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突发性感音神经性听力损失患者炎症通路相关基因的多态性

Polymorphisms in genes involved in inflammatory pathways in patients with sudden sensorineural hearing loss.

作者信息

Hiramatsu Mariko, Teranishi Masaaki, Uchida Yasue, Nishio Naoki, Suzuki Hidenori, Kato Ken, Otake Hironao, Yoshida Tadao, Tagaya Mitsuhiko, Suzuki Hirokazu, Sone Michihiko, Sugiura Saiko, Ando Fujiko, Shimokata Hiroshi, Nakashima Tsutomu

机构信息

Department of Otorhinolaryngology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

出版信息

J Neurogenet. 2012 Sep;26(3-4):387-96. doi: 10.3109/01677063.2011.652266. Epub 2012 Mar 5.

Abstract

Although the etiology of idiopathic sudden sensorineural hearing loss (SSNHL) remains unclear, the pathologically increased permeability of blood vessels, elucidated by gadolinium-enhanced magnetic resonance imaging (MRI), suggests the involvement of inflammation. Because SSNHL is considered a multifactorial disease, possibly caused by interactions between genetic factors and environmental factors, the authors investigated the associations of polymorphisms of inflammatory mediator genes with susceptibility to SSNHL. The authors compared 72 patients affected by SSNHL and 2010 adults (1010 men and 1000 women; mean age 59.2 years; range 40-79) who participated in the National Institute for Longevity Sciences Longitudinal Study of Aging. Multiple logistic regression was used to obtain odds ratios (ORs) for SSNHL in subjects with polymorphisms in the genes IL-6 C - 572G, IL-4R G1902A, IL-10 A - 592C, TNFα C - 863A, TNFRSF1B G593A, VEGF C936T, VEGF C - 2578A, and VEGF G - 1154A, with adjustment for age, gender, and any history of hypertension, diabetes, or dyslipidemia. The per-allele OR for the risk of SSNHL in subjects bearing IL-6 C - 572G was 1.480 (95% confidence interval [CI], 1.037-2.111) in model 1 (no adjustment), 1.463 (CI, 1.022-2.094) in model 2 (adjusted for age and gender), and 1.460 (CI, 1.016-2.097) in model 3 (adjusted for age, gender, and a history of hypertension, diabetes, or dyslipidemia). Under the dominant model of inheritance, the ORs were 1.734 (CI, 1.080-2.783) in model 1, 1.690 (CI, 1.050-2.721) in model 2, and 1.669 (CI, 1.035-2.692) in model 3. The remaining seven polymorphisms failed to show any associations with the risk of SSNHL. These data need to be confirmed on larger series of patients. In conclusion, the IL-6 C - 572G polymorphism is associated with a risk of SSNHL. Because permeability of blood vessels in the inner ear is frequently increased in patients with SSNHL, inflammation of the inner ear might be involved.

摘要

尽管特发性突发性感音神经性听力损失(SSNHL)的病因仍不清楚,但钆增强磁共振成像(MRI)显示的血管病理性通透性增加提示炎症参与其中。由于SSNHL被认为是一种多因素疾病,可能由遗传因素和环境因素之间的相互作用引起,作者研究了炎症介质基因多态性与SSNHL易感性之间的关联。作者比较了72例SSNHL患者和参与国立长寿科学研究所老龄化纵向研究的2010名成年人(1010名男性和1000名女性;平均年龄59.2岁;范围40 - 79岁)。采用多因素logistic回归分析,计算携带IL-6 C - 572G、IL-4R G1902A、IL-10 A - 592C、TNFα C - 863A、TNFRSF1B G593A、VEGF C936T、VEGF C - 2578A和VEGF G - 1154A基因多态性的受试者患SSNHL的比值比(OR),并对年龄、性别以及高血压、糖尿病或血脂异常病史进行校正。在模型1(未校正)中,携带IL-6 C - 572G基因的受试者患SSNHL风险的每等位基因OR为1.480(95%置信区间[CI],1.037 - 2.111);在模型2(校正年龄和性别)中为1.4,63(CI,1.022 - 2.094);在模型3(校正年龄、性别和高血压、糖尿病或血脂异常病史)中为1.460(CI,1.016 - 2.097)。在显性遗传模型下,模型1中的OR为1.734(CI,1.080 - 2.783),模型2中为1.690(CI,1.050 - 2.721),模型3中为1.669(CI,1.035 - 2.692)。其余7种多态性与SSNHL风险未显示出任何关联。这些数据需要在更大规模的患者系列中得到证实。总之,IL-6 C - 572G多态性与SSNHL风险相关。由于SSNHL患者内耳血管通透性经常增加,内耳炎症可能参与其中。

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