Mozaffari Elahe, Doosti Abbas, Arshi Asghar, Faghani Mostafa
Biotechnology Research Center, Islamic Azad University, Shahrekord Branch, Shahrekord, Iran.
Young Researchers and Elite Club, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran.
Iran J Public Health. 2016 Dec;45(12):1625-1635.
Migraine is a common debilitating primary headache disorder with current head pain attacks, which contributes to physical activity dysfunctions in chronic pain phase. PGE2 and PGI2 are two important prostaglandins synthesised by enzymes, involved in migraine pain signals. modulation is essential in treatment and pathogenesis of migraine. This study aimed to investigating the association between gene polymorphisms with the risk of migraine susceptibility in migraine patients with related and unrelated parents.
This case- control study was based on 100 migraine patients and 100 non-migraine subjects in Bushehr province, Iran in 2013. Genomic DNA of blood samples was extracted and genotyping of and gene variants was investigated by PCR-RFLP method. Statistical analyses were accomplished using the SPSS software package.
There was a significant differences in the frequencies of the and genotypes between migraine patients and controls (≤0.05).
, , and genotypes can increase the risk of migraine significantly. As the first study in Iran, we are hopeful to achieve greater results about the relevancy of gene, migraine and pain signals pathway by repeating these experiments on more samples.
偏头痛是一种常见的使人衰弱的原发性头痛疾病,伴有当前的头痛发作,在慢性疼痛阶段会导致身体活动功能障碍。前列腺素E2(PGE2)和前列腺素I2(PGI2)是由酶合成的两种重要前列腺素,参与偏头痛疼痛信号。调节在偏头痛的治疗和发病机制中至关重要。本研究旨在调查有亲属关系和无亲属关系的偏头痛患者中基因多态性与偏头痛易感性风险之间的关联。
本病例对照研究基于2013年伊朗布什尔省的100名偏头痛患者和100名非偏头痛受试者。提取血样的基因组DNA,并通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法研究基因变体的基因分型。使用SPSS软件包进行统计分析。
偏头痛患者和对照组之间基因和基因的基因型频率存在显著差异(≤0.05)。
基因、基因、基因和基因的基因型可显著增加偏头痛风险。作为伊朗的第一项研究,我们希望通过对更多样本重复这些实验,在基因、偏头痛和疼痛信号通路的相关性方面取得更大成果。