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CGRP-induced migraine-like headache in persistent post-traumatic headache attributed to mild traumatic brain injury
OBJECTIVE: To ascertain whether intravenous infusion of calcitonin gene-related peptide (CGRP) can induce migraine-like headache in people with persistent post-traumatic headache attributed to mild traumatic brain injury (TBI) and no pre-existing migraine. METHODS: A non-randomized, single-arm, open...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Milan
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578273/ https://www.ncbi.nlm.nih.gov/pubmed/36253732 http://dx.doi.org/10.1186/s10194-022-01499-5 |
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author | Ashina, Håkan Iljazi, Afrim Al-Khazali, Haidar M. Do, Thien Phu Eigenbrodt, Anna K. Larsen, Eigil L. Andersen, Amalie M. Hansen, Kevin J. Bräuner, Karoline B. Chaudhry, Basit Ali Christensen, Casper E. Amin, Faisal Mohammad Schytz, Henrik W. |
author_facet | Ashina, Håkan Iljazi, Afrim Al-Khazali, Haidar M. Do, Thien Phu Eigenbrodt, Anna K. Larsen, Eigil L. Andersen, Amalie M. Hansen, Kevin J. Bräuner, Karoline B. Chaudhry, Basit Ali Christensen, Casper E. Amin, Faisal Mohammad Schytz, Henrik W. |
author_sort | Ashina, Håkan |
collection | PubMed |
description | OBJECTIVE: To ascertain whether intravenous infusion of calcitonin gene-related peptide (CGRP) can induce migraine-like headache in people with persistent post-traumatic headache attributed to mild traumatic brain injury (TBI) and no pre-existing migraine. METHODS: A non-randomized, single-arm, open-label study at a single site in Denmark. Eligible participants were aged 18 to 65 years and had a known history of persistent post-traumatic headache attributed to mild TBI for ≥ 12 months. All participants received continuous intravenous infusion of CGRP (1.5 µg/min) over 20 min. A headache diary was used to collect outcome data until 12 h after the start of CGRP infusion. The primary end point was the incidence of migraine-like headache during 12-hour observational period. RESULTS: A total of 60 participants completed the study protocol and provided data for the analysis of the primary end point. The median age was 32.5 (IQR, 25.5–43.0) years; 43 participants (72%) were female. Following CGRP infusion, 43 (72%) of 60 participants developed migraine-like headache during the 12-hour observational period. The median time to peak headache intensity was 40 min (IQR, 20–60), and the median peak headache intensity was 6 (IQR, 5–8) on the 11-point numeric rating scale. CONCLUSION: Intravenous infusion of CGRP is a potent inducer of migraine-like headache in people with persistent post-traumatic headache attributed to mild TBI. This observation underscores the importance of CGRP in the genesis of migraine-like headache that is often experienced by individuals who are afflicted by persistent post-traumatic headache. Further research is warranted to ascertain whether other signaling molecules also contribute to the disease mechanisms underlying post-traumatic headache. |
format | Online Article Text |
id | pubmed-9578273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Milan |
record_format | MEDLINE/PubMed |
spelling | pubmed-95782732022-10-19 CGRP-induced migraine-like headache in persistent post-traumatic headache attributed to mild traumatic brain injury Ashina, Håkan Iljazi, Afrim Al-Khazali, Haidar M. Do, Thien Phu Eigenbrodt, Anna K. Larsen, Eigil L. Andersen, Amalie M. Hansen, Kevin J. Bräuner, Karoline B. Chaudhry, Basit Ali Christensen, Casper E. Amin, Faisal Mohammad Schytz, Henrik W. J Headache Pain Research OBJECTIVE: To ascertain whether intravenous infusion of calcitonin gene-related peptide (CGRP) can induce migraine-like headache in people with persistent post-traumatic headache attributed to mild traumatic brain injury (TBI) and no pre-existing migraine. METHODS: A non-randomized, single-arm, open-label study at a single site in Denmark. Eligible participants were aged 18 to 65 years and had a known history of persistent post-traumatic headache attributed to mild TBI for ≥ 12 months. All participants received continuous intravenous infusion of CGRP (1.5 µg/min) over 20 min. A headache diary was used to collect outcome data until 12 h after the start of CGRP infusion. The primary end point was the incidence of migraine-like headache during 12-hour observational period. RESULTS: A total of 60 participants completed the study protocol and provided data for the analysis of the primary end point. The median age was 32.5 (IQR, 25.5–43.0) years; 43 participants (72%) were female. Following CGRP infusion, 43 (72%) of 60 participants developed migraine-like headache during the 12-hour observational period. The median time to peak headache intensity was 40 min (IQR, 20–60), and the median peak headache intensity was 6 (IQR, 5–8) on the 11-point numeric rating scale. CONCLUSION: Intravenous infusion of CGRP is a potent inducer of migraine-like headache in people with persistent post-traumatic headache attributed to mild TBI. This observation underscores the importance of CGRP in the genesis of migraine-like headache that is often experienced by individuals who are afflicted by persistent post-traumatic headache. Further research is warranted to ascertain whether other signaling molecules also contribute to the disease mechanisms underlying post-traumatic headache. Springer Milan 2022-10-17 /pmc/articles/PMC9578273/ /pubmed/36253732 http://dx.doi.org/10.1186/s10194-022-01499-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ashina, Håkan Iljazi, Afrim Al-Khazali, Haidar M. Do, Thien Phu Eigenbrodt, Anna K. Larsen, Eigil L. Andersen, Amalie M. Hansen, Kevin J. Bräuner, Karoline B. Chaudhry, Basit Ali Christensen, Casper E. Amin, Faisal Mohammad Schytz, Henrik W. CGRP-induced migraine-like headache in persistent post-traumatic headache attributed to mild traumatic brain injury |
title | CGRP-induced migraine-like headache in persistent post-traumatic headache attributed to mild traumatic brain injury |
title_full | CGRP-induced migraine-like headache in persistent post-traumatic headache attributed to mild traumatic brain injury |
title_fullStr | CGRP-induced migraine-like headache in persistent post-traumatic headache attributed to mild traumatic brain injury |
title_full_unstemmed | CGRP-induced migraine-like headache in persistent post-traumatic headache attributed to mild traumatic brain injury |
title_short | CGRP-induced migraine-like headache in persistent post-traumatic headache attributed to mild traumatic brain injury |
title_sort | cgrp-induced migraine-like headache in persistent post-traumatic headache attributed to mild traumatic brain injury |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578273/ https://www.ncbi.nlm.nih.gov/pubmed/36253732 http://dx.doi.org/10.1186/s10194-022-01499-5 |
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