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The Association between Different Ocular Dominance and Fixation Preferences in Adolescents with Intermittent Exotropia 青少年间歇性外斜视不同眼优势与注视偏好的关系
Pub Date : 2019-10-25 DOI: 10.3760/CMA.J.ISSN.1674-845X.2019.10.004
Yao Tang, Xiaoning Li, Bin Zhang, Qing-lin Xu, Haoran Wu, Zhikuan Yang
Objective: To investigate the association between different ocular dominance and fixation preferences in adolescents with intermittent exotropia (IXT). Methods: In this case serial study, a total of 43 patients with IXT from Aier Institute of Optometry and Vision Science from July to December 2018 participated. With full refractive error correction, the hole-in-the-card test was used to identify sighting dominance, the near point of convergence test was used to determine motor dominance, and a continuous flash technique based on a Gabor patch was used to determine ocular sensory dominance. The preferred eye for fixation was determined by Mayo's office control scale when observing a target at long distance. The degree of agreement between the dominant eye and the preferred eye for fixation was quantified with Kappa statistics. And the association between the above-mentioned concordance and ocular dominance index (ODI) was analyzed by logistic regression. Results: For a total of 43 patients with IXT, sighting dominance, motor dominance, and sensory dominance showed moderate agreement with fixation preference (the Kappa values were 0.46, 0.43, and 0.68, respectively, P<0.001). When there was a clear sensory dominance, the agreement between the sensory dominant eye and the preferred fixation eye was fairly high (Kappa values was 0.86, P<0.001), while the agreements of the other two kinds of ocular dominance and fixation preference were still moderate (the Kappa values were 0.57 and 0.44, respectively, P<0.01). Logistic regression showed that the probability for the preferred fixation eye to agree with the sensory dominant eye increased with the value of ODI (B=0.53, OR=1.70, P<0.001), the greater the ODI value, the higher the probability for agreement between the sensory dominant eye and the preferred fixation eye. Conclusion: For IXT adolescents, there is a consistent relationship between ocular dominance and fixation preference. The results of sensory ocular dominance are more closely related to the preferred eye for fixation, especially when there is a clear sensory dominance, which is more reliable than a sighting dominance test or motor dominance test. Key words: intermittent exotropia; ocular dominance; fixation preference; adolescents
目的:探讨青少年间歇性外斜视(IXT)不同眼优势与注视偏好的关系。方法:选取2018年7月至12月爱尔视光与视觉科学研究所43例IXT患者进行病例系列研究。在完全屈光误差矫正后,使用卡中孔测试来识别视觉优势,使用近会聚点测试来确定运动优势,使用基于Gabor贴片的连续闪光技术来确定眼感觉优势。在远距离观察目标时,首选的注视眼由Mayo办公室控制量表决定。用Kappa统计量化优势眼和首选眼注视的一致程度。采用logistic回归分析上述一致性与眼优势指数(ODI)的关系。结果:在43例IXT患者中,视觉优势、运动优势和感觉优势与注视偏好表现出中等程度的一致性(Kappa值分别为0.46、0.43和0.68,P<0.001)。当感觉优势明显时,感觉优势眼与首选注视眼的一致性较高(Kappa值为0.86,P<0.001),而其他两种眼的优势眼与注视偏好的一致性仍为中等(Kappa值分别为0.57和0.44,P<0.01)。Logistic回归分析结果表明,首选注视眼与感觉优势眼一致的概率随ODI值的增加而增加(B=0.53, OR=1.70, P<0.001), ODI值越大,感觉优势眼与首选注视眼一致的概率越高。结论:对于IXT青少年,眼优势与注视偏好之间存在一致的关系。感觉眼优势测试的结果与首选注视眼的关系更为密切,特别是当存在明显的感觉优势时,它比视觉优势测试或运动优势测试更可靠。关键词:间歇性外斜视;眼优势;固定的偏好;青少年
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引用次数: 0
Comparison of Refractive Measures of Three Autorefractors in School-Aged Children and Adolescents 学龄儿童和青少年使用三种自折射仪的屈光测量比较
Pub Date : 2019-10-25 DOI: 10.3760/CMA.J.ISSN.1674-845X.2019.10.001
Chunjie Lu, D. Song, Yize Chen, Changsen Tu, X. Mao, Liangde Xu
Objective: To assess the validity, differences and agreements among measurements of refractive status in school-aged children and adolescents using Goaleye RM-9000, Nidek AR-1 and Topcon RM-800. Methods: In this prospective study, 449 individuals (449 right eyes) aged from 9 to 18 from Eye Hospital, Wenzhou Medical University were measured in turns by the three autorefractors for their refractive status in random sequence from May to June, 2019. Then a professional optometrist conducted a subjective refraction for them by phoropter. All measurements by the three autorefractors were compared using a Friedman test, and measurements by the three autorefractors were compared with the subjective refraction respectively using Wilcoxon signed ranks test. Results: The median of spherical equivalent (SE) from Goaleye RM-9000, Nidek AR-1, Topcon RM-800 and the subjective refraction were -2.38(2.63)D, -2.63(2.44)D, -2.75(2.56)D and -2.38(2.50)D, respectively. There were significant differences among the SE of the three autorefractors in the refraction measurement of school-aged children and adolescents (χ2=384.893, P<0.001). There were no significant differences between the SE of Goaleye RM-9000 and subjective refraction (Z=-0.199, P=0.842), There were significant differences between the SE of Nidek AR-1 and subjective refraction (Z=-11.753, P<0.001), There were significant differences between the SE of Topcon RM-800 and subjective refraction (Z=-15.733, P<0.001). Conclusion: The measurements conducted by Goaleye RM-9000 and Nidek AR-1 were more accurate than by Topcon RM-800. There were significant differences among the results of the three autorefractors in the refraction measurement of school-aged children and adolescents. Key words: refractive error; refraction; spherical equivalent; agreement; children and adolescents
