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早期视网膜萎缩可预测急性视神经炎后长期视力损害。

Early retinal atrophy predicts long-term visual impairment after acute optic neuritis.

机构信息

Center of Neuroimmunology, Institut d'Investigacions Biomediques August Pi i Sunyer (IDIBAPS), Barcelona, Spain/Department of Ophthalmology, Hospital Clinic, Barcelona, Spain.

Center of Neuroimmunology, Institut d'Investigacions Biomediques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.

出版信息

Mult Scler. 2018 Aug;24(9):1196-1204. doi: 10.1177/1352458517718628. Epub 2017 Jul 3.

Abstract

BACKGROUND

Visual recovery after optic neuritis (ON) used to be defined as good, although patients frequently complain of poor vision.

METHODS

We carried out a prospective study on 38 consecutive patients with acute ON followed monthly for 6 months and evaluated high- and low-contrast visual acuity (HCVA and LCVA, respectively), quality of vision (National Eye Institute Visual Function Questionnaire-25 (NEI-VFQ-25)), visual fields, and retinal thickness by spectral domain optical coherence tomography (OCT).

RESULTS

We found significant impaired LCVA and color vision in ON eyes 6 months after acute ON, which impact on quality of life. LCVA and color vision were correlated with the thicknesses of the ganglion cell and inner plexiform layer (GCIPL; 2.5% LCVA r = 0.65 and p = 0.0001; color vision r = 0.75 and p < 0.0001) and that of the peripapillary retinal nerve fiber layer (pRNFL; LCVA r = 0.43 and p = 0.0098; color vision r = 0.62 and p < 0.0001). Linear regression models that included the change in the GCIPL and pRNFL thicknesses from baseline to month 1 after onset explained 47% of the change in 2.5% LCVA and 67% of the change of color vision acuity. When adjusting for the value of visual acuity at baseline, predictors of the change in vision from baseline to month 6 achieved similar performance for all three types of vision (HCVA, LCVA, and color vision).

CONCLUSION

Monitoring retinal atrophy by OCT within the first month after ON onset allows individuals at a high risk of residual visual impairment to be identified.

摘要

背景

视神经炎(ON)后的视觉恢复过去被定义为良好,尽管患者经常抱怨视力不佳。

方法

我们对 38 例连续急性 ON 患者进行了前瞻性研究,每月随访 6 个月,并评估高对比度视力(HCVA)和低对比度视力(LCVA)、视力质量(国家眼科研究所视觉功能问卷-25 项(NEI-VFQ-25))、视野和视网膜厚度通过光谱域光学相干断层扫描(OCT)。

结果

我们发现急性 ON 后 6 个月,ON 眼的 LCVA 和色觉明显受损,影响生活质量。LCVA 和色觉与神经节细胞和内丛状层(GCIPL)的厚度相关(2.5% LCVA r = 0.65,p = 0.0001;色觉 r = 0.75,p < 0.0001)和视盘周围视网膜神经纤维层(pRNFL;LCVA r = 0.43,p = 0.0098;色觉 r = 0.62,p < 0.0001)。包括从发病到发病后 1 个月 GCIPL 和 pRNFL 厚度变化在内的线性回归模型解释了 2.5% LCVA 变化的 47%和色觉锐度变化的 67%。在调整视力基线值后,从基线到第 6 个月视力变化的预测因子在所有三种视力类型(HCVA、LCVA 和色觉)中均具有相似的表现。

结论

在 ON 发病后 1 个月内通过 OCT 监测视网膜萎缩,可以识别出视力残留损害风险较高的个体。

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