Tang Qi, Buonfiglio Francesco, Böhm Elsa Wilma, Zhang Liyu, Pfeiffer Norbert, Korb Christina A, Gericke Adrian
Department of Ophthalmology, University Medical Center, Johannes Gutenberg University Mainz, Langenbeckstrasse 1, 55131 Mainz, Germany.
Antioxidants (Basel). 2024 May 12;13(5):594. doi: 10.3390/antiox13050594.
Diabetic retinopathy (DR) represents a severe complication of diabetes mellitus, characterized by irreversible visual impairment resulting from microvascular abnormalities. Since the global prevalence of diabetes continues to escalate, DR has emerged as a prominent area of research interest. The development and progression of DR encompass a complex interplay of pathological and physiological mechanisms, such as high glucose-induced oxidative stress, immune responses, vascular endothelial dysfunction, as well as damage to retinal neurons. Recent years have unveiled the involvement of genomic and epigenetic factors in the formation of DR mechanisms. At present, extensive research explores the potential of biomarkers such as cytokines, molecular and cell therapies, antioxidant interventions, and gene therapy for DR treatment. Notably, certain drugs, such as anti-VEGF agents, antioxidants, inhibitors of inflammatory responses, and protein kinase C (PKC)-β inhibitors, have demonstrated promising outcomes in clinical trials. Within this context, this review article aims to introduce the recent molecular research on DR and highlight the current progress in the field, with a particular focus on the emerging and experimental treatment strategies targeting the immune and redox signaling pathways.
糖尿病视网膜病变(DR)是糖尿病的一种严重并发症,其特征是微血管异常导致不可逆的视力损害。由于全球糖尿病患病率持续上升,DR已成为一个备受关注的重要研究领域。DR的发生和发展涉及病理和生理机制的复杂相互作用,如高糖诱导的氧化应激、免疫反应、血管内皮功能障碍以及视网膜神经元损伤。近年来,基因组和表观遗传因素在DR机制形成中的作用逐渐被揭示。目前,大量研究探索了细胞因子等生物标志物、分子和细胞疗法、抗氧化干预措施以及基因疗法在DR治疗中的潜力。值得注意的是,某些药物,如抗血管内皮生长因子(VEGF)药物、抗氧化剂、炎症反应抑制剂和蛋白激酶C(PKC)-β抑制剂,在临床试验中已显示出有前景的结果。在此背景下,本文旨在介绍DR的最新分子研究,并突出该领域的当前进展,特别关注针对免疫和氧化还原信号通路的新兴和实验性治疗策略。