• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

随着时间的推移,年龄相关性黄斑变性患者的荧光寿命成像眼底镜观察到的玻璃膜疣相关自发荧光的变化。

Changes in drusen-associated autofluorescence over time observed by fluorescence lifetime imaging ophthalmoscopy in age-related macular degeneration.

机构信息

Department of Ophthalmology, University Hospital Jena, Jena, Germany.

Institute for Medical Statistics, Informatics, und Data Sciences, University Hospital Jena, Jena, Germany.

出版信息

Acta Ophthalmol. 2023 Mar;101(2):e154-e166. doi: 10.1111/aos.15238. Epub 2022 Aug 26.

DOI:10.1111/aos.15238
PMID:36017579
Abstract

PURPOSE

To observe fundus autofluorescence (FAF) lifetimes and peak emission wavelength (PEW) of drusen with respect to the pathology of the overlying RPE in the follow-up of AMD-patients.

METHODS

Forty eyes of 38 patients (age: 75.1 ± 7.1 years) with intermediate AMD were included. FAF lifetimes and PEW were recorded by fluorescence lifetime imaging ophthalmoscopy (FLIO). Twenty-six eyes had a follow-up investigation between months 12 and 36, and 10 at months 37-72. AMD progression was retrieved from color fundus photography (CFP) and OCT. Drusen were classified with respect to changes in the overlying RPE into groups no, questionable or faint, and apparent hyperpigmentation based on CFP.

RESULTS

Among the 210 hyperautofluorescent drusen found at baseline, those with hyperpigmentation had longer lifetimes and shorter PEW than those without. Drusen without hyperpigmentation had shorter lifetimes and PEW than neighboring RPE (all p < 0.001) at baseline, but drusen lifetimes increased, and PEW shortened further over follow-up. Eyes, showing AMD progression, had significantly longer FAF lifetimes at baseline than non-progressing eyes: 282 ± 102 ps versus 245 ± 98 ps, p < 0.001 and 365 ± 44 ps vs. 336 ± 48 ps, p = 0.025 for short and long wavelength FLIO channel, respectively.

CONCLUSIONS

Depending on hyperpigmentation properties, drusen show lifetimes and PEW different from that of adjacent RPE which change over the natural history of AMD. This difference and change, however, might reflect progressive dysmorphia of the RPE rather than representing fluorescence of drusen material itself. Nevertheless, the observed FAF changes could make FLIO a useful tool for the early detection of AMD progression risk.

摘要

目的

观察 AMD 患者随访中与 RPE 上层病理相关的玻璃膜疣(drusen)的荧光寿命和峰值发射波长(PEW)。

方法

纳入 38 名患者(年龄:75.1±7.1 岁)的 40 只眼,这些患者均患有中间型 AMD。荧光寿命成像眼底镜(FLIO)记录荧光寿命和 PEW。26 只眼在 12 至 36 个月之间进行了随访调查,10 只眼在 37 至 72 个月之间进行了随访调查。通过彩色眼底照相(CFP)和 OCT 检索 AMD 进展情况。根据 CFP 中 RPE 上层的变化,将 drusen 分为无、可疑或微弱和明显色素沉着组。

结果

在基线时发现的 210 个高自发荧光 drusen 中,那些有色素沉着的 drusen 的寿命比没有色素沉着的 drusen 长,PEW 比没有色素沉着的 drusen 短。在基线时,没有色素沉着的 drusen 比邻近的 RPE 寿命短,PEW 短(均 P<0.001),但随着随访,drusen 寿命增加,PEW 进一步缩短。与非进展性眼相比,显示 AMD 进展的眼在基线时的 FAF 寿命明显更长:282±102 ps 与 245±98 ps,p<0.001 和 365±44 ps 与 336±48 ps,p=0.025,分别用于短波长和长波长 FLIO 通道。

