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Neurol Sci. 2019 Mar 5. doi: 10.1007/s10072-019-03769-8. [Epub ahead of print]

CGRP and headache: a brief review.

Author information

1
Neurology Department, Dartmouth-Hitchcock Medical Center, 1 Medical Center Drive, Lebanon, NH, 03756, USA. Stewart.J.Tepper@Dartmouth.edu.
2
Geisel School of Medicine at Dartmouth, Hanover, NH, USA. Stewart.J.Tepper@Dartmouth.edu.

Abstract

The advent of anti-CGRP medications is an example of translational research made real. Pioneering research by Drs. Lars Edvinsson and Peter Goadsby has yielded the monoclonal antibody therapeutics and will likely also result in the gepants. The availability of MABs represents a watershed moment in the treatment of migraine. These medications have specificity, as they were designed for primary migraine prevention. They work across a group of wide therapeutic targets, episodic migraine, chronic migraine, medication-overuse headache, and episodic cluster headache. They separate from placebo within 1 week, and often show clinical effects within a month or less. They have tolerability similar to placebo. There has been no significant or worrisome safety signal thus far in their use. They manifest unprecedented responder rates at ≥ 75% and even 100%. They lower all acute medication use and can convert patients from chronic migraine to episodic migraine and from acute medication overuse to non-overuse. They work in patients who have already had lack of success with at least 2-4 previous preventive medications. Pent-up demand for designer, well-tolerated, and effective migraine preventive medication in the USA has resulted in more than 100,000 individual patients prescribed erenumab from May to December of 2018, and the numbers continue to increase. The preventive treatment of migraine in the USA has shifted dramatically, and is likely to do so in the rest of the world as well.

KEYWORDS:

CGRP; Calcitonin gene-related peptide; Gepants; Migraine; Monoclonal antibodies

PMID:
30835001
DOI:
10.1007/s10072-019-03769-8

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