An observational study on monoclonal antibodies against calcitonin‐gene‐related peptide and its receptor

降钙素基因相关肽 医学 单克隆抗体 降钙素 观察研究 受体 降钙素受体 内科学 单克隆 抗体 免疫学 神经肽
作者
Francesca Schiano di Cola,Marco Bolchini,Giulia Ceccardi,Salvatore Caratozzolo,Paolo Liberini,Renata Rao,Alessandro Padovani
出处
期刊:European Journal of Neurology [Wiley]
卷期号:30 (6): 1764-1773 被引量:35
标识
DOI:10.1111/ene.15761
摘要

Abstract Background and purpose Based on their pharmacological target, two classes of calcitonin‐gene‐related peptide (CGRP) monoclonal antibodies (mAbs) have been identified: antibodies against the CGRP ligand—galcanezumab, fremanezumab, eptinezumab—and antibodies against the CGRP receptor (CGRP‐R), erenumab. The aim of the present study was to compare anti‐CGRP versus anti‐CGRP‐R mAbs in patients with high frequency episodic and chronic migraine. Methods All patients on monthly treatment with anti‐CGRP mAbs with an available 6 months’ follow‐up at January 2022 were included. Data on efficacy outcome were collected following one (T1), three (T3) and six (T6) months of treatment, and included monthly headache/migraine days, the Migraine Disability Assessment Scale (MIDAS) and Headache Impact Test 6 (HIT‐6) scores, pain intensity, analgesics consumption and response rates (>50% headache days reduction compared to baseline). Results In all, 152 patients were enrolled, of whom 68 were in treatment with anti‐CGRP mAbs (49 galcanezumab, 19 fremanezumab) and 84 with the anti‐CGRP‐R (erenumab). MIDAS scores were significantly lower in the anti‐CGRP group at T1 and T3 (respectively p < 0.02 and p < 0.03) as well as the number of mean migraine days at T3 ( p < 0.01). At T3 and T6 outcome measures were comparable, although a significantly higher percentage of super‐responders was found in the anti‐CGRP group (respectively p < 0.04 and p < 0.05), with a similar overall percentage of responders. Conclusions The present study on a real‐world sample confirms the beneficial effect of both anti‐CGRP and anti‐CGRP‐R mAbs, with a more favorable outcome for anti‐CGRP antibodies.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
长zyzy发布了新的文献求助10
刚刚
LiFei发布了新的文献求助10
刚刚
研友_841dlL完成签到,获得积分10
刚刚
2秒前
2秒前
万能图书馆应助bakerwm采纳,获得10
3秒前
Sally完成签到,获得积分10
3秒前
传奇3应助跨材料采纳,获得10
3秒前
小傅发布了新的文献求助10
3秒前
cdercder应助自然的雁蓉采纳,获得10
4秒前
qing发布了新的文献求助10
5秒前
6秒前
荔枝完成签到 ,获得积分10
6秒前
迷人的芷珍完成签到 ,获得积分10
6秒前
Vincent完成签到,获得积分10
7秒前
8秒前
8秒前
8秒前
9秒前
空勒发布了新的文献求助30
11秒前
小赣同志发布了新的文献求助10
11秒前
小马甲应助cfw采纳,获得20
11秒前
11秒前
所所应助落寞的新晴采纳,获得10
12秒前
小傅完成签到,获得积分10
12秒前
jx完成签到,获得积分10
13秒前
Neal发布了新的文献求助10
14秒前
高贵路灯完成签到,获得积分10
14秒前
14秒前
打打应助科研通管家采纳,获得10
14秒前
跨材料发布了新的文献求助10
15秒前
慕青应助科研通管家采纳,获得10
15秒前
15秒前
15秒前
汉堡包应助科研通管家采纳,获得10
15秒前
所所应助科研通管家采纳,获得10
15秒前
Copyright应助科研通管家采纳,获得10
15秒前
15秒前
15秒前
天天快乐应助科研通管家采纳,获得10
15秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
Molecular Mechanisms of Photosynthesis, 4th Edition 1000
Organic Reactions, Volume 116 1000
Current concepts in cutaneous toxicity : proceedings of the Fourth Conference on Cutaneous Toxicity, Washington, D.C., May 9-11, 1979 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7267366
求助须知:如何正确求助?哪些是违规求助? 8888321
关于积分的说明 18787587
捐赠科研通 6944316
什么是DOI,文献DOI怎么找? 3203320
关于科研通互助平台的介绍 2376235
邀请新用户注册赠送积分活动 2179192