MicroRNAs in neurodegenerative eye disease

Abel Ramón Concepción, Efraín Romo García, Jesús R Álvarez Félix, Silvia Paz Camacho, Elmer López Meza, Itzel Vega Pujalte, Ilse Ochoa Mellado, M. L. Barraza, Carla Angulo Rojo
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引用次数: 1

Abstract

Introduction: Neurodegenerative diseases affect the central nervous system and cause progressive dysfunction. These debilitating and incurable conditions are characterized by loss of neuronal cell function and are often associated with atrophy of the affected nervous system structures. The retina and the optic nerve are considered an extension of the central nervous system due to their embryonic origin and myelination by oligodendrocytes. Thereby, common physiopathological mechanism may be implicated in the neurodegeneration progress, regulated by key molecules as microRNAs. Aim: To determine the expression profile of microRNAs in peripheral blood in patients with neurodegenerative eye diseases such Glaucoma and Alzheimer´s disease. Methods: Observational, multicentric, comparative study. 50 patients distributed into four groups were included for this study: 10 (20%) with Alzheimer's disease, 20 (40%) with Glaucoma and 20 (40%) healthy control individuals. Results: miR-155 was found to be with tendency to overexpression in the Glaucoma group. miR-483 was found to be significatively overexpressed by five times in the Glaucoma group compared to control individuals. No significant changes were observed for Alzheimer’s disease group in both microRNAs. Conclusion: The preliminary results observed in this study, may suggest that the miR155 and miR483 microRNAs show peripheral blood levels that can be measured in a repeatable and reliable way, this opens the way to a new route of early diagnosis and possible treatment for neurodegenerative eye disease like glaucoma.
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神经退行性眼病中的microrna
神经退行性疾病影响中枢神经系统并引起进行性功能障碍。这些使人衰弱和无法治愈的疾病的特征是神经元细胞功能的丧失,通常与受影响的神经系统结构的萎缩有关。视网膜和视神经被认为是中枢神经系统的延伸,因为它们的胚胎起源和髓鞘形成的少突胶质细胞。因此,共同的生理病理机制可能涉及到神经退行性变的进展,由关键分子如microrna调节。目的:探讨青光眼、阿尔茨海默病等神经退行性眼病患者外周血中microrna的表达谱。方法:观察性、多中心、比较研究。50名患者被分为四组:10名阿尔茨海默病患者(20%),20名青光眼患者(40%)和20名健康对照者(40%)。结果:青光眼组miR-155有过表达的倾向。与对照组相比,青光眼组miR-483显着过表达5倍。阿尔茨海默病组两种microrna均未见明显变化。结论:本研究的初步结果可能提示miR155和miR483 microrna显示了可重复可靠测量的外周血水平,这为青光眼等神经退行性眼病的早期诊断和可能的治疗开辟了一条新的途径。
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