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Biosci Rep. 2018 Dec 7;38(6). doi: 10.1042/BSR20181411. Print 2018 Dec 21.
2
Intraocular cytokine profile and autoimmune reactions in retinitis pigmentosa, age-related macular degeneration, glaucoma and cataract.眼内细胞因子谱与视网膜色素变性、年龄相关性黄斑变性、青光眼和白内障的自身免疫反应。
Acta Ophthalmol. 2019 Mar;97(2):185-192. doi: 10.1111/aos.13899. Epub 2018 Oct 8.
3
Cytokine expression in tears of patients with glaucoma or dry eye disease: A prospective, observational cohort study.青光眼或干眼症患者泪液中的细胞因子表达:一项前瞻性观察性队列研究。
Eur J Ophthalmol. 2019 Jul;29(4):437-443. doi: 10.1177/1120672118795399. Epub 2018 Sep 3.
4
[Endothelins and dopamine levels in tears for assessment of neurovascular disorders in glaucoma].[通过检测泪液中内皮素和多巴胺水平评估青光眼的神经血管病变]
Vestn Oftalmol. 2018;134(4):41-46. doi: 10.17116/oftalma201813404141.
5
Commensal microflora-induced T cell responses mediate progressive neurodegeneration in glaucoma.共生微生物诱导的 T 细胞反应介导青光眼的进行性神经退行性变。
Nat Commun. 2018 Aug 10;9(1):3209. doi: 10.1038/s41467-018-05681-9.
6
Tear biomarkers in latanoprost and bimatoprost treated eyes.前列腺素类药物和贝美前列素治疗眼的泪液生物标志物。
PLoS One. 2018 Aug 6;13(8):e0201740. doi: 10.1371/journal.pone.0201740. eCollection 2018.
7
Clinical usefulness of prognostic biomarkers in optic neuritis.视神经炎预后生物标志物的临床应用。
Eur J Neurol. 2018 Apr;25(4):614-618. doi: 10.1111/ene.13553. Epub 2018 Feb 6.
8
Ciliary neurotrophic factor in patients with primary open-angle glaucoma and age-related cataract.原发性开角型青光眼和年龄相关性白内障患者的睫状神经营养因子
Mol Vis. 2017 Nov 17;23:799-809. eCollection 2017.
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Brain-Derived Neurotrophic Factor in Patients with Primary Open-Angle Glaucoma and Age-related Cataract.原发性开角型青光眼和年龄相关性白内障患者的脑源性神经营养因子
Curr Eye Res. 2018 Feb;43(2):224-231. doi: 10.1080/02713683.2017.1396617. Epub 2017 Nov 9.
10
Age-related neurodegenerative disease associated pathways identified in retinal and vitreous proteome from human glaucoma eyes.从人青光眼眼中的视网膜和玻璃体蛋白质组中鉴定出与年龄相关的神经退行性疾病相关途径。
Sci Rep. 2017 Oct 4;7(1):12685. doi: 10.1038/s41598-017-12858-7.

青光眼的分子生物标志物

Molecular Biomarkers for Glaucoma.

作者信息

Beykin Gala, Goldberg Jeffrey L

机构信息

Byers Eye Institute at Stanford University, 2452 Watson Ct, Palo Alto, CA 94303.

出版信息

Curr Ophthalmol Rep. 2019;7(3):171-176. doi: 10.1007/s40135-019-00213-0. Epub 2019 Jul 23.

DOI:10.1007/s40135-019-00213-0
PMID:33133776
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7597904/
Abstract

PURPOSE OF REVIEW

This article summarizes the current studies on molecular biomarkers with potential implications in diagnosis, prognosis, and response to treatment in patients with glaucoma.

RECENT FINDINGS

Important advances have occurred in the understanding of the pathogenesis of glaucomatous neurodegeneration. Protein biomarkers associated with inflammatory, neurodegenerative, and other molecular pathways have been described in glaucoma patients in tear film, aqueous fluid, vitreous fluid, and serum, however, we are still far from having a clear picture of the whole molecular network that relates to the disease and its implications in clinical use.

SUMMARY

Although more studies are needed, current and emerging molecular biomarkers candidates in glaucoma may eventually transition into clinical use and contribute to outline the concept of precision medicine and precision health in glaucoma.

摘要

综述目的

本文总结了目前关于分子生物标志物的研究,这些生物标志物对青光眼患者的诊断、预后及治疗反应可能具有潜在影响。

最新发现

在青光眼性神经变性发病机制的理解方面取得了重要进展。在泪膜、房水、玻璃体和血清中的青光眼患者中,已描述了与炎症、神经退行性变及其他分子途径相关的蛋白质生物标志物,然而,我们距离清晰了解与该疾病相关的整个分子网络及其在临床应用中的意义仍有很大差距。

总结

尽管还需要更多研究,但目前及新出现的青光眼分子生物标志物候选物最终可能会转化为临床应用,并有助于勾勒青光眼精准医学和精准健康的概念。