative phosphorylation, it was not unexpected that mitochondrial mutations interfering with energy production could cause systemic neuromuscular disorders, which have as one of their features hearing impairment. Surprisingly, however, inherited mitochondrial mutations also have been found to be a cause of non-syndromic hearing loss, and predispose to aminoglycoside induced hearing loss, while acquired mitochondrial mutations have been proposed as one of the causes of presbycusis. After a brief review of mitochondrial genetics, we will outline the different mitochondrial mutations associated with hearing loss, describe the audiological features, and discuss the clinical relevance of diagnosing these mutations. Clinical expression of these mitochondrial mutations is dependent on environmental exposures and nuclear-encoded modifier genes. Preventive and therapeutic strategies will depend on identification and avoidance of the environmental exposures, and the identification of the nuclear-encoded modifier genes. Experimental approaches to identify these modifier genes will be presented. The huge majority of human genes are contained in the chromosomes. Although genes in mitochondria represent a tiny fraction of the human genome, both syndromic and non-syndromic hearing loss can be due to inherited mutations of mitochondrial genes. This article provides a brief review of mitochondrial genetics, the different mitochondrial mutations associated with hearing loss, their audiological features, and the clinical relevance of diagnosing these mutations.
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