Gordon M A, McPhee J R, Van de Water T R, Ruben R J
Department of Otolaryngology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY 10467.
Am J Otol. 1992 Sep;13(5):398-407.
Studies of aural and other body tissues suggest that otosclerosis represents the local manifestation of a general disorder of connective tissue. In particular, collagen abnormalities have been described. We have undertaken a pilot study of the in vivo messenger RNA (mRNA) transcription for procollagenase (precursor of collagenase), as well as for stromelysin and tissue inhibitor of metalloprotease (TIMP), an activator and a specific inhibitor of tissue collagenase activity, respectively. Human skin from individuals with surgically confirmed otosclerosis was compared to skin from their family members (clinically positive and clinically negative) and from unrelated normal controls. Preliminary data indicate that on average there are significantly lower levels of mRNA production for stromelysin among individuals with otosclerosis as compared to all others tested. Similar trends were demonstrated for TIMP and procollagenase, although these did not achieve statistical significance. In addition to suggesting a pathogenetic mechanism for the development of the disease, these data could serve as the basis of possible confirmatory tests for early diagnosis of otosclerosis and as a method for evaluating the genotype of offspring of affected individuals prior to their age of clinical manifestation. This could translate into the application of prophylactic treatment regimens in the future. The proposed abnormalities also suggest candidate genes for otosclerosis.
对听觉及其他身体组织的研究表明,耳硬化症是结缔组织普遍紊乱的局部表现。特别是,已有关于胶原蛋白异常的描述。我们开展了一项初步研究,旨在检测体内前胶原酶(胶原酶的前体)、基质溶解素以及金属蛋白酶组织抑制剂(TIMP,分别为组织胶原酶活性的激活剂和特异性抑制剂)的信使核糖核酸(mRNA)转录情况。将经手术确诊为耳硬化症患者的皮肤,与其家庭成员(临床阳性和临床阴性)的皮肤以及无关正常对照者的皮肤进行比较。初步数据表明,与所有其他受试对象相比,耳硬化症患者体内基质溶解素的mRNA产生水平平均显著降低。TIMP和前胶原酶也呈现出类似趋势,尽管未达到统计学显著性。这些数据除了提示该疾病发生发展的致病机制外,还可为耳硬化症早期诊断的可能验证性检测提供基础,并作为一种在受影响个体出现临床表现之前评估其后代基因型的方法。这可能在未来转化为预防性治疗方案的应用。所提出的异常情况也为耳硬化症提示了候选基因。