结论

根据色素沉着的特性,drusen 的寿命和 PEW 与相邻 RPE 不同,并且在 AMD 的自然史中会发生变化。然而,这种差异和变化可能反映了 RPE 的进行性畸形,而不是代表 drusen 物质本身的荧光。尽管如此,观察到的 FAF 变化可能使 FLIO 成为早期检测 AMD 进展风险的有用工具。

相似文献

1
Changes in drusen-associated autofluorescence over time observed by fluorescence lifetime imaging ophthalmoscopy in age-related macular degeneration.随着时间的推移,年龄相关性黄斑变性患者的荧光寿命成像眼底镜观察到的玻璃膜疣相关自发荧光的变化。
Acta Ophthalmol. 2023 Mar;101(2):e154-e166. doi: 10.1111/aos.15238. Epub 2022 Aug 26.
2
Progressive Dysmorphia of Retinal Pigment Epithelium in Age-Related Macular Degeneration Investigated by Fluorescence Lifetime Imaging.荧光寿命成像研究年龄相关性黄斑变性中视网膜色素上皮的进行性形态异常。
Invest Ophthalmol Vis Sci. 2021 Sep 2;62(12):2. doi: 10.1167/iovs.62.12.2.
3
Spectral and lifetime resolution of fundus autofluorescence in advanced age-related macular degeneration revealing different signal sources.眼底自发荧光在晚期年龄相关性黄斑变性中的光谱和寿命分辨率揭示了不同的信号源。
Acta Ophthalmol. 2022 May;100(3):e841-e846. doi: 10.1111/aos.14963. Epub 2021 Jul 13.
4
Fluorescence Lifetime and Spectral Characteristics of Subretinal Drusenoid Deposits and Their Predictive Value for Progression of Age-Related Macular Degeneration.视网膜下硬性脂褐质沉积的荧光寿命和光谱特征及其对年龄相关性黄斑变性进展的预测价值。
Invest Ophthalmol Vis Sci. 2022 Dec 1;63(13):23. doi: 10.1167/iovs.63.13.23.
5
Fundus Autofluorescence Lifetimes and Spectral Features of Soft Drusen and Hyperpigmentation in Age-Related Macular Degeneration.年龄相关性黄斑变性中软性玻璃膜疣和色素沉着的眼底自发荧光寿命及光谱特征
Transl Vis Sci Technol. 2020 Apr 24;9(5):20. doi: 10.1167/tvst.9.5.20. eCollection 2020 Apr.
6
Stages of Drusen-Associated Atrophy in Age-Related Macular Degeneration Visible via Histologically Validated Fundus Autofluorescence.通过经组织学验证的眼底自发荧光观察与年龄相关性黄斑变性相关的玻璃膜疣相关萎缩的阶段。
Ophthalmol Retina. 2021 Aug;5(8):730-742. doi: 10.1016/j.oret.2020.11.006. Epub 2020 Nov 18.
7
Fluorescence Lifetimes of Drusen in Age-Related Macular Degeneration.年龄相关性黄斑变性中玻璃膜疣的荧光寿命
Invest Ophthalmol Vis Sci. 2017 Sep 1;58(11):4856-4862. doi: 10.1167/iovs.17-22184.
8
Prolonged Lifetimes of Histologic Autofluorescence in Ectopic Retinal Pigment Epithelium in Age-Related Macular Degeneration.年龄相关性黄斑变性中异位视网膜色素上皮的组织自发荧光寿命延长。
Invest Ophthalmol Vis Sci. 2022 Dec 1;63(13):5. doi: 10.1167/iovs.63.13.5.
9
Hyperautofluorescent material inside areas of macular atrophy may reveal non-lipofuscin fluorophores in late stage AMD.黄斑萎缩区域内的高自发荧光物质可能揭示晚期年龄相关性黄斑变性中的非脂褐素荧光团。
Acta Ophthalmol. 2025 Feb;103(1):e66-e75. doi: 10.1111/aos.16752. Epub 2024 Aug 23.
10
Spectral fundus autofluorescence peak emission wavelength in ageing and AMD.年龄相关性黄斑变性与光谱眼底自发荧光峰值发射波长。
Acta Ophthalmol. 2022 Sep;100(6):e1223-e1231. doi: 10.1111/aos.15070. Epub 2021 Dec 1.

