Diabetic Retinopathy in Focus: Update on Treatment Advances, Pharmaceutical Approaches, and New Technologies.

IF 4.7 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Adela Laura Ciorba, Sameh Saber, Amir Mohamed Abdelhamid, Noha Keshk, Fatma Elnaghy, Elsayed A Elmorsy, Rasha Abu-Khudir, Rabab S Hamad, Mustafa Ahmed Abdel-Reheim, Alshaimaa A Farrag, Attalla F El-Kott, Sally Negm, Kareem Morsy, Mohammed A AlShehri, Ahmed Gaafar, Simona Cavalu
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Abstract

This review provides an updated overview of the pathogenesis, classification, current management, and emerging therapies for diabetic retinopathy (DR). DR development involves dysregulation of the polyol pathway, formation of advanced glycation end products, activation of protein kinase C, and upregulation of vascular endothelial growth factor (VEGF). Disruption of the retinal neurovascular unit, including neurons, glial cells, and vascular elements, also plays a pivotal role, leading to microvascular damage, neurodegeneration, and inflammation. DR progresses from non-proliferative (NPDR) to proliferative stages (PDR) characterized by retinal neovascularization. Management emphasizes glycemic and blood pressure control, with advanced stages treated using laser photocoagulation, vitrectomy, and intravitreal anti-VEGF injections. Novel imaging technologies like optical coherence tomography angiography (OCTA) and electroretinography (ERG) enable early diagnosis and disease monitoring. Genetic factors, including VEGF polymorphisms and genes linked to oxidative stress and angiogenesis, significantly influence DR susceptibility. Innovative treatments under investigation include nanotechnology-based drug delivery, microRNA-targeted therapies, and AAV-mediated gene therapies aimed at anti-angiogenic pathways. Stem cell-based strategies utilizing adipose, bone marrow, amniotic, and umbilical cord-derived. It shows promise for retinal repair and neuroprotection. Future directions encompass CRISPR-Cas9 gene editing for precise genomic interventions, personalized medicine approaches, and integrated screening programs powered by artificial intelligence. A multifaceted approach involving risk factor modification, lifestyle interventions, advanced therapeutics, and cost-effectiveness analysis is essential to reduce the public health burden of diabetic retinopathy.

糖尿病视网膜病变的焦点:最新的治疗进展,药物方法和新技术。
本文综述了糖尿病视网膜病变(DR)的发病机制、分类、目前的治疗和新出现的治疗方法。DR的发展涉及多元醇通路的失调、晚期糖基化终产物的形成、蛋白激酶C的激活和血管内皮生长因子(VEGF)的上调。视网膜神经血管单元(包括神经元、神经胶质细胞和血管元件)的破坏也起着关键作用,导致微血管损伤、神经变性和炎症。DR由非增生性(NPDR)发展到以视网膜新生血管为特征的增生性阶段(PDR)。治疗强调血糖和血压控制,晚期治疗采用激光光凝、玻璃体切除术和玻璃体内抗vegf注射。光学相干断层血管造影(OCTA)和视网膜电图(ERG)等新型成像技术能够实现早期诊断和疾病监测。遗传因素,包括VEGF多态性和与氧化应激和血管生成相关的基因,显著影响DR易感性。正在研究的创新治疗方法包括基于纳米技术的药物递送、微rna靶向治疗和针对抗血管生成途径的aav介导的基因治疗。利用脂肪、骨髓、羊膜和脐带来源的干细胞为基础的策略。它有望修复视网膜和保护神经。未来的发展方向包括用于精确基因组干预的CRISPR-Cas9基因编辑、个性化医学方法以及由人工智能驱动的综合筛查计划。涉及危险因素改变、生活方式干预、先进治疗和成本效益分析的多方面方法对于减轻糖尿病视网膜病变的公共卫生负担至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.60
自引率
2.20%
发文量
248
审稿时长
50 days
期刊介绍: The journal publishes research articles, review articles and scientific commentaries on all aspects of the pharmaceutical sciences with emphasis on conceptual novelty and scientific quality. The Editors welcome articles in this multidisciplinary field, with a focus on topics relevant for drug discovery and development. More specifically, the Journal publishes reports on medicinal chemistry, pharmacology, drug absorption and metabolism, pharmacokinetics and pharmacodynamics, pharmaceutical and biomedical analysis, drug delivery (including gene delivery), drug targeting, pharmaceutical technology, pharmaceutical biotechnology and clinical drug evaluation. The journal will typically not give priority to manuscripts focusing primarily on organic synthesis, natural products, adaptation of analytical approaches, or discussions pertaining to drug policy making. Scientific commentaries and review articles are generally by invitation only or by consent of the Editors. Proceedings of scientific meetings may be published as special issues or supplements to the Journal.
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