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本文引用的文献

1
Tear fluid small molecular antioxidants profiling shows lowered glutathione in keratoconus.泪液小分子抗氧化剂分析显示,圆锥角膜患者谷胱甘肽水平降低。
Exp Eye Res. 2012 Oct;103:41-6. doi: 10.1016/j.exer.2012.07.010. Epub 2012 Aug 10.
2
Proteases, proteolysis and inflammatory molecules in the tears of people with keratoconus.角膜膨隆患者泪液中的蛋白酶、蛋白水解和炎症分子。
Acta Ophthalmol. 2012 Jun;90(4):e303-9. doi: 10.1111/j.1755-3768.2011.02369.x. Epub 2012 Mar 13.
3
Oxidative stress in keratoconus?圆锥角膜中的氧化应激?
Invest Ophthalmol Vis Sci. 2011 Nov 4;52(12):8592-7. doi: 10.1167/iovs.11-7732.
4
Oxidative stress in diseases of the human cornea.人类角膜疾病中的氧化应激
Free Radic Biol Med. 2008 Oct 15;45(8):1047-55. doi: 10.1016/j.freeradbiomed.2008.07.021. Epub 2008 Aug 3.
5
Hypersensitive response to oxidative stress in keratoconus corneal fibroblasts.圆锥角膜角膜成纤维细胞对氧化应激的超敏反应。
Invest Ophthalmol Vis Sci. 2008 Oct;49(10):4361-9. doi: 10.1167/iovs.08-1969. Epub 2008 May 30.
6
Abnormal rubbing and keratectasia.异常摩擦与角膜扩张。
Eye Contact Lens. 2007 Nov;33(6 Pt 1):265-71. doi: 10.1097/ICL.0b013e31814fb64b.
7
SOD1: a candidate gene for keratoconus.超氧化物歧化酶1:圆锥角膜的一个候选基因。
Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3345-51. doi: 10.1167/iovs.05-1500.
8
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.
9
Increased stress-induced generation of reactive oxygen species and apoptosis in human keratoconus fibroblasts.应激诱导人圆锥角膜成纤维细胞中活性氧生成增加及细胞凋亡。
Invest Ophthalmol Vis Sci. 2006 May;47(5):1902-10. doi: 10.1167/iovs.05-0828.
10
A new automated colorimetric method for measuring total oxidant status.一种用于测量总氧化剂状态的新型自动比色法。
Clin Biochem. 2005 Dec;38(12):1103-11. doi: 10.1016/j.clinbiochem.2005.08.008. Epub 2005 Oct 7.

圆锥角膜患者全身氧化应激增加。

Increased systemic oxidative stress in patients with keratoconus.

作者信息

Toprak I, Kucukatay V, Yildirim C, Kilic-Toprak E, Kilic-Erkek O

机构信息

Department of Ophthalmology, Servergazi State Hospital, Denizli, Turkey.

Department of Physiology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.

出版信息

Eye (Lond). 2014 Mar;28(3):285-9. doi: 10.1038/eye.2013.262. Epub 2013 Dec 6.

DOI:10.1038/eye.2013.262
PMID:24310241
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3965806/
Abstract

PURPOSE

To establish the effect of systemic oxidative stress on the pathogenesis of keratoconus by measuring serum total oxidant status (TOS) and total antioxidant status (TAS) in patients with keratoconus.

METHODS

Twenty-five patients with keratoconus (keratoconus group) and 25 age-sex-matched healthy subjects (control group) were enrolled in the study. Exclusion criteria were smoking habit, history of any other corneal pathology, systemic disease or inflammation, and current antioxidant or anti-inflammatory therapies. All participants underwent a detailed ophthalmological examination and corneal topography. Serum samples were obtained from all participants. Oxidative stress markers (TAS and TOS) were measured using a commercial kit and oxidative stress index (OSI) was calculated.

RESULTS

The study comprised 25 patients with keratoconus (mean age of 26.4±1.7 years) and 25 healthy control subjects (mean age of 26.6±1.7 years) (P>0.05). The serum TOS and OSI values were significantly higher in patients with keratoconus compared with those of the controls (P=0.036 and 0.037, respectively). However, serum TAS did not show significant difference between the keratoconus and control groups (P=0.497).

CONCLUSIONS

The higher levels of serum oxidant status and OSI in patients with keratoconus suggest that systemic oxidative stress might be involved in the pathogenesis of keratoconus.

摘要

目的

通过测量圆锥角膜患者血清总氧化剂状态(TOS)和总抗氧化剂状态(TAS),确定全身氧化应激在圆锥角膜发病机制中的作用。

方法

本研究纳入25例圆锥角膜患者(圆锥角膜组)和25例年龄、性别匹配的健康受试者(对照组)。排除标准包括吸烟习惯、任何其他角膜病变史、全身疾病或炎症史以及当前的抗氧化或抗炎治疗。所有参与者均接受详细的眼科检查和角膜地形图检查。采集所有参与者的血清样本。使用商用试剂盒测量氧化应激标志物(TAS和TOS)并计算氧化应激指数(OSI)。

结果

本研究包括25例圆锥角膜患者(平均年龄26.4±1.7岁)和25例健康对照者(平均年龄26.6±1.7岁)(P>0.05)。与对照组相比,圆锥角膜患者的血清TOS和OSI值显著更高(分别为P=0.036和0.037)。然而,圆锥角膜组和对照组之间的血清TAS没有显著差异(P=0.497)。

结论

圆锥角膜患者血清氧化剂状态和OSI水平较高,提示全身氧化应激可能参与圆锥角膜的发病机制。