Mode and site of action of therapies targeting CGRP signaling

Abstract Targeting CGRP has proved to be efficacious, tolerable, and safe to treat migraine; however, many patients with migraine do not benefit from drugs that antagonize the CGRPergic system. Therefore, this review focuses on summarizing the general pharmacology of the different types of treatment...

詳細記述

書誌詳細
出版年:The Journal of Headache and Pain
主要な著者: Alejandro Labastida-Ramírez, Edoardo Caronna, Cédric Gollion, Emily Stanyer, Austeja Dapkute, Diana Braniste, Hoda Naghshineh, Liga Meksa, Nino Chkhitunidze, Tamari Gudadze, Patricia Pozo-Rosich, Rami Burstein, Jan Hoffmann
フォーマット: 論文
言語:英語
出版事項: BMC 2023-09-01
主題:
オンライン・アクセス:https://doi.org/10.1186/s10194-023-01644-8
_version_ 1851901281182941184
author Alejandro Labastida-Ramírez
Edoardo Caronna
Cédric Gollion
Emily Stanyer
Austeja Dapkute
Diana Braniste
Hoda Naghshineh
Liga Meksa
Nino Chkhitunidze
Tamari Gudadze
Patricia Pozo-Rosich
Rami Burstein
Jan Hoffmann
author_facet Alejandro Labastida-Ramírez
Edoardo Caronna
Cédric Gollion
Emily Stanyer
Austeja Dapkute
Diana Braniste
Hoda Naghshineh
Liga Meksa
Nino Chkhitunidze
Tamari Gudadze
Patricia Pozo-Rosich
Rami Burstein
Jan Hoffmann
author_sort Alejandro Labastida-Ramírez
collection DOAJ
container_title The Journal of Headache and Pain
description Abstract Targeting CGRP has proved to be efficacious, tolerable, and safe to treat migraine; however, many patients with migraine do not benefit from drugs that antagonize the CGRPergic system. Therefore, this review focuses on summarizing the general pharmacology of the different types of treatments currently available, which target directly or indirectly the CGRP receptor or its ligand. Moreover, the latest evidence regarding the selectivity and site of action of CGRP small molecule antagonists (gepants) and monoclonal antibodies is critically discussed. Finally, the reasons behind non-responders to anti-CGRP drugs and rationale for combining and/or switching between these therapies are addressed.
format Article
id doaj-art-e362add4199b46bbb5eb14bc92a5cd98
institution Directory of Open Access Journals
issn 1129-2377
language English
publishDate 2023-09-01
publisher BMC
record_format Article
spelling doaj-art-e362add4199b46bbb5eb14bc92a5cd982025-08-19T22:05:44ZengBMCThe Journal of Headache and Pain1129-23772023-09-0124111410.1186/s10194-023-01644-8Mode and site of action of therapies targeting CGRP signalingAlejandro Labastida-Ramírez0Edoardo Caronna1Cédric Gollion2Emily Stanyer3Austeja Dapkute4Diana Braniste5Hoda Naghshineh6Liga Meksa7Nino Chkhitunidze8Tamari Gudadze9Patricia Pozo-Rosich10Rami Burstein11Jan Hoffmann12Wolfson Centre for Age-Related Diseases, Institute of Psychiatry, Psychology & Neuroscience, King’s College LondonHeadache Unit, Neurology Department, Vall d’Hebron Universitary HospitalDepartment of Neurology, University Hospital of ToulouseWolfson Centre for Age-Related Diseases, Institute of Psychiatry, Psychology & Neuroscience, King’s College LondonCentre of Neurology, Vilnius UniversityInstitute of Neurology and NeurosurgeryHeadache Department, Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical ScienceHeadache Unit, Neurology and Neurosurgery Department, Riga East University Hospital GailezersDepartment of Neurology, Caucasus Medical CentreDepartment of Neurology, Christian Hospital UnnaHeadache Unit, Neurology Department, Vall d’Hebron Universitary HospitalDepartment of Anesthesia, Critical Care and Pain Medicine, Beth Israel Deaconess Medical CenterWolfson Centre for Age-Related Diseases, Institute of Psychiatry, Psychology & Neuroscience, King’s College LondonAbstract Targeting CGRP has proved to be efficacious, tolerable, and safe to treat migraine; however, many patients with migraine do not benefit from drugs that antagonize the CGRPergic system. Therefore, this review focuses on summarizing the general pharmacology of the different types of treatments currently available, which target directly or indirectly the CGRP receptor or its ligand. Moreover, the latest evidence regarding the selectivity and site of action of CGRP small molecule antagonists (gepants) and monoclonal antibodies is critically discussed. Finally, the reasons behind non-responders to anti-CGRP drugs and rationale for combining and/or switching between these therapies are addressed.https://doi.org/10.1186/s10194-023-01644-8AmylinAnti-CGRPCalcitoninHeadacheMigraineTrigeminal
spellingShingle Alejandro Labastida-Ramírez
Edoardo Caronna
Cédric Gollion
Emily Stanyer
Austeja Dapkute
Diana Braniste
Hoda Naghshineh
Liga Meksa
Nino Chkhitunidze
Tamari Gudadze
Patricia Pozo-Rosich
Rami Burstein
Jan Hoffmann
Mode and site of action of therapies targeting CGRP signaling
Amylin
Anti-CGRP
Calcitonin
Headache
Migraine
Trigeminal
title Mode and site of action of therapies targeting CGRP signaling
title_full Mode and site of action of therapies targeting CGRP signaling
title_fullStr Mode and site of action of therapies targeting CGRP signaling
title_full_unstemmed Mode and site of action of therapies targeting CGRP signaling
title_short Mode and site of action of therapies targeting CGRP signaling
title_sort mode and site of action of therapies targeting cgrp signaling
topic Amylin
Anti-CGRP
Calcitonin
Headache
Migraine
Trigeminal
url https://doi.org/10.1186/s10194-023-01644-8
work_keys_str_mv AT alejandrolabastidaramirez modeandsiteofactionoftherapiestargetingcgrpsignaling
AT edoardocaronna modeandsiteofactionoftherapiestargetingcgrpsignaling
AT cedricgollion modeandsiteofactionoftherapiestargetingcgrpsignaling
AT emilystanyer modeandsiteofactionoftherapiestargetingcgrpsignaling
AT austejadapkute modeandsiteofactionoftherapiestargetingcgrpsignaling
AT dianabraniste modeandsiteofactionoftherapiestargetingcgrpsignaling
AT hodanaghshineh modeandsiteofactionoftherapiestargetingcgrpsignaling
AT ligameksa modeandsiteofactionoftherapiestargetingcgrpsignaling
AT ninochkhitunidze modeandsiteofactionoftherapiestargetingcgrpsignaling
AT tamarigudadze modeandsiteofactionoftherapiestargetingcgrpsignaling
AT patriciapozorosich modeandsiteofactionoftherapiestargetingcgrpsignaling
AT ramiburstein modeandsiteofactionoftherapiestargetingcgrpsignaling
AT janhoffmann modeandsiteofactionoftherapiestargetingcgrpsignaling