Abstract | BACKGROUND: Subcutaneous histamine at low concentrations interacts with H3-receptors and may constitute a new therapeutic drug in migraine prophylaxis. It acts by limiting the excessive inflammatory response involved in migraine pathophysiology. OBJECTIVE: Describe the results of a 15-year trial administering histamine at low concentrations. METHODS: Different study designs were used with subcutaneous histamine (10 microg/ml in Evan's solution) twice weekly, with an initial administration of microg (0.1 ml) and gradually increasing the dose to 10 microg (1.0 ml) over a 12-week period together with placebo, sodium valproate and topiramate. A Friedman-type rank ANOVA test was used to assess the difference between basal values and different design outcomes. RESULTS: Data recorded during the 12-week period showed a significant reduction in variables from both treatment groups ( histamine) compared with basaline stage results (p < 0.001). The histamine group reported a reduction of headache frequency (50%), decrease in pain intensity (51%), length of migraine attacks (45%) and painkiller use (52%). CONCLUSIONS: The present study provides evidence on the safety and efficiency of subcutaneous histamine administered at a dose of 1-10 microg twice weekly. This treatment constitutes a new therapeutic alternative, and provides a clinical and pharmacological basis for the use of H3 histaminergic agonists in migraine prophylaxis.
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Authors | Rebeca O Millán-Guerrero, Rebeca Isais-Millán |
Journal | Gaceta medica de Mexico
(Gac Med Mex)
2008 Jul-Aug
Vol. 144
Issue 4
Pg. 291-5
ISSN: 0016-3813 [Print] Mexico |
Vernacular Title | Nueva alternativa terapéutica en profilaxis de migraña con histamina como agonista de receptores H3. |
PMID | 18942262
(Publication Type: English Abstract, Journal Article)
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Chemical References |
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Topics |
- Adult
- Female
- Histamine Agonists
(therapeutic use)
- Humans
- Male
- Migraine Disorders
(prevention & control)
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