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Feasibility of serum CGRP measurement as a biomarker of chronic migraine: a critical reappraisal

BACKGROUND: Calcitonin gene-related peptide (CGRP) has been reported as elevated in chronic migraine. We aimed to validate the role of interictal serum CGRP concentration in peripheral blood samples as a biomarker of chronic migraine. METHODS: We prospectively recruited patients with episodic and ch...

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Autores principales: Lee, Mi Ji, Lee, Sook-Yeon, Cho, Soohyun, Kang, Eun-Suk, Chung, Chin-Sang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6045522/
https://www.ncbi.nlm.nih.gov/pubmed/30006780
http://dx.doi.org/10.1186/s10194-018-0883-x
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author Lee, Mi Ji
Lee, Sook-Yeon
Cho, Soohyun
Kang, Eun-Suk
Chung, Chin-Sang
author_facet Lee, Mi Ji
Lee, Sook-Yeon
Cho, Soohyun
Kang, Eun-Suk
Chung, Chin-Sang
author_sort Lee, Mi Ji
collection PubMed
description BACKGROUND: Calcitonin gene-related peptide (CGRP) has been reported as elevated in chronic migraine. We aimed to validate the role of interictal serum CGRP concentration in peripheral blood samples as a biomarker of chronic migraine. METHODS: We prospectively recruited patients with episodic and chronic migraine and normal controls (NCs) in the Samsung Medical Center between August 2015 and May 2016. Blood samples were collected interictally from antecubital veins per prespecified protocol. Serum CGRP measurement was performed in the central laboratory by a single experienced technician blinded to clinical information. Migraine subtype, headache days in the previous month, and the presence and characteristics of headache at ±2 days of measurement were evaluated at every visit. RESULTS: A total of 156 migraineurs (106 episodic and 50 chronic) and 27 NCs were recruited in this study. Compared to NCs (75.7 ± 20.07 pg/mL) and patients with episodic migraine (67.0 ± 20.70 pg/mL), patients with chronic migraine did not show an interictal elevation of serum CGRP levels (64.9 ± 15.32 pg/mL). Serum CGRP concentration was not associated with headache status (ictal vs. interictal), migraine subtype (migraine with vs. without aura), use of preventive or acute medications, and comorbid medication overuse. Higher serum CGRP concentration did not predict treatment response in patients with chronic migraine. CONCLUSIONS: Serum CGRP concentration may not be a feasible biomarker for chronic migraine. Further validation is necessary before CGRP can be used in the clinical practice. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s10194-018-0883-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-60455222018-07-30 Feasibility of serum CGRP measurement as a biomarker of chronic migraine: a critical reappraisal Lee, Mi Ji Lee, Sook-Yeon Cho, Soohyun Kang, Eun-Suk Chung, Chin-Sang J Headache Pain Research Article BACKGROUND: Calcitonin gene-related peptide (CGRP) has been reported as elevated in chronic migraine. We aimed to validate the role of interictal serum CGRP concentration in peripheral blood samples as a biomarker of chronic migraine. METHODS: We prospectively recruited patients with episodic and chronic migraine and normal controls (NCs) in the Samsung Medical Center between August 2015 and May 2016. Blood samples were collected interictally from antecubital veins per prespecified protocol. Serum CGRP measurement was performed in the central laboratory by a single experienced technician blinded to clinical information. Migraine subtype, headache days in the previous month, and the presence and characteristics of headache at ±2 days of measurement were evaluated at every visit. RESULTS: A total of 156 migraineurs (106 episodic and 50 chronic) and 27 NCs were recruited in this study. Compared to NCs (75.7 ± 20.07 pg/mL) and patients with episodic migraine (67.0 ± 20.70 pg/mL), patients with chronic migraine did not show an interictal elevation of serum CGRP levels (64.9 ± 15.32 pg/mL). Serum CGRP concentration was not associated with headache status (ictal vs. interictal), migraine subtype (migraine with vs. without aura), use of preventive or acute medications, and comorbid medication overuse. Higher serum CGRP concentration did not predict treatment response in patients with chronic migraine. CONCLUSIONS: Serum CGRP concentration may not be a feasible biomarker for chronic migraine. Further validation is necessary before CGRP can be used in the clinical practice. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s10194-018-0883-x) contains supplementary material, which is available to authorized users. Springer Milan 2018-07-13 /pmc/articles/PMC6045522/ /pubmed/30006780 http://dx.doi.org/10.1186/s10194-018-0883-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Article
Lee, Mi Ji
Lee, Sook-Yeon
Cho, Soohyun
Kang, Eun-Suk
Chung, Chin-Sang
Feasibility of serum CGRP measurement as a biomarker of chronic migraine: a critical reappraisal
title Feasibility of serum CGRP measurement as a biomarker of chronic migraine: a critical reappraisal
title_full Feasibility of serum CGRP measurement as a biomarker of chronic migraine: a critical reappraisal
title_fullStr Feasibility of serum CGRP measurement as a biomarker of chronic migraine: a critical reappraisal
title_full_unstemmed Feasibility of serum CGRP measurement as a biomarker of chronic migraine: a critical reappraisal
title_short Feasibility of serum CGRP measurement as a biomarker of chronic migraine: a critical reappraisal
title_sort feasibility of serum cgrp measurement as a biomarker of chronic migraine: a critical reappraisal
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6045522/
https://www.ncbi.nlm.nih.gov/pubmed/30006780
http://dx.doi.org/10.1186/s10194-018-0883-x
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