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PACAP38- 和 VIP 诱导的丛集性头痛发作与血浆 CGRP 或肥大细胞活化标志物的变化无关。

PACAP38- and VIP-induced cluster headache attacks are not associated with changes of plasma CGRP or markers of mast cell activation.

机构信息

Danish Headache Center, Department of Neurology, Rigshospitalet Glostrup, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

RefLab ApS, Copenhagen, Denmark.

出版信息

Cephalalgia. 2022 Jul;42(8):687-695. doi: 10.1177/03331024211056248. Epub 2021 Nov 25.

Abstract

BACKGROUND

Pituitary adenylate cyclase-activating polypeptide-38 (PACAP38) and vasoactive intestinal polypeptide can provoke cluster headache attacks in up to half of cluster headache patients in their active phase. At present, it is unknown whether provoked attacks are mediated via calcitonin gene-related peptide or mast cell activation.

METHODS

All enrolled patients with cluster headache were randomly allocated to receive a continuous infusion of either PACAP38 (10 pmol/kg/min) or vasoactive intestinal polypeptide (8 pmol/kg/min) over 20 min. We collected clinical data and measured plasma levels of calcitonin gene-related peptide and markers of mast cell activation (tryptase and histamine) at fixed time points: at baseline (T), at the end of the infusion (T), 10 min after the infusion (T), and 70 min after the infusion (T).

RESULTS

Blood was collected from episodic cluster headache patients in active phase (n = 14), episodic cluster headache patients in remission (n = 15), and chronic cluster headache patients (n = 15). At baseline, plasma levels of calcitonin gene-related peptide, tryptase, and histamine were not different among the three study groups. Plasma levels of calcitonin gene-related peptide ( = 0.7074), tryptase ( = 0.6673), or histamine ( = 0.4792) remained unchanged during provoked attacks compared to attack-free patients.

CONCLUSION

Cluster headache attacks provoked by either PACAP38 or vasoactive intestinal polypeptide were not accompanied by alterations of plasma calcitonin gene-related peptide, tryptase or histamine. The provoked attacks may not be mediated by calcitonin gene-related peptide or mast cell activation.: The study is registered at ClinicalTrials.gov (NCT03814226).

摘要

背景

垂体腺苷酸环化酶激活肽-38(PACAP38)和血管活性肠肽可诱发高达一半活跃期丛集性头痛患者的头痛发作。目前,尚不清楚诱发性头痛是否通过降钙素基因相关肽或肥大细胞激活来介导。

方法

所有入组的丛集性头痛患者均随机接受 PACAP38(10pmol/kg/min)或血管活性肠肽(8pmol/kg/min)连续输注 20 分钟。我们在固定时间点采集临床数据并测量降钙素基因相关肽和肥大细胞活化标志物(类胰蛋白酶和组胺)的血浆水平:基线时(T)、输注结束时(T)、输注后 10 分钟(T)和输注后 70 分钟(T)。

结果

采集处于活跃期的发作性丛集性头痛患者(n=14)、缓解期的发作性丛集性头痛患者(n=15)和慢性丛集性头痛患者(n=15)的血液。在基线时,三组研究患者的降钙素基因相关肽、类胰蛋白酶和组胺的血浆水平无差异。与无头痛发作的患者相比,PACAP38 或血管活性肠肽诱发的头痛发作期间,降钙素基因相关肽( =0.7074)、类胰蛋白酶( =0.6673)或组胺( =0.4792)的血浆水平没有变化。

结论

PACAP38 或血管活性肠肽诱发的丛集性头痛发作不会引起降钙素基因相关肽、类胰蛋白酶或组胺的血浆变化。这些诱发性头痛发作可能不是由降钙素基因相关肽或肥大细胞激活介导的。该研究在 ClinicalTrials.gov 注册(NCT03814226)。

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