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Visualization of microneuromas by using in vivo confocal microscopy: An objective biomarker for the diagnosis of neuropathic corneal pain?应用活体共聚焦显微镜观察微神经瘤:诊断神经病理性角膜痛的客观生物标志物?
Ocul Surf. 2020 Oct;18(4):651-656. doi: 10.1016/j.jtos.2020.07.004. Epub 2020 Jul 11.
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Corneal nerve fiber loss in diabetes with chronic kidney disease.糖尿病合并慢性肾脏病患者的角膜神经纤维损伤
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In Vivo Confocal Microscopy Automated Morphometric Analysis of Corneal Subbasal Nerve Plexus in Patients With Dry Eye Treated With Different Sources of Homologous Serum Eye Drops.体内共聚焦显微镜对不同来源同源血清滴眼剂治疗的干眼患者角膜基底部神经丛的自动形态计量分析。
Cornea. 2019 Nov;38(11):1412-1417. doi: 10.1097/ICO.0000000000002005.
5
The Relationship Between Corneal Dendritic Cells, Corneal Nerve Morphology and Tear Inflammatory Mediators and Neuropeptides in Healthy Individuals.健康人群角膜内神经形态与神经肽及泪液中炎症介质和神经肽与角膜树突细胞的关系
Curr Eye Res. 2019 Aug;44(8):840-848. doi: 10.1080/02713683.2019.1600196. Epub 2019 Apr 15.
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Efficacy of autologous serum tears for treatment of neuropathic corneal pain.自体血清滴眼液治疗神经病理性角膜痛的疗效。
Ocul Surf. 2019 Jul;17(3):532-539. doi: 10.1016/j.jtos.2019.01.009. Epub 2019 Jan 24.
7
In vivo confocal microscopy morphometric analysis of corneal subbasal nerve plexus in dry eye disease using newly developed fully automated system.使用新开发的全自动系统对干眼症患者角膜基底神经丛进行体内共焦显微镜形态计量分析。
Graefes Arch Clin Exp Ophthalmol. 2019 Mar;257(3):583-589. doi: 10.1007/s00417-018-04225-7. Epub 2019 Jan 14.
8
Clinically Relevant Immune-Cellular Metrics of Inflammation in Meibomian Gland Dysfunction.睑板腺功能障碍的炎症的临床相关免疫细胞指标。
Invest Ophthalmol Vis Sci. 2018 Dec 3;59(15):6111-6123. doi: 10.1167/iovs.18-25571.
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The Chemokine Receptor CXCR4 Mediates Recruitment of CD11c+ Conventional Dendritic Cells Into the Inflamed Murine Cornea.趋化因子受体 CXCR4 介导 CD11c+ 常规树突状细胞募集到炎症性的小鼠角膜中。
Invest Ophthalmol Vis Sci. 2018 Nov 1;59(13):5671-5681. doi: 10.1167/iovs.18-25084.
10
In Vivo Confocal Microscopy Shows Alterations in Nerve Density and Dendritiform Cell Density in Fuchs' Endothelial Corneal Dystrophy.体内共聚焦显微镜显示 Fuchs 内皮角膜营养不良中神经密度和树突状细胞密度的改变。
Am J Ophthalmol. 2018 Dec;196:136-144. doi: 10.1016/j.ajo.2018.08.040. Epub 2018 Sep 6.

不同亚型干眼疾病中角膜神经的改变:一项活体共聚焦显微镜研究。

Alterations in corneal nerves in different subtypes of dry eye disease: An in vivo confocal microscopy study.

机构信息

Center for Translational Ocular Immunology and Cornea Service, Department of Ophthalmology, Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USA.

Ocular Surface Imaging Center, Cornea & Refractive Surgery Service, Massachusetts Eye & Ear Infirmary, Department of Ophthalmology, Harvard Medical School, Boston, MA, USA.

出版信息

Ocul Surf. 2021 Oct;22:135-142. doi: 10.1016/j.jtos.2021.08.004. Epub 2021 Aug 15.

DOI:10.1016/j.jtos.2021.08.004
PMID:34407488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11549962/
Abstract

PURPOSE

To evaluate corneal subbasal nerve alterations in evaporative and aqueous-deficient dry eye disease (DED) as compared to controls.

METHODS

In this retrospective, cross-sectional, controlled study, eyes with a tear break-up time of less than 10 s were classified as DED. Those with an anesthetized Schirmer's strip of less than 5 mm were classified as aqueous-deficient DED. Three representative in vivo confocal microscopy images were graded for each subject for total, main, and branch nerve density and numbers.

RESULTS

Compared to 42 healthy subjects (42 eyes), the 70 patients with DED (139 eyes) showed lower total (18,579.0 ± 687.7 μm/mm vs. 21,014.7 ± 706.5, p = 0.026) and main (7,718.9 ± 273.9 vs. 9,561.4 ± 369.8, p < 0.001) nerve density, as well as lower total (15.5 ± 0.7/frame vs. 20.5 ± 1.3, p = 0.001), main (3.0 ± 0.1 vs. 3.8 ± 0.2, p = 0.001) and branch (12.5 ± 0.7 vs. 16.5 ± 1.2, p = 0.004) nerve numbers. Compared to the evaporative DED group, the aqueous-deficient DED group showed reduced total nerve density (19,969.9 ± 830.7 vs. 15,942.2 ± 1,135.7, p = 0.006), branch nerve density (11,964.9 ± 749.8 vs. 8,765.9 ± 798.5, p = 0.006), total nerves number (16.9 ± 0.8/frame vs. 13.0 ± 1.2, p = 0.002), and branch nerve number (13.8 ± 0.8 vs. 10.2 ± 1.1, p = 0.002).

CONCLUSIONS

Patients with DED demonstrate compromised corneal subbasal nerves, which is more pronounced in aqueous-deficient DED. This suggests a role for neurosensory abnormalities in the pathophysiology of DED.

摘要

目的

评估蒸发过强型和水液缺乏型干眼(DED)与正常对照者的角膜基底神经改变。

方法

本回顾性、横断面、对照研究中,泪膜破裂时间(tear break-up time,BUT)<10s 的眼被分类为 DED;Schirmer 试验无麻醉条<5mm 的眼被分类为水液缺乏型 DED。对每个患者的 3 个有代表性的活体共聚焦显微镜图像进行总神经密度、主神经密度和分支神经密度以及数量的分级。

结果

与 42 名健康受试者(42 只眼)相比,70 例 DED 患者(139 只眼)的总神经密度(18579.0±687.7μm/mm 比 21014.7±706.5,p=0.026)和主神经密度(7718.9±273.9μm/mm 比 9561.4±369.8μm/mm,p<0.001)均较低,总神经数量(15.5±0.7/帧比 20.5±1.3,p=0.001)、主神经数量(3.0±0.1/帧比 3.8±0.2/帧,p=0.001)和分支神经数量(12.5±0.7/帧比 16.5±1.2/帧,p=0.004)也较低。与蒸发过强型 DED 组相比,水液缺乏型 DED 组的总神经密度(19969.9±830.7μm/mm 比 15942.2±1135.7μm/mm,p=0.006)、分支神经密度(11964.9±749.8μm/mm 比 8765.9±798.5μm/mm,p=0.006)、总神经数量(16.9±0.8/帧比 13.0±1.2/帧,p=0.002)和分支神经数量(13.8±0.8/帧比 10.2±1.1/帧,p=0.002)均较低。

结论

DED 患者的角膜基底神经受损,水液缺乏型 DED 更为明显。这提示神经感觉异常可能在 DED 的病理生理学中发挥作用。