• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

非动脉炎性前部缺血性视神经病变的结构-功能分析及结局的年龄相关差异

Structure-Function Analysis of Nonarteritic Anterior Ischemic Optic Neuropathy and Age-Related Differences in Outcome.

作者信息

Sun Ming-Hui, Liao Yaping Joyce

机构信息

Department of Ophthalmology (MHS, YJL), Stanford University School of Medicine, Stanford, California; and Department of Ophthalmology (MHS), Chang Gung Memorial Hospital, Chang Gung University, Taoyuan, Taiwan.

出版信息

J Neuroophthalmol. 2017 Sep;37(3):258-264. doi: 10.1097/WNO.0000000000000521.

DOI:10.1097/WNO.0000000000000521
PMID:28538035
Abstract

BACKGROUND

The optic nerve head is vulnerable to ischemia leading to anterior ischemic optic neuropathy (AION), the most common acute optic neuropathy in those older than 50 years of age.

METHODS

We performed a cross-sectional study of 55 nonarteritic anterior ischemic optic neuropathy (NAION) eyes in 34 patients to assess clinical outcome and perform structure-function correlations.

RESULTS

The peak age of NAION onset was between 50 and 55 years. Sixty-seven percent of patients presented with their first event between the ages of 40 and 60 years, and 32% presented at ≤50 years. Those with NAION onset at age ≤50 years did not have significantly better visual outcome per logMAR visual acuity, automated perimetric mean deviation (PMD) or optical coherence tomography (OCT) measurements. Kaplan-Meier survival curve and multivariate Cox proportional regression analysis showed that age >50 years at NAION onset was associated with greater risk of second eye involvement, with hazard ratio of 20. Older age at onset was significantly correlated with greater thinning of the ganglion cell complex (GCC) (P = 0.022) but not with logMAR visual acuity, PMD, or thinning of retinal nerve fiber layer (RNFL). Using area under receiver operating characteristic curve analyses, we found that thinning of RNFL and GCC was best able to predict visual outcome, and that mean RNFL thickness >65 μm or macular GCC thickness >55 μm significantly correlated with good visual field outcome.

CONCLUSIONS

We showed that NAION onset at age >50 years had a greater risk of second eye involvement. Patients with OCT mean RNFL thickness >65 μm and mean macular ganglion cell complex thickness >55 μm had better visual outcomes.

摘要

背景

视神经乳头易受缺血影响,导致前部缺血性视神经病变(AION),这是50岁以上人群中最常见的急性视神经病变。

方法

我们对34例患者的55只非动脉性前部缺血性视神经病变(NAION)眼进行了横断面研究,以评估临床结局并进行结构-功能相关性分析。

结果

NAION发病的高峰年龄在50至55岁之间。67%的患者首次发病年龄在40至60岁之间,32%的患者发病年龄≤50岁。发病年龄≤50岁的NAION患者,根据对数最小分辨角视力、自动视野平均偏差(PMD)或光学相干断层扫描(OCT)测量,其视力结局并无显著更好。Kaplan-Meier生存曲线和多变量Cox比例回归分析显示,NAION发病时年龄>50岁与对侧眼受累风险更高相关,风险比为20。发病时年龄较大与神经节细胞复合体(GCC)变薄更显著相关(P = 0.022),但与对数最小分辨角视力、PMD或视网膜神经纤维层(RNFL)变薄无关。通过受试者工作特征曲线下面积分析,我们发现RNFL和GCC变薄最能预测视力结局,且平均RNFL厚度>65μm或黄斑GCC厚度>55μm与良好的视野结局显著相关。

