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光学相干断层扫描成像中的高反射点与糖尿病视网膜病变中的炎症标志物。

Hyper-reflective dots in optical coherence tomography imaging and inflammation markers in diabetic retinopathy.

机构信息

School of Optometry and Vision Science and New Zealand National Eye Centre, The University of Auckland, Auckland, New Zealand.

Universiti Sultan Zainal Abidin, Kuala Terengganu, Malaysia.

出版信息

J Anat. 2023 Oct;243(4):697-705. doi: 10.1111/joa.13889. Epub 2023 May 24.


DOI:10.1111/joa.13889
PMID:37222261
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10485584/
Abstract

The aim of this study is to correlate small dot hyper-reflective foci (HRF) observed in spectral domain optical coherence tomography (SD-OCT) scans of an animal model of hyperglycaemia with focal electroretinography (fERG) response and immunolabelling of retinal markers. The eyes of an animal model of hyperglycaemia showing signs of diabetic retinopathy (DR) were imaged using SD-OCT. Areas showing dot HRF were further evaluated using fERG. Retinal areas enclosing the HRF were dissected and serially sectioned, stained and labelled for glial fibrillary acidic protein (GFAP) and a microglial marker (Iba-1). Small dot HRF were frequently seen in OCT scans in all retinal quadrants in the inner nuclear layer or outer nuclear layer in the DR rat model. Retinal function in the HRF and adjacent areas was reduced compared with normal control rats. Microglial activation was detected by Iba-1 labelling and retinal stress identified by GFAP expression in Müller cells observed in discrete areas around small dot HRF. Small dot HRF seen in OCT images of the retina are associated with a local microglial response. This study provides the first evidence of dot HRF correlating with microglial activation, which may allow clinicians to better evaluate the microglia-mediated inflammatory component of progressive diseases showing HRF.

摘要

本研究旨在将高血糖动物模型的光谱域光学相干断层扫描(SD-OCT)图像中小点状高反射焦点(HRF)与焦点视网膜电图(fERG)反应和视网膜标记物的免疫标记相关联。使用 SD-OCT 对出现糖尿病视网膜病变(DR)迹象的高血糖动物模型的眼睛进行成像。使用 fERG 进一步评估显示点状 HRF 的区域。包含 HRF 的视网膜区域被解剖并连续切片、染色和标记神经胶质纤维酸性蛋白(GFAP)和小胶质细胞标记物(Iba-1)。在 DR 大鼠模型的内核层或外核层的所有视网膜象限的 OCT 扫描中,经常可以看到小点状 HRF。与正常对照大鼠相比,HRF 和相邻区域的视网膜功能降低。通过 Iba-1 标记检测到小胶质细胞活化,并在离散的小点状 HRF 周围区域观察到 Müller 细胞中 GFAP 表达,确定视网膜应激。OCT 图像中观察到的小点状 HRF 与局部小胶质细胞反应相关。这项研究首次提供了点状 HRF 与小胶质细胞活化相关的证据,这可能使临床医生能够更好地评估显示 HRF 的进行性疾病中小胶质细胞介导的炎症成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ed5/10485584/247355922427/JOA-243-697-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ed5/10485584/9bb0cdb33e69/JOA-243-697-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ed5/10485584/0634565bc3b6/JOA-243-697-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ed5/10485584/ca1ce14eac93/JOA-243-697-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ed5/10485584/247355922427/JOA-243-697-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ed5/10485584/9bb0cdb33e69/JOA-243-697-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ed5/10485584/0634565bc3b6/JOA-243-697-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ed5/10485584/ca1ce14eac93/JOA-243-697-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ed5/10485584/247355922427/JOA-243-697-g001.jpg

相似文献

[1]
Hyper-reflective dots in optical coherence tomography imaging and inflammation markers in diabetic retinopathy.

J Anat. 2023-10

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Topographic associations of hyperreflective materials in diabetic retinopathy: a multimodal correlation with microvascular pathology, structural remodeling and systemic metabolic dysregulation.

Front Med (Lausanne). 2025-7-16

[2]
Retinal Hyperreflective Foci Are Biomarkers of Ocular Disease: A Scoping Review With Evidence From Humans and Insights From Animal Models.

J Ophthalmol. 2025-5-29

[3]
The TP53 Arg72Pro polymorphism predicts visual and neurodegenerative outcomes in retinal detachment.

Cell Death Dis. 2025-5-26

[4]
Hyperreflective Retinal Foci (HRF): Definition and Role of an Invaluable OCT Sign.

J Clin Med. 2025-4-27

[5]
Letter to the Editor Regarding "Intraretinal Hyper-Reflective Foci Are Almost Universally Present and Co-Localize With Intraretinal Fluid in Diabetic Macular Edema".

Invest Ophthalmol Vis Sci. 2025-2-3

[6]
Hyperreflective retinal foci are associated with retinal degeneration after optic neuritis in neuromyelitis optica spectrum disorders and multiple sclerosis.

Eur J Neurol. 2025-1

[7]
Hyper-reflective foci changes in RRMS under natalizumab therapy.

Front Immunol. 2024

[8]
Proliferative gliosis, a rare finding following multilayered inverted internal limiting membrane flap technique for concurrent macular hole and retinal detachment: Case series.

Am J Ophthalmol Case Rep. 2024-2-29

[9]
Presumed Müller Cell Activation in Multiple Evanescent White Dot Syndrome.

Invest Ophthalmol Vis Sci. 2023-10-3

本文引用的文献

[1]
Hyper-reflective retinal foci as possible in vivo imaging biomarker of microglia activation in von Hippel-Lindau disease.

PLoS One. 2022

[2]
Retinal Hyperreflecting Foci Associate With Cortical Pathology in Multiple Sclerosis.

Neurol Neuroimmunol Neuroinflamm. 2022-7

[3]
Contribution of Müller Cells in the Diabetic Retinopathy Development: Focus on Oxidative Stress and Inflammation.

Antioxidants (Basel). 2022-3-23

[4]
Optical coherence tomography as retinal imaging biomarker of neuroinflammation/neurodegeneration in systemic disorders in adults and children.

Eye (Lond). 2023-2

[5]
Significance of Hyperreflective Foci as an Optical Coherence Tomography Biomarker in Retinal Diseases: Characterization and Clinical Implications.

J Ophthalmol. 2021-12-17

[6]
Clinical electroretinography in diabetic retinopathy: a review.

Surv Ophthalmol. 2022

[7]
Association between Inflammatory Factors in the Aqueous Humor and Hyperreflective Foci in Patients with Intractable Macular Edema Treated with Antivascular Endothelial Growth Factor.

Dis Markers. 2021

[8]
The Role of Inflammation in Diabetic Retinopathy.

Front Immunol. 2020

[9]
Hyperreflective Foci in the Retina of Active Relapse-Onset Multiple Sclerosis.

Ophthalmology. 2020-12

[10]
Connexin Hemichannel Block Using Orally Delivered Tonabersat Improves Outcomes in Animal Models of Retinal Disease.

Neurotherapeutics. 2020-1

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