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添加超微化N-棕榈酰乙醇酰胺对伴先兆偏头痛患者的影响:一项初步研究。

Effects of Add-On Ultramicronized N-Palmitol Ethanol Amide in Patients Suffering of Migraine With Aura: A Pilot Study.

作者信息

Chirchiglia Domenico, Cione Erika, Caroleo Maria C, Wang Minyan, Di Mizio Giulio, Faedda Noemi, Giacolini Teodosio, Siviglia Serena, Guidetti Vincenzo, Gallelli Luca

机构信息

Department of Medical and Surgical Science, School of Medicine, University of Catanzaro, Catanzaro, Italy.

Department of Pharmacy Health and Nutritional Sciences, University of Calabria, Rende, Italy.

出版信息

Front Neurol. 2018 Aug 17;9:674. doi: 10.3389/fneur.2018.00674. eCollection 2018.

Abstract

Palmitoyl ethanol amide (PEA) is an endogenously produced substance showing anti-nociceptive effect through both receptor and non-receptor mediated effects at the level of different cellular and tissue sites. This study showed the results of a single blind study that was conducted to evaluate both the safety and the efficacy of ultramicronized PEA (umPEA; 1,200 mg/day) for up 90 days in patients suffering of Migraine with Aura (MA) treated with NSAIDs. A total of 20 patients, 8 male (33-56-years, average 41.4 ± 7.8) and 12 female (19-61-years, average 38.5 ± 11.9) with MA were admitted to our observation and diagnosed according to ICHD-3 criteria, they received umPEA (1,200 mg/day) in combination with NSAIDs for up to 90 days. They were revaluated at 30, 60, and 90 days after treatment. umPEA administration induced a statistically significant and time dependent pain relief. In particular, these effects were evident at 60 days (male = 0.01189; female = <0.01) and they lasted until the end of the study (male = 0.0066; female = 0.01473). Although further studies are needed, our findings indicate that in patients suffering of MA treatment with umPEA had good efficacy and safety which candidate this compound as a therapeutic tool in pain migraine management.

摘要

棕榈酰乙醇酰胺(PEA)是一种内源性产生的物质,通过在不同细胞和组织部位水平上的受体介导和非受体介导作用发挥抗伤害感受效应。本研究展示了一项单盲研究的结果,该研究旨在评估超微粒化PEA(umPEA;1200毫克/天)在使用非甾体抗炎药治疗的伴有先兆偏头痛(MA)患者中长达90天的安全性和有效性。共有20例MA患者,8例男性(33 - 56岁,平均41.4±7.8)和12例女性(19 - 61岁,平均38.5±11.9)纳入我们的观察,并根据国际头痛疾病分类第三版(ICHD - 3)标准进行诊断,他们接受umPEA(1200毫克/天)联合非甾体抗炎药治疗长达90天。在治疗后30天、60天和90天对他们进行重新评估。umPEA给药诱导了具有统计学意义且随时间变化的疼痛缓解。特别是,这些效应在60天时明显(男性=0.01189;女性=<0.01),并且一直持续到研究结束(男性=0.0066;女性=0.01473)。尽管需要进一步研究,但我们的研究结果表明,在MA患者中,umPEA治疗具有良好的疗效和安全性,这使该化合物有望成为偏头痛疼痛管理的治疗工具。

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