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Combining treatments for migraine prophylaxis: the state-of-the-art

  • Lanfranco Pellesi
  • , David Garcia-Azorin
  • , Eloisa Rubio-Beltrán
  • , Wook Seok Ha
  • , Roberta Messina
  • , Raffaele Ornello
  • , Igor Petrusic
  • , Bianca Raffaelli
  • , Alejandro Labastida-Ramirez
  • , Ruth Ruscheweyh
  • , Claudio Tana
  • , Doga Vuralli
  • , Marta Waliszewska-Prosół
  • , Wei Wang
  • , William Wells-Gatnik
  • University of Southern Denmark
  • University of Valladolid
  • Hospital Universitario Río Hortega
  • King's College London
  • Yonsei University
  • San Raffaele Scientific Institute
  • Vita-Salute San Raffaele University
  • University of L'Aquila
  • University of Belgrade Faculty of Physical Chemistry
  • Charité – Universitätsmedizin Berlin
  • Charité-Universitätsmedizin Berlin
  • University of Manchester
  • Ludwig Maximilian University of Munich
  • Center of Excellence on Headache
  • Gazi University
  • Wrocław Medical University
  • Department of Neurology
  • Capital Medical University
  • University of Rome La Sapienza

Araştırma sonucu: Dergiye katkıİnceleme makalesibilirkişi

30 Alıntılar (Scopus)

Özet

Combination treatments for migraine prophylaxis present a promising approach to addressing the diverse and complex mechanisms underlying migraine. This review explores the potential of combining oral conventional prophylactics, onabotulinumtoxin A, monoclonal antibodies (mAbs) targeting the calcitonin gene-related peptide (CGRP) pathway, and small molecule CGRP receptor antagonists (gepants). Among the most promising strategies, dual CGRP inhibition through mAbs and gepants may enhance efficacy by targeting both the CGRP peptide and its receptor, while the combination of onabotulinumtoxin A with CGRP treatments offers synergistic pain relief. Oral non-CGRP treatments, which are accessible and often prescribed for patients with comorbid conditions, provide an affordable and practical option in combination regimens. Despite the potential of these combinations, there is a lack of evidence to support their widespread inclusion in clinical guidelines. The high cost of certain combinations, such as onabotulinumtoxin A with a CGRP mAb or dual anti-CGRP mAbs, presents feasibility challenges. Further large-scale trials are needed to establish safe and effective combination protocols and solidify their role in clinical practice, particularly for treatment-resistant patients.

Orijinal dilİngilizce
Makale numarası214
DergiJournal of Headache and Pain
Hacim25
Basın numarası1
DOI'lar
Yayın durumuYayınlandı - Ara 2024
Harici olarak yayınlandıEvet

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