遗传变异IL18 -105G>A和-137G>C与偏头痛易感性相关

Aline Vitali da Silva, Beatriz Rabello Espinosa, Tainah Mendes Ahrens, A. Antonucci, V. A. Bello, Regina Célia Poli Frederico, Carlos Eduardo Coral de Oliveira, E. V. Reiche, A. Simão
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引用次数: 0

摘要

关于偏头痛的神经源性炎症和神经炎症的研究很少。然而,有证据表明,免疫系统可能对偏头痛患者的三叉神经激活和皮质扩散抑制产生影响。白细胞介素(IL)-18是一种促炎细胞因子,在偏头痛患者中已证实其血浆水平升高。然而,到目前为止,IL-18的遗传变异尚未在偏头痛的背景下进行研究。目的探讨遗传变异IL18 -105G>A (rs360717)和IL18 -137G>C (rs187238)与偏头痛易感性及其临床特征的关系。研究对象和方法:病例对照研究包括307名参与者,其中152人诊断为偏头痛,155人为健康对照组,按性别、年龄、种族和体重指数配对。对临床和人口学资料进行评估。研究人员对偏头痛患者进行了结构化访谈,其中包含偏头痛类型(有或没有先兆、发作性或慢性)、发病年龄、发作频率、引发头痛的伴随症状等信息。患者还回答了有效的问卷,以评估偏头痛的丧失能力(偏头痛残疾评估- MIDAS)和影响(头痛影响测试- HIT-6),异常性疼痛的存在(ASC-12),以及焦虑症状(状态焦虑量表- STAI 1和2),抑郁(贝克抑郁量表)和听觉亢进量表。采用聚合酶链反应(PCR)鉴定遗传变异IL18 -105G>A (rs360717)和IL18 -137G>C (rs187238),并使用Step One热循环仪(Applied Biosystems)评估PCR产物的荧光水平。采用显性、共显性、隐性和过显性遗传模型进行分析。(要查看完整的摘要,请查看PDF)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic variants IL18 -105G>A and -137G>C associated with susceptibility to migraine
IntroductionFew studies have been conducted into neurogenic inflammation and neuroinflammation in respect of migraine. However, evidence suggests that the immune system may exert an influence over trigeminal activation and cortical spreading depression in individuals suffering from migraine. The interleukin (IL)-18 is a pro-inflammatory cytokine and increased plasma levels have been confirmed in individuals with migraine. However, as yet, the genetic variants of IL-18 have not been investigated in the context of migraine. ObjectiveTo investigate the association between genetic variants IL18 -105G>A (rs360717) and IL18 -137G>C (rs187238) and susceptibility to migraine and its clinical characteristics. Subjects and MethodsCase control study comprising 307 participants, of whom 152 had a diagnosis of migraine and 155 were healthy controls, paired by sex, age, ethnicity and BMI. The clinical and demographic data were evaluated. The patients with migraine were interviewed using a structured form containing information about the type of migraine (with or without aura, episodic or chronic), age at onset of the disease, frequency of attacks, accompanying symptoms that triggered headaches. The patients also answered validated questionnaires to evaluate incapacity (Migraine Disability Assessment - MIDAS) and impact (Headache Impact Test - HIT-6) for migraine, the presence of allodynia (ASC-12), as well as symptoms of anxiety (State Anxiety Inventory - STAI 1 and 2), depression (Beck Depression Inventory) and a hyperacusis scale.The genetic variants IL18 -105G>A (rs360717) and IL18 -137G>C (rs187238) were identified using polymerase chain reaction (PCR) and the fluorescence levels of PCR products were evaluated using a Step One thermocycler (Applied Biosystems). The analyses were conducted using the dominant, codominant, recessive and overdominant genetic models. (To see the complete abstract, please, check out the PDF). 
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