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正常眼压性青光眼:发病机制与遗传学

Normal-tension glaucoma: Pathogenesis and genetics.

作者信息

Trivli Alexandra, Koliarakis Ioannis, Terzidou Chryssa, Goulielmos George N, Siganos Charalambos S, Spandidos Demetrios A, Dalianis Georgios, Detorakis Efstathios T

机构信息

Department of Ophthalmology, Konstantopouleio-Patission General Hospital, 14233 Athens, Greece.

Section of Molecular Pathology and Human Genetics, Department of Internal Medicine, School of Medicine, University of Crete, 71003 Heraklion, Greece.

出版信息

Exp Ther Med. 2019 Jan;17(1):563-574. doi: 10.3892/etm.2018.7011. Epub 2018 Nov 26.


DOI:10.3892/etm.2018.7011
PMID:30651837
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6307418/
Abstract

Normal-tension glaucoma (NTG) is a multifactorial optic neuropathy which, similar to open-angle glaucomas, is characterized by progressive retinal ganglion cell death and glaucomatous visual field loss. The major distinction of NTG from open-angle glaucomas is that the intraocular pressure (IOP) does not exceed the normal range. Missing the major risk factor and target of therapy, the elevated IOP, NTG poses a clinical challenge. Several insightful reviews have been published on the pathophysiology of NTG describing the possible underlying mechanisms. The current literature available also suggests that a significant percentage of patients with NTG (as high as 21%) have a family history of glaucoma, indicating a genetic predisposition to the disease. These facts strengthen the indication that NTG remains an enigmatic process. The aim of this review was to summarize the vascular, mechanical and genetic components considered to be responsible for NTG development and to discuss the mechanisms through which they are involved in the pathogenesis of NTG.

摘要

正常眼压性青光眼(NTG)是一种多因素性视神经病变,与开角型青光眼相似,其特征为视网膜神经节细胞进行性死亡和青光眼性视野缺损。NTG与开角型青光眼的主要区别在于眼压(IOP)不超过正常范围。由于缺少主要危险因素和治疗靶点——升高的眼压,NTG带来了临床挑战。关于NTG的病理生理学已发表了几篇有见地的综述,描述了可能的潜在机制。现有文献还表明,相当比例的NTG患者(高达21%)有青光眼家族史,提示该病存在遗传易感性。这些事实进一步表明NTG仍是一个谜一样的过程。本综述的目的是总结被认为与NTG发生相关的血管、机械和遗传因素,并讨论它们参与NTG发病机制的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0937/6307418/06ec01c147a0/etm-17-01-0563-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0937/6307418/06ec01c147a0/etm-17-01-0563-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0937/6307418/06ec01c147a0/etm-17-01-0563-g00.jpg

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Normal-tension glaucoma: Pathogenesis and genetics.

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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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本文引用的文献

[1]
Normal-Tension Glaucoma Has Normal Intracranial Pressure: A Prospective Study of Intracranial Pressure and Intraocular Pressure in Different Body Positions.

Ophthalmology. 2017-10-31

[2]
Functional Activity of Matrix Metalloproteinases 2 and 9 in Tears of Patients With Glaucoma.

Invest Ophthalmol Vis Sci. 2017-5-1

[3]
Translaminar pressure in Caucasian normal tension glaucoma patients.

Acta Ophthalmol. 2017-11

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Visual Field Change and 24-Hour IOP-Related Profile with a Contact Lens Sensor in Treated Glaucoma Patients.

Ophthalmology. 2016-1-21

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Translamina Cribrosa Pressure Difference as Potential Element in the Pathogenesis of Glaucomatous Optic Neuropathy.

Asia Pac J Ophthalmol (Phila). 2016

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Candidate genes involved in the susceptibility of primary open angle glaucoma.

Gene. 2016-2-15

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Biomed Res Int. 2015

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Eye (Lond). 2015-10

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Relationship between daytime variability of blood pressure or ocular perfusion pressure and glaucomatous visual field progression.

Am J Ophthalmol. 2015-9

[10]
Analysis of the expression and polymorphism of APOE, HSP, BDNF, and GRIN2B genes associated with the neurodegeneration process in the pathogenesis of primary open angle glaucoma.

Biomed Res Int. 2015

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