Gallelli Luca, Cione Erika, Caroleo Maria Cristina, Carotenuto Marco, Lagana Pasqualina, Siniscalchi Antonio, Guidetti Vincenzo
University of Catanzaro, Clinical Pharmacology Unit, Mater Domini University Hospital - Chair of Pharmacology, Department of Health Science, School of Medicine, Catanzaro, Italy.
Department of Pharmacy Health and Nutritional Sciences, University of Calabria, Rende (CS), Catanzaro, Italy.
Microrna. 2017 Dec 6;6(3):152-156. doi: 10.2174/2211536606666170913152821.
Migraine is a prevalent neurovascular disorders with a complex pathophysiology and therapeutic options characterized by important side effects or problems related to drug abuse. No specific biomarkers are recognized to be univocal for this subclinical condition, yet. In this concern microRNAs (miRNAs) have been suggested as potentially useful screening/diagnostic tool, and research is underway to recognize the most effective candidate(s). In this concern in the present review we Herein we highlighted miRs involvement in pain and migraine, as well as drug response and efficacy focusing also on miRs panel results from mice model with multiple induced pain conditions, and human patients with migraine in order to understand if there are similar miRs expression pattern may useful into human translational studies.
During human migraine attack specific miRs were found dysregulated, as well as in mouse models with different pain conditions. Amongst all the miRs screened in mice/human suffering of pain the miR-590-5p was found alterated. This latter miR, in mice is modulated by celecoxib, while in human is dysregulated in the complex regional pain syndrome, condition where migraine assume a risk factor for its development. Recently has been reported that pharmacological treatments, indirectly can pertubate miRNA expression results. Therefore, miR-590-5p could assume an interesting double meaning for a clinical point of view. It can be considered biomarker of general pain, including migraine and also biomarker to evaluate the efficacy of the drug treatment. This could be of great importance in infant-juvenile segment, where the diagnosis of migraine is very challenging. In this view, since therapy is often started with NSAIDs herein we discuss also how the discovery of the new role of miRNAs in determining drug efficacy open a new scenario in the pain-migraine tailored therapy and pharmacogenomics concept.
miRNAs could have a pleiotropic meaning in the clinical management of migraine and could represent biomarkers of pathology, of drug efficacy as well as drug adherence to the treatment.
偏头痛是一种常见的神经血管疾病,其病理生理复杂,治疗选择具有重要副作用或与药物滥用相关的问题。目前尚未发现针对这种亚临床状况的特异性生物标志物。在此背景下,微小RNA(miRNA)被认为可能是有用的筛查/诊断工具,相关研究正在寻找最有效的候选者。在此,我们在本综述中强调了miRNA在疼痛和偏头痛中的作用,以及药物反应和疗效,重点关注了多种诱导疼痛条件的小鼠模型和偏头痛患者的miRNA谱结果,以了解是否存在相似的miRNA表达模式,这可能对人类转化研究有用。
在人类偏头痛发作期间,以及在具有不同疼痛状况的小鼠模型中,均发现特定的miRNA表达失调。在所有筛选的疼痛小鼠/人类中,miR-590-5p被发现发生改变。后一种miRNA在小鼠中受塞来昔布调节,而在人类复杂区域疼痛综合征中表达失调,在该综合征中偏头痛是其发展的危险因素。最近有报道称,药物治疗可间接影响miRNA表达结果。因此,从临床角度来看,miR-590-5p可能具有有趣的双重意义。它可被视为包括偏头痛在内的一般疼痛的生物标志物,也是评估药物治疗疗效的生物标志物。这在婴幼儿期可能非常重要,因为偏头痛的诊断极具挑战性。从这个角度来看,由于治疗通常从非甾体抗炎药开始,我们还讨论了miRNA在确定药物疗效方面新作用的发现如何为疼痛 - 偏头痛的个性化治疗和药物基因组学概念开辟了新的前景。
miRNA在偏头痛的临床管理中可能具有多效性意义,可代表病理、药物疗效以及药物治疗依从性的生物标志物。