Uchida Yasue, Sugiura Saiko, Nakashima Tsutomu, Ando Fujiko, Shimokata Hiroshi
Department of Otorhinolaryngology, National Center for Geriatrics and Gerontology, Obu City, Aichi Prefecture, Japan.
J Neurogenet. 2011 Oct;25(3):82-7. doi: 10.3109/01677063.2011.591462. Epub 2011 Jul 14.
Protein kinase C-eta (PRKCH) gene has been recently identified as a susceptible risk locus for cerebral infarction and hemorrhage in the Asian populations. The inner ear artery, a usual branch of anterior inferior cerebellar artery, is an end artery with minimal collaterals, therefore, the inner ear is particularly vulnerable to ischemia. The potential association between the development of stroke and sudden sensorineural hearing loss (SSNHL) has been implied. The authors hypothesized that the PRKCH polymorphism predisposing to stroke is associated with SSNHL risk, in view of brain magnetic resonance imaging (MRI) findings. The authors compared 33 cases of prevalent SSNHL with other cases among 2188 adults aged 40 to 79 years who participated in the Study of Aging, to assess the impact of PRKCH 1425G/A polymorphism in consideration of brain MRI findings. Multiple logistic regression was used to obtain odds ratios (ORs) for SSNHL, with adjustment for other possibly influential factors under additive model of minor allele. The per-allele OR for SSNHL risk was 1.770 (95% confidence interval: 1.024-3.060) after adjustments. The effect of the 1425A-allele varied by white matter lesion (WML) status. A significant impact of the A-allele on SSNHL risk increment was observed in higher-WML group, but not in no- or mild-WML group. The 1425A-allele of PRKCH has probably contributed to the susceptibility to SSNHL, despite the etiological heterogeneity of SSNHL, and the impact of the PRKCH 1425A variation observed in this study may imply underlying vascular pathogenesis of SSNHL.
蛋白激酶C-η(PRKCH)基因最近被确定为亚洲人群中脑梗死和脑出血的一个易感风险位点。内耳动脉是小脑前下动脉的一个常见分支,是一条侧支极少的终末动脉,因此,内耳特别容易发生缺血。中风的发生与突发性感音神经性听力损失(SSNHL)之间的潜在关联已被暗示。鉴于脑磁共振成像(MRI)结果,作者推测易患中风的PRKCH基因多态性与SSNHL风险相关。作者在参与衰老研究的2188名40至79岁的成年人中,将33例现患SSNHL患者与其他患者进行比较,以评估PRKCH 1425G/A基因多态性在考虑脑MRI结果时的影响。采用多因素logistic回归分析,在小等位基因的加性模型下,对其他可能有影响的因素进行校正,以获得SSNHL的比值比(OR)。校正后,SSNHL风险的每等位基因OR为1.770(95%置信区间:1.024-3.060)。1425A等位基因的效应因白质病变(WML)状态而异。在高WML组中观察到A等位基因对SSNHL风险增加有显著影响,但在无或轻度WML组中未观察到。尽管SSNHL的病因存在异质性,但PRKCH的1425A等位基因可能导致了对SSNHL的易感性,本研究中观察到的PRKCH 1425A变异的影响可能暗示了SSNHL潜在的血管发病机制。