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糖尿病视网膜病变与血管内皮生长因子基因插入/缺失多态性。

Diabetic Retinopathy and Vascular Endothelial Growth Factor Gene Insertion/Deletion Polymorphism.

机构信息

Department of Biotechnology Faculty of Life Sciences and Informatics, Balochistan University of Information Technology Engineering and Management Sciences, Quetta, Balochistan, Pakistan.

Department of Biotechnology Faculty of Life Sciences and Informatics, Balochistan University of Information Technology Engineering and Management Sciences, Quetta, Balochistan, Pakistan.

出版信息

Can J Diabetes. 2020 Apr;44(3):287-291. doi: 10.1016/j.jcjd.2019.08.005. Epub 2019 Aug 25.

Abstract

Diabetic retinopathy (DR) is a microvascular complication of the retina of the eye and represents a major cause of blindness worldwide. It is a complex disorder characterized by both genetic and environmental factors. The vascular endothelial growth factor (VEGF) gene is among the main candidate genes for DR, as it is also involved in several other diseases, such as microvascular complications of diabetes mellitus and cancer. The VEGF gene is extremely polymorphic. The 18-bp fragment (insertion/deletion) polymorphism at the -2549 position of the promoter region of the VEGF gene is of great importance. In this review, we highlight the DR and VEGF gene (insertion/deletion) polymorphism. In addition, we assess this association in various DR populations and in other microvascular complications, such as diabetic nephropathy, diabetic peripheral neuropathy and cancer.

摘要

糖尿病性视网膜病变(DR)是眼底视网膜的一种微血管并发症,是全球范围内导致失明的主要原因。它是一种复杂的疾病,既有遗传因素又有环境因素。血管内皮生长因子(VEGF)基因是 DR 的主要候选基因之一,因为它也涉及到其他几种疾病,如糖尿病的微血管并发症和癌症。VEGF 基因是高度多态性的。VEGF 基因启动子区域-2549 位的 18bp 片段(插入/缺失)多态性非常重要。在这篇综述中,我们重点介绍了 DR 和 VEGF 基因(插入/缺失)多态性。此外,我们还评估了这种关联在不同的 DR 人群以及其他微血管并发症中的存在情况,如糖尿病肾病、糖尿病周围神经病变和癌症。

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