目的:评价Goaleye RM-9000、Nidek AR-1和Topcon RM-800测量学龄儿童和青少年屈光状态的有效性、差异和一致性。方法:本前瞻性研究于2019年5月至6月随机顺序对温州医科大学眼科医院9 ~ 18岁的449例(449只右眼)患者进行自折射仪轮流测量。然后由专业验光师用照相机为他们进行主观折射。用Friedman检验比较三个自折射仪的测量值,用Wilcoxon符号秩检验比较三个自折射仪的测量值与主观折射值。结果:Goaleye RM-9000、Nidek AR-1、Topcon RM-800的球等效(SE)中位数和主观屈光分别为-2.38(2.63)D、-2.63(2.44)D、-2.75(2.56)D和-2.38(2.50)D。三种自折射仪在学龄儿童和青少年屈光测量中的SE差异有统计学意义(χ2=384.893, P<0.001)。Goaleye RM-9000的SE与主观屈光无显著差异(Z=-0.199, P=0.842), Nidek AR-1的SE与主观屈光有显著差异(Z=-11.753, P<0.001), Topcon RM-800的SE与主观屈光有显著差异(Z=-15.733, P<0.001)。结论:Goaleye RM-9000和Nidek AR-1的测量精度高于Topcon RM-800。三种自折射仪对学龄儿童和青少年的屈光度测量结果有显著性差异。关键词:屈光不正;折射;球形等效;协议;儿童和青少年
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引用次数: 1
Clinical Observation of Wavefront-Guided Transepithelial Photorefractive Keratectomy with Simultaneous Accelerated Corneal Collagen Cross-Linking in Early Keratoconic Patients 波前引导经上皮性光屈光性角膜切除术同时加速角膜胶原交联治疗早期角膜锥形患者的临床观察
Pub Date : 2019-10-25 DOI: 10.3760/CMA.J.ISSN.1674-845X.2019.10.006
Fen Chen, Dan Shen, X. Lei, Qian Chen, Peng Song, Kai Liao, Qingyan Zeng
Objective: To observe the efficacy and safety of wavefront-guided transepithelial photorefractive keratectomy (WG-TransPRK) with simultaneous accelerated corneal collagen cross-linking (A-CXL) in early-stage keratoconus. Methods: In this retrospective study, twelve eyes of 7 patients with early keratoconus underwent simultaneous WG-TransPRK with A-CXL. Visual acuity, refractive status, topography, confocal microscopy and aberrations were examined before treatment and 1 week, 1 month, 3 months, 6 months, and 12 months after surgery. Data were analyzed by paired t test. Results: Twelve months after the surgery, the average UCVA improved from 0.77±0.25 LogMAR to 0.34±0.26 LogMAR (P=0.001), the average BCVA improved from 0.18±0.21 LogMAR to 0.05±0.09 LogMAR (P=0.034). The K1, K2 spherical equivalent of the cornea were reduced from 43.85±1.72 D and 46.64±2.36 D to 40.63±2.13 D (t=9.48, P=0.001) and 42.27±1.89 D (t=8.29, P=0.001), respectively. And Kmax decreasing from 48.88±3.62 D to 45.43±1.54 D (t=3.02, P=0.014). Sub-basal nerve density decreased (P=0.001). The anterior and mid-stromal keratocyte density was reduced also (P<0.05). No significant change was detected in the deep stromal and endothelial cell density. The aberration parameters decreased in the 4 mm diameter analysis area (P<0.05). Conclusion: WG-TransPRK combined with simultaneous A-CXL is safe and effective for the treatment of early-stage keratoconus, with an improvement in visual acuity. Key words: photorefractive keratectomy; corneal collagen cross-linking; keratoconus; aberration
目的:观察波前引导经上皮性光屈光性角膜切除术(WG-TransPRK)联合加速角膜胶原交联(A-CXL)治疗早期圆锥角膜的疗效和安全性。方法:回顾性研究7例早期圆锥角膜患者12眼同时行WG-TransPRK和A-CXL。治疗前及术后1周、1个月、3个月、6个月、12个月检查视力、屈光状态、地形、共聚焦显微镜和像差。数据分析采用配对t检验。结果:术后12个月,平均UCVA由0.77±0.25 LogMAR改善至0.34±0.26 LogMAR (P=0.001),平均BCVA由0.18±0.21 LogMAR改善至0.05±0.09 LogMAR (P=0.034)。角膜K1、K2的球面等效度分别从43.85±1.72 D和46.64±2.36 D降至40.63±2.13 D (t=9.48, P=0.001)和42.27±1.89 D (t=8.29, P=0.001)。Kmax由48.88±3.62 D降至45.43±1.54 D (t=3.02, P=0.014)。基底下神经密度降低(P=0.001)。前基质、中基质角质细胞密度明显降低(P<0.05)。深层间质和内皮细胞密度未见明显变化。在直径为4 mm的分析区,像差参数降低(P<0.05)。结论:WG-TransPRK联合A-CXL治疗早期圆锥角膜安全有效,视力明显改善。关键词:光屈光性角膜切除术;角膜胶原交联;圆锥形角膜;像差
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引用次数: 0
Clinical Efficacy and Posterior Corneal Elevation of Small Incision Lenticule Extraction in High Myopes 高近视眼小切口晶状体拔除术的临床疗效及角膜后抬高
Pub Date : 2019-10-25 DOI: 10.3760/CMA.J.ISSN.1674-845X.2019.10.009
Luci M. Chen, Xiaoying Wu, D. Wen, B. Xiao, Shuang-zhen Liu, Chenling Li, Shengfa Hu
