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Comment on: Glucagon-Like Peptide-1 Receptor Agonist Use and Risk of Cataract Development. 评论:胰高血糖素样肽-1受体激动剂的使用和白内障发展的风险。
IF 4.2 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-12-29 DOI: 10.1016/j.ajo.2025.11.050
Ha-Neul Yu, Isdin Oke, Julius T Oatts
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引用次数: 0
Association of Sodium-Glucose Cotransporter 2 Inhibitors and Glucagon-Like Peptide-1 Receptor Agonists With Risk of Cataract 钠-葡萄糖共转运蛋白2抑制剂和胰高血糖素样肽-1受体激动剂与白内障风险的关系
IF 4.2 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-12-26 DOI: 10.1016/j.ajo.2025.12.025
Bing-Hua Lin , Shu-Han Chuang , Lien-Chen Wu , Yu-Pin Chen , Yi-Jie Kuo , Cheng-Hsien Chang

Purpose

To evaluate the risk of age-related cataract (ARC) among patients with type 2 diabetes mellitus (T2DM) using sodium-glucose cotransporter 2 inhibitors (SGLT2i) or glucagon-like peptide-1 receptor agonists (GLP-1 RA) as second-line antihyperglycemic agents.

Design

Population-based retrospective cohort study.

Participants

Adults aged over 40 years with a diagnosis of T2DM between January 2015 and June 2025 were identified from the TriNetX Global Network. The patients were categorized into three cohorts: (1) SGLT2i plus metformin, (2) GLP-1 RA plus metformin, and (3) metformin monotherapy. Patients with aphakia or pseudophakia, orbital injuries, secondary cataracts, or congenital ocular malformations were excluded.

Methods

Pairwise comparisons were performed with a 3-year follow-up. Baseline characteristics were balanced using 1:1 propensity score matching for demographics, comorbidities, T2DM severity, and cataract risk factors. Cox proportional hazards models were applied to estimate hazard ratios (HRs) and 95% confidence intervals (CIs).

Main Outcome Measures

The primary outcome was the incidence of ARC events, defined as a diagnosis of ARC or cataract surgery, with stratified analyses conducted by demographics, glycemic control, and comorbidities.

Results

After matching, three pairwise comparisons included 34,259 (SGLT2i vs metformin; mean age, 62.8 years; 35.1% female), 50,877 (GLP-1 RA vs metformin; mean age, 58.3 years; 54.8% female), and 23,022 (SGLT2i vs GLP-1 RA; mean age, 61.0 years; 40.8% female) patients. Adjunctive SGLT2i or GLP-1 RA was associated with a reduced risk of ARC events (SGLT2i, HR: 0.82, 95% CI: 0.76-0.89; GLP-1 RA, HR: 0.93, 95% CI: 0.87-0.99). The protective effect of SGLT2i was greater than that of GLP-1 RA (HR: 0.84, 95% CI: 0.76-0.92). However, in patients with advanced age, obesity, or diabetic retinopathy, the association attenuated. When analyzed as separate outcomes, adjunctive use of SGLT2i and GLP-1 RA remained associated with a reduced risk of ARC diagnosis, while the risk of cataract surgery did not differ significantly (SGLT2i, HR: 1.14, 95% CI: 0.95-1.34; GLP-1 RA, HR: 1.01, 95% CI: 0.79-1.26).

