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Early diagnosis of keratoconus using corneal biomechanics and OCT derived technologies. 角膜生物力学及OCT技术在圆锥角膜早期诊断中的应用。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-05-12 DOI: 10.1186/s40662-025-00435-3
Xiaorui Wang, Sayo Maeno, Yixin Wang, Shizuka Koh, Shihao Chen, Andrew J Quantock, Siân R Morgan, Sally Hayes, Colm McAlinden

Background: Early detection of keratoconus is essential for maximizing the potential of cross-linking treatments designed to halt keratoconus progression, minimizing the risks of iatrogenic ectasia as well as reducing the need for corneal transplantation. This review focuses on the progress that has been made in the early detection of keratoconus using biomechanical and topographical properties derived from three different technologies, namely the ocular response analyser (ORA), corneal visualization Scheimpflug tonometer (Corvis ST) and optical coherence tomography (OCT).

Method: A PubMed search was performed using the keywords of 'early keratoconus', 'subclinical keratoconus', 'forme fruste keratoconus', 'very asymmetric ectasia with normal topography/tomography' and 'ocular response analyser' and/or 'Corvis ST'/'corneal visualized Scheimpflug tomographer/tomography' and/or 'optical coherence tomography/tomographer'.

Results: The integration of biomechanical parameters and corneal morphological data from the topography/tomography or OCT, or the assessment of bilateral asymmetry, has demonstrated improvement in the accuracy of diagnosing early-stage keratoconus.

Conclusions: As measurement principles differ depending on the technique used for keratoconus assessment, comprehensive metrics may be needed to reflect subtle anterior or posterior corneal changes and help identify eyes with very early ectasia. Although clinical experts have always, and will most likely, continue to play a pivotal role in decision-making for early keratoconus diagnosis, future developments in technology and AI may lead to enhanced early detection in the future.

背景:圆锥角膜的早期发现对于最大限度地发挥交联治疗的潜力至关重要,交联治疗旨在阻止圆锥角膜的进展,最大限度地减少医源性扩张的风险,并减少角膜移植的需要。本文综述了利用眼反应分析仪(ORA)、角膜可视化Scheimpflug眼压计(Corvis ST)和光学相干断层扫描(OCT)三种不同技术获得的生物力学和地形特性在圆锥角膜早期检测方面的进展。方法:使用关键词“早期圆锥角膜”、“亚临床圆锥角膜”、“形成状圆锥角膜”、“非常不对称扩张与正常地形/断层扫描”和“眼反应分析仪”和/或“Corvis ST”/“角膜可视化Scheimpflug断层扫描/断层扫描”和/或“光学相干断层扫描/断层扫描”进行PubMed搜索。结果:结合生物力学参数和来自于地形/断层扫描或OCT的角膜形态数据,或评估双侧不对称性,可以提高早期圆锥角膜的诊断准确性。结论:由于圆锥角膜评估的测量原理因技术的不同而不同,因此可能需要综合的指标来反映细微的角膜前或后变化,并有助于识别早期扩张的眼睛。尽管临床专家一直并极有可能继续在圆锥角膜早期诊断的决策中发挥关键作用,但未来技术和人工智能的发展可能会提高未来的早期发现能力。
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引用次数: 0
Obesity negatively impacts corneal nerves in patients with diabetes mellitus. 肥胖对糖尿病患者角膜神经有负面影响。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-04-23 DOI: 10.1186/s40662-025-00433-5
Calesta Hui Yi Teo, Chang Liu, Mingyi Yu, Isabelle Xin Yu Lee, Ansa Anam, Ching-Yu Cheng, Yadana Htunwai, Jasmine Shimin Koh, Suresh Rama Chandran, Yu-Chi Liu

Background: To investigate the relationship between obesity and corneal nerve metrics in patients with type 2 diabetes mellitus (DM).

Methods: This cross-sectional study included a total of 385 healthy controls and 663 patients with DM. Metrics for corneal nerve and epithelial cells were evaluated using in-vivo confocal microscopy (IVCM). Corneal nerve and epithelial cell parameters were quantified and compared between patients with and without obesity and across six different body mass index (BMI) categories. Multivariable regression analyses were conducted to determine the association between corneal nerve metrics and BMI in patients with DM.

Results: Of the DM participants, 162 (25.4%) had obesity. Compared to the non-obese group, patients with obesity had significantly lower corneal nerve fiber density (CNFD, P < 0.0001), corneal nerve fiber length (CNFL, P = 0.002), and corneal nerve branch density (CNBD, P = 0.005). Analyses across different BMI categories showed a progressive decline in corneal nerve parameters including CNFD (P < 0.0001), CNFL (P < 0.0001), CNBD (P < 0.0001), corneal nerve fiber total branch density (P = 0.003), corneal nerve fiber area (P = 0.04), and corneal nerve fiber fractal dimension (P = 0.02) with increasing obesity severity. Multivariable regression analyses demonstrated that lower CNFD (β: - 0.21, 95% CI: - 0.29 to - 0.13, P < 0.0001), shorter CNFL (β: - 0.12, 95% CI: - 0.17 to - 0.07, P < 0.0001), and lower CNBD (β: - 0.17, 95% CI: - 0.30 to - 0.04, P = 0.01) were significantly associated with BMI after adjusting for confounders. There were no significant differences in the corneal epithelial parameters between the obese and non-obese groups.

Conclusions: General obesity, specifically higher BMI, adversely affects corneal nerve health in individuals with DM. Evaluation of corneal nerves and resultant keratopathy should be considered in patients with DM and concomitant obesity.

