INSERM, UMRS1138, Team 17, From Physiopathology of Ocular Diseases to Clinical Development, Université Paris Descartes Sorbonne Paris Cité, Centre de Recherche des Cordeliers, 15 rue de l'Ecole de Médecine, 75006 Paris, France; Department of Ophthalmology, University of Lausanne, Jules-Gonin Eye Hospital, Fondation Asile des Aveugles, Avenue de France 15, 1004 Lausanne, Switzerland.
Department of Ophthalmology, University of Lausanne, Jules-Gonin Eye Hospital, Fondation Asile des Aveugles, Avenue de France 15, 1004 Lausanne, Switzerland.
Prog Retin Eye Res. 2018 Mar;63:20-68. doi: 10.1016/j.preteyeres.2017.10.006. Epub 2017 Nov 7.
Macular edema consists of intra- or subretinal fluid accumulation in the macular region. It occurs during the course of numerous retinal disorders and can cause severe impairment of central vision. Major causes of macular edema include diabetes, branch and central retinal vein occlusion, choroidal neovascularization, posterior uveitis, postoperative inflammation and central serous chorioretinopathy. The healthy retina is maintained in a relatively dehydrated, transparent state compatible with optimal light transmission by multiple active and passive systems. Fluid accumulation results from an imbalance between processes governing fluid entry and exit, and is driven by Starling equation when inner or outer blood-retinal barriers are disrupted. The multiple and intricate mechanisms involved in retinal hydro-ionic homeostasis, their molecular and cellular basis, and how their deregulation lead to retinal edema, are addressed in this review. Analyzing the distribution of junction proteins and water channels in the human macula, several hypotheses are raised to explain why edema forms specifically in the macular region. "Pure" clinical phenotypes of macular edema, that result presumably from a single causative mechanism, are detailed. Finally, diabetic macular edema is investigated, as a complex multifactorial pathogenic example. This comprehensive review on the current understanding of macular edema and its mechanisms opens perspectives to identify new preventive and therapeutic strategies for this sight-threatening condition.
黄斑水肿是指黄斑区视网膜内或下的液体蓄积。它发生在许多视网膜疾病的过程中,并可导致严重的中心视力损害。黄斑水肿的主要原因包括糖尿病、分支和中央视网膜静脉阻塞、脉络膜新生血管、后葡萄膜炎、术后炎症和中心性浆液性脉络膜视网膜病变。健康的视网膜保持在相对脱水、透明的状态,有利于光的最佳透过,这是由多个主动和被动系统共同作用的结果。液体蓄积是由于控制液体进入和流出的过程之间的失衡引起的,当内或外血视网膜屏障被破坏时,这种失衡是由 Starling 方程驱动的。本文综述了视网膜水离子动态平衡的多种复杂机制、其分子和细胞基础,以及它们的失调如何导致视网膜水肿。分析了人眼黄斑区连接蛋白和水通道的分布,提出了几个假设来解释为什么水肿只在黄斑区形成。详细描述了“纯”黄斑水肿的临床表型,推测它们是由单一致病机制引起的。最后,研究了糖尿病性黄斑水肿,作为一种复杂的多因素致病范例。对黄斑水肿及其机制的当前认识进行了全面综述,为这一眼部致盲疾病的新的预防和治疗策略的确定提供了新的思路。