Conclusions

Adjunctive use of SGLT2i or GLP-1 RA was associated with a lower risk of ARC, with a stronger effect for SGLT2i; however, neither agent reduced the risk of cataract surgery. Further studies are needed to clarify the underlying biological pathways and validate our findings.
目的评价钠-葡萄糖共转运蛋白2抑制剂(SGLT2i)或胰高血糖素样肽-1受体激动剂(GLP-1 RA)作为二线降糖药物对2型糖尿病(T2DM)患者发生年龄相关性白内障(ARC)的风险。设计基于人群的回顾性队列研究。2015年1月至2025年6月期间诊断为2型糖尿病的40岁以上成年人从TriNetX全球网络中确定。患者被分为三个队列:(1)SGLT2i +二甲双胍,(2)GLP-1 RA +二甲双胍,(3)二甲双胍单药治疗。排除无晶状体或假性晶状体、眼窝损伤、继发性白内障或先天性眼畸形的患者。方法采用3年随访进行两组比较。基线特征采用1:1倾向评分匹配人口统计学、合并症、T2DM严重程度和白内障危险因素进行平衡。采用Cox比例风险模型估计风险比(hr)和95%置信区间(ci)。主要结局指标主要结局指标是ARC事件的发生率,定义为ARC或白内障手术的诊断,并根据人口统计学、血糖控制和合并症进行分层分析。结果匹配后,三组两两比较包括34,259例(SGLT2i vs二甲双胍,平均年龄62.8岁,女性占35.1%)、50,877例(GLP-1 RA vs二甲双胍,平均年龄58.3岁,女性占54.8%)和23,022例(SGLT2i vs GLP-1 RA,平均年龄61.0岁,女性占40.8%)患者。辅助SGLT2i或GLP-1 RA与降低ARC事件的风险相关(SGLT2i, HR: 0.82, 95% CI: 0.76-0.89; GLP-1 RA, HR: 0.93, 95% CI: 0.87-0.99)。SGLT2i的保护作用大于GLP-1 RA (HR: 0.84, 95% CI: 0.76 ~ 0.92)。然而,在老年、肥胖或糖尿病视网膜病变患者中,相关性减弱。当作为单独的结果进行分析时,辅助使用SGLT2i和GLP-1 RA仍然与ARC诊断风险降低相关,而白内障手术的风险没有显着差异(SGLT2i, HR: 1.14, 95% CI: 0.95-1.34; GLP-1 RA, HR: 1.01, 95% CI: 0.79-1.26)。结论联合使用SGLT2i或GLP-1 RA与较低的ARC风险相关,且对SGLT2i的作用更强;然而,这两种药物都不能降低白内障手术的风险。需要进一步的研究来阐明潜在的生物学途径并验证我们的发现。
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引用次数: 0
The AJO and Academic Freedom: Then and Now AJO和学术自由:过去和现在
IF 4.2 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-12-26 DOI: 10.1016/j.ajo.2025.12.023
Richard K. Parrish
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引用次数: 0
Elevated Retinal Neovascularization on Widefield Optical Coherence Tomography Angiography Predicts Complications in High-Risk Proliferative Diabetic Retinopathy 宽视场OCTA RNV升高预测高危PDR并发症
IF 4.2 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-12-24 DOI: 10.1016/j.ajo.2025.12.017
AN-LUN WU , JINYI HAO , LIQIN GAO , YUKUN GUO , TRISTAN T. HORMEL , CHRISTINA J. FLAXEL , MERINA THOMAS , BENJAMIN K. YOUNG , STEVEN T. BAILEY , DONG-WOUK PARK , YALI JIA , THOMAS S. HWANG

Purpose

To determine whether retinal neovascularization (RNV) metrics derived from single-shot widefield swept-source OCT angiography (SS-OCTA) predict subsequent vision-threatening complications in eyes with high-risk proliferative diabetic retinopathy (PDR).

Design

Prospective case series.

Participants

Eyes clinically graded as high-risk PDR at a tertiary care center, followed up for at least 6 months.

Methods

Eligible eyes underwent single-shot 26 × 21-mm SS-OCTA imaging (DREAM OCT, Intalight Inc.). A validated deep learning-based algorithm segmented the vitreous cavity slab to generate en face OCTA images for automated detection and quantification of RNV membrane and the vascular areas. Lesions were classified as elevated when they were separated from the internal limiting membrane (ILM) and attached when there was no space between the lesion and the ILM. We analyzed baseline OCTA-derived metrics for their predicting eyes that developed new or recurrent vitreous hemorrhage (VH) or tractional retinal detachment (TRD) during follow-up.

Main outcome measures

Incidence of new or recurrent vitreous hemorrhage and traction retinal detachment.

Results

Over a median follow-up period of 291 days (range, 180-466), 8 of 18 eyes (44.4%) developed complications, with 7 (38.9%) developing VH and 1 (5.6%) developing TRD. Among the 115 identified RNV lesions, 87 (75.7%) were located outside the arcades. Compared to eyes without complications, eyes with complications had a larger median total RNV membrane area (25.72 mm² vs 1.33 mm²; P = .006) and a larger median total RNV vascular area (9.72 mm² vs 0.76 mm²; P = .010). Eyes with complications had a larger elevated RNV membrane area (5.13 mm² vs 0.10 mm²; P = .009) and vascular area (2.69 mm² vs 0.05 mm²; P = .007), whereas attached RNV metrics were not significantly different between groups. Total RNV membrane area demonstrated the highest predictive performance for identifying eyes at risk of complications (AUC = 0.888), with a sensitivity of 87.5% and a specificity of 80.0% at a cutoff value of 3.40 mm².