Objective: To investigate the safety, efficacy, predictability, stability and posterior corneal elevation of small incision lenticule extraction (SMILE) for high myopia. Methods: This study was a descriptive longitudinal study. A retrospective analysis was performed on 37 patients (67 eyes) with high myopia (spherical equivalent, -10.75--6.25 D) who underwent SMILE in the Ophthalmology Department of Xiangya Hospital, Central South University in 2016. Uncorrected visual acuity (UCVA), best corrected visual acuity (BCVA), refractive error, intraocular pressure (IOP), axial length, and corneal topography were measured preoperatively and postoperatively at 1 day, 1 month, 3 months and 6 months. The data before and after surgery and the influencing factors were analyzed by a generalized estimation equation. Results: The UCVA (LogMAR) of the high myopes was -0.1 (-0.2, 0), the effective index was 0.83±0.20, the BCVA (LogMAR) was -0.2 (-0.2, -0.2), and the safety index was 1.03±0.16 at 6 months after SMILE. The degree of myopia increased gradually from 1 month to 6 months postoperatively. The refractive error was -0.25 (-0.50, 0) D and regression was -0.25 (-0.50, 0) D at 6 months after SMILE. UCVA was positively correlated with age, refractive error and regression and was negatively correlated with age after surgery. The difference value of the posterior corneal surface was 0.030±0.006 mm before and 0.046±0.012 mm 6 months after surgery, which was lower than that in the first month, and was not statistically different at 3 months. Difference and Δdifference at 6 months were positively correlated with mPTA (modified percent tissue altered). Conclusions: This study demonstrates SMILE to be a safe, effective, predictable and stable procedure for the treatment of high myopia, with a slight myopic regression at 6 months after surgery, especially in elders. The posterior corneal surface shifts forward postoperatively and partially recovers after 3 months; the amounts are associated with mPTA. Key words: small incision lenticule extraction; high myopia; posterior corneal surface
目的:探讨小切口晶状体摘出术(SMILE)治疗高度近视的安全性、有效性、可预见性、稳定性及角膜后抬高情况。方法:本研究为描述性纵向研究。回顾性分析2016年在中南大学湘雅医院眼科行SMILE手术的37例(67只眼)高度近视(球面等效度-10.75—6.25 D)患者。分别于术前、术后1天、1个月、3个月、6个月测量未矫正视力(UCVA)、最佳矫正视力(BCVA)、屈光不正、眼内压(IOP)、眼轴长度和角膜地形图。采用广义估计方程对手术前后数据及影响因素进行分析。结果:SMILE术后6个月,高近视眼UCVA (LogMAR)为-0.1(-0.2,0),有效指数为0.83±0.20,BCVA (LogMAR)为-0.2(-0.2,-0.2),安全指数为1.03±0.16。术后1 ~ 6个月近视程度逐渐增加。术后6个月,患者屈光误差为-0.25 (-0.50,0)D,视力回归为-0.25 (-0.50,0)D。UCVA与年龄、屈光不正、视力退化呈正相关,与术后年龄负相关。术后6个月角膜后表面差值分别为0.030±0.006 mm和0.046±0.012 mm,均低于术后1个月,3个月时差异无统计学意义。6个月时的差异和Δdifference与mPTA(组织改变百分比)呈正相关。结论:SMILE是一种安全、有效、可预测、稳定的治疗高度近视的方法,术后6个月近视有轻微消退,尤其是老年人。术后角膜后表面前移,3个月后部分恢复;数量与mPTA有关。关键词:小切口晶状体摘除;高度近视;后角膜表面
{"title":"Clinical Efficacy and Posterior Corneal Elevation of Small Incision Lenticule Extraction in High Myopes","authors":"Luci M. Chen, Xiaoying Wu, D. Wen, B. Xiao, Shuang-zhen Liu, Chenling Li, Shengfa Hu","doi":"10.3760/CMA.J.ISSN.1674-845X.2019.10.009","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1674-845X.2019.10.009","url":null,"abstract":"Objective: \u0000To investigate the safety, efficacy, predictability, stability and posterior corneal elevation of small incision lenticule extraction (SMILE) for high myopia. \u0000 \u0000 \u0000Methods: \u0000This study was a descriptive longitudinal study. A retrospective analysis was performed on 37 patients (67 eyes) with high myopia (spherical equivalent, -10.75--6.25 D) who underwent SMILE in the Ophthalmology Department of Xiangya Hospital, Central South University in 2016. Uncorrected visual acuity (UCVA), best corrected visual acuity (BCVA), refractive error, intraocular pressure (IOP), axial length, and corneal topography were measured preoperatively and postoperatively at 1 day, 1 month, 3 months and 6 months. The data before and after surgery and the influencing factors were analyzed by a generalized estimation equation. \u0000 \u0000 \u0000Results: \u0000The UCVA (LogMAR) of the high myopes was -0.1 (-0.2, 0), the effective index was 0.83±0.20, the BCVA (LogMAR) was -0.2 (-0.2, -0.2), and the safety index was 1.03±0.16 at 6 months after SMILE. The degree of myopia increased gradually from 1 month to 6 months postoperatively. The refractive error was -0.25 (-0.50, 0) D and regression was -0.25 (-0.50, 0) D at 6 months after SMILE. UCVA was positively correlated with age, refractive error and regression and was negatively correlated with age after surgery. The difference value of the posterior corneal surface was 0.030±0.006 mm before and 0.046±0.012 mm 6 months after surgery, which was lower than that in the first month, and was not statistically different at 3 months. Difference and Δdifference at 6 months were positively correlated with mPTA (modified percent tissue altered). \u0000 \u0000 \u0000Conclusions: \u0000This study demonstrates SMILE to be a safe, effective, predictable and stable procedure for the treatment of high myopia, with a slight myopic regression at 6 months after surgery, especially in elders. The posterior corneal surface shifts forward postoperatively and partially recovers after 3 months; the amounts are associated with mPTA. \u0000 \u0000 \u0000Key words: \u0000small incision lenticule extraction; high myopia; posterior corneal surface","PeriodicalId":10142,"journal":{"name":"Chinese Journal of Optometry & Ophthalmology","volume":"19 1","pages":"776-782"},"PeriodicalIF":0.0,"publicationDate":"2019-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90794391","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Therapeutic Effect of Intense Pulsed Light Combined with Meibomian Gland Expression in the Treatment of Meibomian Gland Dysfunction 强脉冲光联合睑板腺表达治疗睑板腺功能障碍的疗效观察
