Migraine in the Triptan Era: Lessons From Epidemiology, Pathophysiology, and Clinical Science

被引:41
作者
Bigal, Marcelo E. [1 ]
Ferrari, Michel [2 ]
Silberstein, Stephen D. [3 ]
Lipton, Richard B. [4 ,5 ,6 ]
Goadsby, Peter J. [7 ]
机构
[1] Merck Res Labs, Whitehouse Stn, NJ USA
[2] LUMC, Chair Leiden Ctr Translat Neurosci, Leiden, Netherlands
[3] Jefferson Headache Ctr, Philadelphia, PA USA
[4] Albert Einstein Coll Med, Dept Neurol, Bronx, NY 10467 USA
[5] Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10467 USA
[6] Montefiore Headache Ctr, Bronx, NY USA
[7] Univ Calif San Francisco, Dept Neurol, Headache Grp, San Francisco, CA 94143 USA
来源
HEADACHE | 2009年 / 49卷
关键词
triptans; migraine epidemiology; pathophysiology; CORTICAL SPREADING DEPRESSION; FAMILIAL HEMIPLEGIC MIGRAINE; MEDICATION-OVERUSE HEADACHE; BRAIN-STEM ACTIVATION; QUALITY-OF-LIFE; EXTRACEREBRAL CIRCULATION; TRIGEMINOVASCULAR SYSTEM; VASCULAR MALFORMATION; PLASMA EXTRAVASATION; PREMONITORY SYMPTOMS;
D O I
10.1111/j.1526-4610.2008.01336.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The triptan era has been a time of remarkable progress for migraine diagnosis and treatment. In this paper, we review some of the advances achieved in migraine science during this era focusing on 3 themes: lessons from clinical practice, lessons from epidemiology and lessons from pathophysiology. Science has shown that migraine is a disorder of the brain, and that the key events happen in the the trigeminal neuronal pathways, not on blood vessels. Clinical science has led to the observation that migraine sometimes progresses or remits. This in turn led to longitudinal epidemiologic studies focusing on factors that determine migraine prognosis. In addition, these studies raised questions about the mechanisms of migraine progression, including the role of allodynia, obesity, inflammation, and medications as determinants of progression. This in turn opens a new set of scientific questions about the neurobiologic determinants of migraine, as well as of its clinical course, and exciting opportunities to develop new therapies for this highly disabling brain disorder.
引用
收藏
页码:S21 / S33
页数:13
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