Conclusions

Widefield SS-OCTA is useful for evaluating RNV burden and its axial relationship to the ILM in high-risk PDR. Elevated baseline RNV, incorporating spatial and anatomic features, predicts subsequent tractional complications such as VH and TRD. These imaging biomarkers may complement current clinical staging of PDR.
目的探讨单次广角扫描源OCT血管造影(SS-OCTA)视网膜新生血管(RNV)指标是否能预测高风险增殖性糖尿病视网膜病变(PDR)患者随后出现的视力威胁并发症。DesignProspective案例系列。参与者在三级医疗中心被临床分级为高风险PDR,随访至少6个月。方法对符合条件的眼睛进行26 × 21 mm SS-OCTA单次成像(DREAM OCT, Intalight Inc.)。经过验证的基于深度学习的算法对玻璃体腔板进行分割,生成正面OCTA图像,用于RNV膜和血管区域的自动检测和定量。当病变与内限制膜(ILM)分离时,病变被归类为升高,当病变与内限制膜之间没有空间时,病变被归类为附着。我们分析了基线octa衍生指标,用于预测随访期间发生新的或复发性玻璃体出血(VH)或牵引性视网膜脱离(TRD)的眼睛。主要观察指标:新发或复发玻璃体出血及牵引性视网膜脱离的发生率。结果18只眼中有8只(44.4%)发生并发症,其中7只(38.9%)发生VH, 1只(5.6%)发生TRD。在115例确诊的RNV病变中,87例(75.7%)位于拱廊外。与无并发症的眼睛相比,有并发症的眼睛中位总RNV膜面积更大(25.72 mm²vs 1.33 mm²;P = )。006)和更大的中位总RNV血管面积(9.72 mm²vs 0.76 mm²;P = .010)。并发症眼RNV膜面积升高较大(5.13 mm²vs 0.10 mm²;P = )。009)和血管面积(2.69 mm²vs 0.05 mm²;P = 。007),而附加的RNV指标在组间无显著差异。总RNV膜面积在识别并发症风险方面表现出最高的预测性能(AUC = 0.888),在截止值为3.40 mm²时,敏感性为87.5%,特异性为80.0%。结论swdefield SS-OCTA可用于评价高危PDR患者RNV负荷及其与ILM的轴向关系。基线RNV升高,结合空间和解剖特征,预测随后的牵拉并发症,如VH和TRD。这些成像生物标志物可以补充当前PDR的临床分期。
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引用次数: 0
Geographic and Phenotypic Variability in RHO-Associated Retinopathy: Evidence From a Chinese Cohort and Global Literature rho相关视网膜病变的地理和表型变异:来自中国队列和全球文献的证据
IF 4.2 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-12-23 DOI: 10.1016/j.ajo.2025.12.020
CHENYUE HANG , TIANYUAN ZHAO , ZHIXUAN CHEN , HONG WANG , LIN CHEN , TING ZHANG , YUTIAN JIAO , TONG LI , JUNRAN SUN , SUQIN YU , YUANYUAN GONG , HAO ZHOU , XUJUN JIANG , XINXIN LIU , HUIXUN JIA , KAIRONG ZHENG , XIAOLING WAN , JIEQIONG CHEN , XIAODONG SUN

Purpose

To investigate the genotype-phenotype correlation in RHO-associated retinopathy, with a focus on delineating an ethnic-specific variant spectrum and comparing clinical severity across biological classes and common variants.

Design

Retrospective cohort study and literature review.

Methods

We systematically reviewed all published cases of RHO-associated retinal diseases (2196 patients, 1278 probands) and analyzed clinical, genetic, and imaging data from our institutional cohort (80 probands). Variants were categorized by type and by biological class (Class 1-7), and phenotypes were compared across different biological classes and three common variants.

Results

A marked geographic divergence was observed: P23H was common in North America but rare in other populations, whereas P347L and R135W were major common variants in European and Asian populations. Genotype-phenotype analysis revealed that Class 2 variants were associated with later onset and slower visual decline, whereas Class 1 and Class 3 variants correlated with earlier onset (P < .0001) and more aggressive phenotypes. Notably, R135W (Class 3) emerged as an under-recognized but highly aggressive variant, with earlier onset (P < .01) and potentially earlier macular involvement.

