医学
痛觉超敏
偏头痛
发作性
慢性偏头痛
定量感官测试
麻醉
前瞻性队列研究
感觉系统
痛觉过敏
内科学
癫痫
神经科学
伤害
受体
精神科
心理学
作者
Sait Ashina,Agustin Melo‐Carrillo,Edina Szabó,David Borsook,Rami Burstein
出处
期刊:Cephalalgia
[SAGE]
日期:2023-02-14
卷期号:43 (3): 3331024221147881-3331024221147881
被引量:42
标识
DOI:10.1177/03331024221147881
摘要
Background Migraine is a complex neurological disorder involving generalized abnormalities in processing sensory information. Adopting evidence that central sensitization imposes major hurdles in the treatment of migraine, we hypothesized that it is the non-ictal (rather than ictal) allodynia that may determine the outcome of migraine prevention with peripherally-acting drugs. Methods To test this hypothesis, we used Quantitative Sensory Testing to determine whether it is possible to identify a patient’s response to prophylactic treatment with galcanezumab based on presence/absence of cephalic and/or extracephalic allodynia during the pre-treatment non-ictal phase of migraine. Results Using strict criteria for allodynia (heat 32–40°C, cold 32–20°C, mechanical <60 g), we report that (a) the incidence of pre-treatment non-ictal cephalic allodynia was 21% in the 24 responders (>50% decrease in monthly migraine days) and 85% in the 19 non-responders; (b) the incidence of non-ictal extracephalic allodynia distinguishes responders from non-responders less accurately; and that (c) the incidence of non-ictal cephalic allodynia was similar in the chronic migraine and high-frequency episodic migraine groups. Conclusions Clinically, the findings suggest that presence/absence of non-ictal allodynia can be used to identify galcanezumab responders with nearly 80% accuracy and galcanezumab non-responders with nearly 85% accuracy. Mechanistically, the presence of non-ictal allodynia (reflecting a state of activity-independent central sensitization) in both chronic migraine and high-frequency episodic migraine patients raises the possibility that the state of non-ictal allodynia may be attributed to physiological properties of central trigeminovascular neurons that are due to the genetic load of the individual patient rather than their migraine frequency.
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