Department of Pathophysiology, School of Pharmacy, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan.
Mol Cell Biochem. 2012 Apr;363(1-2):357-66. doi: 10.1007/s11010-011-1188-4. Epub 2011 Dec 23.
Migraine is a multifactorial disease with various factors, such as genetic polymorphisms and personality traits, but the contribution of those factors is not clear. To clarify the pathogenesis of migraine, the contributions of genetic polymorphisms and personality traits were simultaneously investigated using multivariate analysis. Ninety-one migraine patients and 119 non-headache healthy volunteers were enrolled. The 12 gene polymorphisms analysis and NEO-FFI personality test were performed. At first, the univariate analysis was performed to extract the contributing factors to pathogenesis of migraine. We then extracted the factors that independently contributed to the pathogenesis of migraine using multivariate stepwise logistic regression analysis. Using the multivariate analysis, three gene polymorphisms including monoamine oxidase A (MAOA) T941G, methylenetetrahydrofolate reductase (MTHFR) C677T, and tumor necrosis factor beta (TNF-β) G252Α, and the neuroticism and conscientiousness scores in NEO-FFI were selected as significant factors that independently contributed to the pathogenesis of migraine. Their odds ratios were 1.099 (per point of neuroticism score), 1.080 (per point of conscientiousness score), 2.272 (T and T/T or T/G vs G and G/G genotype of MAOA), 1.939 (C/T or T/T vs C/C genotype of MTHFR), and 2.748 (G/A or A/A vs G/G genotype of TNF-β), respectively. We suggested that multiple factors, such as gene polymorphisms and personality traits, contribute to the pathogenesis of migraine. The contribution of polymorphisms, such as MAOA T941G, MTHFR C677T, and TNF-β G252A, were more important than personality traits in the pathogenesis of migraine, a multifactorial disorder.
偏头痛是一种多因素疾病,有多种因素,如遗传多态性和人格特质,但这些因素的贡献尚不清楚。为了阐明偏头痛的发病机制,我们同时使用多元分析研究了遗传多态性和人格特质的贡献。纳入 91 例偏头痛患者和 119 名非头痛健康志愿者。进行了 12 个基因多态性分析和 NEO-FFI 人格测试。首先,进行单变量分析以提取偏头痛发病机制的致病因素。然后,我们使用多元逐步逻辑回归分析提取独立导致偏头痛发病机制的因素。使用多元分析,包括单胺氧化酶 A (MAOA) T941G、亚甲基四氢叶酸还原酶 (MTHFR) C677T 和肿瘤坏死因子-β (TNF-β) G252A 在内的三个基因多态性以及 NEO-FFI 中的神经质和尽责性评分被选为独立导致偏头痛发病机制的重要因素。它们的优势比分别为 1.099(神经质评分每增加 1 分)、1.080(尽责性评分每增加 1 分)、2.272(MAOA 的 T 和 T/T 或 T/G 与 G 和 G/G 基因型相比)、1.939(MTHFR 的 C/T 或 T/T 与 C/C 基因型相比)和 2.748(TNF-β 的 G/A 或 A/A 与 G/G 基因型相比)。我们认为,多种因素,如基因多态性和人格特质,导致偏头痛的发病机制。多态性的贡献,如 MAOA T941G、MTHFR C677T 和 TNF-β G252A,在偏头痛这种多因素疾病的发病机制中比人格特质更为重要。