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本文引用的文献

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Systemic and ocular fluid compounds as potential biomarkers in age-related macular degeneration.全身和眼内液化合物作为年龄相关性黄斑变性的潜在生物标志物
Surv Ophthalmol. 2018 Jan-Feb;63(1):9-39. doi: 10.1016/j.survophthal.2017.05.003. Epub 2017 May 15.
2
Clinical Relevance of Biomarkers of Oxidative Stress.氧化应激生物标志物的临床相关性
Antioxid Redox Signal. 2015 Nov 10;23(14):1144-70. doi: 10.1089/ars.2015.6317. Epub 2015 Oct 26.
3
Increased systemic oxidative stress in patients with keratoconus.圆锥角膜患者全身氧化应激增加。
Eye (Lond). 2014 Mar;28(3):285-9. doi: 10.1038/eye.2013.262. Epub 2013 Dec 6.
4
Vascular reactivity of optic nerve head and retinal blood vessels in glaucoma--a review.青光眼患者视神经头和视网膜血管的血管反应性——综述。
Microcirculation. 2010 Oct;17(7):568-81. doi: 10.1111/j.1549-8719.2010.00045.x.
5
Variability of serum oxidative stress biomarkers relative to biochemical data and clinical parameters of glaucoma patients.青光眼患者血清氧化应激生物标志物相对于生化数据和临床参数的变异性。
Mol Vis. 2010 Jul 9;16:1260-71.
6
The role of advanced oxidation protein products and total thiols in diabetic retinopathy.晚期氧化蛋白产物和总硫醇在糖尿病视网膜病变中的作用。
Eur J Ophthalmol. 2008 Sep-Oct;18(5):792-8. doi: 10.1177/112067210801800521.
7
Oxygen and blood flow: players in the pathogenesis of glaucoma.氧气与血流:青光眼发病机制中的因素
Mol Vis. 2008 Jan 31;14:224-33.
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Oxidative stress is an early event in hydrostatic pressure induced retinal ganglion cell damage.氧化应激是静水压诱导视网膜神经节细胞损伤过程中的早期事件。
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9
Oxidative stress in hepatitis C infected end-stage renal disease subjects.丙型肝炎感染的终末期肾病患者的氧化应激
BMC Infect Dis. 2006 Jul 14;6:114. doi: 10.1186/1471-2334-6-114.
10
Pseudoexfoliation syndrome and its antioxidative protection deficiency as risk factors for age-related cataract.假性剥脱综合征及其抗氧化保护缺陷作为年龄相关性白内障的危险因素
Eur J Ophthalmol. 2006 Mar-Apr;16(2):268-73. doi: 10.1177/112067210601600212.

非动脉炎性前部缺血性视神经病变中的系统性氧化应激。

Systemic oxidative stress in non-arteritic anterior ischemic optic neuropathy.

机构信息

Department of Ophtalmology, Kayseri Training and Research Hospital, Kayseri, Turkey.

Department of Ophthalmology, Faculty of Medicine, Erciyes University, Kayseri, Turkey.

出版信息

Eye (Lond). 2019 Jul;33(7):1140-1144. doi: 10.1038/s41433-019-0388-0. Epub 2019 Mar 4.

DOI:10.1038/s41433-019-0388-0
PMID:30833666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6707156/
Abstract

PURPOSE

To investigate whether the serum total oxidant status (TOS), total antioxidant status (TAS), advanced oxidation protein products (AOPP), and thiol parameters could play a role in the pathogenesis of non-arteritic anterior ischemic optic neuropathy (NA-AION).

METHODS

In this study, 18 newly diagnosed NA-AION patients and 17 healthy subjects (control group) were included. Serum plasma TOS and TAS, AOPP, and thiol parameters were measured by spectrophotometric method and the results were compared.

RESULTS

Mean age of the patients and the controls were 60.8 ± 8.4 and 61.9 ± 9.4 years, respectively (p = 0.729). There were no significant differences between the patients and the control group with regard to the values of TAS, TOS, AOPP, and thiol (p = 0.869, p = 0.863, p = 0.040, p = 0.314; respectively). There was a positive correlation between TOS and thiol (p = 0.002, r = 0.681).

CONCLUSION

We found no significant relationship between systemic oxidative parameters and NA-AION. However, this study should be accepted as a pilot investigation and needs to be validated.

摘要

目的

探讨血清总氧化剂状态(TOS)、总抗氧化状态(TAS)、晚期氧化蛋白产物(AOPP)和巯基参数是否在非动脉炎性前部缺血性视神经病变(NA-AION)发病机制中起作用。

方法

本研究纳入了 18 例新诊断的 NA-AION 患者和 17 例健康受试者(对照组)。采用分光光度法测定血清血浆 TOS 和 TAS、AOPP 和巯基参数,并比较结果。

结果

患者和对照组的平均年龄分别为 60.8±8.4 岁和 61.9±9.4 岁(p=0.729)。患者与对照组之间 TAS、TOS、AOPP 和巯基的差异无统计学意义(p=0.869、p=0.863、p=0.040、p=0.314)。TOS 与巯基之间存在正相关(p=0.002,r=0.681)。

结论

我们未发现全身氧化参数与 NA-AION 之间存在显著关系。然而,这项研究应被视为初步研究,需要进一步验证。