Andrés-Blasco Irene, Gallego-Martínez Alex, Casaroli-Marano Ricardo Pedro, Di Lauro Salvatore, Arévalo Jose Fernando, Pinazo-Durán Maria Dolores
Ophthalmic Research Unit "Santiago Grisolía"/Fisabio, 46017 Valencia, Spain.
Cellular and Molecular Ophthalmo-Biology Group, Department of Surgery, Faculty of Medicina and Odontology, University of Valencia, 46017 Valencia, Spain.
J Clin Med. 2024 Dec 5;13(23):7426. doi: 10.3390/jcm13237426.
Diabetic macular edema (DME) is a leading cause of vision impairment and blindness among diabetic patients, requiring effective diagnostic and monitoring strategies. This systematic review aims to synthesize current knowledge on molecular biomarkers associated with DME, focusing on their potential to improve diagnostic accuracy and disease management. A comprehensive search was conducted in PubMed, Embase, Medline, and the Cochrane Central Register of Controlled Trials, covering literature from 2004 to 2023. Out of 1074 articles initially identified, 48 relevant articles were included in this systematic review. We found that molecules involved in several cellular processes, such as neuroinflammation, oxidative stress, vascular dysfunction, apoptosis, and cell-to-cell communication, exhibit differential expression profiles in various biological fluids when comparing diabetic individuals with or without macular edema. The study of these molecules could lead to the proper identification of specific biomarkers that may improve the diagnosis, prognosis, and therapeutic management of DME patients.
糖尿病性黄斑水肿(DME)是糖尿病患者视力损害和失明的主要原因,需要有效的诊断和监测策略。本系统评价旨在综合目前关于与DME相关的分子生物标志物的知识,重点关注其提高诊断准确性和疾病管理的潜力。我们在PubMed、Embase、Medline和Cochrane对照试验中央登记册中进行了全面检索,涵盖了2004年至2023年的文献。在最初识别的1074篇文章中,有48篇相关文章被纳入本系统评价。我们发现,在比较有或没有黄斑水肿的糖尿病个体时,参与神经炎症、氧化应激、血管功能障碍、细胞凋亡和细胞间通讯等多种细胞过程的分子,在各种生物体液中表现出不同的表达谱。对这些分子的研究可能有助于正确识别特定的生物标志物,从而改善DME患者的诊断、预后和治疗管理。