Pub Date : 2019-10-25 DOI: 10.3760/CMA.J.ISSN.1674-845X.2019.10.008
Men-Zhao Wang, Chen Dan, Liping Li, Huilin Liu, C. Min, Wu Xiaoman, Qingyan Zeng
Objective: To evaluate the short-term therapeutic effect of intense pulsed light combined with meibomian gland expression (IPL/MGX) for the treatment of meibomian gland dysfunction (MGD). Methods: This was a prospective single-arm clinical study that included 55 MGD patients, in which 48 patients (96 eyes) finished the follow-up. IPL/MGX treatment was administered in both eyes, once every 3 weeks for 3 sessions. Testing was performed before treatment and 1 week after treatment and included the ocular surface disease index (OSDI), a questionnaire survey, tear film break-up time, corneal staining, meibomian gland function and imaging, conjunctival bulbar redness, confocal microscope examination of the meibomian gland and mites, etc. A paired t test, Wilcoxon rank sum test and Spearman rank correlation were used for statistical analysis. Results: Ocular surface disease index (t=2.300, P=0.024) meibomian gland expression score and meibum quality score (Z=-3.617, P<0.001; t=2.472, P=0.017), corneal staining score and bulbar redness score (Z=-2.757, P=0.006; t=2.040, P=0.044), inflammatory cell density (t=4.765, P<0.001), and total number of demodex mites in the follicle (t=2.121, P=0.037) were all improved after treatment. The patients with a meibomian gland dropout area of less than 50% had significant improvement of subjective symptoms, ocular surface inflammation and meibomian gland function after treatment. Patients with a meibomian gland dropout area of more than 70% showed no significant improvement before and after treatment. Conclusion: IPL/MGX can significantly improve the subjective symptoms and meibomian gland function of MGD patients with mild atrophy of the meibomian gland, alleviate the inflammation of the ocular surface, reduce the number of demodex mites, and relieve damage onthe ocular surface. Key words: intense pulsed light; meibomian gland expression; meibomian gland dysfunction; in vivo confocal microscopy
目的:评价强脉冲光联合睑板腺表达(IPL/MGX)治疗睑板腺功能障碍(MGD)的短期疗效。方法:这是一项前瞻性单臂临床研究,纳入55例MGD患者,其中48例(96只眼)完成随访。双眼进行IPL/MGX治疗,每3周1次,共3个疗程。治疗前及治疗后1周检测,包括眼表疾病指数(OSDI)、问卷调查、泪膜破裂时间、角膜染色、睑板腺功能及影像学、结膜球红度、睑板腺及螨共聚焦显微镜检查等。采用配对t检验、Wilcoxon秩和检验和Spearman秩相关进行统计分析。结果:眼表疾病指数(t=2.300, P=0.024)睑板腺表达评分和睑板质量评分(Z=-3.617, P<0.001;t=2.472, P=0.017),角膜染色评分和球红度评分(Z=-2.757, P=0.006;t=2.040, P=0.044)、炎性细胞密度(t=4.765, P<0.001)、毛囊蠕形螨总数(t=2.121, P=0.037)均改善。睑板腺脱落面积小于50%的患者经治疗后主观症状、眼表炎症及睑板腺功能均有明显改善。睑板腺脱落面积大于70%的患者治疗前后无明显改善。结论:IPL/MGX可显著改善轻度睑板腺萎缩MGD患者的主观症状和睑板腺功能,减轻眼表炎症,减少蠕形螨数量,减轻眼表损伤。关键词:强脉冲光;睑板腺表达;睑板腺功能障碍;体内共聚焦显微镜
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引用次数: 1
Repeatability and Reproducibility of Axial Length Obtained by the IOLMaster 500 in 2 – 6 Year-Old Children iolmaster500测定2 - 6岁儿童眼轴长度的重复性和再现性
Pub Date : 2019-09-25 DOI: 10.3760/CMA.J.ISSN.1674-845X.2019.09.003
Guanshun Yu, Q. Zheng, Yili Jin, Hengli Lian, Miaojun Yan, Ruru Chen, Qin-Mei Wang
Objective: To assess the repeatability and reproducibility of axial length obtained by the optical biometer IOLMaster 500 in children aged 2-6 years. Methods: One hundred and two right eyes from 102 children were included in this cross-sectional study from Eye Hospital, Wenzhou Medical University from December 2016 to March 2017. Each eye was measured by two experienced operators using the IOLMaster 500 with 3 consecutive measurements. To evaluate intraoperator repeatability using repeated measurement ANOVA, Bland-Altman plots, and use paired samples t test and so on to analyze data. Results: The axial length obtained by the IOLMaster 500 showed high repeatability (95%LoA within -0.04 to 0.04 mm, and ICC was 1.000). The reproducibility of axial length was also high (95%LoA within -0.04 to 0.03 mm, Sw<0.01mm, 2.77 Sw<0.03 mm, CoV<0.05%). The width of the 95%LoA was reduced by 42.86% using averaged results rather than the result of a single measurement. Conclusions: Axial lengths obtained by the IOLMaster 500 in children aged 2-6 years shows high repeatability and reproducibility. In addition, the mean value of 3 consecutive measurements is better than that of a single measurement. Key words: IOLMaster 500; axial length; A scan; repeatability; reproducibility; children