引用本文的文献

1
Fundus autofluorescence lifetimes in age-related macular degeneration versus healthy controls in a pseudophakic population.假晶状体人群中年龄相关性黄斑变性与健康对照者的眼底自发荧光寿命
Acta Ophthalmol. 2025 Sep;103(6):e394-e400. doi: 10.1111/aos.17519. Epub 2025 May 14.
2
Fluorescence Lifetime Imaging Ophthalmoscopy, Vision, and Chorioretinal Asymmetries in Aging and Age-Related Macular Degeneration: ALSTAR2.荧光寿命成像检眼镜、视力以及衰老和年龄相关性黄斑变性中的脉络膜视网膜不对称性:ALSTAR2
Invest Ophthalmol Vis Sci. 2025 Apr 1;66(4):56. doi: 10.1167/iovs.66.4.56.
3
Fundus Autofluorescence Variation in Geographic Atrophy of Age-Related Macular Degeneration: A Clinicopathologic Correlation.
年龄相关性黄斑变性地图样萎缩中的眼底自发荧光变化:临床病理相关性研究
Invest Ophthalmol Vis Sci. 2025 Jan 2;66(1):49. doi: 10.1167/iovs.66.1.49.
4
Hyperautofluorescent material inside areas of macular atrophy may reveal non-lipofuscin fluorophores in late stage AMD.黄斑萎缩区域内的高自发荧光物质可能揭示晚期年龄相关性黄斑变性中的非脂褐素荧光团。
Acta Ophthalmol. 2025 Feb;103(1):e66-e75. doi: 10.1111/aos.16752. Epub 2024 Aug 23.
5
Near Infrared Autofluorescence Lifetime Imaging of Human Retinal Pigment Epithelium Using Adaptive Optics Scanning Light Ophthalmoscopy.自适应光学扫描激光检眼镜对人视网膜色素上皮的近红外荧光寿命成像。
Invest Ophthalmol Vis Sci. 2024 May 1;65(5):27. doi: 10.1167/iovs.65.5.27.
6
Fluorescence Lifetime Imaging of Human Retinal Pigment Epithelium in Pentosan Polysulfate Toxicity Using Adaptive Optics Scanning Light Ophthalmoscopy.自适应光学扫描激光检眼镜观察戊聚糖多硫酸盐毒性对人视网膜色素上皮细胞的荧光寿命成像。
Invest Ophthalmol Vis Sci. 2024 Apr 1;65(4):27. doi: 10.1167/iovs.65.4.27.
7
Fluorescence Lifetime Imaging Ophthalmoscopy of Mouse Models of Age-related Macular Degeneration.荧光寿命成像眼底镜在年龄相关性黄斑变性小鼠模型中的应用。
Transl Vis Sci Technol. 2024 Jan 2;13(1):24. doi: 10.1167/tvst.13.1.24.
8
Lipofuscin, Its Origin, Properties, and Contribution to Retinal Fluorescence as a Potential Biomarker of Oxidative Damage to the Retina.脂褐素,其起源、特性以及作为视网膜氧化损伤潜在生物标志物对视网膜荧光的贡献。
Antioxidants (Basel). 2023 Dec 13;12(12):2111. doi: 10.3390/antiox12122111.
9
Multimodal imaging and deep learning in geographic atrophy secondary to age-related macular degeneration.多模态成像和深度学习在年龄相关性黄斑变性继发的地图状萎缩中的应用。
Acta Ophthalmol. 2023 Dec;101(8):881-890. doi: 10.1111/aos.15796.