背景:探讨2型糖尿病(DM)患者肥胖与角膜神经指标的关系。方法:这项横断面研究包括385名健康对照和663名糖尿病患者。使用体内共聚焦显微镜(IVCM)评估角膜神经和上皮细胞的指标。将角膜神经和上皮细胞参数量化,并在肥胖和非肥胖患者以及六种不同的体重指数(BMI)类别中进行比较。我们进行了多变量回归分析,以确定DM患者角膜神经指标与BMI之间的关系。结果:在DM参与者中,162人(25.4%)患有肥胖症。与非肥胖组相比,肥胖患者角膜神经纤维密度(CNFD, P < 0.0001)、角膜神经纤维长度(CNFL, P = 0.002)、角膜神经分支密度(CNBD, P = 0.005)均显著降低。不同BMI类别的分析显示,随着肥胖严重程度的增加,角膜神经参数CNFD (P < 0.0001)、CNFL (P < 0.0001)、CNBD (P < 0.0001)、角膜神经纤维总分支密度(P = 0.003)、角膜神经纤维面积(P = 0.04)和角膜神经纤维分形维数(P = 0.02)逐渐下降。多变量回归分析表明,调整混杂因素后,较低的CNFD (β: - 0.21, 95% CI: - 0.29至- 0.13,P < 0.0001)、较短的CNFL (β: - 0.12, 95% CI: - 0.17至- 0.07,P < 0.0001)和较低的CNBD (β: - 0.17, 95% CI: - 0.30至- 0.04,P = 0.01)与BMI显著相关。肥胖组和非肥胖组的角膜上皮参数无显著差异。结论:一般肥胖,特别是较高的BMI,会对糖尿病患者的角膜神经健康产生不利影响。糖尿病合并肥胖患者应考虑评估角膜神经和由此产生的角膜病变。
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引用次数: 0
Sturge-Weber syndrome secondary glaucoma: From Pathogenesis to Treatment. 斯特奇-韦伯综合征继发性青光眼:从发病机理到治疗。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-04-17 DOI: 10.1186/s40662-025-00432-6
Tingli Wen, Lixiang Wang, Hongmei Luo, Li Tang

Sturge-Weber syndrome (SWS) is a rare form of neurocutaneous disorder characterized by the involvement of neurologic, cutaneous and ocular problems. Among all SWS-related ocular abnormalities, glaucoma is the most common complication with a bimodal onset time. The occurrence of gene mutations in GNAQ has been identified as a cause of SWS. Recent studies have indicated that macrophages and mutations in GNA11 or GNB2 are also involved in the pathogenesis of SWS. Different mechanisms such as elevated episcleral venous pressure and focal venous hypertension can result in SWS secondary glaucoma (SG). In addition to glaucoma-related manifestations, SG may be associated with the typical site of facial port-wine birthmarks, choroidal vascular malformation and other ocular features. Medication and surgery are still the mainstay for SG. ROCK inhibitors have shown good performance in the control of intraocular pressure in SG but have not been verified in large sample populations. Due to the anatomical abnormalities, the incidence of surgical complications is higher. Non-penetrating surgical procedures, known for their safety and hypotensive characteristics, may be preferable instead. In general, the treatment of SG is a challenging undertaking. Early detection and treatment are crucial to preserve the visual function of patients with SWS. This review provides an overview of its pathogenesis, clinical manifestations, therapeutic agents, surgeries, and recent advances in the field of SG. The aim is to offer the latest perspectives and insights for the understanding and diagnosis of this disease.

斯特奇-韦伯综合征(SWS)是一种罕见的神经皮肤疾病,其特征是累及神经、皮肤和眼部问题。在所有sws相关的眼部异常中,青光眼是最常见的并发症,具有双峰发病时间。GNAQ基因突变的发生已被确定为SWS的原因之一。最近的研究表明,巨噬细胞和GNA11或GNB2突变也参与了SWS的发病机制。不同的机制,如膜外静脉压升高和局灶性静脉高压可导致SWS继发性青光眼(SG)。除了青光眼相关的表现外,SG还可能与面部葡萄酒型胎记的典型部位、脉络膜血管畸形和其他眼部特征有关。药物和手术仍然是治疗SG的主要手段。ROCK抑制剂在控制SG患者眼压方面表现良好,但尚未在大样本人群中得到验证。由于解剖异常,手术并发症的发生率较高。非穿透性手术以其安全性和降压特性而闻名,可能是更好的选择。一般来说,SG的治疗是一项具有挑战性的工作。早期发现和治疗对于保护SWS患者的视觉功能至关重要。本文就其发病机制、临床表现、治疗药物、手术方法及近年来研究进展作一综述。其目的是为了解和诊断这种疾病提供最新的观点和见解。
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引用次数: 0
Genetic landscape of uveal melanoma in Southeast Asia: high 1q gains and unique patterns of metastasis risk. 东南亚葡萄膜黑色素瘤的遗传景观:高q增益和独特的转移风险模式。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-04-16 DOI: 10.1186/s40662-025-00430-8
Chuanfei Chen, Mona Meng Wang, Alvin Soon Tiong Lim, Evelyn Yee Hsieh Heng, Sim Leng Tien, Sunny Yu Shen, Gavin Siew Wei Tan, Jason Yongsheng Chan, Anita Sook Yee Chan

Purpose: This retrospective cohort study aims to investigate chromosomal aberrations in Southeast Asian (SEA) uveal melanoma (UM) patients, evaluate their impact on clinical outcomes, and compare findings with the TCGA-Uveal Melanoma (TCGA-UM) dataset to explore potential genetic differences.

Methods: Formalin-fixed paraffin-embedded (FFPE) tumour samples from 20 UM patients diagnosed between 2004 and 2018 were initially analysed using the OncoScan™ CNV Array to detect chromosomal aberrations, with 14 samples yielding valid results for cytogenetic analysis. BAP1 immunohistochemistry was performed on all 20 samples to assess BAP1 protein expression using automated immunostaining techniques validated in the Clinical Pathology Laboratory of the Singapore General Hospital. Clinical data were retrospectively reviewed, and chromosomal aberration frequencies were compared with the TCGA-UM dataset.

