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首页> 外文期刊>Pharmacogenetics and genomics >Genotypes of the MTHFR C677T and MTRR A66G genes act independently to reduce migraine disability in response to vitamin supplementation
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Genotypes of the MTHFR C677T and MTRR A66G genes act independently to reduce migraine disability in response to vitamin supplementation

机译:MTHFR C677T和MTRR A66G基因的基因型独立发挥作用,以减少因补充维生素引起的偏头痛

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BACKGROUND: Migraine is a chronic disabling neurovascular condition that may in part be caused by endothelial and cerebrovascular disruption induced by hyperhomocysteinaemia. We have previously provided evidence indicating that reduction of homocysteine by vitamin supplementation can reduce the occurrence of migraine in women. The current study examined the genotypic effects of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) gene variants on the occurrence of migraine in response to vitamin supplementation. METHODS: This was a 6-month randomized, double-blinded placebo-controlled trial of daily vitamin B supplementation (B6, B9 and B12) on reduction of homocysteine and of the occurrence of migraine in 206 female patients diagnosed with migraine with aura. RESULTS: Vitamin supplementation significantly reduced homocysteine levels (P<0.001), severity of headache in migraine (P=0.017) and high migraine disability (P=0.022) in migraineurs compared with the placebo effect (P>0.1). When the vitamin-treated group was stratified by genotype, the C allele carriers of the MTHFR C677T variant showed a higher reduction in homocysteine levels (P<0.001), severity of pain in migraine (P=0.01) and percentage of high migraine disability (P=0.009) compared with those with the TT genotypes. Similarly, the A allele carriers of the MTRR A66G variants showed a higher level of reduction in homocysteine levels (P<0.001), severity of pain in migraine (P=0.002) and percentage of high migraine disability (P=0.006) compared with those with the GG genotypes. Genotypic analysis for both genes combined indicated that the treatment effect modification of the MTRR variant was independent of the MTHFR variant. CONCLUSION: This provided further evidence that vitamin supplementation is effective in reducing migraine and also that both MTHFR and MTRR gene variants are acting independently to influence treatment response in female migraineurs.
机译:背景:偏头痛是一种慢性致残性神经血管疾病,可能部分由高同型半胱氨酸血症引起的内皮和脑血管破坏引起。我们先前提供的证据表明,通过补充维生素减少同型半胱氨酸可以减少女性偏头痛的发生。目前的研究检查了亚甲基四氢叶酸还原酶(MTHFR)和蛋氨酸合酶还原酶(MTRR)基因变体对偏头痛发生的基因型影响,以补充维生素。方法:这是一项为期6个月的随机,双盲安慰剂对照试验,每天补充维生素B(B6,B9和B12),以减少206名诊断为先兆偏头痛的女性患者的同型半胱氨酸减少和偏头痛的发生。结果:与安慰剂相比,补充维生素可以显着降低偏头痛的同型半胱氨酸水平(P <0.001),偏头痛的严重程度(P = 0.017)和偏头痛高发性(P = 0.022)。当按基因型对维生素治疗组进行分层时,MTHFR C677T变体的C等位基因携带者高半胱氨酸水平降低(P <0.001),偏头痛疼痛严重程度(P = 0.01)和高偏头痛残疾百分比(P = 0.001)。 P = 0.009)与TT基因型的相比。同样,与那些相比,MTRR A66G变体的A等位基因携带者在同型半胱氨酸水平的降低(P <0.001),偏头痛的严重程度(P = 0.002)和高偏头痛致残率(P = 0.006)方面表现出更高的降低水平。 GG基因型。对两个基因组合的基因型分析表明,MTRR变体的治疗效果修饰独立于MTHFR变体。结论:这提供了进一步的证据,表明补充维生素可有效减少偏头痛,并且MTHFR和MTRR基因变体均独立发挥作用,影响女性偏头痛的治疗反应。

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