目的:评价光学生物计IOLMaster 500测定眼球轴长在2 ~ 6岁儿童中的重复性和再现性。方法:选取2016年12月至2017年3月温州医科大学眼科医院102例患儿的102只右眼进行横断面研究。每只眼睛由两名经验丰富的操作员使用IOLMaster 500进行3次连续测量。采用重复测量方差分析、Bland-Altman图、配对样本t检验等方法评价操作者内部重复性。结果:IOLMaster 500测定的轴向长度具有较高的重复性(95%LoA在-0.04 ~ 0.04 mm范围内,ICC为1.000)。轴向长度的重现性也较高(95%LoA在-0.04 ~ 0.03 mm范围内,Sw<0.01mm, 2.77 Sw<0.03 mm, CoV<0.05%)。使用平均结果而不是单次测量结果,95%LoA的宽度减小了42.86%。结论:IOLMaster 500测定的2-6岁儿童眼轴长度具有较高的重复性和再现性。此外,连续3次测量的平均值优于单次测量的平均值。关键词:iolmaster500;轴向长度;一个扫描;可重复性;再现性;孩子们
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引用次数: 0
AAV-Mediated EPO Gene Reduction Inhibits Choroidal Neovascularization aav介导的EPO基因减少抑制脉络膜新生血管
Pub Date : 2019-09-25 DOI: 10.3760/CMA.J.ISSN.1674-845X.2019.09.001
Yi-Xiao Wang, Teng-Teng Yao, Yao Tong, Ya-Li Zhou, Yuan Yang, Zhao-yang Wang
Objective: To probe the role of Erythropoietin (EPO) in the progress of choroidal neovascularization (CNV). AAV-mediated EPO shRNA was used to target retinal pigment epithelium (RPE) in order to find a potential therapeutic approach to neovascular age-related macular degeneration (nAMD). Methods: This study was based on a controlled comparison experimental design. The in vitro efficiency of the EPO shRNA plasmid was tested in HEK293T cell culture. Two-month-old C57/B6J mice were used in this study. The right eyes were the experimental group and were injected with AAV1-sCBA-GFP-EPO-shRNA subretinally. The left eyes were the control group and were injected with AAV1-sCBA-GFP subretinally. Laser burns were performed to induce choroidal neovascularization in each eye 3 weeks after injection. Fundus images were taken immediately after that to make sure RPE was infected by the virus and the animal model was constructed successfully. The mice were sacrificed 15 days after laser photocoagulation, RPE flat-mounts were used to quantify the area of the CNV lesions. Statistical comparisons between groups were analyzed with a student's t test. Results: EPO shRNA had a statistically significantly efficiency (t=6.080, P=0.022) in HEK293T cell culture. The gene reduction rate of EPO shRNA was 69.6%. Successful virus transfection and model construction could be seen on fundus images. The average area of CNV lesions in the experimental eyes was 44.7% less than that in the control eyes. This reduction was also statistically significant (t=4.279, P=0.001). Conclusions: AAV-mediated EPO shRNA significantly reduces the progress of CNV lesions. This suggests that knocking down the EPO gene with AAV-mediated EPO shRNA can be a potential treatment for nAMD in the future. Key words: adeno-associated virus; choroidal neovascularization; erythropoietin; neovascular age-related macular degeneration
目的:探讨促红细胞生成素(EPO)在脉络膜新生血管(CNV)过程中的作用。利用aav介导的EPO shRNA靶向视网膜色素上皮(RPE),寻找一种治疗新生血管性年龄相关性黄斑变性(nAMD)的潜在方法。方法:采用对照比较试验设计。在HEK293T细胞培养中检测了EPO shRNA质粒的体外表达效率。本研究采用两个月大的C57/B6J小鼠。以右眼为实验组,在视网膜下注射AAV1-sCBA-GFP-EPO-shRNA。左眼为对照组,在视网膜下注射AAV1-sCBA-GFP。注射后3周,每只眼行激光灼烧诱导脉络膜新生血管形成。随即拍摄眼底图像,确认RPE感染病毒,成功构建动物模型。激光光凝15天后处死小鼠,用RPE平载仪定量CNV病变面积。组间统计比较采用学生t检验进行分析。结果:在HEK293T细胞培养中,EPO shRNA的效率有统计学意义(t=6.080, P=0.022)。EPO shRNA基因还原率为69.6%。在眼底图像上可以看到成功的病毒转染和模型构建。实验眼CNV病变面积比对照组平均小44.7%。这种减少也具有统计学意义(t=4.279, P=0.001)。结论:aav介导的EPO shRNA可显著降低CNV病变的进展。这表明,用aav介导的EPO shRNA敲除EPO基因可能是未来治疗nAMD的一种潜在方法。关键词:腺相关病毒;脉络膜新生血管形成;促红细胞生成素;新生血管性年龄相关性黄斑变性
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引用次数: 0
The Short-Term Outcome of Treatment with Corticosteroids and Immunosuppressive Drugs for Non-Infectious Posterior Scleritis 皮质类固醇和免疫抑制药物治疗非感染性后巩膜炎的短期疗效
Pub Date : 2019-09-25 DOI: 10.3760/CMA.J.ISSN.1674-845X.2019.09.007
Zhizhang Dong, Yifeng Gan, Haihua Zheng, Mei Li
Objective: To explore the short-term clinical outcome of treatment with corticosteroids and immunosuppressive drugs for non-infectious posterior scleritis. Methods: Twenty patients (20 eyes) who were diagnosed with posterior scleritis from January 2012 to October 2017 in the Department Ophthalmology of the Second Affiliated Hospital of Wenzhou Medical University were recruited for this retrospective series of case study. Clinical findings were documented before and after treatment for all patients. Patients also underwent testing for best corrected visual acuity, intraocular pressure, fundus examination, and posterior retinal examination with B-scan ultrasound. Examinations were performed at 1 week, 2 weeks, 1 month, 3 months and 6 months after the start of treatment. All results were