Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
Otol Neurotol. 2009 Dec;30(8):1021-32. doi: 10.1097/MAO.0b013e3181a86509.
Otosclerosis is a major cause of acquired hearing loss in adult life affecting exclusively the human temporal bone. Until recently, the etiopathogenesis of otosclerosis was still a matter of debate. Genetic research, however, has evolved enormously the last years and unveiled important clues regarding the cause of otosclerosis. The objective of this article is to review the genetics of otosclerosis with special attention for the links to the bone homeostasis of the otic capsule.
A detailed literature study was performed focusing on the recent genetic findings in otosclerosis and the special bone turnover of the otic capsule. A PubMed search and own research data were used to bring the relevant information for this review together.
Unlike all other bones in the human skeleton, the otic capsule undergoes very little remodeling after development, possibly due to local inner ear factors. Otosclerosis is a process of pathologic increased bone turnover in the otic capsule, which in most cases leads to stapes fixation, resulting in a conductive hearing loss. Although environmental factors such as estrogens, fluoride, and viral infection have been implicated, it is clear that genetic factors play a significant role in the manifestation of otosclerosis. From a genetic viewpoint, otosclerosis is considered to be a complex disease with rare autosomal dominant forms caused by a single gene. Already, 7 monogenic loci have been published, but none of the genes involved have been identified. For the complex form of otosclerosis, caused by an interaction between genetic and environmental factors, the first susceptibility genes were identified by case-control association studies. All 3 replicated genes, TGFB1, BMP2, and BMP4, are a part of the transforming growth factor-beta1 pathway. Data from both genetic association studies and gene expression analysis of otosclerotic bone showed that the TGF-beta1 pathway is most likely an important factor in the pathogenesis of otosclerosis.
耳硬化症是成人获得性听力损失的主要原因,仅影响人类颞骨。直到最近,耳硬化症的病因仍然存在争议。然而,遗传研究在过去几年中取得了巨大进展,揭示了耳硬化症病因的重要线索。本文的目的是综述耳硬化症的遗传学,特别关注耳硬化症与耳囊骨稳态的联系。
进行了详细的文献研究,重点关注耳硬化症的最新遗传发现以及耳囊的特殊骨转换。使用 PubMed 搜索和自己的研究数据将相关信息汇集在一起,用于本综述。
与人体骨骼中的所有其他骨骼不同,耳囊在发育后几乎没有进行重塑,这可能是由于内耳局部因素所致。耳硬化症是耳囊病理性骨转换增加的过程,在大多数情况下导致镫骨固定,导致传导性听力损失。尽管已经涉及环境因素,如雌激素、氟化物和病毒感染,但显然遗传因素在耳硬化症的表现中起重要作用。从遗传的角度来看,耳硬化症被认为是一种复杂的疾病,罕见的常染色体显性形式由单个基因引起。已经发表了 7 个单基因座,但尚未确定涉及的基因。对于由遗传和环境因素相互作用引起的复杂形式的耳硬化症,通过病例对照关联研究确定了第一个易感基因。所有 3 个复制的基因,TGFB1、BMP2 和 BMP4,都是转化生长因子-β1 途径的一部分。来自遗传关联研究和耳硬化症骨基因表达分析的数据表明,TGF-β1 途径很可能是耳硬化症发病机制的重要因素。