Results: A total of 78 chromosomal gains, 48 losses, and two cases of copy-neutral loss of heterozygosity (CN-LOH) were identified. Compared to the TCGA-UM cohort, SEA patients exhibited a lower frequency of monosomy 3 (14% vs. 53%) and a higher incidence of chromosome 1q gains (20% vs. 6%). Gains in chromosome 1q were significantly associated (P = 0.0289) with shorter progression-free survival (PFS). In comparison, gains in chromosome 9q were correlated with longer PFS in SEA patients, a trend not observed in the TCGA-UM cohort. BAP1 loss was detected in 20% of cases and was associated with reduced survival rates, consistent with TCGA data.

Conclusions: This study highlights significant genetic differences between SEA and Western UM patients, particularly the lower incidence of monosomy 3 in SEA patients. This preliminary observation raises concerns about the reliability of using BAP1 loss alone, assessed through gene expression or immunostaining, as a sole marker for metastasis surveillance and risk stratification in Asian UM patients. These findings underscore the need for further research to determine whether additional genetic markers are required to improve prognostic accuracy in this population. Expanding molecular profiling in SEA would improve risk stratification and inform treatment strategies, while collaborative research with larger cohorts is essential to validate these findings and refine prognostic models globally.

目的:本回顾性队列研究旨在调查东南亚(SEA)葡萄膜黑色素瘤(UM)患者的染色体畸变,评估其对临床结果的影响,并将结果与tcga -葡萄膜黑色素瘤(TCGA-UM)数据集进行比较,以探索潜在的遗传差异。方法:对2004年至2018年间诊断的20例UM患者的福尔马林固定石蜡包埋(FFPE)肿瘤样本进行初步分析,使用OncoScan™CNV阵列检测染色体畸变,其中14个样本获得有效结果用于细胞遗传学分析。对所有20个样本进行BAP1免疫组化,使用经新加坡综合医院临床病理实验室验证的自动免疫染色技术评估BAP1蛋白表达。回顾性回顾临床资料,并将染色体畸变频率与TCGA-UM数据集进行比较。结果:共鉴定出78例染色体获得,48例缺失,2例拷贝中性杂合性缺失(CN-LOH)。与TCGA-UM队列相比,SEA患者表现出较低的3号单体频率(14%对53%)和较高的1q染色体发生率(20%对6%)。染色体1q的增加与较短的无进展生存期(PFS)显著相关(P = 0.0289)。相比之下,染色体9q的增加与SEA患者PFS的延长相关,TCGA-UM队列中没有观察到这种趋势。在20%的病例中检测到BAP1缺失,并与生存率降低相关,与TCGA数据一致。结论:本研究强调SEA患者与Western UM患者之间存在显著的遗传差异,特别是SEA患者中单体3的发生率较低。这一初步观察结果引起了人们对单独使用BAP1缺失,通过基因表达或免疫染色评估,作为亚洲UM患者转移监测和风险分层的唯一标志的可靠性的担忧。这些发现强调了进一步研究的必要性,以确定是否需要额外的遗传标记来提高该人群的预后准确性。扩大SEA的分子谱分析将改善风险分层并为治疗策略提供信息,而与更大队列的合作研究对于验证这些发现和完善全球预后模型至关重要。
{"title":"Genetic landscape of uveal melanoma in Southeast Asia: high 1q gains and unique patterns of metastasis risk.","authors":"Chuanfei Chen, Mona Meng Wang, Alvin Soon Tiong Lim, Evelyn Yee Hsieh Heng, Sim Leng Tien, Sunny Yu Shen, Gavin Siew Wei Tan, Jason Yongsheng Chan, Anita Sook Yee Chan","doi":"10.1186/s40662-025-00430-8","DOIUrl":"https://doi.org/10.1186/s40662-025-00430-8","url":null,"abstract":"<p><strong>Purpose: </strong>This retrospective cohort study aims to investigate chromosomal aberrations in Southeast Asian (SEA) uveal melanoma (UM) patients, evaluate their impact on clinical outcomes, and compare findings with the TCGA-Uveal Melanoma (TCGA-UM) dataset to explore potential genetic differences.</p><p><strong>Methods: </strong>Formalin-fixed paraffin-embedded (FFPE) tumour samples from 20 UM patients diagnosed between 2004 and 2018 were initially analysed using the OncoScan™ CNV Array to detect chromosomal aberrations, with 14 samples yielding valid results for cytogenetic analysis. BAP1 immunohistochemistry was performed on all 20 samples to assess BAP1 protein expression using automated immunostaining techniques validated in the Clinical Pathology Laboratory of the Singapore General Hospital. Clinical data were retrospectively reviewed, and chromosomal aberration frequencies were compared with the TCGA-UM dataset.</p><p><strong>Results: </strong>A total of 78 chromosomal gains, 48 losses, and two cases of copy-neutral loss of heterozygosity (CN-LOH) were identified. Compared to the TCGA-UM cohort, SEA patients exhibited a lower frequency of monosomy 3 (14% vs. 53%) and a higher incidence of chromosome 1q gains (20% vs. 6%). Gains in chromosome 1q were significantly associated (P = 0.0289) with shorter progression-free survival (PFS). In comparison, gains in chromosome 9q were correlated with longer PFS in SEA patients, a trend not observed in the TCGA-UM cohort. BAP1 loss was detected in 20% of cases and was associated with reduced survival rates, consistent with TCGA data.</p><p><strong>Conclusions: </strong>This study highlights significant genetic differences between SEA and Western UM patients, particularly the lower incidence of monosomy 3 in SEA patients. This preliminary observation raises concerns about the reliability of using BAP1 loss alone, assessed through gene expression or immunostaining, as a sole marker for metastasis surveillance and risk stratification in Asian UM patients. These findings underscore the need for further research to determine whether additional genetic markers are required to improve prognostic accuracy in this population. Expanding molecular profiling in SEA would improve risk stratification and inform treatment strategies, while collaborative research with larger cohorts is essential to validate these findings and refine prognostic models globally.</p>","PeriodicalId":12194,"journal":{"name":"Eye and Vision","volume":"12 1","pages":"15"},"PeriodicalIF":4.1,"publicationDate":"2025-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12001427/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144005159","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Efficacy of botulinum toxin and surgery in managing acute acquired comitant esotropia. 肉毒杆菌毒素与手术治疗急性获得性共同性内斜视的疗效。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-04-01 DOI: 10.1186/s40662-025-00431-7
Xiangxiang Liu, Jiayu Chen, Jie Hao, Zhaojun Meng, Weibin Chen, Huijian Li, Jing Fu

Background: Acute acquired comitant esotropia (AACE) can significantly impair binocular vision, and its prevalence is increasing. This study aims to compare the effectiveness of botulinum toxin (BTX) injections with strabismus surgery in patients diagnosed with AACE and to investigate the factors predicting success.

