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Photophobia: shared pathophysiology underlying dry eye disease, migraine and traumatic brain injury leading to central neuroplasticity of the trigeminothalamic pathway

机译:镜噬菌体:分享疾病性疾病,偏头痛和创伤性脑损伤,导致三际塔的途径中央神经塑性

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Photophobia is a potentially debilitating symptom often found in dry eye disease (DE), migraine and traumatic brain injury (TBI).We conducted a review of the literature via a PubMed search of English language articles with a focus on how photophobia may relate to a shared pathophysiology across DE, migraine and TBI.DE, migraine and TBI are common conditions in the general population, are often comorbid, and share photophobia as a symptom. Across the three conditions, neural dysregulation of peripheral and central nervous system components is implicated in photophobia in various animal models and in humans. Enhanced activity of the neuropeptide calcitonin gene-related peptide (CGRP) is closely linked to photophobia. Current therapies for photophobia include glasses which shield the eyes from specific wavelengths, botulinum toxin, and inhibition of CGRP and its receptor. Many individuals have persistent photophobia despite the use of these therapies, and thus, development of new therapies is needed.The presence of photophobia in DE, migraine and TBI suggests shared trigeminothalamic pathophysiologic mechanisms, as explained by central neuroplasticity and hypersensitivity mediated by neuropeptide CGRP. Treatment strategies which target neural pathways (ie, oral neuromodulators, transcutaneous nerve stimulation) should be considered in patients with persistent photophobia, specifically in individuals with DE whose symptoms are not controlled with traditional therapies.
机译:镜噬菌体是一种潜在的衰弱症状,通常在干眼症(DE),偏头痛和创伤性脑损伤(TBI)中发现。我们通过PUBMED搜索英语语言文章进行了审查,专注于镜川如何与a有关在DE,偏头痛和TBI.de中,偏头痛和TBI共同的病理生理学是一般人群的常见条件,通常是合并的,并作为症状分享噬菌体。在三个条件下,外周和中枢神经系统组分的神经缺陷涉及各种动物模型和人类的镜噬菌体。神经肽转基因基因相关肽(CGRP)的增强活性与镜噬菌体密切相关。用于噬菌体的当前疗法包括遮挡来自特定波长,肉毒杆菌毒素和CGRP及其受体的抑制作用的眼镜。尽管使用这些疗法,许多人具有持久的票针,因此,需要开发新疗法。偏头痛和TBI的镜噬菌关的存在表明共享的三峰母植物病理学机制,如神经血型术和由神经肽CGRP介导的中枢性神经塑性和超敏反应所解释的。应考虑患有神经途径(即口腔神经调节剂,经皮神经刺激)的治疗策略,特别是在持续的噬菌体患者中,特别是在患有传统疗法的DE的个体中。

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