Genetic variants IL1B +3954C>T and -511C>T associated with incapacity and allodynia in migraine

Aline Vitali da Silva, B. Khouri, Debora Villas Boas Rezende, Ana Paula Gallina Pezzini, Beatriz Rabello Espinosa, Tainah Mendes Ahrens, A. Antonucci, V. A. Bello, Regina Célia Poli Frederico, Carlos Eduardo Coral, E. V. Reiche, A. Simão
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Abstract

IntroductionThe main mechanisms in the physiopathology of migraine are cortical spreading depression and trigeminal activation with the release of CGRP. Neurogenic inflammation and neuroinflammation can exert an influence over both these mechanisms, but there are still a number of gaps in our understanding. Interleukin (IL)- 1β is a pro-inflammatory cytokine whose levels of plasma increase during the attack phase of migraine. Thus far, its genetic variants have not been well studied. ObjectiveTo investigate the association between the genetic variants IL1B +3954C>T (rs1143634) and -511C>T (rs16944) 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 IL1B +3954C>T (rs1143634) and -511C>T (rs16944) 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 over- dominant genetic models. Categorical data were evaluated via the chi-squared test or Fisher’s exact test, and continuous data were evaluated using the Mann-Whitney test.  (To see the complete abstract, please, check out the PDF).
遗传变异IL1B +3954C>T和-511C>T与偏头痛患者能力丧失和异常性疼痛相关
偏头痛的生理病理机制主要是皮层扩张性抑制和CGRP释放激活三叉神经。神经源性炎症和神经炎症可以对这两种机制施加影响,但在我们的理解中仍有许多空白。白细胞介素(IL)- 1β是一种促炎细胞因子,其血浆水平在偏头痛发作期升高。到目前为止,它的基因变异还没有得到很好的研究。目的探讨遗传变异IL1B +3954C>T (rs1143634)和-511C>T (rs16944)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IL1B +3954C>T (rs1143634)和-511C>T (rs16944),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。分类资料采用卡方检验或Fisher精确检验进行评价,连续资料采用Mann-Whitney检验进行评价。(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。
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