结论

我们表明,NAION发病年龄>50岁时对侧眼受累风险更高。OCT平均RNFL厚度>65μm且平均黄斑神经节细胞复合体厚度>55μm的患者视力结局更好。

相似文献

1
Structure-Function Analysis of Nonarteritic Anterior Ischemic Optic Neuropathy and Age-Related Differences in Outcome.非动脉炎性前部缺血性视神经病变的结构-功能分析及结局的年龄相关差异
J Neuroophthalmol. 2017 Sep;37(3):258-264. doi: 10.1097/WNO.0000000000000521.
2
Ganglion cell analysis at acute episode of nonarteritic anterior ischemic optic neuropathy to predict irreversible damage. A prospective study.非动脉炎性前部缺血性视神经病变急性期的神经节细胞分析以预测不可逆损伤。一项前瞻性研究。
Graefes Arch Clin Exp Ophthalmol. 2016 Sep;254(9):1793-800. doi: 10.1007/s00417-016-3425-8. Epub 2016 Jul 15.
3
Comparison of peripapillary retinal nerve fiber layer loss and visual outcome in fellow eyes following sequential bilateral non-arteritic anterior ischemic optic neuropathy.双侧非动脉性前部缺血性视神经病变先后发病后,对侧眼视乳头周围视网膜神经纤维层损失与视觉预后的比较。
Curr Eye Res. 2015 May;40(6):632-7. doi: 10.3109/02713683.2014.952829. Epub 2014 Aug 25.
4
Optic nerve head morphology in primary open-angle glaucoma and nonarteritic anterior ischaemic optic neuropathy measured with spectral domain optical coherence tomography.应用谱域光学相干断层扫描测量原发性开角型青光眼和非动脉炎性前部缺血性视神经病变的视神经头形态。
Acta Ophthalmol. 2018 Dec;96(8):e1018-e1024. doi: 10.1111/aos.13804. Epub 2018 Sep 21.
5
Follow-up of nonarteritic anterior ischemic optic neuropathy with optical coherence tomography.非动脉炎性前部缺血性视神经病变的光学相干断层扫描随访
Ophthalmology. 2007 Dec;114(12):2338-44. doi: 10.1016/j.ophtha.2007.05.042. Epub 2007 Aug 27.
6
Retinal Ganglion Cell Loss Precedes Retinal Nerve Fiber Thinning in Nonarteritic Anterior Ischemic Optic Neuropathy.在非动脉炎性前部缺血性视神经病变中,视网膜神经节细胞丢失先于视网膜神经纤维变薄。
J Neuroophthalmol. 2016 Jun;36(2):141-6. doi: 10.1097/WNO.0000000000000345.
7
Change of Retinal Nerve Layer Thickness in Non-Arteritic Anterior Ischemic Optic Neuropathy Revealed by Fourier Domain Optical Coherence Tomography.傅里叶域光学相干断层扫描揭示非动脉炎性前部缺血性视神经病变中视网膜神经纤维层厚度的变化
Curr Eye Res. 2016 Aug;41(8):1076-1081. doi: 10.3109/02713683.2015.1084640. Epub 2015 Nov 18.
8
Papillomacular bundle and inner retinal thicknesses correlate with visual acuity in nonarteritic anterior ischemic optic neuropathy.乳头黄斑束和内层视网膜厚度与前部非动脉炎性缺血性视神经病变的视力相关。
Invest Ophthalmol Vis Sci. 2015 Jan 13;56(2):682-92. doi: 10.1167/iovs.14-15314.
9
Macular thickness predictive of visual field sensitivity in ischaemic optic neuropathy.黄斑厚度可预测缺血性视神经病变的视野敏感性。
Acta Ophthalmol. 2012 Sep;90(6):e463-9. doi: 10.1111/j.1755-3768.2012.02467.x. Epub 2012 Jun 13.
10
Spectral-Domain Optical Coherence Tomography of the Vitreopapillary Interface in Acute Nonarteritic Anterior Ischemic Optic Neuropathy.急性非动脉炎性前部缺血性视神经病变中玻璃体内视乳头界面的谱域光相干断层扫描。
Am J Ophthalmol. 2018 Nov;195:199-208. doi: 10.1016/j.ajo.2018.08.002. Epub 2018 Aug 8.

引用本文的文献

1
Hematological indicators and ocular parameters in patients with non-arteritic anterior ischemic optic neuropathy.非动脉炎性前部缺血性视神经病变患者的血液学指标和眼部参数
Int Ophthalmol. 2025 Aug 13;45(1):333. doi: 10.1007/s10792-025-03714-z.
2
Variability of relationship between inner-retinal structural changes and visual dysfunction in optic neuropathy.视神经病变中外层视网膜结构变化与视觉功能障碍关系的可变性。
Sci Rep. 2024 May 27;14(1):12069. doi: 10.1038/s41598-024-62704-w.
3
Synergistic Protection of Retinal Ganglion Cells (RGCs) by SARM1 Inactivation with CNTF in a Rodent Model of Nonarteritic Anterior Ischemic Optic Neuropathy.
SARM1 失活与 CNTF 协同保护在非动脉炎性前部缺血性视神经病变啮齿动物模型中的视网膜神经节细胞(RGC)。
Cells. 2024 Jan 23;13(3):202. doi: 10.3390/cells13030202.
4
Peripapillary and macular microvasculature features of non-arteritic anterior ischemic optic neuropathy.非动脉炎性前部缺血性视神经病变的视乳头周围和黄斑部微血管特征
Front Med (Lausanne). 2023 Jan 12;9:1033838. doi: 10.3389/fmed.2022.1033838. eCollection 2022.
5
Factors Associated With Visual Acuity in Non-arteritic Ischemic Optic Neuropathy Patients: A Five-Year Cross-Sectional Study.非动脉炎性缺血性视神经病变患者视力相关因素:一项为期五年的横断面研究。
Cureus. 2022 Sep 14;14(9):e29156. doi: 10.7759/cureus.29156. eCollection 2022 Sep.
6
Risk factors and visual outcome of Non-Arteritic Ischemic Optic Neuropathy (NAION): Experience of a tertiary center in Kuwait.非动脉炎性缺血性视神经病变(NAION)的风险因素和视觉预后:科威特一家三级中心的经验。
PLoS One. 2021 Feb 18;16(2):e0247126. doi: 10.1371/journal.pone.0247126. eCollection 2021.
7
Analysis of Macular Microperimetry Characteristics in Non-Arteritic Anterior Ischemic Optic Neuropathy.非动脉炎性前部缺血性视神经病变的黄斑微视野特征分析
Med Sci Monit. 2020 Nov 20;26:e928274. doi: 10.12659/MSM.928274.
8
Early diagnostic value of optical coherence tomography in the clinical prediction model for optic nerve injury in saddle space occupying patients.光学相干断层扫描在鞍区占位患者视神经损伤临床预测模型中的早期诊断价值
Saudi J Biol Sci. 2020 Mar;27(3):820-826. doi: 10.1016/j.sjbs.2019.12.043. Epub 2020 Jan 8.
9
Neuroenhancement and neuroprotection by oral solution citicoline in non-arteritic ischemic optic neuropathy as a model of neurodegeneration: A randomized pilot study.口服胞磷胆碱治疗非动脉炎性前部缺血性视神经病变模型的神经增强和神经保护作用:一项随机初步研究。
PLoS One. 2019 Jul 26;14(7):e0220435. doi: 10.1371/journal.pone.0220435. eCollection 2019.
10
Direct targeting of the mouse optic nerve for therapeutic delivery.直接靶向小鼠视神经进行治疗性给药。
J Neurosci Methods. 2019 Feb 1;313:1-5. doi: 10.1016/j.jneumeth.2018.10.038. Epub 2018 Oct 31.