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Plasma Calcitonin Gene-Related Peptide: A Potential Biomarker for Diagnosis and Therapeutic Responses in Pediatric Migraine

机译:血浆降钙素基因相关肽:小儿偏头痛的诊断和治疗反应的潜在生物标志物

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摘要

>Background: Plasma calcitonin gene-related peptide (CGRP) plays a key role in the migraine pathophysiology. This study aimed to investigate its role in predicting diagnosis and outcome of pharmacotherapy in pediatric migraine.>Methods: We prospectively recruited 120 subjects, who never took migraine-preventive agents in a pediatric clinic, including 68 patients with migraine, 30 with non-migraine headache (NM), and 22 non-headache (NH) age-matched controls. Short-term therapeutic response was measured for at least 2 weeks after the start of therapy. Responders were defined with >50% headache reduction. Plasma CGRP concentrations were measured by ELISA.>Results: In the migraine group, more patients required acute therapy, as compared to the NM group (62/68, 91% vs. 5/30, 15%, p = 0.001). The mean plasma CGRP level in migraineurs either during (291 ± 60 pg/ml) or between (240 ± 48) attacks was higher than in NM patients (51 ± 5 pg/ml, p = 0.006 and 0.018, respectively) and NH controls (53 ± 6 pg/ml, p = 0.016 and 0.045, respectively). Forty-seven patients (69%) needed preventive treatments and had higher plasma CGRP levels (364 ± 62 pg/ml, n = 47) than those not (183 ± 54 pg/ml, n = 21) (p = 0.031). Topiramate responders had higher plasma CGRP levels than non-responders (437 ± 131 pg/ml, n = 14 vs. 67 ± 19 pg/ml, n = 6, p = 0.021). Survival curves of plasma CGRP levels also showed those with higher CGRP levels responded better to topiramate. Differences were not found in the other preventives.>Conclusion: The plasma CGRP level can differentiate migraine from non-migraine headache. It may also serve as a reference for the therapeutic strategy since it is higher in patients requiring migraine prevention and responsive to short-term topiramate treatment. These results are clinically significant, especially for the young children who cannot clearly describe their headache symptoms and may provide new insights into the clinical practice for the diagnosis and treatment of pediatric migraine.
机译:>背景:血浆降钙素基因相关肽(CGRP)在偏头痛的病理生理中起着关键作用。这项研究旨在探讨其在预测小儿偏头痛的药物治疗诊断和结果中的作用。>方法:我们前瞻性招募了120名从未在儿科诊所服用偏头痛预防药的受试者,其中包括68例偏头痛患者,30名非偏头痛(NM)和22名非头痛(NH)年龄匹配的对照组。开始治疗后至少2周测量短期治疗反应。定义为响应者头痛减少> 50%。通过ELISA测定血浆CGRP浓度。>结果:与NM组相比,偏头痛组中需要急性治疗的患者更多(62 / 68,91%对5 / 30,15%, p = 0.001)。偏头痛患者发作期间(291±60 pg / ml)或发作之间(240±48)的平均血浆CGRP水平高于NM患者(分别为51±5 pg / ml,p = 0.006和0.018)和NH对照(53±6 pg / ml,p分别为0.016和0.045)。 47名患者(69%)需要预防性治疗,血浆CGRP水平(364±62 pg / ml,n = 47)高于非CGRP(183±54 pg / ml,n = 21)(p = 0.031)。托吡酯应答者的血浆CGRP水平高于非应答者(437±131 pg / ml,n = 14 vs. 67±19 pg / ml,n = 6,p = 0.021)。血浆CGRP水平的生存曲线还显示,CGRP水平较高的患者对托吡酯反应更好。在其他预防措施中未发现差异。>结论:血浆CGRP水平可以区分偏头痛和非偏头痛。它也可以作为治疗策略的参考,因为它在需要偏头痛预防且对短期托吡酯治疗有反应的患者中较高。这些结果具有重要的临床意义,尤其是对于无法清晰描述其头痛症状并可能为小儿偏头痛的诊断和治疗的临床实践提供新见解的幼儿。

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