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唾液降钙素基因相关肽可监测不同偏头痛阶段:CGRP(依赖/不依赖)发作。

Salivary CGRP can monitor the different migraine phases: CGRP (in)dependent attacks.

机构信息

Headache Unit, Neurology Department, Vall d'Hebron University Hospital, Barcelona, Spain.

Headache and Neurological Pain Research Group, Vall d'Hebron Research Institute, Departament de Medicina, Universitat Autònoma de Barcelona, Barcelona, Spain.

出版信息

Cephalalgia. 2022 Mar;42(3):186-196. doi: 10.1177/03331024211040467. Epub 2021 Oct 4.

Abstract

BACKGROUND

CGRP plays a key role in the transmission and modulation of nociceptive signals and is a critical component in the pathogenesis of migraine.

OBJECTIVE

To assess saliva as a substrate to measure CGRP by comparing interictal levels in patients with episodic migraine and controls; and to evaluate CGRP's temporal profile during migraine attacks.

METHODS

This prospective observational pilot study included young women with episodic migraine and healthy controls. We monitored salivary CGRP-like immunoreactivity (CGRP-LI) during 30 consecutive days and during migraine attacks. We considered six timepoints for the analysis: interictal (72h headache free), preictal (PRE-24h before the attack), ictal (headache onset, after 2h, after 8h), postictal (POST-24h after the attack). CGRP levels were quantified by ELISA.

RESULTS

44 women (22 with episodic migraine, 22 healthy controls) were recruited. Differences in interictal salivary levels of CGRP between patients and controls (Me [IQR]: 98.0 [80.3] (95% CI 56.6, 124.0) vs. 54.3 [44.0] (95% CI 42.2, 70.1) pg/mL, p = 0.034) were found. An increase in CGRP levels during migraine attacks was detected (pre:169.0 [95% CI 104.2-234.0]; headache onset: 247.0 [181.9-312.0]; after 2h: 143.0 [77.6-208.0]; after 8h: 169.0 [103.5-234.0], post: 173.0 [107.8-238.0]). Patients were classified as having CGRP-dependent (79.6%) and non-CGRP dependent migraine attacks (20.4%) according to the magnitude of change between preictal and ictal phase. Accompanying symptoms such as photophobia and phonophobia were significantly associated to the first group.

CONCLUSIONS

Salivary CGRP-LI levels, which interictally are elevated in episodic migraine patients, usually increase during a migraine attack in the majority of patients. However, not every attack is CGRP-dependent, which in turn, might explain different underlying pathophysiology and response to treatment.

摘要

背景

降钙素基因相关肽(CGRP)在痛觉信号的传递和调节中发挥着关键作用,是偏头痛发病机制的关键组成部分。

目的

通过比较发作性偏头痛患者和对照组的间歇期水平,评估唾液作为测量 CGRP 的基质;并评估偏头痛发作期间 CGRP 的时间分布。

方法

这项前瞻性观察性初步研究纳入了年轻的发作性偏头痛女性患者和健康对照者。我们在 30 天内监测唾液中 CGRP 样免疫反应性(CGRP-LI),并在偏头痛发作期间进行监测。我们考虑了六个时间点进行分析:间歇期(头痛发作前 72 小时无头痛)、发作前期(头痛发作前 24 小时 PRE-24h)、发作期(头痛发作时,发作后 2 小时和 8 小时)、发作后期(头痛发作后 24 小时 POST-24h)。通过 ELISA 定量 CGRP 水平。

结果

共纳入 44 名女性(22 名偏头痛患者,22 名健康对照者)。患者与对照组在间歇期唾液 CGRP 水平方面存在差异(中位数 [IQR]:98.0 [80.3](95%CI56.6,124.0)与 54.3 [44.0](95%CI42.2,70.1)pg/mL,p=0.034)。在偏头痛发作期间检测到 CGRP 水平升高(发作前期:169.0 [95%CI104.2-234.0];头痛发作时:247.0 [181.9-312.0];发作后 2 小时:143.0 [77.6-208.0];发作后 8 小时:169.0 [103.5-234.0];发作后期:173.0 [107.8-238.0])。根据发作前期和发作期之间的变化幅度,将患者分为 CGRP 依赖性偏头痛发作(79.6%)和非 CGRP 依赖性偏头痛发作(20.4%)。畏光和畏声等伴随症状与第一组显著相关。

结论

在发作性偏头痛患者中,间歇期的唾液 CGRP-LI 水平升高,在大多数患者中,偏头痛发作期间通常会升高。然而,并非每个发作都是 CGRP 依赖性的,这反过来可能解释了不同的潜在病理生理学和对治疗的反应。

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