Methods: Sixty AACE patients were included in this prospective comparative clinical study. Twenty-seven patients underwent incisional strabismus surgery (surgery group) and 33 patients received BTX injection (chemodenervation group). Patients were followed up visit at 1, 3, and 6 months post-treatment. The primary outcome was the success rate at 6 months post-treatment, defined as a horizontal deviation of 10 prism diopters (PD) or less with confirmed binocular single vision. Secondary outcomes included risk factors for the recurrence of AACE.

Results: The present study included 27 patients in the surgery group and 33 in the chemodenervation group. No significant differences were observed in the motor success rate at 1 and 3 months post-treatment between the two groups. However, the surgery group had a significantly higher motor success rate compared to the chemodenervation group at 6 months post-treatment (100% vs. 69.7%, P < 0.001). The success rate of achieving stereopsis at near ≤ 100 arcsec in the chemodenervation group was significantly higher than in the surgery group at 1 month post-treatment (51.5% vs. 14.8%, P < 0.001). By the 6 months post-treatment, no significant differences were observed in sensory outcomes between the chemodenervation and surgery groups (P > 0.05 for all). In the chemodenervation group, patients with an anisometropia less than 1 dioptor (D)demonstrate significantly higher motor success rate, and better sensory outcomes, including stereopsis at near (84%, 21/25) and stereopsis at near ≤ 100 arcsec (56%, 14/25), compared to those with anisometropia of 1 D or more (P = 0.044).

Conclusion: The success rate after BTX injection was similar to that of surgery for 3 months but lower at 6 months post-treatment. Patients who received BTX showed restoration of stereopsis within the initial first postoperative month, with sustained preservation of this function across 6 months post-treatment. Anisometropia of 1 D may indicate suitability for BTX injection as a preferred treatment option for AACE. Trial registration This study was registered on the Chinese Clinical Trial Registry (ChiCTR2100053717. Registered 28 November 2021. https://www.chictr.org.cn/showprojEN.html?proj=140975 ).

背景:急性获得性共同性内斜视(AACE)严重损害双眼视力,其发病率呈上升趋势。本研究旨在比较AACE患者斜视手术与注射肉毒杆菌毒素(BTX)的疗效,并探讨影响手术成功的因素。方法:对60例AACE患者进行前瞻性比较临床研究。27例患者行切口斜视手术(手术组),33例患者行BTX注射(化学神经支配组)。分别于治疗后1、3、6个月对患者进行随访。主要结果是治疗后6个月的成功率,定义为水平偏差在10棱镜屈光度(PD)或以下,确认双眼单视力。次要结局包括AACE复发的危险因素。结果:手术组27例,化学神经支配组33例。两组治疗后1个月和3个月的运动成功率无显著差异。然而,在治疗后6个月,手术组的运动成功率明显高于化学神经支配组(100% vs 69.7%, P < 0.05)。在化学神经支配组中,与屈光参差大于等于1度的患者相比,屈光参差小于1度(D)的患者表现出更高的运动成功率和更好的感觉结果,包括近视(84%,21/25)和近视(56%,14/25)(P = 0.044)。结论:BTX注射后3个月的成功率与手术后相似,但治疗后6个月的成功率较手术后低。接受BTX治疗的患者在术后第一个月内恢复了立体视觉,并在治疗后6个月内持续保持了这种功能。1d的屈光参差可能表明BTX注射作为AACE的首选治疗方案的适宜性。本研究已在中国临床试验注册中心注册(ChiCTR2100053717)。注册于2021年11月28日。https://www.chictr.org.cn/showprojEN.html?proj=140975)。
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引用次数: 0
Randomized controlled trial on corneal denervation, neuroinflammation and ocular surface in corneal lenticule extraction for advanced refractive correction (CLEAR) and small incision lenticule extraction (SMILE). 高级屈光矫正(CLEAR)和小切口角膜晶状体摘除术(SMILE)中角膜去神经支配、神经炎症和眼表的随机对照试验。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-04-01 DOI: 10.1186/s40662-025-00429-1
Mingyi Yu, Chang Liu, Isabelle Xin Yu Lee, Victor Wei-Tse Hsu, Regina Kay Ting Wong, Ansa Anam, Rong Lim, Jodhbir S Mehta, Yu-Chi Liu

Background: To investigate and compare the corneal denervation, tear neuromediators, and ocular surface changes following corneal lenticule extraction for advanced refractive correction (CLEAR) versus small incision lenticule extraction (SMILE).

Methods: In this randomized clinical trial, 19 patients were randomized to undergo CLEAR in one eye and SMILE in the other eye. Ocular surface assessments, in vivo confocal microscopy for seven corneal nerve parameters, four corneal dendritic cell parameters, three corneal epithelial parameters, and tear neuromediator analysis were performed preoperatively and 1, 3, 6 and 12 months postoperatively.

Results: There were no significant differences in all ocular surface assessments between CLEAR and SMILE throughout postoperative 1 year. CLEAR and SMILE led to significant and comparable reductions of corneal nerve fiber density (CNFD), nerve branch density, total branch density, nerve fiber length, area, and fiber fractal dimension, which did not restore even at 1 year. The reduction in CNFD was significantly correlated with the corrected spherical equivalent in both surgical types. Although post-SMILE eyes had significantly higher nerve growth factor concentrations at 1 month, there was no significant difference in substance P and calcitonin gene-related peptide (CGRP) concentrations between SMILE and CLEAR.

