Non-medical treatment for late age-related macular degeneration

Q4 Medicine
A. K. Drakon, A. G. Kurguzova, V. Sheludchenko, N. Korchazhkina
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引用次数: 0

Abstract

Age-related macular degeneration (AMD) is the leading cause of blindness in people over 55 in developed countries. Moreover, the number of these patients will increase growth as life expectancy increases. It is estimated that late AMD accounts for half of blindness and low vision cases in European countries. A myriad of studies is currently underway to discover cutting-edge, effective therapeutic modalities. Gene therapy is a novel alternative to regular intravitreal injections of anti-VEGF agents for late wet AMD. This technique’s heart is a specific gene delivery to target cells to generate natural VEGF inhibitors. Gene therapy affecting the complement system to deactivate its end product, the membrane attack complex, is reasonable in late atrophic AMD. Studies on stem cell therapy for late atrophic AMD undergo as well. It was demonstrated that retinal pigment epithelium (RPE) cells derived from human embryonic stem cells or induced pluripotent stem cells express typical RPE markers that can phagocytize photoreceptor segments. Electrical stimulation and magnet therapy are already introduced into clinical practice to rehabilitate patients with late AMD. Magnetic and electrical fields improve impulse transmitting, activate intracellular and tissue regeneration of the retina. Recent findings are promising but require further in-depth studies. Keywords: age-related macular degeneration, retinal scar, gene therapy, stem cells, physiotherapy, rehabilitative medicine. For citation: Drakon A.K., Kurguzova A.G., Sheludchenko V.M., Korchazhkina N.B. Non-medical treatment for late age-related macular degeneration. Russian Journal of Clinical Ophthalmology. 2021;21(4):215–219 (in Russ.). DOI: 10.32364/2311-7729-2021-21-4-215-219.
晚期老年性黄斑变性的非药物治疗
在发达国家,年龄相关性黄斑变性(AMD)是55岁以上人群失明的主要原因。此外,随着预期寿命的延长,这些患者的数量也会增加。据估计,晚期AMD占欧洲国家失明和低视力病例的一半。无数的研究目前正在进行中,以发现尖端的,有效的治疗方式。基因治疗是一种新的替代常规玻璃体内注射抗vegf药物治疗晚期湿性AMD。这项技术的核心是将特定的基因传递到靶细胞,以产生天然的VEGF抑制剂。影响补体系统使其最终产物膜攻击复合物失活的基因治疗在晚期萎缩性AMD中是合理的。干细胞治疗晚期萎缩性AMD的研究也在进行中。研究表明,来源于人胚胎干细胞或诱导多能干细胞的视网膜色素上皮细胞(RPE)表达典型的RPE标记物,可以吞噬光感受器片段。电刺激和磁疗已被引入临床实践,以恢复晚期AMD患者。磁场和电场改善脉冲传输,激活视网膜细胞内和组织再生。最近的发现很有希望,但需要进一步深入研究。关键词:老年性黄斑变性,视网膜瘢痕,基因治疗,干细胞,物理治疗,康复医学引用本文:Drakon a.k., Kurguzova a.g., Sheludchenko v.m., Korchazhkina N.B.老年黄斑变性的非药物治疗。俄罗斯临床眼科学杂志,2021;21(4):215-219。DOI: 10.32364 / 2311-7729-2021-21-4-215-219。
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
0.60
自引率
0.00%
发文量
21
审稿时长
20 weeks
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