Conclusions

Our study represents the largest study integrating ethnic, genotypic, and clinical data in RHO-associated retinopathy. The findings highlight substantial inter-ethnic differences in common variants and underscore the clinical relevance of biological classification in predicting disease course. In particular, R135W and P347L warrants closer clinical attention due to their aggressive trajectory, which may inform prioritization in gene therapy trials and individualized patient management.
目的研究rho相关视网膜病变的基因型-表型相关性,重点描述种族特异性变异谱,并比较不同生物类别和常见变异的临床严重程度。设计回顾性队列研究及文献回顾。方法:我们系统地回顾了所有已发表的rro相关视网膜疾病病例(2196例患者,1278个先证者),并分析了我们的机构队列(80个先证者)的临床、遗传和影像学资料。变异按类型和生物类别(1-7类)分类,并比较了不同生物类别和三种常见变异的表型。结果P23H基因在北美人群中较为常见,在其他人群中较为少见,而P347L和R135W基因在欧洲和亚洲人群中较为常见。基因型-表型分析显示,2类变异与发病较晚和较慢的视力下降有关,而1类和3类变异与发病较早(P < .0001)和更具侵袭性的表型相关。值得注意的是,R135W(3类)是一种未被充分认识但具有高度侵袭性的变异,发病时间更早(P < 0.01),可能更早累及黄斑。sour研究是整合rho相关视网膜病变种族、基因型和临床数据的最大研究。研究结果强调了常见变异的实质性种族间差异,并强调了生物学分类在预测疾病进程中的临床相关性。特别是,R135W和P347L由于其侵袭性轨迹,值得更密切的临床关注,这可能为基因治疗试验和个体化患者管理的优先级提供信息。
{"title":"Geographic and Phenotypic Variability in RHO-Associated Retinopathy: Evidence From a Chinese Cohort and Global Literature","authors":"CHENYUE HANG ,&nbsp;TIANYUAN ZHAO ,&nbsp;ZHIXUAN CHEN ,&nbsp;HONG WANG ,&nbsp;LIN CHEN ,&nbsp;TING ZHANG ,&nbsp;YUTIAN JIAO ,&nbsp;TONG LI ,&nbsp;JUNRAN SUN ,&nbsp;SUQIN YU ,&nbsp;YUANYUAN GONG ,&nbsp;HAO ZHOU ,&nbsp;XUJUN JIANG ,&nbsp;XINXIN LIU ,&nbsp;HUIXUN JIA ,&nbsp;KAIRONG ZHENG ,&nbsp;XIAOLING WAN ,&nbsp;JIEQIONG CHEN ,&nbsp;XIAODONG SUN","doi":"10.1016/j.ajo.2025.12.020","DOIUrl":"10.1016/j.ajo.2025.12.020","url":null,"abstract":"<div><h3>Purpose</h3><div>To investigate the genotype-phenotype correlation in <em>RHO</em>-associated retinopathy, with a focus on delineating an ethnic-specific variant spectrum and comparing clinical severity across biological classes and common variants.</div></div><div><h3>Design</h3><div>Retrospective cohort study and literature review.</div></div><div><h3>Methods</h3><div>We systematically reviewed all published cases of <em>RHO</em>-associated retinal diseases (2196 patients, 1278 probands) and analyzed clinical, genetic, and imaging data from our institutional cohort (80 probands). Variants were categorized by type and by biological class (Class 1-7), and phenotypes were compared across different biological classes and three common variants.</div></div><div><h3>Results</h3><div>A marked geographic divergence was observed: P23H was common in North America but rare in other populations, whereas P347L and R135W were major common variants in European and Asian populations. Genotype-phenotype analysis revealed that Class 2 variants were associated with later onset and slower visual decline, whereas Class 1 and Class 3 variants correlated with earlier onset (<em>P</em> &lt; .0001) and more aggressive phenotypes. Notably, R135W (Class 3) emerged as an under-recognized but highly aggressive variant, with earlier onset (<em>P</em> &lt; .01) and potentially earlier macular involvement.</div></div><div><h3>Conclusions</h3><div>Our study represents the largest study integrating ethnic, genotypic, and clinical data in <em>RHO</em>-associated retinopathy. The findings highlight substantial inter-ethnic differences in common variants and underscore the clinical relevance of biological classification in predicting disease course. In particular, R135W and P347L warrants closer clinical attention due to their aggressive trajectory, which may inform prioritization in gene therapy trials and individualized patient management.</div></div>","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":"284 ","pages":"Pages 1-11"},"PeriodicalIF":4.2,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145823647","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Natural History of CNGA1-Associated Retinitis Pigmentosa in a Large Chinese Cohort Revealing an Optimal Intervention Window cnga1相关视网膜色素变性的自然历史揭示了一个最佳的干预窗口
IF 4.2 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-12-23 DOI: 10.1016/j.ajo.2025.12.018
YUE LIU , DINGDING ZHANG , YUNYU ZHOU , YAMEI LI , XIAOXU HAN , ZIXI SUN , XING WEI , HUI LI , XUAN ZOU , RUIFANG SUI

Purpose

To detail the natural history, clinical manifestations, and molecular characteristics of a large Chinese cohort of patients with CNGA1-associated retinitis pigmentosa (CNGA1-RP).

Design

Single-center, retrospective case series.

Participants

A total of 58 Chinese patients with CNGA1-RP from 52 families were enrolled between 2011 and 2025.

Methods

Longitudinal data were available for 20 individuals, with the longest follow-up of 11 years. All participants underwent comprehensive clinical evaluations and genetic analysis. The impact of age on best-corrected visual acuity (BCVA) and visual field (VF) was evaluated using restricted cubic spline (RCS) analysis. Retinal multimodal imaging was acquired, including optical coherence tomography (OCT), ultra-widefield (UWF) scanning laser ophthalmoscope (SLO) and UWF fundus autofluorescence (FAF). Moreover, electroretinogram (ERG) was performed.

Main Outcome Measures

Clinical symptoms, age-related changes in BCVA and VF, retinal multimodal imaging features, molecular characteristics.

