Novel therapies for diabetic retinopathy

IF 1.5 4区 医学 Q4 IMMUNOLOGY
Magdalena Kupis, Katarzyna Samelska, J. Szaflik, P. Skopiński
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引用次数: 4

Abstract

Diabetes mellitus (DM) is a metabolic disease characterized by high blood glucose levels as well as microvascular and macrovascular changes. According to the latest statistics the growth of DM incidence is very fast. Diabetic retinopathy (DR) – one of the common DM complications – is the leading cause of blindness among professionally active people. Traditional treatment of DR including drugs controlling hyperglycemia, laser therapy, vitrectomy, and intravitreal injections of anti-VEGF is effectively administered with the effect of neovascularization and macular edema prevention. However, new potential DR therapies – focusing on a longer therapeutic effect and potentially fewer side effects – are being widely investigated. Gene therapy – targeting retinal vasculopathy or targeting retinal protection, mesenchymal stem cell injections, SGLT2 inhibitors, and islet cell transplantation have been proved to stop DR progression. The majority of the new treatment research was performed on an animal model and did not reach the final study stage. A further future human model and randomized studies with optimized delivery vectors will hopefully confirm positive outcomes of the new DR therapies.
糖尿病视网膜病变的新疗法
糖尿病(DM)是一种以高血糖及微血管和大血管改变为特征的代谢性疾病。据最新统计,糖尿病的发病率增长非常快。糖尿病视网膜病变(DR)是常见的糖尿病并发症之一,是职业活跃人群失明的主要原因。DR的传统治疗方法包括控制高血糖药物、激光治疗、玻璃体切割、玻璃体内注射抗vegf等,具有新生血管和预防黄斑水肿的作用。然而,新的潜在DR疗法——专注于更长的治疗效果和潜在更少的副作用——正在被广泛研究。基因治疗-针对视网膜血管病变或视网膜保护,间充质干细胞注射,SGLT2抑制剂和胰岛细胞移植已被证明可以阻止DR的进展。大多数新的治疗研究是在动物模型上进行的,并没有进入最后的研究阶段。未来进一步的人类模型和随机研究优化的传递载体将有望证实新的DR疗法的积极结果。
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
3.00
自引率
0.00%
发文量
17
审稿时长
6-12 weeks
期刊介绍: Central European Journal of Immunology is a English-language quarterly aimed mainly at immunologists.
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