https://researchopenworld.com/migraine-a-review-of-basic-clinical-and-translational-approaches-to-new-treatment/#

Jared Wahl, T. Vanderah
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Abstract

Migraine is a debilitating neurological primary headache disorder characterized by recurring unipolar headaches lasting 4–72 hours with accompaniment of nausea and sensory sensitivities. Migraine is the most common headache disorder resulting in seeking of medical care [1, 2], in addition to being one of the most debilitating chronic disease conditions in terms of both morbidity and lost economic productivity. Migraine incidence has been observed since ancient times to disproportionately affect women, and most current epidemiological assessments put current incidence estimates at 12% overall for US populations, with an incidence of 18% in women and 6% in men when stratified by sex. This dimorphism of incidence is crucial when assessing overall health of a community, specifically when concerning women’s health and therefore must be taken into consideration when developing both clinical and basic models of migraine to enact the best possible outcomes of combined translational research efforts. While major recent advances have been made in the field of pharmacologic intervention for migraine with the recent approval of the anti CGRP and anti CGRP receptor antibody medications, prohibitive cost and limited access have made older treatments, such as the triptans and NSAIDs, still the most commonly utilized medications to combat migraine attacks. Current preclinical research models are heavily interested in modulation of the neuropeptide CGRP, and the phenomenon of cortical spreading depression (CSD), believed to be the underlying trigger of migraine with aura, via pharmacological intervention. Modulations of these phenomena has found to be correlated with menstrual events in women, tying back to the overarching theme of higher morbidity in women. With the advent of pharmacogenomics and personalized medicine, a new epoch of potential customizable treatments looms on the horizon, endearing those afflicted with this severely debilitating condition a new glimmer of hope as research progresses into its next phase. Acronyms: AMPP: American Migraine Prevalence and Prevention study. NIH: National Institute of Health. ICHD-3: International Classification of Headache Disorders, 3rd edition. NHIS: National Health Interview Survey. NSAID: Non-Steroidal Anti-Inflammatory Drug. CGRP: Calcitonin Gene Related Peptide. 5HT1: 5-Hydroxytryptamine (Serotonin) Receptor, Subfamily 1. FDA: Food and Drug Administration. CNS: Central Nervous System. MOH: Medication Overuse Headache. PGE2: Prostaglandin E2. CSD: Cortical Spreading depression. fMRI: Functional Magnetic Resonance Imaging. GWAS: Genome Wide Association Study. SNP: Single Nucleotide Polymorphism.
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https://researchopenworld.com/migraine-a-review-of-basic-clinical-and-translational-approaches-to-new-treatment/#
偏头痛是一种使人衰弱的神经性原发性头痛疾病,其特点是反复发作的单极性头痛,持续4-72小时,伴有恶心和感觉敏感。偏头痛是最常见的导致就医的头痛疾病[1,2],此外,就发病率和经济生产力损失而言,偏头痛也是最使人衰弱的慢性疾病之一。自古以来,人们就观察到偏头痛对女性的影响不成比例,目前大多数流行病学评估认为,美国人口目前的发病率估计为12%,按性别分层时,女性发病率为18%,男性发病率为6%。在评估一个社区的整体健康时,这种发病率的二态性是至关重要的,特别是在涉及妇女健康时,因此在开发偏头痛的临床和基础模型时必须考虑到这一点,以制定联合转化研究努力的最佳结果。随着抗CGRP和抗CGRP受体抗体药物的批准,最近在偏头痛的药物干预领域取得了重大进展,但高昂的成本和有限的获取使得旧的治疗方法,如曲坦类药物和非甾体抗炎药,仍然是最常用的治疗偏头痛的药物。目前的临床前研究模型非常关注神经肽CGRP的调节,以及通过药物干预被认为是先兆偏头痛的潜在触发因素的皮质扩张性抑制(CSD)现象。这些现象的调节已被发现与女性的月经事件相关,并与女性发病率较高的首要主题联系起来。随着药物基因组学和个性化医学的出现,一个潜在的定制治疗的新时代隐约出现在地平线上,随着研究进入下一阶段,那些受这种严重衰弱疾病折磨的人看到了新的希望。缩写词:AMPP:美国偏头痛患病率和预防研究。美国国立卫生研究院。ICHD-3:国际头痛疾病分类,第三版。全国健康访谈调查。非甾体抗炎药。CGRP:降钙素基因相关肽5HT1: 5-羟色胺(5-羟色胺)受体,亚家族1FDA:食品和药物管理局。CNS:中枢神经系统。卫生部:药物过度使用头痛。PGE2:前列腺素E2。CSD:皮质扩张性凹陷。功能磁共振成像。全基因组关联研究。SNP:单核苷酸多态性。
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