Results

Night blindness was the universal initial symptom, with most patients (88%) experiencing onset during childhood. BCVA remained stable (0.09 logMAR) until age of 30.7 years, followed by a progressive decline at 0.029 logMAR per year; by age of 72 years, 32% of patients had developed blindness (BCVA > 1.30 logMAR). VF impairment began in childhood and progressed to tunnel vision (VF ≤ 10°) at a median age of 39.4 years. A high degree of interocular symmetry was observed for both BCVA and VF. FAF imaging revealed a macular hyper-autofluorescent (hyperAF) ring in 73% of patients. Genetic analysis identified 14 novel pathogenic variants in CNGA1, and c.265delC was confirmed as a hotspot variant with an allele frequency of 72% in the Chinese population. Furthermore, homozygous carriers of this hotspot variant exhibited more severe phenotypes.

Conclusions

Our study characterized the natural history of CNGA1-RP and identified c.265delC as a hotspot variant in the Chinese population. Based on the quantitative data, VA loss in CNGA1-RP is late-onset and slow-progressing, whereas VF loss occurs earlier and more severely. The optimal window of intervention for CNGA1-RP in the Chinese population appears to be between the 3rd and 4th decade of life.
目的探讨中国cnga1相关性视网膜色素变性(CNGA1-RP)患者的自然病史、临床表现和分子特征。设计单中心回顾性病例系列。2011年至2025年间,共有58名来自52个家庭的CNGA1-RP患者入组。方法收集20例患者的纵向资料,最长随访时间为11年。所有参与者都进行了全面的临床评估和基因分析。采用限制性三次样条(RCS)分析评价年龄对最佳矫正视力(BCVA)和视野(VF)的影响。获得视网膜多模态成像,包括光学相干断层扫描(OCT)、超宽视场(UWF)扫描激光检眼镜(SLO)和超宽视场眼底自体荧光(FAF)。并行视网膜电图(ERG)检查。临床症状、BCVA和VF的年龄相关变化、视网膜多模态成像特征、分子特征。结果夜盲症是常见的首发症状,大多数患者(88%)在儿童期发病。BCVA在30.7岁前保持稳定(0.09 logMAR),随后以每年0.029 logMAR的速度逐渐下降;到72岁时,32%的患者发生失明(BCVA > 1.30 logMAR)。VF损害始于儿童时期,在中位年龄39.4岁时发展为隧道性视力(VF≤10°)。BCVA和VF均有高度眼间对称性。FAF成像显示73%的患者有黄斑超自体荧光环。遗传分析发现CNGA1有14个新的致病变异,其中c.265delC在中国人群中被确认为热点变异,等位基因频率为72%。此外,该热点变异的纯合携带者表现出更严重的表型。结论我们研究了CNGA1-RP的自然历史,确定了c.265delC是中国人群中的热点变异。定量数据显示,CNGA1-RP的VA损失是晚发性的、进展缓慢的,而VF损失发生的更早、更严重。在中国人群中,CNGA1-RP的最佳干预窗口似乎是在生命的第三和第四个十年之间。
{"title":"Natural History of CNGA1-Associated Retinitis Pigmentosa in a Large Chinese Cohort Revealing an Optimal Intervention Window","authors":"YUE LIU ,&nbsp;DINGDING ZHANG ,&nbsp;YUNYU ZHOU ,&nbsp;YAMEI LI ,&nbsp;XIAOXU HAN ,&nbsp;ZIXI SUN ,&nbsp;XING WEI ,&nbsp;HUI LI ,&nbsp;XUAN ZOU ,&nbsp;RUIFANG SUI","doi":"10.1016/j.ajo.2025.12.018","DOIUrl":"10.1016/j.ajo.2025.12.018","url":null,"abstract":"<div><h3>Purpose</h3><div>To detail the natural history, clinical manifestations, and molecular characteristics of a large Chinese cohort of patients with <em>CNGA1</em>-associated retinitis pigmentosa (<em>CNGA1-RP</em>).</div></div><div><h3>Design</h3><div>Single-center, retrospective case series.</div></div><div><h3>Participants</h3><div>A total of 58 Chinese patients with <em>CNGA1-RP</em> from 52 families were enrolled between 2011 and 2025.</div></div><div><h3>Methods</h3><div>Longitudinal data were available for 20 individuals, with the longest follow-up of 11 years. All participants underwent comprehensive clinical evaluations and genetic analysis. The impact of age on best-corrected visual acuity (BCVA) and visual field (VF) was evaluated using restricted cubic spline (RCS) analysis. Retinal multimodal imaging was acquired, including optical coherence tomography (OCT), ultra-widefield (UWF) scanning laser ophthalmoscope (SLO) and UWF fundus autofluorescence (FAF). Moreover, electroretinogram (ERG) was performed.