Baike E V, Vitkovsky Yu A, Dutova A A
Research Institute of Molecular Medicine, Chita State Medical Academy, Chita, Russia, 672090.
Vestn Otorinolaringol. 2017;82(3):14-18. doi: 10.17116/otorino201782314-18.
The objective of the present work was to study the influence of allelic variant associations of 1-beta interleukin (C3953T, &511C, T31C), interleukin-6 (C174G), and tumour necrosis factor-alpha (G308A) gene polymorphisms on the serum cytokine level in the patients presenting with chronic suppurative otitis media. A total of 299 patients at the age varying from 16 to 55 years with this condition divided into three groups were examined. Group 1 was comprised of 146 patients suffering from the tubotympanic form of chronic suppurative otitis media (CSOM). Group 2 was composed of 153 patients with epitympanic antral form of this condition. The control group included 183 subjects who have never suffered pathological changes in the middle ear. Human genomic DNA was analyzed with the use of the polymerase chain reaction (PCR). The serum cytokine levels were measured by the solid-state enzyme immunoassay in the beginning and at the end of the treatment period. The study has demonstrated that 56.2% of the healthy residents of the trans-Baikal region had the C/T Il-1b (C3953T) genotype. 79.1% of the patients presenting with the carious carious-destructive form of chronic suppurative otitis media were the heterozygous carriers of the T511C gene of 1-beta interleukin and had the maximally high concentrations of this interleukin in the blood serum. A rise in the production of the pro-inflammatory mediator (IL-6) was found to be related to the severity of the inflammatory process in the middle ear. The TNF-alpha content in the patients with CSOM during the active period of the disease proved to increase by a factor of 6 in comparison with that in the subjects of the control group irrespective of the type of mutation.
本研究的目的是探讨白细胞介素 -1β(C3953T、&511C、T31C)、白细胞介素 -6(C174G)和肿瘤坏死因子 -α(G308A)基因多态性的等位基因变异关联对慢性化脓性中耳炎患者血清细胞因子水平的影响。共检查了299例年龄在16至55岁之间的该疾病患者,并将其分为三组。第一组由146例患有鼓室型慢性化脓性中耳炎(CSOM)的患者组成。第二组由153例患有上鼓室窦型该疾病的患者组成。对照组包括183名中耳从未发生过病理变化的受试者。使用聚合酶链反应(PCR)分析人类基因组DNA。在治疗期开始和结束时,通过固相酶免疫测定法测量血清细胞因子水平。研究表明,外贝加尔地区56.2%的健康居民具有C/T Il-1β(C3953T)基因型。79.1%患有龋蚀性破坏性慢性化脓性中耳炎的患者是白细胞介素 -1β T511C基因的杂合携带者,且血清中该白细胞介素的浓度最高。发现促炎介质(IL-6)的产生增加与中耳炎症过程的严重程度有关。与对照组受试者相比,CSOM患者在疾病活动期的TNF-α含量无论突变类型如何均增加了6倍。