quantitatively and statistically analyzed by variance analysis. Results: Before treatment, 18 patients (90%) had complained about pain and worsening vision, 13 patients had anterior uveitis and anterior scleritis, 17 eyes had optic disc swelling, and 18 eyes had retinal phlebectasia. After two weeks of treatment, 18 patients (90%) had relief from pain symptoms and 7 patients (35%) had improved visual acuity. Anterior inflammation eased in all patients after 1 month of treatment. Optic disc edema and retinal phlebectasia were alleviated in 10 eyes, the retinal/choroidal folds gradually resolved, and symptoms were eased in all cases after 3 months of treatment. Almost all abnormalities in the fundus disappeared after 6 months of treatment. After treatment, B-scan ultrasound examination showed that eyeball thickness was reduced and accompanied by "T" syndrome remission, with an average of 2.82±0.63 mm, 2.01±0.68 mm, 1.86±0.44 mm, 1.68±0.45 mm, and 1.43±0.65 mm after treatment for 1 week, 2 weeks, 1 month, 3 months and 6 months, respectively, compared to 3.24±0.78 mm before treatment. Compared to pre-treatment, the difference from 2 weeks after treatment was statistically significant (t=13.76, P=0.0017). Symptoms were alleviated in about 17 cases after two weeks of treatment with an effective rate of 30% (6 cases). Effectiveness was at 45% (9 cases) after 3 months of treatment, and 5 patients (25%) were cured. Conclusions: Aggressive therapy with systemic corticosteroids and immunosuppressive agents to treat posterior scleritis always achieves good resolution in a short period of time with a favorable visual outcome but long-term therapy is often required to prevent recurrence. B-scan ultrasound is the most useful option for assessing the therapeutic effect during follow-up. Key words: sclera; posterior scleritis; clinical treatment; uveitis
目的:探讨糖皮质激素联合免疫抑制药物治疗非感染性后巩膜炎的近期临床疗效。方法:选取2012年1月至2017年10月温州医科大学第二附属医院眼科诊断为后巩膜炎的患者20例(20只眼)进行回顾性系列病例研究。所有患者在治疗前后均记录了临床表现。患者还接受了最佳矫正视力、眼压、眼底检查和后视网膜b超检查。分别于治疗开始后1周、2周、1个月、3个月和6个月进行检查。所有结果均采用方差分析进行定量统计分析。结果:治疗前,18例患者(90%)出现疼痛和视力下降,13例患者出现前葡萄膜炎和前巩膜炎,17眼视盘肿胀,18眼视网膜静脉扩张。治疗2周后,18例(90%)患者疼痛症状缓解,7例(35%)患者视力改善。治疗1个月后,所有患者的前侧炎症均有所缓解。10眼视盘水肿、视网膜静脉扩张减轻,视网膜/脉络膜皱襞逐渐消失,治疗3个月后症状全部缓解。治疗6个月后,眼底异常几乎全部消失。治疗后b超检查显示眼球厚度减轻并伴有“T”综合征缓解,治疗1周、2周、1个月、3个月、6个月平均分别为2.82±0.63 mm、2.01±0.68 mm、1.86±0.44 mm、1.68±0.45 mm、1.43±0.65 mm,而治疗前为3.24±0.78 mm。治疗后2周与治疗前比较,差异有统计学意义(t=13.76, P=0.0017)。治疗2周后症状缓解约17例,有效率30%(6例)。治疗3个月后,有效率为45%(9例),治愈5例(25%)。结论:采用全身皮质类固醇和免疫抑制剂积极治疗后巩膜炎总能在短时间内获得良好的解决和良好的视觉效果,但往往需要长期治疗以防止复发。在随访期间,b超扫描是评估治疗效果的最有用的选择。关键词:巩膜;后巩膜炎;临床治疗;葡萄膜炎
{"title":"The Short-Term Outcome of Treatment with Corticosteroids and Immunosuppressive Drugs for Non-Infectious Posterior Scleritis","authors":"Zhizhang Dong, Yifeng Gan, Haihua Zheng, Mei Li","doi":"10.3760/CMA.J.ISSN.1674-845X.2019.09.007","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1674-845X.2019.09.007","url":null,"abstract":"Objective: \u0000To explore the short-term clinical outcome of treatment with corticosteroids and immunosuppressive drugs for non-infectious posterior scleritis. \u0000 \u0000 \u0000Methods: \u0000Twenty patients (20 eyes) who were diagnosed with posterior scleritis from January 2012 to October 2017 in the Department Ophthalmology of the Second Affiliated Hospital of Wenzhou Medical University were recruited for this retrospective series of case study. Clinical findings were documented before and after treatment for all patients. Patients also underwent testing for best corrected visual acuity, intraocular pressure, fundus examination, and posterior retinal examination with B-scan ultrasound. Examinations were performed at 1 week, 2 weeks, 1 month, 3 months and 6 months after the start of treatment. All results were quantitatively and statistically analyzed by variance analysis. \u0000 \u0000 \u0000Results: \u0000Before treatment, 18 patients (90%) had complained about pain and worsening vision, 13 patients had anterior uveitis and anterior scleritis, 17 eyes had optic disc swelling, and 18 eyes had retinal phlebectasia. After two weeks of treatment, 18 patients (90%) had relief from pain symptoms and 7 patients (35%) had improved visual acuity. Anterior inflammation eased in all patients after 1 month of treatment. Optic disc edema and retinal phlebectasia were alleviated in 10 eyes, the retinal/choroidal folds gradually resolved, and symptoms were eased in all cases after 3 months of treatment. Almost all abnormalities in the fundus disappeared after 6 months of treatment. After treatment, B-scan ultrasound examination showed that eyeball thickness was reduced and accompanied by \"T\" syndrome remission, with an average of 2.82±0.63 