Conclusions: CLEAR and SMILE had comparable effects on ocular surface, corneal denervation and postoperative neuroinflammation. Corneal nerve metrics did not restore even at 1 year for both procedures.

Trial registration number: ClinicalTrials.gov NCT06774651, registration on 14 January 2025, https://clinicaltrials.gov/study/NCT06774651 .

背景:研究和比较先进屈光矫正(CLEAR)和小切口晶状体摘除(SMILE)后角膜去神经控制、撕裂神经介质和眼表的变化。方法:在本随机临床试验中,19例患者随机接受一只眼CLEAR和另一只眼SMILE。术前、术后1、3、6、12个月分别进行眼表评估、角膜7个神经参数、4个角膜树突状细胞参数、3个角膜上皮参数的体内共聚焦显微镜检查和泪液神经介质分析。结果:术后1年内,CLEAR和SMILE的所有眼表评估均无显著差异。CLEAR和SMILE可显著降低角膜神经纤维密度(CNFD)、神经分支密度、总分支密度、神经纤维长度、面积和纤维分形维数,即使在1年后也没有恢复。在两种手术类型中,CNFD的减少与校正的球形当量显著相关。尽管术后1个月时,SMILE组的神经生长因子浓度明显升高,但在P物质和降钙素基因相关肽(CGRP)浓度方面,SMILE组与CLEAR组无显著差异。结论:CLEAR和SMILE在眼表、角膜去神经支配和术后神经炎症方面具有相当的效果。两种手术的角膜神经指标在1年后也没有恢复。试验注册号:ClinicalTrials.gov NCT06774651,注册日期为2025年1月14日,网址:https://clinicaltrials.gov/study/NCT06774651。
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引用次数: 0
Associations between RetNet gene polymorphisms and the efficacy of orthokeratology for myopia control: a retrospective clinical study. RetNet基因多态性与角膜塑形术控制近视疗效之间的关系:一项回顾性临床研究。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-03-17 DOI: 10.1186/s40662-025-00426-4
Ruijing Xia, Xiangyi Yu, Hao Wu, Lulu Peng, Zhenlin Du, Xiaoguang Yu, Shilai Xing, Fan Lu, Xinjie Mao

Background: This study investigated how clinical and genetic factors impact the effectiveness of orthokeratology lenses in myopia.

Methods: A retrospective clinical study was conducted with a sample of 545 children aged 8-12 years who had myopia and have initially worn orthokeratology lenses for one year. Whole-genome sequencing (WGS) was also performed on 60 participants in two groups, one with rapid axial length (AL) progression of larger than 0.33 mm and the other with slow AL progression of less than 0.09 mm. The RetNet database was used to screen candidate genes that may contribute to the effectiveness of orthokeratology lenses in controlling myopia.

Results: Children with greater baseline AL, greater spherical equivalent (SE) and greater age had better myopia control with orthokeratology lenses. A significant excess of nonsynonymous variants was observed among those with slow myopia progression, and these were prominently enriched in retinal disease-related genes. Subsequently, RIMS2 [odds ratio (OR) = 0.01, P = 0.0097] and LCA5 (OR = 9.27, P = 0.0089) were found to harbor an excess number of nonsynonymous variants in patients with slow progression of high myopia. Two intronic common variants rs36006402 in SLC7A14 and rs2285814 in CLUAP1 were strongly associated with AL growth. The identification of these novel genes associated with the effectiveness of orthokeratology lens therapy in myopic children provides insight into the genetic mechanism of orthokeratology treatment.

Conclusion: The effectiveness of orthokeratology lens treatment relates to interindividual variability in the control of AL growth in myopic eyes. The efficacy increased when patients carried more nonsynonymous variants in retinal disease-related gene sets. These data serve as reference for genetic counselling and the management of patients who choose orthokeratology lenses to control myopia.

