Department of Pathophysiology, Showa University School of Pharmacy, Shinagawa-ku, Tokyo 142-8555, Japan.
Neurol Sci. 2012 Apr;33(2):453-61. doi: 10.1007/s10072-011-0716-z. Epub 2011 Aug 6.
Moderate to severe migraine attacks are treated with triptans. However, about 25% of migraineurs fail to respond to triptans. We investigated the involvement of gene polymorphisms, personality traits and characteristics of headache, and made a scoring system for prediction of clinical response to triptans in patients with migraine. Gene polymorphisms including serotonin (5-HT)(1B) receptor G861C and dopamine receptor 2 (DRD2) C939T, personality traits and characteristics of headache were investigated in 46 consistent responders and 14 inconsistent responders to triptans. The multivariate stepwise logistic regression analysis revealed that age, periorbital/deep orbital pain and C/C genotype carrier at DRD2 C939T were significant factors that contributed independently to the negative response to triptans in patients with migraine. Their odds ratios were 6.329 (40-69 vs. 20-39 years, 95% CI 1.441-27.778), 6.772 (no vs. yes, periorbital/deep orbital pain, 95% CI 1.159-39.580) and 14.085 (non-C/C vs. C/C genotype at DRD2 C939T, 95% CI 1.253-166.667), respectively. The predictive index (PI) of clinical response to triptans in patients with migraine was calculated using these three factors. The score in inconsistent responders (1.6 ± 0.6) was significantly higher than that in consistent responders (0.8 ± 0.7, P < 0.001). Sensibility of low-score (RI = 0) group was 100%, and specificity of high-score (PI ≥ 2) group was 87%. The proposed scoring system should in the future be the object of larger studies to confirm its validity.
中重度偏头痛发作采用曲坦类药物治疗。然而,约 25%的偏头痛患者对曲坦类药物无反应。我们研究了基因多态性、人格特质和头痛特征与曲坦类药物临床反应之间的关系,并建立了预测偏头痛患者曲坦类药物临床反应的评分系统。在 46 例对曲坦类药物反应一致的患者和 14 例反应不一致的患者中,研究了包括 5-羟色胺(5-HT)(1B)受体 G861C 和多巴胺受体 2(DRD2)C939T 在内的基因多态性、人格特质和头痛特征。多变量逐步逻辑回归分析显示,年龄、眶周/深部疼痛和 DRD2 C939T 的 C/C 基因型携带者是偏头痛患者对曲坦类药物反应阴性的独立危险因素。其比值比分别为 6.329(40-69 岁 vs. 20-39 岁,95%可信区间 1.441-27.778)、6.772(无 vs. 有,眶周/深部疼痛,95%可信区间 1.159-39.580)和 14.085(非-C/C 基因型 vs. DRD2 C939T 的 C/C 基因型,95%可信区间 1.253-166.667)。使用这三个因素计算偏头痛患者对曲坦类药物临床反应的预测指数(PI)。反应不一致患者的得分(1.6 ± 0.6)显著高于反应一致患者(0.8 ± 0.7,P < 0.001)。低评分(RI = 0)组的敏感性为 100%,高评分(PI ≥ 2)组的特异性为 87%。该评分系统未来需要更大规模的研究来验证其有效性。