mm, 2.01±0.68 mm, 1.86±0.44 mm, 1.68±0.45 mm, and 1.43±0.65 mm after treatment for 1 week, 2 weeks, 1 month, 3 months and 6 months, respectively, compared to 3.24±0.78 mm before treatment. Compared to pre-treatment, the difference from 2 weeks after treatment was statistically significant (t=13.76, P=0.0017). Symptoms were alleviated in about 17 cases after two weeks of treatment with an effective rate of 30% (6 cases). Effectiveness was at 45% (9 cases) after 3 months of treatment, and 5 patients (25%) were cured. \u0000 \u0000 \u0000Conclusions: \u0000Aggressive therapy with systemic corticosteroids and immunosuppressive agents to treat posterior scleritis always achieves good resolution in a short period of time with a favorable visual outcome but long-term therapy is often required to prevent recurrence. B-scan ultrasound is the most useful option for assessing the therapeutic effect during follow-up. \u0000 \u0000 \u0000Key words: \u0000sclera; posterior scleritis; clinical treatment; uveitis","PeriodicalId":10142,"journal":{"name":"Chinese Journal of Optometry & Ophthalmology","volume":"56 79 1","pages":"682-688"},"PeriodicalIF":0.0,"publicationDate":"2019-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83587092","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effects of Corneal Electrical Stimulation on the Anterior Ischemic Optic Neuropathy in Diabetic Rats 角膜电刺激对糖尿病大鼠前缺血性视神经病变的影响
Pub Date : 2019-09-25 DOI: 10.3760/CMA.J.ISSN.1674-845X.2019.09.008
Bei Cheng, Qichang Wang, Luo-sheng Tang
Objective: To observe and evaluate the effect of corneal electrical stimulation on anterior ischemic optic neuropathy (AION) in diabetic rats. Methods: In this experimental study, 40 healthy male Sprague-Dawley rats were randomly grouped, and 8 of them were selected as the normal group. For the remaining 32 rats, the diabetic rat model was established by intraperitoneal injection of streptozotocin, and 8 of the rat models were randomly selected as the diabetic group. Meanwhile, the remaining 24 diabetic rats were treated with rose bengal combined with 532 nm laser to construct the AION rat model. Afterwards, the above-mentioned AION rat models were randomly divided into three groups with 8 in each group, including the AION rat group (received no treatment), the electrical stimulation group and the sham electrical stimulation group. The electrical stimulation group was given corneal electrical stimulation with the following parameters: Current of 1 mA, frequency of 20 Hz, wave width of 1 ms/phase, and stimulation time of 1 hour once every other day for 2 weeks. The sham electrical stimulation group had an electrode placed in the same position as that of the electrical stimulation group, but the power was not connected. After 2 weeks, rats in the 5 above-mentioned groups were analyzed with fundus color photography, optical coherence tomography (OCT) and visual evoked potentials (VEP). Moreover, after the rats were sacrificed, the retina and optic nerve were frozen and sectioned, and hematoxylin and eosin stains were applied to the tissues. LSD-t tests and one-way analysis of variance were used to analyze the data. Results: The average retinal thickness of the superior optic disc was 211±13 μm in the normal rat group, 206±16 μm in the diabetic rat group, 240±54 μm in the AION rat group, 216±11 μm in the sham stimulation group, and 198±4 μm in the electrical stimulation group. There were significant differences in the average retinal thickness of the superior optic disc among the five groups (F=2.854, P=0.038). Of them, the average retinal thickness of the superior optic disc in the AION group was greater than the retinal thickness in the normal group, the diabetic group and the electrical stimulation group, and the differences were statistically significant (P 0.05), or between the AION group and the sham stimulation group (P>0.05). VEP revealed that the N1 latency of the AION group was longer than that of the electrical stimulation group, and the difference was statistically significant (t=4.1, P<0.001). The P1 latency of the AION group was extended compared to latencies in the normal group, the diabetic group, the sham electrical stimulation group and the electrical stimulation group, and the differences were statistically significant (t=4.1, 2.5, 2.6, 3.2, P<0.05). In addition, the amplitude of N1-P1 in the electrical stimulation group increased relative to that in the sham electrical stimulation group, and the difference was statist