</div></div><div><h3>Main Outcome Measures</h3><div>Clinical symptoms, age-related changes in BCVA and VF, retinal multimodal imaging features, molecular characteristics.</div></div><div><h3>Results</h3><div>Night blindness was the universal initial symptom, with most patients (88%) experiencing onset during childhood. BCVA remained stable (0.09 logMAR) until age of 30.7 years, followed by a progressive decline at 0.029 logMAR per year; by age of 72 years, 32% of patients had developed blindness (BCVA <strong>&gt;</strong> 1.30 logMAR). VF impairment began in childhood and progressed to tunnel vision (VF ≤ 10°) at a median age of 39.4 years. A high degree of interocular symmetry was observed for both BCVA and VF. FAF imaging revealed a macular hyper-autofluorescent (hyperAF) ring in 73% of patients. Genetic analysis identified 14 novel pathogenic variants in <em>CNGA1</em>, and c.265delC was confirmed as a hotspot variant with an allele frequency of 72% in the Chinese population. Furthermore, homozygous carriers of this hotspot variant exhibited more severe phenotypes.</div></div><div><h3>Conclusions</h3><div>Our study characterized the natural history of <em>CNGA1</em>-RP and identified c.265delC as a hotspot variant in the Chinese population. Based on the quantitative data, VA loss in <em>CNGA1</em>-RP is late-onset and slow-progressing, whereas VF loss occurs earlier and more severely. The optimal window of intervention for <em>CNGA1</em>-RP in the Chinese population appears to be between the 3rd and 4th decade of life.</div></div>","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":"283 ","pages":"Pages 299-312"},"PeriodicalIF":4.2,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145822822","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Gonioscopy Assisted Transluminal Trabeculotomy (GATT) as a viable intervention for Neovascular Glaucoma 经腔镜辅助小梁切开术(GATT)作为新生血管性青光眼可行的干预手段
IF 4.2 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-12-23 DOI: 10.1016/j.ajo.2025.12.016
Avilasha Mohapatra, Vyshak Suresh, Sushmita Kaushik
{"title":"Gonioscopy Assisted Transluminal Trabeculotomy (GATT) as a viable intervention for Neovascular Glaucoma","authors":"Avilasha Mohapatra,&nbsp;Vyshak Suresh,&nbsp;Sushmita Kaushik","doi":"10.1016/j.ajo.2025.12.016","DOIUrl":"10.1016/j.ajo.2025.12.016","url":null,"abstract":"","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":"283 ","pages":"Pages e1-e2"},"PeriodicalIF":4.2,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145822821","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Interpreting Imaging in the Era of Artificial Intelligence: Future Possibilities in Ocular Inflammatory Disease 解读人工智能时代的影像:眼炎性疾病的未来可能性
IF 4.2 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-12-22 DOI: 10.1016/j.ajo.2025.12.019
K. MATTHEW MCKAY , LEOPOLD SCHMETTERER , SRINIVAS R. SADDA , LUCIA SOBRIN

