2001
DOI: 10.1007/s101940170041
|View full text |Cite
|
Sign up to set email alerts
|

Anti-epileptic drugs in the preventive treatment of migraine headache: a brief review

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
5
0

Year Published

2003
2003
2022
2022

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(5 citation statements)
references
References 12 publications
0
5
0
Order By: Relevance
“…18 However, botulinum toxin A has not been demonstrated to be more efficacious than placebo for episodic migraine 19 and is only approved for the prevention of chronic migraine in the USA and Europe. The results of our study suggest that galcanezumab, a CGRP monoclonal antibody, may be more rapidly acting than many other conventional preventive treatments currently available 20,21 and may overcome the challenges associated with conventional preventive treatments, including lack of efficacy, low adherence, and high discontinuation rates. 5,6,22 The current study showed that approximately half of the patients receiving galcanezumab experienced ≥50% response at each week from weeks 1 to 4.…”
Section: Discussionmentioning
confidence: 79%
“…18 However, botulinum toxin A has not been demonstrated to be more efficacious than placebo for episodic migraine 19 and is only approved for the prevention of chronic migraine in the USA and Europe. The results of our study suggest that galcanezumab, a CGRP monoclonal antibody, may be more rapidly acting than many other conventional preventive treatments currently available 20,21 and may overcome the challenges associated with conventional preventive treatments, including lack of efficacy, low adherence, and high discontinuation rates. 5,6,22 The current study showed that approximately half of the patients receiving galcanezumab experienced ≥50% response at each week from weeks 1 to 4.…”
Section: Discussionmentioning
confidence: 79%
“…Inhibition of NMDA in turn inhibits glutamate, which has been implicated in cortical spreading depression propagation, central sensitization and activation of nociceptive neurons ( 8 ). Other parenteral treatment options include dihydroergotamine, which inhibits vasoconstriction, and CGRP release at 5HT1B/D receptors ( 13 ), chlorpromazine which antagonizes dopamine ( 14 ) and sodium valproate, which inhibits GABA uptake and inhibits voltage-sensitive channels while stimulating GABA synthesis ( 15 ).…”
Section: Discussionmentioning
confidence: 99%
“…There do not seem to have been formal systematic studies or controlled clinical trials of pharmacological agents in the management of these rather uncommon aura situations. However, there are reports based on small numbers of cases that certain measures, such as the use of antiseizure medications or calcium channel antagonists, may be effective in preventing their occurrence or in shortening their durations [18,19].…”
Section: The Migraine Auramentioning
confidence: 99%
“…The available literature reports that various drugs believed to act at other receptor types that have already been identified as probably playing a role in the pathogenesis of migraine headache are currently under investigation or are being developed [19,42,43]. The receptors involved in their actions include pituitary adenyl cyclase activating peptide receptors, certain classes of glutamate receptor, orexin receptors, receptors of the endocannabinoid system [44], and perhaps receptors subserving the near final stage headacheproducing molecular mechanism by blocking nitric oxide synthase activity or ATP-sensitive potassium channels [45].…”
Section: Agents Acting At Other Receptor Typesmentioning
confidence: 99%