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本文引用的文献

1
Corneal innervation and cellular changes after corneal transplantation: an in vivo confocal microscopy study.角膜移植术后角膜神经支配与细胞变化:一项活体共聚焦显微镜研究。
Invest Ophthalmol Vis Sci. 2007 Feb;48(2):621-6. doi: 10.1167/iovs.06-0538.
2
The human corneal endothelium.人角膜内皮
Am J Ophthalmol. 1966 May;61(5 Pt 1):835-41. doi: 10.1016/0002-9394(66)90921-4.
3
Laser in situ keratomileusis in patients with corneal guttata and family history of Fuchs' endothelial dystrophy.患有角膜滴状变性且有Fuchs内皮营养不良家族史的患者的准分子原位角膜磨镶术。
J Cataract Refract Surg. 2005 Dec;31(12):2281-6. doi: 10.1016/j.jcrs.2004.05.061.
4
The effect of age on the corneal subbasal nerve plexus.年龄对角膜基底神经丛的影响。
Cornea. 2005 Aug;24(6):705-9. doi: 10.1097/01.ico.0000154387.51355.39.
5
Age-related modifications of corneal sensitivity.角膜敏感性的年龄相关变化。
Ophthalmologica. 2004 Sep-Oct;218(5):350-5. doi: 10.1159/000079478.
6
Long-term keratocyte deficits in the corneal stroma after LASIK.准分子激光原位角膜磨镶术后角膜基质中长期存在的角膜细胞缺陷。
Ophthalmology. 2004 Jul;111(7):1356-61. doi: 10.1016/j.ophtha.2003.10.027.
7
Keratocyte density in the human cornea after photorefractive keratectomy.准分子激光角膜切削术后人眼角膜基质细胞密度
Arch Ophthalmol. 2003 Jun;121(6):770-6. doi: 10.1001/archopht.121.6.770.
8
Assessing the sub-basal nerve plexus of the living healthy human cornea by in vivo confocal microscopy.通过活体共聚焦显微镜评估健康人类活体角膜的基底膜下神经丛。
Clin Exp Ophthalmol. 2002 Jun;30(3):187-90. doi: 10.1046/j.1442-9071.2002.00507.x.
9
Depth and age-dependent distribution of keratocytes in healthy human corneas: a study using scanning-slit confocal microscopy in vivo.健康人角膜中角膜细胞的深度和年龄依赖性分布:一项使用活体扫描裂隙共聚焦显微镜的研究。
J Cataract Refract Surg. 2002 Apr;28(4):611-6. doi: 10.1016/s0886-3350(01)01227-5.
10
A population study of the normal cornea using an in vivo, slit-scanning confocal microscope.一项使用活体裂隙扫描共聚焦显微镜对正常角膜进行的群体研究。
Optom Vis Sci. 2001 Oct;78(10):706-11. doi: 10.1097/00006324-200110000-00010.

正常人角膜的年龄相关性差异:一项激光扫描活体共聚焦显微镜研究。

Age-related differences in the normal human cornea: a laser scanning in vivo confocal microscopy study.

作者信息

Niederer R L, Perumal D, Sherwin T, McGhee C N J

机构信息

Department of Ophthalmology, Faculty of Medical and Health Sciences, The University of Auckland, Private Bag 92019, Auckland, New Zealand

出版信息

Br J Ophthalmol. 2007 Sep;91(9):1165-9. doi: 10.1136/bjo.2006.112656. Epub 2007 Mar 27.

DOI:10.1136/bjo.2006.112656
PMID:17389741
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1954900/
Abstract

AIMS

To quantify and establish baseline normative data for age-related differences in cellular and innervation density in the normal, healthy, human cornea using laser scanning in vivo confocal microscopy.

METHODS

Cross-sectional study of 85 normal subjects assessed via corneal topography and laser scanning in vivo confocal microscopy.

RESULTS

Mean age was 38+/-16 years (range 18-87 years) and 60% of subjects were female. Anterior keratocyte density declined by 0.9% per year (r = -0.423, p<0.001), posterior keratocyte density declined by 0.3% per year (r = -0.250, p = 0.021) and endothelial cell density declined by 0.5% per year (r = -0.615, p<0.001). Sub-basal nerve fibre density declined by 0.9% per year (r = -0.423, p<0.001). No association was observed between age and basal epithelial cell density, or between age and central corneal thickness, corneal astigmatism or horizontal corneal diameter (p>0.05). No association was observed between subject gender and corneal cell or innervation density.

CONCLUSIONS

Using laser scanning in vivo confocal microscopy this study highlights a significant, and relatively linear, reduction in keratocyte and endothelial cell density with increasing subject age. Interestingly, corneal sub-basal nerve fibre density also significantly decreases with increasing age. In vivo laser scanning confocal microscopy provides a safe, non-invasive method for the establishment of normative data and assessment of alterations in human corneal microstructure following surgery or disease processes.

摘要

目的

使用激光扫描活体共聚焦显微镜,量化并建立正常、健康人角膜细胞和神经支配密度与年龄相关差异的基线标准数据。

方法

通过角膜地形图和激光扫描活体共聚焦显微镜对85名正常受试者进行横断面研究。

结果

平均年龄为38±16岁(范围18 - 87岁),60%的受试者为女性。前基质层角膜细胞密度每年下降0.9%(r = -0.423,p<0.001),后基质层角膜细胞密度每年下降0.3%(r = -0.250,p = 0.021),内皮细胞密度每年下降0.5%(r = -0.615,p<0.001)。基底膜下神经纤维密度每年下降0.9%(r = -0.423,p<0.001)。未观察到年龄与基底上皮细胞密度之间、年龄与中央角膜厚度、角膜散光或水平角膜直径之间存在关联(p>0.05)。未观察到受试者性别与角膜细胞或神经支配密度之间存在关联。

结论

本研究使用激光扫描活体共聚焦显微镜发现,随着受试者年龄增加,角膜细胞和内皮细胞密度显著且相对呈线性下降。有趣的是,角膜基底膜下神经纤维密度也随年龄增加而显著降低。活体激光扫描共聚焦显微镜为建立标准数据以及评估手术或疾病过程后人角膜微观结构的改变提供了一种安全、非侵入性的方法。