背景:本研究探讨了临床和遗传因素对角膜塑形镜治疗近视效果的影响。方法:回顾性临床研究545例8-12岁近视儿童,初次配戴角膜塑形镜1年。对60名参与者进行了全基因组测序(WGS),分为两组,一组是轴向长度(AL)快速进展大于0.33 mm,另一组是AL缓慢进展小于0.09 mm。RetNet数据库用于筛选可能有助于角膜塑形镜控制近视有效性的候选基因。结果:基线AL、球等效(SE)和年龄越大的儿童配戴角膜塑形镜控制近视效果越好。在近视进展缓慢的患者中观察到显著过量的非同义变异,这些变异在视网膜疾病相关基因中显著富集。随后,我们发现RIMS2[比值比(OR) = 0.01, P = 0.0097]和LCA5 (OR = 9.27, P = 0.0089)在进展缓慢的高度近视患者中存在过多的非同义变异。SLC7A14的两个内含子共同变异rs36006402和CLUAP1的rs2285814与AL生长密切相关。这些与角膜塑形镜治疗近视儿童有效性相关的新基因的鉴定为角膜塑形镜治疗的遗传机制提供了深入的见解。结论:角膜塑形镜治疗的效果与控制近视眼AL生长的个体差异有关。当患者携带更多视网膜疾病相关基因组的非同义变体时,疗效增加。这些数据可为选择角膜塑形镜控制近视患者的遗传咨询和管理提供参考。
{"title":"Associations between RetNet gene polymorphisms and the efficacy of orthokeratology for myopia control: a retrospective clinical study.","authors":"Ruijing Xia, Xiangyi Yu, Hao Wu, Lulu Peng, Zhenlin Du, Xiaoguang Yu, Shilai Xing, Fan Lu, Xinjie Mao","doi":"10.1186/s40662-025-00426-4","DOIUrl":"10.1186/s40662-025-00426-4","url":null,"abstract":"<p><strong>Background: </strong>This study investigated how clinical and genetic factors impact the effectiveness of orthokeratology lenses in myopia.</p><p><strong>Methods: </strong>A retrospective clinical study was conducted with a sample of 545 children aged 8-12 years who had myopia and have initially worn orthokeratology lenses for one year. Whole-genome sequencing (WGS) was also performed on 60 participants in two groups, one with rapid axial length (AL) progression of larger than 0.33 mm and the other with slow AL progression of less than 0.09 mm. The RetNet database was used to screen candidate genes that may contribute to the effectiveness of orthokeratology lenses in controlling myopia.</p><p><strong>Results: </strong>Children with greater baseline AL, greater spherical equivalent (SE) and greater age had better myopia control with orthokeratology lenses. A significant excess of nonsynonymous variants was observed among those with slow myopia progression, and these were prominently enriched in retinal disease-related genes. Subsequently, RIMS2 [odds ratio (OR) = 0.01, P = 0.0097] and LCA5 (OR = 9.27, P = 0.0089) were found to harbor an excess number of nonsynonymous variants in patients with slow progression of high myopia. Two intronic common variants rs36006402 in SLC7A14 and rs2285814 in CLUAP1 were strongly associated with AL growth. The identification of these novel genes associated with the effectiveness of orthokeratology lens therapy in myopic children provides insight into the genetic mechanism of orthokeratology treatment.</p><p><strong>Conclusion: </strong>The effectiveness of orthokeratology lens treatment relates to interindividual variability in the control of AL growth in myopic eyes. The efficacy increased when patients carried more nonsynonymous variants in retinal disease-related gene sets. These data serve as reference for genetic counselling and the management of patients who choose orthokeratology lenses to control myopia.</p>","PeriodicalId":12194,"journal":{"name":"Eye and Vision","volume":"12 1","pages":"13"},"PeriodicalIF":4.1,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11912624/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143647666","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Iridectomy combined with posterior approach anterior chamber gas injection technique: a novel technique for the treatment of extensive Descemet's membrane detachment. 虹膜切除术联合后入路前房气体注射技术:一种治疗大面积Descemet膜脱离的新技术。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-03-09 DOI: 10.1186/s40662-025-00428-2
Yu Shen, Yongqiao Chen, Fei Yin, Luyi Zhang, Xiaoxia Li, Jing Wu, Miaoqin Wu

Background: To present the iridectomy combined with posterior approach anterior chamber gas injection technique for the treatment of extensive Descemet's membrane detachment (DMD), which is a novel surgical approach for the management of DMD after phacoemulsification.

Case presentation: The surgical technique was performed on a 68-year-old female with a history of cataract phacoemulsification surgery and two times of anterior chamber gas injection to treat DMD. After creating a scleral tunnel at 4 o'clock of the limbus, the iris root in that direction was cut off. This was confirmed via an iris root incision indicating that the syringe needle entered the posterior chamber through the scleral tunnel. The anterior chamber was filled about 3/4 with 16% C3F8. After surgery, patients were required to maintain a supine position without pillows. One month post-surgery, the cornea was transparent, DMD had fully recovered, and the best corrected visual acuity improved to 20/20.

Conclusions: The iridectomy combined with a posterior approach anterior chamber gas injection technique can be used as an alternative surgical option for the management of extensive DMD in patients who have undergone several ineffective anterior chamber gas injection surgeries.

背景:介绍虹膜切除联合后路前房气体注射技术治疗广泛性Descemet膜脱离(DMD),这是一种治疗超声乳化术后DMD的新手术入路。病例介绍:该手术技术应用于一位68岁女性,有白内障超声乳化手术史,两次前房气体注射治疗DMD。在角膜缘的4点钟位置形成巩膜隧道后,这个方向的虹膜根被切断。这是通过虹膜根部切口证实的,表明注射器针头通过巩膜隧道进入后房。前房约3/4填充了16%的C3F8。术后患者需保持仰卧位,不带枕头。术后1个月,角膜透明,DMD完全恢复,最佳矫正视力提高至20/20。结论:虹膜切除术联合后路前房注气技术可作为治疗多次前房注气手术无效的广泛性DMD患者的替代手术选择。
{"title":"Iridectomy combined with posterior approach anterior chamber gas injection technique: a novel technique for the treatment of extensive Descemet's membrane detachment.","authors":"Yu Shen, Yongqiao Chen, Fei Yin, Luyi Zhang, Xiaoxia Li, Jing Wu, Miaoqin Wu","doi":"10.1186/s40662-025-00428-2","DOIUrl":"10.1186/s40662-025-00428-2","url":null,"abstract":"<p><strong>Background: </strong>To present the iridectomy combined with posterior approach anterior chamber gas injection technique for the treatment of extensive Descemet's membrane detachment (DMD), which is a novel surgical approach for the management of DMD after phacoemulsification.</p><p><strong>Case presentation: </strong>The surgical technique was performed on a 68-year-old female with a history of cataract phacoemulsification surgery and two times of anterior chamber gas injection to treat DMD. After creating a scleral tunnel at 4 o'clock of the limbus, the iris root in that direction was cut off. This was confirmed via an iris root incision indicating that the syringe needle entered the posterior chamber through the scleral tunnel. The anterior chamber was filled about 3/4 with 16% C3F8. After surgery, patients were required to maintain a supine position without pillows. One month post-surgery, the cornea was transparent, DMD had fully recovered, and the best corrected visual acuity improved to 20/20.</p><p><strong>Conclusions: </strong>The iridectomy combined with a posterior approach anterior chamber gas injection technique can be used as an alternative surgical option for the management of extensive DMD in patients who have undergone several ineffective anterior chamber gas injection surgeries.</p>","PeriodicalId":12194,"journal":{"name":"Eye and Vision","volume":"12 1","pages":"11"},"PeriodicalIF":4.1,"publicationDate":"2025-03-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11890721/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143585349","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Myopia control efficacy of spectacle lenses with highly aspherical lenslets: results of a 5-year follow-up study. 高度非球面眼镜镜片控制近视的效果:一项5年随访研究结果。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-03-05 DOI: 10.1186/s40662-025-00427-3
Xue Li, Yingying Huang, Chenyao Liu, Xindan Chang, Zaifeng Cui, Qiulin Yang, Björn Drobe, Mark A Bullimore, Hao Chen, Jinhua Bao

Purpose: To evaluate myopia control efficacy in myopic children wearing spectacle lenses with highly aspherical lenslets (HAL) for 5 years.