目的:观察和评价角膜电刺激对糖尿病大鼠前缺血性视神经病变(AION)的影响。方法:选取健康雄性Sprague-Dawley大鼠40只,随机分组,其中8只为正常组。其余32只大鼠,通过腹腔注射链脲佐菌素建立糖尿病大鼠模型,随机选取8只大鼠模型作为糖尿病组。同时,将24只糖尿病大鼠用玫瑰花联合532 nm激光治疗,建立AION大鼠模型。随后,将上述AION大鼠模型随机分为3组,每组8只,分别为AION大鼠组(未给药)、电刺激组和假电刺激组。电刺激组给予角膜电刺激,电流为1 mA,频率为20 Hz,波宽为1 ms/相,刺激时间为1小时,每隔一天1次,持续2周。假电刺激组与电刺激组在相同位置放置电极,但未接通电源。2周后,用眼底彩色摄影、光学相干断层扫描(OCT)和视觉诱发电位(VEP)对上述5组大鼠进行分析。处死大鼠后,冷冻视网膜和视神经切片,对组织进行苏木精和伊红染色。采用LSD-t检验和单因素方差分析对数据进行分析。结果:正常大鼠组上视盘视网膜平均厚度为211±13 μm,糖尿病大鼠组为206±16 μm, AION大鼠组为240±54 μm,假刺激组为216±11 μm,电刺激组为198±4 μm。五组患者上视盘视网膜平均厚度差异有统计学意义(F=2.854, P=0.038)。其中,AION组上视盘视网膜平均厚度大于正常组、糖尿病组和电刺激组,差异均有统计学意义(P < 0.05); AION组与假刺激组之间差异均有统计学意义(P < 0.05)。VEP显示AION组N1潜伏期长于电刺激组,差异有统计学意义(t=4.1, P<0.001)。AION组P1潜伏期较正常组、糖尿病组、假电刺激组、电刺激组延长,差异均有统计学意义(t=4.1、2.5、2.6、3.2,P<0.05)。此外,电刺激组N1-P1的振幅较假电刺激组增加,差异有统计学意义(t=4.0, P<0.001)。结论:角膜电刺激可促进高血糖状态AION大鼠视盘变薄,加速视盘水肿消退,部分改善视功能。关键词:角膜电刺激;糖尿病大鼠;前路缺血性视神经病变;光学相干层析成像
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引用次数: 0
The Effect of Y27632 on Retinal Tissue Histomorphology in Rats with Acute Retinal Ischemia-Reperfusion Y27632对急性视网膜缺血再灌注大鼠视网膜组织形态学的影响
Pub Date : 2019-09-25 DOI: 10.3760/CMA.J.ISSN.1674-845X.2019.09.002
L. Yin, Shu-Hong Zhang, Jing Zhu, Chao Sun, Xun Bao, Yong Yao
Objective: To study the effect of rho kinase inhibitor Y27632 on retinal histomorphology in rats with retinal ischemia-reperfusion injury. Methods: In this experimental study, sixty SD rats were randomly divided into 4 groups, 15 in each group: normal group, ischemia-reperfusion injury group (IRI group), saline group, and Y27632 group. Twenty-four hours (10 rats) and 168 hours (5 rats) after the induction of ischemia-reperfusion, the rats were sacrificed and the retinas were stained with HE and ADP. Histopathological change in the retina was examined and the thickness of the retina was measured. Data were analyzed by one-way ANOVA. Results: The retinal structure was clear and the structure of the three layer cells was orderly in the normal group. In the IRI group, after 24 hours of reperfusion, retinal thickness increased, the inner and outer plexiform layers were loose, the retinal ganglion cells and the inner and outer nuclear layers showed evidence of edema and were disordered and the retinal ganglion cells were reduced. After 168 hours, retinal edema subsided, and thickness was reduced and atrophic. The number of ganglion cells and inner and outer nuclear cells decreased. Capillaries were seen in the anterior retina and nerve fiber layer. After 24 hours of reperfusion, the retinal thickness of the IRI group was greater than that of the nomal group (P=0.005), and the thickness of the Y27632 group was lower than that of the saline group (P=0.032). After 168 hours of reperfusion, the retinal thickness of the IRI group was lower than that of nomal group (P<0.001), and the thickness of the Y27632 group was higher than that of the saline group (P=0.025). In the norml group, the retinal blood vessels were distributed uniformly and radially around the papillae, and the structure of the capillary network was clear. After 24 hours of reperfusion, retinal vessels in the IRI group were thinner, more rigid and had less branching. Large non-perfusion areas were observed around the retina and around the optic papilla, and neovascularization buds were gradually reticulated around the non-perfusion area. In the Y27632 group, there was a non-perfusion area around the optic papilla and the middle retina, and neovascularization was around the non-perfusion area. The area of the non-perfusion zone in 4PD of the posterior pole was significantly less than that in the IRI andsaline groups. Conclusions: Y27632 intravitreal injection can reduce retinal edema, apoptosis of retinal ganglion cells, retinal neovascularization and retinal atrophy in the early stage of retinal ischemia-reperfusion. It has a protective effect on the optic nerve. Key words: glaucoma; ischemia; reperfusion injury; Rho kinase; Y27632; rats
目的:研究rho激酶抑制剂Y27632对视网膜缺血再灌注损伤大鼠视网膜组织形态学的影响。方法:将60只SD大鼠随机分为4组,每组15只:正常组、缺血再灌注损伤组(IRI组)、生理盐水组、Y27632组。缺血再灌注诱导后24 h(10只)和168 h(5只)处死大鼠,用HE和ADP染色视网膜。观察视网膜组织病理变化,测量视网膜厚度。数据采用单因素方差分析。结果:正常组视网膜结构清晰,三层细胞结构有序。IRI组视网膜再灌注24h后,视网膜厚度增加,内外网状层疏松,视网膜神经节细胞及内外核层明显水肿紊乱,视网膜神经节细胞减少。168 h后,视网膜水肿消退,厚度减少萎缩。神经节细胞和内外核细胞数量减少。前视网膜和神经纤维层可见毛细血管。再灌注24h后,IRI组视网膜厚度大于正常组(P=0.005), Y27632组视网膜厚度低于生理盐水组(P=0.032)。再灌注168 h后,IRI组视网膜厚度低于正常组(P<0.001), Y27632组视网膜厚度高于生理盐水组(P=0.025)。正常组视网膜血管在乳头周围呈放射状均匀分布,毛细血管网结构清晰。再灌注24小时后,IRI组视网膜血管更薄、更坚硬、分支更少。视网膜周围及视乳头周围可见大片非灌注区,非灌注区周围逐渐网状新生血管芽。Y27632组视乳头和视网膜中部周围有非灌注区,非灌注区周围有新生血管形成。后极4PD非灌注区面积明显小于IRI组和生理盐水组。结论:玻璃体内注射Y27632可减少视网膜缺血再灌注早期视网膜水肿、视网膜神经节细胞凋亡、视网膜新生血管和视网膜萎缩。它对视神经有保护作用。关键词:青光眼;缺血;再灌注损伤;ρ激酶;Y27632;老鼠
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引用次数: 0
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Chinese Journal of Optometry & Ophthalmology
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