Amblyopia is a visual development deficit caused by abnormal visual experience in early life, mainly manifesting as defected visual acuity and binocular visual impairment, which is considered to reflect abnormal development of the brain rather than organic lesions of the eye. Previous studies have reported abnormal spontaneous brain activity in patients with amblyopia. However, the location of abnormal spontaneous activity in patients with amblyopia and the association between abnormal brain function activity and clinical deficits remain unclear. The purpose of this study is to analyze spontaneous brain functional activity abnormalities in patients with amblyopia and their associations with clinical defects using resting-state functional magnetic resonance imaging (fMRI) data. In this study, 31 patients with amblyopia and 31 healthy controls were enrolled for resting-state fMRI scanning. The results showed that spontaneous activity in the right angular gyrus, left posterior cerebellum, and left cingulate gyrus were significantly lower in patients with amblyopia than in controls, and spontaneous activity in the right middle temporal gyrus was significantly higher in patients with amblyopia. In addition, the spontaneous activity of the left cerebellum in patients with amblyopia was negatively associated with the best-corrected visual acuity of the amblyopic eye, and the spontaneous activity of the right middle temporal gyrus was positively associated with the stereoacuity. This study found that adult patients with amblyopia showed abnormal spontaneous activity in the angular gyrus, cerebellum, middle temporal gyrus, and cingulate gyrus. Furthermore, the functional abnormalities in the cerebellum and middle temporal gyrus may be associated with visual acuity defects and stereopsis deficiency in patients with amblyopia. These findings help explain the neural mechanism of amblyopia, thus promoting the improvement of the treatment strategy for amblyopia.
ObjectiveTo evaluate the changes in subfoveal choroidal thickness (SFCT) in amblyopic eyes.MethodsA evidence-based medicine study. Chinese and English as search terms for amblyopia and choroid was used to search literature in Wanfang, CNKI, and PubMed of National Library of Medicine. Incomplete or irrelevant literature and review literature were excluded. The literature was meta-analyzed using STATA 15.0. The weighted mean difference (WMD) and 95% confidence interval (CI) were selected as the estimated value of effect size, and subgroup analysis and sensitivity analysis were used to detect the source of heterogeneity.ResultsAccording to the search strategy, 75 articles were initially retrieved, and 15 articles were finally included for meta-analysis. A total of 650 patients with amblyopia, aged 3 to 65 years old, were included. The enhanced depth imaging technology of spectral domain optical coherence tomography was used to measure SFCT. The results of meta analysis showed that SFCT of amblyopic eyes was more effective than the contralateral eye (WMD=18.89 μm, 95% CI 14.81-22.98 μm, P＜0.001) and normal eyes were thicken (WMD=39.49 μm, 95% CI 33.88-45.09 μm, P＜0.001). There was no statistically significant difference in SFCT between anisometropic and strabismic amblyopia eyes (WMD=－5.03 μm, 95% CI －19.50-9.44 μm, P=0.495).ConclusionsThe SFCT of amblyopic eyes in amblyopic patients is thicker than that of the contralateral eye and normal eyes. There is no difference in SFCT between anisometropia and strabismus amblyopia.
【摘要】 目的 探讨儿童弱视治疗效果与疗程的关系。 方法 对2002年5月-2007年5月收治的25例弱视患儿进行戴镜、遮盖、红光闪烁及精细作业训练。3个月复查一次，12个月重新验光，随访12~60个月。 结果 25例弱视患儿经12~60个月随访，25例患儿均治愈，治愈疗程最少3个月，最长达60个月，平均24个月。 结论 儿童弱视只要早期发现，在12岁之前进行干预，早期治疗均可获得治愈。【Abstract】 Objective To discuss the relationship between the effect and duration of the treatment for children amblyopia. Methods Patients diagnosed as amblyopia were administered wearing glasses, occlusion, flashing red, and fine training from May 2002 to May 2007. Reexamination was done 3 months later after the treatment, and the refraction examination was done after 12 months. The follow-up time was from 12 to 60 months. Results The results showed that all of the 25 amblyopic children were cured. The treatment duration was from three months to 50 months with an average of 24 months. Conclusion As long as the amblyopia is detected at the early stage and treated before age 12, all the children can be cured.
目的:分析探讨单眼散光弱视患儿对比敏感度(CS)视功能的受损特点。方法:对正常儿童组36例、单眼散光弱视组34例、单眼非散光弱视组33例,共103例,用静态F.A.C.T图表和计算机Gabor斑CS检查程序分别检查患儿对侧眼、弱视眼及90°和180°两主子午线方向上的对比敏感度。结果:①单眼散光弱视组和单眼非散光弱视组的对侧眼、弱视眼的CS值在所有空间频率均较正常组的CS降低(Plt;0.05),表现为中、高空间频率区CS的明显受损(Plt;0.01)。②单眼散光弱视组的弱视眼在90°和180°两主子午线方向上的对比敏感度有显著差异(Plt;0.01)。结论:弱视儿童的对侧眼不正常。用计算机Gabor斑检查可以了解弱视散光儿童不同子午线上的CS存在的差异,明确定位弱子午线,并可以针对子午线性弱视,进一步开展知觉学习的治疗。
Purpose To identify the expression of alternatively spliced mRNA isoforms of the NMDA-R1 in the visual cortex of strabismic cats. Methods Two pai rs of normal and strabismic cats were used．The amblyopic cats had been made monocularly esotropic (by tenotomy) at the age of weeks，resulting in behavioral am blyopia．Animals were sacrificed about 6 months by intraperitoneal administration of Nembutal．Cryostat sections of fresh，frozen central visual cortex of the ats were cut to 20 micron thickness．A series of digoxygenin-labelled oligonucle otide probes basing on the human gene sequence were used for ISH．Control probes included sense oligonucleotides and short segment probes which were adjacent to ，but did not，span the splice junctions．A computer-assisted systematic morphometric ounting procedure was used to enumerate hybridising cells． Results The number of positive cells expressing NMDA-R1 mRNA in t he strabismic amblyopic cats was decreased，notably in layer IV of visual cortex (P＜0．0001)．The pattern of isoform expression varied between normal and strabismic amblyopic cats with decreased numbers of 1-a，1- b and 1-1 isoforms and apparently increased expression of 1-3 P ＜0．0001)，whereas no significant difference was found for the 1-2 and 1-4 isoforms (P＞0．05)． Conclusion Transcriptional inhibition of NMDA-R1 mRNA and of specifie isoforms may underlie the change in receptor expression．Alternatively，preferentialloss of neurones bearing particular NMDA-R1 isoforms and compensation with a proportional increase in cells expressing other isoforms may occurr during the critical period of visual plasticity． (Chin J Ocul Fundus Dis，2000，16：71-138)