应用erenumab预防治疗偏头痛患者血清CGRP。

Simone de Vries Lentsch, Ingrid M Garrelds, A H Jan Danser, Gisela M Terwindt, Antoinette MaassenVanDenBrink
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引用次数: 9

摘要

目的:测定偏头痛患者在开始erenumab治疗前后血清降钙素基因相关肽(CGRP)样免疫反应性(CGRP- li)水平,以评价其与临床治疗反应的关系。方法:应用erenumab治疗前(T0)和治疗后(T1) 2 ~ 4周采集肘窝血液。使用每日头痛电子日记监测临床反应。用放射免疫法评估血清CGRP-LI水平,比较T0和T1之间的差异,校正偏头痛减轻。此外,对于T0和T1,以偏头痛减少为结果,血清CGRP-LI为自变量,校正基线时的年龄、性别和每月偏头痛天数(MMD),构建线性回归模型。结果:血清CGRP-LI在T0和T1之间无显著差异(p = 0.30)。然而,时间与烟雾病的减少之间存在相互作用(p = 0.01)。erenumab治疗后第3个月MMD的绝对减少与开始erenumab治疗后2-4周T1时的血清CGRP-LI相关(p = 0.003),但与T0时的血清CGRP-LI无关(p = 0.24)。结论:erenumab治疗开始后2-4周降低血清CGRP-LI与治疗3个月后偏头痛天数的较高减少有关。尽管潜在的机制仍有待确定,但这表明,在开始使用erenumab后不久,CGRP水平的变化对其临床效果很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Serum CGRP in migraine patients using erenumab as preventive treatment.

Serum CGRP in migraine patients using erenumab as preventive treatment.

Aim: Serum levels of Calcitonin Gene-Related Peptide (CGRP)-like immunoreactivity (CGRP-LI) in migraine patients before and after starting treatment with erenumab were measured to evaluate the association with clinical treatment response.

Methods: Blood samples were collected from the cubital fossa before (T0) and 2-4 weeks after (T1) starting treatment with erenumab. Clinical response was monitored using a daily headache e-diary. Serum levels of CGRP-LI, assessed using radioimmunoassay, were compared between T0 and T1, correcting for migraine reduction. In addition, for both T0 and T1, linear regression models were constructed using migraine reduction as outcome and serum CGRP-LI as independent variable, corrected for age, gender and monthly migraine days (MMD) at baseline.

Results: Serum CGRP-LI did not differ between T0 and T1 (p = 0.30). However, there was an interaction between time and reduction in MMD (p = 0.01). Absolute reduction in MMD in the third month after treatment with erenumab was associated with serum CGRP-LI at T1, 2-4 weeks after starting treatment with erenumab (p = 0.003), but not with serum CGRP-LI at T0 (p = 0.24).

Conclusion: Lower serum CGRP-LI 2-4 weeks after starting treatment with erenumab was associated with a higher reduction in migraine days after three months of treatment. Although the underlying mechanisms remain to be determined, this suggests that changes in CGRP levels, shortly after starting erenumab, are important for its clinical effect.

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