Purpose

Uveitis encompasses a heterogeneous group of ocular inflammatory diseases with a high risk of permanent vision loss. Accurate diagnosis and disease monitoring are dependent on integrating disparate clinical data from patient history, examination findings and multimodal imaging, which is complex and time-consuming. The advent of artificial intelligence (AI) in the field of ophthalmology has provided new opportunities for automation of data gathering and interpretation, particularly for imaging data through deep learning algorithms. This article will review the current abilities, limitations, and future promise for the application of AI to the interpretation of multimodal imaging in the field of uveitis.

Methods

Review article.

Results

AI has provided new opportunities for automation of data gathering and interpretation in the field of uveitis, particularly for analysis of imaging data using deep learning techniques. Tools for diagnostic support, grading of intraocular inflammation, and quantification of disease features by multimodal imaging are under development.

Conclusion

Application of AI in the field of uveitis is in its infancy but holds promise for improving efficiency and quality of patient care.
目的葡萄膜炎是一种异质性的眼部炎症性疾病,具有永久性视力丧失的高风险。准确的诊断和疾病监测依赖于整合来自患者病史、检查结果和多模式成像的不同临床数据,这既复杂又耗时。人工智能(AI)在眼科领域的出现为数据收集和解释的自动化提供了新的机会,特别是通过深度学习算法进行成像数据。本文将回顾人工智能在葡萄膜炎领域多模态成像解释中的当前能力、局限性和未来前景。MethodsReview文章。结果为葡萄膜炎领域的数据采集和解释自动化提供了新的机会,特别是使用深度学习技术对成像数据进行分析。目前正在开发用于诊断支持、眼内炎症分级和通过多模态成像对疾病特征进行量化的工具。结论人工智能在葡萄膜炎领域的应用尚处于起步阶段,但有望提高患者护理的效率和质量。
{"title":"Interpreting Imaging in the Era of Artificial Intelligence: Future Possibilities in Ocular Inflammatory Disease","authors":"K. MATTHEW MCKAY ,&nbsp;LEOPOLD SCHMETTERER ,&nbsp;SRINIVAS R. SADDA ,&nbsp;LUCIA SOBRIN","doi":"10.1016/j.ajo.2025.12.019","DOIUrl":"10.1016/j.ajo.2025.12.019","url":null,"abstract":"<div><h3>Purpose</h3><div>Uveitis encompasses a heterogeneous group of ocular inflammatory diseases with a high risk of permanent vision loss. Accurate diagnosis and disease monitoring are dependent on integrating disparate clinical data from patient history, examination findings and multimodal imaging, which is complex and time-consuming. The advent of artificial intelligence (AI) in the field of ophthalmology has provided new opportunities for automation of data gathering and interpretation, particularly for imaging data through deep learning algorithms. This article will review the current abilities, limitations, and future promise for the application of AI to the interpretation of multimodal imaging in the field of uveitis.</div></div><div><h3>Methods</h3><div>Review article.</div></div><div><h3>Results</h3><div>AI has provided new opportunities for automation of data gathering and interpretation in the field of uveitis, particularly for analysis of imaging data using deep learning techniques. Tools for diagnostic support, grading of intraocular inflammation, and quantification of disease features by multimodal imaging are under development.</div></div><div><h3>Conclusion</h3><div>Application of AI in the field of uveitis is in its infancy but holds promise for improving efficiency and quality of patient care.</div></div>","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":"283 ","pages":"Pages 291-298"},"PeriodicalIF":4.2,"publicationDate":"2025-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145822823","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Potential Eye Disorders in People With and Without Type 2 Diabetes Mellitus Exposed to GLP-1 Receptor Agonists: An Examination of the FAERS (FDA Adverse Event Reporting System) Database 暴露于GLP-1受体激动剂的2型糖尿病患者和非2型糖尿病患者的潜在眼病FAERS (FDA不良事件报告系统)数据库的检查
IF 4.2 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-12-20 DOI: 10.1016/j.ajo.2025.12.015
Mya Murray , Fabrizio Schifano , Stefania Chiappini , John Martin Corkery , Amira Guirguis

Purpose

As use of glucagon-like peptide-1 receptor agonists (GLP-1RAs) for Type 2 diabetes (T2DM) and weight management increases, emerging research identifies various adverse drug reactions. This study aimed to expand this research base, focusing on eye disorders in people with and without T2DM, a novel consideration.

Design

A retrospective clinical cohort disproportionality analysis of reports made to the Food and Drug Administration Adverse Event Reporting System (FAERS).

Methods

FAERS was queried regarding selected GLP-1RAs. Python 3.11 was adopted to develop a program, quantifying reported cases between January 2017 - September 2025 (January 2022-September 2025 for tirzepatide) meeting the criteria for cases with and without T2DM. Main outcome measures Reporting Odds Ratios (RORs) >4.000 and 95% confidence intervals were calculated, with metformin and orlistat as controls.

Results

Compared to metformin, semaglutide showed increased reporting of optic ischemic neuropathy (ROR: 12.269 [0.915-1.967]), cataract (ROR: 31.879 [2.463-4.461]) and retinopathy (ROR: 5.185 [0.556-2.736]) in T2DM patients, and retinopathy (ROR: 9.424 [1.081-3.406]) and retinal hemorrhage (ROR: 10.253 [0.319-4.336]) in non-T2DM patients. Tirzepatide showed increased reporting of optic ischemic neuropathy (ROR: 4.619 [0.726-2.335]) and macular degeneration (ROR: 15.579 [0.554-4.938]) in T2DM patients and eye swelling (ROR: 6.475 [0.407-3.329]) in non-T2DM patients. Liraglutide showed increased reporting of cataract (ROR: 53.866 [2.945-5.028]), diabetic retinopathy (ROR: 18.162 [1.753-4.045]) and macular degeneration (ROR: 26.261 [1.076-5.460]) in T2DM patients and cataract (ROR: 9.628 [1.387-3.142]) and macular degeneration (ROR: 9.557 [0.110-4.405]) in non-T2DM patients.