Methods: This is a randomized, double-masked extended trial. Myopic children aged 8 to 13 years who were originally allocated to the HAL group in the 2-year clinical trial. The HAL group underwent a 5-year assessment for myopia progression using cycloplegic spherical equivalent refraction (SER) and axial length (AL). An extrapolated single-vision spectacle lenses (ESVL) group was used as a control group. The 5-year myopia progression and axial elongation of the ESVL group was calculated based on the 2-year data from the single-vision spectacle lenses group in the same clinical trial, and the data for the following 3 years was estimated by assuming an annual reduction in SER by 9.7% and in AL by 15%. A generalized linear model approach was used to evaluate the treatment efficacy. The validity of the ESVL group was evaluated by comparing myopia progression in the first year of the 3-year estimates with a single-vision spectacle lenses (SVL2) group from a 1-year extended study of the same clinical trial.

Results: Forty-three participants from the original HAL group completed the 5-year visit (74%). Five-year myopia progression [mean ± standard error (SE)] in the HAL group was - 1.27 ± 0.14 D. Compared with the ESVL (- 3.03 ± 0.18 D), myopia progression was - 1.75 ± 0.24 D less for the HAL group (P < 0.001). The mean AL elongation over 5 years was 0.67 ± 0.06 mm for the HAL group compared with 1.40 mm in the ESVL group (P < 0.001), AL elongation was slower by 0.72 ± 0.10 mm for the HAL group (P < 0.001). No significant differences were found for myopia (- 0.58 ± 0.04 D vs. - 0.56 ± 0.05 D) or AL elongation (0.28 ± 0.02 mm vs. 0.28 ± 0.02 mm) between the ESVL group and SVL2 group (PSER = 0.83; PAL = 0.93) in year 3.

Conclusions: In this 5-year study, HAL spectacles reduced the rate of myopia progression and axial elongation, preventing the equivalent of 3 years of myopia progression and axial elongation. Long-term use of HAL spectacles also decreased the incidence of high myopia. Extrapolated control groups are valid for evaluating myopia progression in long-term studies. Trial registration The study was registered at the Chinese Clinical Trial Registry (ChiCTR2100047262), https://www.chictr.org.cn/showproj.html?proj=127182 .

目的:评价近视儿童配戴高度非球面镜片(HAL) 5年控制近视的效果。方法:这是一项随机、双盲的扩展试验。在为期2年的临床试验中,最初被分配到HAL组的8至13岁的近视儿童。HAL组接受了5年的近视进展评估,使用单眼瘫痪的等效球面屈光度(SER)和眼轴长度(AL)。外推单视力镜片组(ESVL)作为对照组。ESVL组的5年近视进展和轴向伸长率是根据同一临床试验中单视力镜片组2年的数据计算的,之后3年的数据是假设SER每年减少9.7%,AL每年减少15%来估计的。采用广义线性模型方法评价治疗效果。ESVL组的有效性是通过比较3年估计第一年的近视进展情况与来自同一临床试验的1年扩展研究的单视力镜片组(SVL2)来评估的。结果:来自原HAL组的43名参与者完成了5年的随访(74%)。HAL组5年近视进展[平均±标准误差(SE)]为- 1.27±0.14 D,与ESVL组(- 3.03±0.18 D)相比,HAL组的近视进展缩短了- 1.75±0.24 D (P SER = 0.83;PAL = 0.93)。结论:在这项为期5年的研究中,HAL眼镜降低了近视进展和轴向伸长的速度,防止了相当于3年的近视进展和轴向伸长。长期使用HAL眼镜也降低了高度近视的发生率。在长期研究中,外推的对照组对于评估近视进展是有效的。本研究在中国临床试验注册中心注册(ChiCTR2100047262), https://www.chictr.org.cn/showproj.html?proj=127182。
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引用次数: 0
Preoperative edema severity affects outcomes after Descemet membrane endothelial keratoplasty for Fuchs endothelial corneal dystrophy: a cohort study. 术前水肿严重程度影响富克斯内皮性角膜营养不良患者行Descemet膜内皮角膜移植术后的预后:一项队列研究。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-03-01 DOI: 10.1186/s40662-025-00425-5
Maximilian Friedrich, Hyeck-Soo Son, Jasper Lind, Maximilian Hammer, Lizaveta Chychko, Timur Mert Yildirim, Gerd Uwe Auffarth, Victor Aristide Augustin

Background: In patients with Fuchs endothelial corneal dystrophy (FECD), the most beneficial stage to perform Descemet membrane endothelial keratoplasty (DMEK) remains uncertain. The goal of this study was to compare the surgical outcomes after DMEK in FECD patients with subclinical corneal edema and clinical corneal edema to test the hypothesis of whether performing surgery in subclinical corneal edema stages achieves better surgical outcomes.

Methods: In this prospective, observational, single-institution cohort study, 106 pseudophakic eyes of 85 patients with FECD were divided into two groups depending on the presence of preoperative subclinical and clinical corneal edema. Subclinical corneal edema was diagnosed if more than one of the following criteria was present in Scheimpflug tomography: loss of regular isopachs, displacement of the thinnest point of the cornea, and focal posterior corneal surface depression. Clinical corneal edema was diagnosed with slit-lamp biomicroscopy. The primary outcome was the corrected distance visual acuity (CDVA) 4 months after DMEK. Secondary outcomes were central corneal thickness (CCT), thinnest corneal thickness (TCT), and total corneal density (TCD) in Scheimpflug tomography, as well as endothelial cell loss (ECL) and the re-bubbling rate. The differences between both groups were analyzed using clustered Wilcoxon rank-sum tests or a Chi-squared test.

