Precision Medicine in migraine management

IF 1 4区 医学 Q3 EMERGENCY MEDICINE
Signa Vitae Pub Date : 2021-09-15 DOI:10.22514/sv.2021.206
Theodora Barkoula
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Abstract

Migraine is a common disorder that negatively affects a significant percentage of patients, with corresponding social and economic costs. It is a neurovascular disease whose pathophysiological mechanisms are still being examined. While cortical spreading depression (CSD) and dysfunction of the trigeminovascular system appear to play a key role in the onset of migraine aura and pain, the study of human genome has shown the involvement of several genes and neuropeptides in its pathogenesis. New data make it necessary to search for targeted methods in the diagnosis and treatment of the disease, as current therapeutic approaches in many cases show little effectiveness and significant side effects. Nowadays, the rapid development of genetics opens new horizons in the approach of migraine through the prism of Medical Precision. Precision Medicine (PM) is a new approach to the treatment and prevention of the disease, which combines the individualized approach of the patient with the design and implementation of appropriate treatment. It differs radically from the "one size fits all" approach, leading to a better understanding of the pathophysiological mechanisms of the disease and the development of innovative diagnostic and treatment options. It combines the expression of genome and the correlation of science of Biochemistry with the comorbidity of the patient, in order to achieve the optimal clinical result. The purpose of this essay is to present the current therapeutic approaches for migraine treatment and to investigate their applicability, according to the new data of Medical Precision. The investigation and identification of new genetic, epigenetic, biochemical and other biomarkers will enable the patient to be better approached, more targeted treatment and reduced disease’s management costs.
精准医学治疗偏头痛
偏头痛是一种常见的疾病,对相当比例的患者产生负面影响,并带来相应的社会和经济成本。它是一种神经血管疾病,其病理生理机制仍在研究中。虽然皮层扩张性抑制(CSD)和三叉神经系统功能障碍似乎在偏头痛先兆和疼痛的发病中起关键作用,但人类基因组的研究表明,其发病机制涉及多个基因和神经肽。新的数据使得有必要在疾病的诊断和治疗中寻找有针对性的方法,因为目前的治疗方法在许多情况下显示效果甚微且副作用显著。如今,遗传学的快速发展通过医学精密的棱镜为偏头痛的治疗开辟了新的视野。精准医学(PM)是一种治疗和预防疾病的新方法,它将患者的个体化方法与适当治疗的设计和实施相结合。它从根本上不同于“一刀切”的方法,导致更好地了解疾病的病理生理机制和创新的诊断和治疗方案的发展。它将基因组的表达和生物化学科学与患者合并症的相关性结合起来,以达到最佳的临床效果。本文的目的是介绍目前偏头痛治疗的治疗方法,并根据医学精密的新数据探讨其适用性。研究和鉴定新的遗传、表观遗传、生化和其他生物标志物将使患者能够更好地接近,更有针对性地治疗,降低疾病的管理成本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Signa Vitae
Signa Vitae 医学-急救医学
CiteScore
1.30
自引率
9.10%
发文量
0
审稿时长
3 months
期刊介绍: Signa Vitae is a completely open-access,peer-reviewed journal dedicate to deliver the leading edge research in anaesthesia, intensive care and emergency medicine to publics. The journal’s intention is to be practice-oriented, so we focus on the clinical practice and fundamental understanding of adult, pediatric and neonatal intensive care, as well as anesthesia and emergency medicine. Although Signa Vitae is primarily a clinical journal, we welcome submissions of basic science papers if the authors can demonstrate their clinical relevance. The Signa Vitae journal encourages scientists and academicians all around the world to share their original writings in the form of original research, review, mini-review, systematic review, short communication, case report, letter to the editor, commentary, rapid report, news and views, as well as meeting report. Full texts of all published articles, can be downloaded for free from our web site.
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