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Photophobia and migraine outcome during treatment with galcanezumab

BACKGROUND: Calcitonin gene-related peptide (CGRP) plays a pivotal role in migraine physiology, not only regarding migraine pain but also associated symptoms such as photophobia. The aim of the present study was to assess monoclonal antibodies targeting CGRP efficacy not only in terms of headache an...

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Autores principales: Schiano di Cola, Francesca, Ceccardi, Giulia, Bolchini, Marco, Caratozzolo, Salvatore, Liberini, Paolo, Padovani, Alessandro, Rao, Renata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889984/
https://www.ncbi.nlm.nih.gov/pubmed/36742057
http://dx.doi.org/10.3389/fneur.2022.1088036
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author Schiano di Cola, Francesca
Ceccardi, Giulia
Bolchini, Marco
Caratozzolo, Salvatore
Liberini, Paolo
Padovani, Alessandro
Rao, Renata
author_facet Schiano di Cola, Francesca
Ceccardi, Giulia
Bolchini, Marco
Caratozzolo, Salvatore
Liberini, Paolo
Padovani, Alessandro
Rao, Renata
author_sort Schiano di Cola, Francesca
collection PubMed
description BACKGROUND: Calcitonin gene-related peptide (CGRP) plays a pivotal role in migraine physiology, not only regarding migraine pain but also associated symptoms such as photophobia. The aim of the present study was to assess monoclonal antibodies targeting CGRP efficacy not only in terms of headache and migraine frequency and disability but also in reducing ictal photophobia. MATERIAL AND METHODS: This is a retrospective observational study, conducted at the Headache Center–ASST Spedali Civili Brescia. All patients in monthly treatment with galcanezumab with at least a 6-month follow-up in September 2022 with reported severe photophobia during migraine attacks were included. Data regarding headache frequency, analgesics consumption, and migraine disability were collected quarterly. Moreover, patients were asked the following information regarding photophobia: (1) whether they noticed an improvement in photophobia during migraine attacks since galcanezumab introduction; (2) the degree of photophobia improvement (low, moderate, and high); and (3) timing photophobia improvement. RESULTS: Forty-seven patients were enrolled in the present study as they met the inclusion criteria. Seventeen patients had a diagnosis of high-frequency episodic migraine and 30 of chronic migraine. From baseline to T3 and T6, a significant improvement in terms of headache days (19.2 ± 7.6 vs. 8.6 ± 6.8 vs. 7.7 ± 5.7; p < 0.0001), migraine days (10.4 ± 6.7 vs. 2.9 ± 4.3 vs. 3.6 ± 2.8; p < 0.0001), analgesics consumption (25.1 ± 28.2 vs. 7.6 ± 7.5 vs. 7.6 ± 8.1; p < 0.0001), MIDAS score (82.1 ± 48.4 vs. 21.6 ± 17.6 vs. 18.1 ± 20.5; p < 0.0001), and HIT-6 score (66.2 ± 6.2 vs. 57.2 ± 8.6 vs. 56.6 ± 7.6; p < 0.0001) was found. Thirty-two patients (68.1%) reported a significant improvement in ictal photophobia, with over half of the patients reporting it within the first month of treatment. Photophobia improvement was more frequent in patients with episodic migraine (p = 0.02) and triptans responders (p = 0.03). CONCLUSIONS: The present study confirms previous reports regarding galcanezumab efficacy beyond migraine frequency. In particular, over 60% of patients, in our cohort, documented a significant improvement also in reducing ictal photophobia. This improvement was, in most patients, moderate to high, and within the first 6 months of treatment, regardless of the clinical response on migraine frequency.
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spelling pubmed-98899842023-02-02 Photophobia and migraine outcome during treatment with galcanezumab Schiano di Cola, Francesca Ceccardi, Giulia Bolchini, Marco Caratozzolo, Salvatore Liberini, Paolo Padovani, Alessandro Rao, Renata Front Neurol Neurology BACKGROUND: Calcitonin gene-related peptide (CGRP) plays a pivotal role in migraine physiology, not only regarding migraine pain but also associated symptoms such as photophobia. The aim of the present study was to assess monoclonal antibodies targeting CGRP efficacy not only in terms of headache and migraine frequency and disability but also in reducing ictal photophobia. MATERIAL AND METHODS: This is a retrospective observational study, conducted at the Headache Center–ASST Spedali Civili Brescia. All patients in monthly treatment with galcanezumab with at least a 6-month follow-up in September 2022 with reported severe photophobia during migraine attacks were included. Data regarding headache frequency, analgesics consumption, and migraine disability were collected quarterly. Moreover, patients were asked the following information regarding photophobia: (1) whether they noticed an improvement in photophobia during migraine attacks since galcanezumab introduction; (2) the degree of photophobia improvement (low, moderate, and high); and (3) timing photophobia improvement. RESULTS: Forty-seven patients were enrolled in the present study as they met the inclusion criteria. Seventeen patients had a diagnosis of high-frequency episodic migraine and 30 of chronic migraine. From baseline to T3 and T6, a significant improvement in terms of headache days (19.2 ± 7.6 vs. 8.6 ± 6.8 vs. 7.7 ± 5.7; p < 0.0001), migraine days (10.4 ± 6.7 vs. 2.9 ± 4.3 vs. 3.6 ± 2.8; p < 0.0001), analgesics consumption (25.1 ± 28.2 vs. 7.6 ± 7.5 vs. 7.6 ± 8.1; p < 0.0001), MIDAS score (82.1 ± 48.4 vs. 21.6 ± 17.6 vs. 18.1 ± 20.5; p < 0.0001), and HIT-6 score (66.2 ± 6.2 vs. 57.2 ± 8.6 vs. 56.6 ± 7.6; p < 0.0001) was found. Thirty-two patients (68.1%) reported a significant improvement in ictal photophobia, with over half of the patients reporting it within the first month of treatment. Photophobia improvement was more frequent in patients with episodic migraine (p = 0.02) and triptans responders (p = 0.03). CONCLUSIONS: The present study confirms previous reports regarding galcanezumab efficacy beyond migraine frequency. In particular, over 60% of patients, in our cohort, documented a significant improvement also in reducing ictal photophobia. This improvement was, in most patients, moderate to high, and within the first 6 months of treatment, regardless of the clinical response on migraine frequency. Frontiers Media S.A. 2023-01-18 /pmc/articles/PMC9889984/ /pubmed/36742057 http://dx.doi.org/10.3389/fneur.2022.1088036 Text en Copyright © 2023 Schiano di Cola, Ceccardi, Bolchini, Caratozzolo, Liberini, Padovani and Rao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Schiano di Cola, Francesca
Ceccardi, Giulia
Bolchini, Marco
Caratozzolo, Salvatore
Liberini, Paolo
Padovani, Alessandro
Rao, Renata
Photophobia and migraine outcome during treatment with galcanezumab
title Photophobia and migraine outcome during treatment with galcanezumab
title_full Photophobia and migraine outcome during treatment with galcanezumab
title_fullStr Photophobia and migraine outcome during treatment with galcanezumab
title_full_unstemmed Photophobia and migraine outcome during treatment with galcanezumab
title_short Photophobia and migraine outcome during treatment with galcanezumab
title_sort photophobia and migraine outcome during treatment with galcanezumab
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889984/
https://www.ncbi.nlm.nih.gov/pubmed/36742057
http://dx.doi.org/10.3389/fneur.2022.1088036
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