Results: Postoperative CDVA was significantly better in the group with subclinical edema (0.18 ± 0.12 logMAR) compared to the group with clinical edema (0.24 ± 0.19 logMAR; P = 0.026). Four months after DMEK, TCD was higher in the group with preoperative clinical edema [31.7 ± 8.3 gray scale units (GSU)] compared to the group with subclinical edema (27.8 ± 6.1 GSU; P = 0.005). The postoperative CCT, TCT, ECL, and re-bubbling rates did not differ significantly between both groups (all P > 0.05).

Conclusions: DMEK for FECD yielded better visual acuity after 4 months when performed in the early stage of FECD compared to a later stage with clinical edema. This may be attributable to persistent corneal fibrosis after DMEK in eyes with preoperative clinically evident corneal edema, as suggested by higher postoperative corneal density in eyes with clinical edema. Consequently, the findings advocate for the consideration of earlier DMEK in FECD patients to achieve better surgical recovery.

背景:在Fuchs内皮性角膜营养不良(FECD)患者中,实施Descemet膜内皮角膜移植术(DMEK)的最有利阶段仍不确定。本研究的目的是比较feecd亚临床角膜水肿患者与临床角膜水肿患者行DMEK后的手术效果,以验证在亚临床角膜水肿期进行手术是否能获得更好的手术效果。方法:在这项前瞻性、观察性、单机构队列研究中,根据术前亚临床和临床角膜水肿的存在将85例FECD患者的106只假性晶状眼分为两组。如果在Scheimpflug断层扫描中出现以下标准之一以上,则诊断为亚临床角膜水肿:正常等厚缺失,角膜最薄点移位,角膜后表面局灶性凹陷。应用裂隙灯生物显微镜诊断临床角膜水肿。主要观察指标为DMEK术后4个月的矫正距离视力(CDVA)。次要结果为角膜中央厚度(CCT)、最薄角膜厚度(TCT)和角膜总密度(TCD),以及内皮细胞损失(ECL)和再泡率。两组间的差异采用聚类Wilcoxon秩和检验或卡方检验进行分析。结果:亚临床水肿组术后CDVA(0.18±0.12 logMAR)明显优于临床水肿组(0.24±0.19 logMAR;p = 0.026)。DMEK后4个月,术前临床水肿组TCD[31.7±8.3灰度单位(GSU)]高于亚临床水肿组(27.8±6.1 GSU;p = 0.005)。两组术后CCT、TCT、ECL、再泡率差异无统计学意义(均P < 0.05)。结论:与临床水肿晚期相比,FECD早期DMEK在4个月后获得了更好的视力。这可能是由于术前有明显的角膜水肿的眼睛在DMEK后角膜持续纤维化,临床水肿的眼睛术后角膜密度较高。因此,研究结果提倡在FECD患者中考虑早期DMEK以获得更好的手术恢复。
{"title":"Preoperative edema severity affects outcomes after Descemet membrane endothelial keratoplasty for Fuchs endothelial corneal dystrophy: a cohort study.","authors":"Maximilian Friedrich, Hyeck-Soo Son, Jasper Lind, Maximilian Hammer, Lizaveta Chychko, Timur Mert Yildirim, Gerd Uwe Auffarth, Victor Aristide Augustin","doi":"10.1186/s40662-025-00425-5","DOIUrl":"10.1186/s40662-025-00425-5","url":null,"abstract":"<p><strong>Background: </strong>In patients with Fuchs endothelial corneal dystrophy (FECD), the most beneficial stage to perform Descemet membrane endothelial keratoplasty (DMEK) remains uncertain. The goal of this study was to compare the surgical outcomes after DMEK in FECD patients with subclinical corneal edema and clinical corneal edema to test the hypothesis of whether performing surgery in subclinical corneal edema stages achieves better surgical outcomes.</p><p><strong>Methods: </strong>In this prospective, observational, single-institution cohort study, 106 pseudophakic eyes of 85 patients with FECD were divided into two groups depending on the presence of preoperative subclinical and clinical corneal edema. Subclinical corneal edema was diagnosed if more than one of the following criteria was present in Scheimpflug tomography: loss of regular isopachs, displacement of the thinnest point of the cornea, and focal posterior corneal surface depression. Clinical corneal edema was diagnosed with slit-lamp biomicroscopy. The primary outcome was the corrected distance visual acuity (CDVA) 4 months after DMEK. Secondary outcomes were central corneal thickness (CCT), thinnest corneal thickness (TCT), and total corneal density (TCD) in Scheimpflug tomography, as well as endothelial cell loss (ECL) and the re-bubbling rate. The differences between both groups were analyzed using clustered Wilcoxon rank-sum tests or a Chi-squared test.</p><p><strong>Results: </strong>Postoperative CDVA was significantly better in the group with subclinical edema (0.18 ± 0.12 logMAR) compared to the group with clinical edema (0.24 ± 0.19 logMAR; P = 0.026). Four months after DMEK, TCD was higher in the group with preoperative clinical edema [31.7 ± 8.3 gray scale units (GSU)] compared to the group with subclinical edema (27.8 ± 6.1 GSU; P = 0.005). The postoperative CCT, TCT, ECL, and re-bubbling rates did not differ significantly between both groups (all P > 0.05).</p><p><strong>Conclusions: </strong>DMEK for FECD yielded better visual acuity after 4 months when performed in the early stage of FECD compared to a later stage with clinical edema. This may be attributable to persistent corneal fibrosis after DMEK in eyes with preoperative clinically evident corneal edema, as suggested by higher postoperative corneal density in eyes with clinical edema. Consequently, the findings advocate for the consideration of earlier DMEK in FECD patients to achieve better surgical recovery.</p>","PeriodicalId":12194,"journal":{"name":"Eye and Vision","volume":"12 1","pages":"9"},"PeriodicalIF":4.1,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11871603/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143531573","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Eye and Vision
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