眼睛里的幽灵血管萎缩性老年性黄斑变性中的游离细胞绒毛膜域

IF 3 2区 医学 Q1 OPHTHALMOLOGY
Robert F. Mullins , Miles J. Flamme-Wiese , Emma M. Navratil , Erin A. Boese , Katayoun Varzavand , Megan J. Riker , Kai Wang , Edwin M. Stone , Budd A. Tucker
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引用次数: 0

摘要

绒毛膜是脉络膜内部的一个致密血管床,为感光细胞和视网膜色素上皮(RPE)提供营养。虽然绒毛膜密度的下降与年龄相关性黄斑变性(AMD)有关,但这些变化是原发性的还是继发性的,一直存在争议。在这项研究中,我们通过量化用 UEA-I 凝集素标记的 99 例人类供体黄斑中的 "幽灵 "血管来描述绒毛膜缺失的特征,结果发现在早期-中期 AMD 中绒毛膜缺失显著增加,而在 RPE 完整的区域,地理萎缩的差异更大。对眼睛进行了CFH Tyr402His基因位点的基因分型,His等位基因的同卵眼比其他基因型的眼显示出明显更多的幽灵血管。如果只评估非AMD眼球,His等位基因眼球的幽灵血管密度会增加,但这一趋势没有达到统计学意义。这些结果支持了这样一种观点,即绒毛膜死亡往往先于 RPE 退化,而这种损失是治疗 AMD 的一个重要考虑因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ghost vessels in the eye: Cell free choriocapillaris domains in atrophic age-related macular degeneration
The choriocapillaris is a dense vascular bed in the inner choroid that supplies the photoreceptor cells and retinal pigment epithelium (RPE). While loss of choriocapillaris density has been described in association with age-related macular degeneration (AMD), whether these changes are primary or secondary to RPE degenerative changes in AMD has been debated. In this study we characterized choriocapillaris loss by quantifying “ghost” vessels in a series of 99 human donor maculae labeled with the UEA-I lectin, and found significant increases in early-intermediate AMD and a greater difference in geographic atrophy in areas with intact RPE. Eyes were genotyped at the CFH Tyr402His locus, and those homozygous for the His allele showed significantly more ghost vessels than those with other genotypes. When only non-AMD eyes were evaluated, His homozygotes had increased ghost vessel density but this trend did not reach statistical significance. These results support the notion that choriocapillaris death often precedes RPE degeneration in AMD and that this loss is an important therapeutic consideration for AMD.
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来源期刊
Experimental eye research
Experimental eye research 医学-眼科学
CiteScore
6.80
自引率
5.90%
发文量
323
审稿时长
66 days
期刊介绍: The primary goal of Experimental Eye Research is to publish original research papers on all aspects of experimental biology of the eye and ocular tissues that seek to define the mechanisms of normal function and/or disease. Studies of ocular tissues that encompass the disciplines of cell biology, developmental biology, genetics, molecular biology, physiology, biochemistry, biophysics, immunology or microbiology are most welcomed. Manuscripts that are purely clinical or in a surgical area of ophthalmology are not appropriate for submission to Experimental Eye Research and if received will be returned without review.
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