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A proof-of-concept study on CGRP plasma levels of migraineurs during a 6-month treatment with ERENUMAB
The introduction of monoclonal antibodies (mAbs) against calcitonin-gene related peptide (CGRP) or CGRP receptors in the treatment of migraine raised concerns on the possible risks associated to the long-term inhibition of CGRP physiological functions. In this proof-of-concept study, we have measure...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Milan
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579961/ https://www.ncbi.nlm.nih.gov/pubmed/33087040 http://dx.doi.org/10.1186/s10194-020-01193-4 |
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author | Tringali, Giuseppe Vollono, Catello Calabresi, Paolo Navarra, Pierluigi |
author_facet | Tringali, Giuseppe Vollono, Catello Calabresi, Paolo Navarra, Pierluigi |
author_sort | Tringali, Giuseppe |
collection | PubMed |
description | The introduction of monoclonal antibodies (mAbs) against calcitonin-gene related peptide (CGRP) or CGRP receptors in the treatment of migraine raised concerns on the possible risks associated to the long-term inhibition of CGRP physiological functions. In this proof-of-concept study, we have measured the circulating levels of CGRP in 7 patients with high-frequency episodic migraine receiving the anti-CGRP receptor mAb erenumab for at least 6 months, to test the hypothesis that long-term blockade of CGRP receptors induces an increase in systemic CGRP levels via a classical up-regulation mechanism. Plasma CGRP levels were measured by a validated radioimmunoassay at baseline, and after 1 and 6 months of treatment with erenumab, 70 mg given sc every 4 weeks. We found (data expressed as the means ± SD): 38.34 ± 30.74 pg CGRP/ml of plasma at baseline, 38.19 ± 29.23 pg/ml after 1 month and 53.89 ± 28.03 pg/ml after 6 months of treatment. Thus, the average increase in plasma CGRP levels after 6 months of treatment was about + 40% compared to both baseline and 1-month treatments; such difference was not statistically significant because of high SD values in all groups. These preliminary findings need to be confirmed in larger, sufficiently powered experiments. |
format | Online Article Text |
id | pubmed-7579961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Milan |
record_format | MEDLINE/PubMed |
spelling | pubmed-75799612020-10-22 A proof-of-concept study on CGRP plasma levels of migraineurs during a 6-month treatment with ERENUMAB Tringali, Giuseppe Vollono, Catello Calabresi, Paolo Navarra, Pierluigi J Headache Pain Short Report The introduction of monoclonal antibodies (mAbs) against calcitonin-gene related peptide (CGRP) or CGRP receptors in the treatment of migraine raised concerns on the possible risks associated to the long-term inhibition of CGRP physiological functions. In this proof-of-concept study, we have measured the circulating levels of CGRP in 7 patients with high-frequency episodic migraine receiving the anti-CGRP receptor mAb erenumab for at least 6 months, to test the hypothesis that long-term blockade of CGRP receptors induces an increase in systemic CGRP levels via a classical up-regulation mechanism. Plasma CGRP levels were measured by a validated radioimmunoassay at baseline, and after 1 and 6 months of treatment with erenumab, 70 mg given sc every 4 weeks. We found (data expressed as the means ± SD): 38.34 ± 30.74 pg CGRP/ml of plasma at baseline, 38.19 ± 29.23 pg/ml after 1 month and 53.89 ± 28.03 pg/ml after 6 months of treatment. Thus, the average increase in plasma CGRP levels after 6 months of treatment was about + 40% compared to both baseline and 1-month treatments; such difference was not statistically significant because of high SD values in all groups. These preliminary findings need to be confirmed in larger, sufficiently powered experiments. Springer Milan 2020-10-21 /pmc/articles/PMC7579961/ /pubmed/33087040 http://dx.doi.org/10.1186/s10194-020-01193-4 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 | Short Report Tringali, Giuseppe Vollono, Catello Calabresi, Paolo Navarra, Pierluigi A proof-of-concept study on CGRP plasma levels of migraineurs during a 6-month treatment with ERENUMAB |
title | A proof-of-concept study on CGRP plasma levels of migraineurs during a 6-month treatment with ERENUMAB |
title_full | A proof-of-concept study on CGRP plasma levels of migraineurs during a 6-month treatment with ERENUMAB |
title_fullStr | A proof-of-concept study on CGRP plasma levels of migraineurs during a 6-month treatment with ERENUMAB |
title_full_unstemmed | A proof-of-concept study on CGRP plasma levels of migraineurs during a 6-month treatment with ERENUMAB |
title_short | A proof-of-concept study on CGRP plasma levels of migraineurs during a 6-month treatment with ERENUMAB |
title_sort | proof-of-concept study on cgrp plasma levels of migraineurs during a 6-month treatment with erenumab |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579961/ https://www.ncbi.nlm.nih.gov/pubmed/33087040 http://dx.doi.org/10.1186/s10194-020-01193-4 |
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