Conclusions

These results provide a signal of increased reporting of various eye disorders with GLP-1RA use compared to metformin across T2DM and non-T2DM patient cases. Further research is required to support these findings and confirm a biological causation.
随着胰高血糖素样肽-1受体激动剂(GLP-1RAs)用于2型糖尿病(T2DM)和体重管理的增加,新研究发现了各种药物不良反应。本研究旨在扩大这一研究基础,重点关注T2DM患者和非T2DM患者的眼部疾病,这是一个新的考虑。设计对提交给美国食品和药物管理局不良事件报告系统(FAERS)的报告进行回顾性临床队列歧化分析。方法对选定的GLP-1RAs进行faers查询。采用Python 3.11开发程序,量化2017年1月至2025年9月(替西帕肽为2022年1月至2025年9月)符合T2DM和非T2DM标准的报告病例。以二甲双胍和奥利司他为对照,计算报告优势比(RORs) >; 000和95%置信区间。结果与二甲双胍相比,西马鲁肽在T2DM患者中视神经缺血性病变(ROR: 12.269[0.915-1.967])、白内障(ROR: 31.879[2.463-4.461])和视网膜病变(ROR: 5.185[0.556-2.736])的报告增加,在非T2DM患者中视网膜病变(ROR: 9.424[1.081-3.406])和视网膜出血(ROR: 10.253[0.319-4.336])的报告增加。替西帕肽显示T2DM患者视神经缺血性病变(ROR: 4.619[0.726-2.335])和黄斑变性(ROR: 15.579[0.554-4.938])报告增加,非T2DM患者眼肿胀(ROR: 6.475[0.407-3.329])报告增加。利拉鲁肽显示T2DM患者中白内障(ROR: 53.866[2.945-5.028])、糖尿病视网膜病变(ROR: 18.162[1.753-4.045])和黄斑变性(ROR: 26.261[1.076-5.460])的报告增加,非T2DM患者中白内障(ROR: 9.628[1.387-3.142])和黄斑变性(ROR: 9.557[0.110-4.405])的报告增加。这些结果提供了一个信号,与二甲双胍相比,在T2DM和非T2DM患者中,GLP-1RA的使用增加了各种眼病的报告。需要进一步的研究来支持这些发现并确认生物学上的原因。
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引用次数: 0
The Relationship Between Corneal Stiffness Distribution and Tomography in Keratoconus Patients 圆锥角膜患者角膜硬度分布与断层扫描的关系
IF 4.2 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-12-19 DOI: 10.1016/j.ajo.2025.12.011
Nan-Ji Lu , Marta Jiménez-García , Ahmed Elsheikh , Ahmed Makarem , Carina Koppen , Jos J. Rozema

Purpose

To characterize the regional distribution of corneal stiffness in keratoconus (KC) and explore its relationship with tomographic parameters.

Design

Prospective, cross-sectional observational study.

Subjects

One hundred eleven eyes from 111 KC patients.

Methods

All eyes underwent Scheimpflug-based tomography and air-puff tonometry (Pentacam and Corvis). Stress-Strain Index (SSI) maps were generated to quantify overall and regional stiffness. Maximum, minimum, and mean SSI values, as well as regional values, were correlated with keratometric and pachymetric indices.

Main Outcome Measures

Regional SSI values and their correlations with keratometric and pachymetric parameters.

Results

SSI maps showed non-uniform stiffness, with the lowest values predominantly in the inferior-temporal region. The mean SSI at the thinnest pachymetry point (Pmin; 0.68 ± 0.16) was higher than at the steepest keratometry point (Kmax; 0.63 ± 0.19; P = .036). In overall analyses, the strongest correlation was between SSI-map minimum and Pmin (R² = 0.51), while mean SSI correlated weakly with tomography (R² = 0.11-0.19). In regional analyses, SSI correlated most strongly with Kmax in the central region (R² = 0.74), followed by the midperipheral inferior (R² = 0.38) and temporal (R² = 0.23) regions. SSI correlations with Pmin were most evident in the central (R² = 0.52), paracentral inferior (R² = 0.45), and inferior-temporal (R² = 0.31) regions.

Conclusions

Biomechanical weakening in KC varies regionally. Strong correlations with disease severity occurred in the central and inferior-temporal regions — especially with Kmax and Pmin, highlighting the role of regional mechanical stiffness and collagen architecture in corneal deformation.
目的探讨圆锥角膜(KC)角膜硬度的区域分布特征及其与层析成像参数的关系。前瞻性、横断面观察性研究。实验对象111例KC患者的111只眼睛。方法所有眼行Scheimpflug-based断层扫描和气肿眼压测量(Pentacam和Corvis)。生成应力应变指数(SSI)图来量化整体和区域刚度。最大、最小和平均SSI值以及区域值与角膜测量和厚测指数相关。主要观察指标:区域SSI值及其与角膜测量和角膜厚度测量参数的相关性。结果sssi图显示刚度不均匀,最低值主要在颞下区。最薄角测点的平均SSI (Pmin; 0.68 ± 0.16)高于最陡角测点的平均SSI (Kmax; 0.63 ± 0.19;P = 0.036)。在整体分析中,SSI-map最小值与Pmin之间的相关性最强(R² = 0.51),而平均SSI与断层扫描的相关性较弱(R² = 0.11-0.19)。在区域分析中,SSI与Kmax在中枢区相关性最强(R² = 0.74),其次是中外周下枢区(R² = 0.38)和颞区(R² = 0.23)。SSI与Pmin的相关性在中央区(R² = 0.52)、旁中央区(R² = 0.45)和颞下区(R² = 0.31)最为明显。结论KC的生物力学减弱存在区域差异。与疾病严重程度的强相关性发生在中央和下颞区,尤其是Kmax和Pmin,突出了区域机械刚度和胶原蛋白结构在角膜变形中的作用。
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引用次数: 0
期刊
American Journal of Ophthalmology
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