Revisiting the Efficacy of Sumatriptan Therapy During the Aura Phase of Migraine

被引:31
作者
Aurora, Sheena K. [1 ]
Barrodale, Patricia M. [1 ]
McDonald, Susan A. [2 ]
Jakubowski, Moshe [3 ]
Burstein, Rami [3 ,4 ]
机构
[1] Swedish Med Ctr, Seattle, WA USA
[2] GlaxoSmithKline Inc, Res Triangle Pk, NC USA
[3] Beth Israel Deaconess Med Ctr, Dept Anesthesia & Crit Care, Boston, MA 02215 USA
[4] Harvard Univ, Sch Med, Program Neurosci, Boston, MA 02115 USA
来源
HEADACHE | 2009年 / 49卷 / 07期
关键词
central sensitization; allodynia; headache; trigeminal; pain; nociception; BLOOD-BRAIN-BARRIER; DISRUPTION; NEURONS; PAIN;
D O I
10.1111/j.1526-4610.2009.01429.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Objective.- To reexamine the efficacy of terminating migraine headache by administration of sumatriptan during the visual-aura phase of the attack. Background.- Although the antimigraine action of triptans is most effective soon after onset of the headache, treatment during the aura phase has been found to be ineffective. Methods.- Nineteen subjects having migraine with aura were studied using a 4-way crossover, open-label design. Each patient was asked to treat 8 consecutive attacks with 100 mg of sumatriptan RT: 3 attacks treated at a timing of the patient's discretion (baseline); 1 attack treated 4 hours after onset of pain (late); 2 attacks treated within 1 hour of onset of pain (early); 2 attacks treated during the aura phase - before the onset of pain (aura). Pain level and cutaneous allodynia were reported by the patients at the onset of pain, at the time of treatment, and 2 and 24 hours after treatment. Results.- Sumatriptan treatment during the aura preempted the development of headache in 34/38 (89%) attacks. The same patients were rendered pain-free in 30/38 (79%) of attacks treated within 1 hour of pain onset, and in 4/19 (21%) of attacks treated 4 hours after the onset of pain. The incidence of allodynia at the time of treatment was 2/38 (5%) in attacks treated during aura, 8/38 (21%) in attacks treated early, and 14/19 (74%) in attacks treated late. Conclusion.- Considering the discrepancy between the present and previous clinical studies, it is worthwhile revisiting the efficacy of preemptive triptan therapy during the aura phase of migraine attacks, using larger-scale, 3-way, crossover, placebo-controlled studies.
引用
收藏
页码:1001 / 1004
页数:4
相关论文
共 10 条
[1]
Tissue injury regulates serotonin 1D receptor expression: Implications for the control of migraine and inflammatory pain [J].
Ahn, Andrew H. ;
Basbaum, Allan I. .
JOURNAL OF NEUROSCIENCE, 2006, 26 (32) :8332-8338
[2]
SUBCUTANEOUS SUMATRIPTAN DURING THE MIGRAINE AURA [J].
BATES, D ;
ASHFORD, E ;
DAWSON, R ;
ENSINK, FBM ;
GILHUS, NE ;
OLESEN, J ;
PILGRIM, AJ ;
SHEVLIN, P .
NEUROLOGY, 1994, 44 (09) :1587-1592
[3]
Defeating migraine pain with triptans: A race against the development of cutaneous allodynia [J].
Burstein, R ;
Collins, B ;
Jakubowski, M .
ANNALS OF NEUROLOGY, 2004, 55 (01) :19-26
[4]
Can oral 311C90, a novel 5-HT1D agonist, prevent migraine headache when taken during an aura? [J].
Dowson, A .
EUROPEAN NEUROLOGY, 1996, 36 :28-31
[5]
HARPER AM, 1977, LANCET, V1, P1034
[6]
PRECLINICAL STUDIES ON THE ANTIMIGRAINE DRUG, SUMATRIPTAN [J].
HUMPHREY, PPA ;
FENIUK, W ;
MARRIOTT, AS ;
TANNER, RJN ;
JACKSON, MR ;
TUCKER, ML .
EUROPEAN NEUROLOGY, 1991, 31 (05) :282-290
[7]
INHIBITION BY SUMATRIPTAN OF CENTRAL TRIGEMINAL NEURONS ONLY AFTER BLOOD-BRAIN-BARRIER DISRUPTION [J].
KAUBE, H ;
HOSKIN, KL ;
GOADSBY, PJ .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 109 (03) :788-792
[8]
Disruption of communication between peripheral and central trigeminovascular neurons mediates the antimigraine action of 5HT1B/1D receptor agonists [J].
Levy, D ;
Jakubowski, M ;
Burstein, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (12) :4274-4279
[9]
No effect of eletriptan administration during the aura phase of migraine [J].
Olesen, J ;
Diener, HC ;
Schoenen, J ;
Hettiarachchi, J .
EUROPEAN JOURNAL OF NEUROLOGY, 2004, 11 (10) :671-677
[10]
Pharmacokinetic profile of a new form of sumatriptan tablets in healthy volunteers [J].
Walls, C ;
Lewis, A ;
Bullman, J ;
Boswell, D ;
Summers, SJ ;
Dow, A ;
Sidhu, J .
CURRENT MEDICAL RESEARCH AND OPINION, 2004, 20 (06) :803-809