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Genetics of Otosclerosis

耳硬化病 镫骨 医学 骨重建 听力损失 成骨不全 病理 遗传学 解剖 生物 听力学 中耳 内科学
作者
Melissa Thys,Guy Van Camp
出处
期刊:Otology & Neurotology [Lippincott Williams & Wilkins]
卷期号:30 (8): 1021-1032 被引量:48
标识
DOI:10.1097/mao.0b013e3181a86509
摘要

Objectives: 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. Data Sources: 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. Conclusion: 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-β1 pathway. Data from both genetic association studies and gene expression analysis of otosclerotic bone showed that the TGF-β1 pathway is most likely an important factor in the pathogenesis of otosclerosis.

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