Short-Term Rates of Visual Field Change Predict Glaucoma Progression.

Q2 Medicine
Mohsen Adelpour, Sasan Moghimi, Takashi Nishida, Leo Meller, Kelvin H Du, Alireza Kamalipour, Natchada Tansuebchueasai, Golnoush Mahmoudinezhad, Linda M Zangwill, Robert N Weinreb
{"title":"Short-Term Rates of Visual Field Change Predict Glaucoma Progression.","authors":"Mohsen Adelpour, Sasan Moghimi, Takashi Nishida, Leo Meller, Kelvin H Du, Alireza Kamalipour, Natchada Tansuebchueasai, Golnoush Mahmoudinezhad, Linda M Zangwill, Robert N Weinreb","doi":"10.1016/j.ogla.2025.05.006","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To explore the prognostic significance of short-term rates of visual field (VF) mean deviation (MD) change in predicting progression across various levels of glaucoma severity.</p><p><strong>Design: </strong>Observational cohort.</p><p><strong>Participants: </strong>A total of 349 eyes from 254 patients followed up to 5 years.</p><p><strong>Methods: </strong>Primary open-angle glaucoma eyes were included with ≥ 5 24-2 VFs tests during the initial 2 years over a period of up to 5 years. Two assessment methods, Guided Progression Analysis (GPA) and a United States Food and Drug Administration (FDA)-consistent end point, were utilized to identify progression events. Rates of change in VF MD during the initial 2 years were calculated, and survival models were employed to evaluate the risk of faster initial VF MD loss on the development of GPA and FDA-consistent end points.</p><p><strong>Main outcomes and measures: </strong>Risk of progression based on initial MD change rates.</p><p><strong>Results: </strong>Over a mean follow-up of 4.3 years, progression was observed in 17.2% (GPA end point) and 24.9% (FDA-consistent end point) of eyes. Faster initial rates of VF MD loss significantly increased the progression risk (hazard ratio [HR] per 0.1 dB/year faster for GPA: 1.16, 95% confidence interval [CI]: 1.12-1.20; HR for FDA: 1.16, 95% confidence interval: 1.12-1.21; both P < 0.001) with survival-adjusted R<sup>2</sup> values of 0.67 for GPA and 0.75 for FDA-consistent end points. Global initial 2-year slopes showed the highest predictive accuracy for FDA progression events, with adjusted R<sup>2</sup> values of 0.75 overall, 0.71 for early glaucoma, and 0.42 for moderate-to-advanced glaucoma. Superior and inferior sectoral slopes demonstrated lower abilities to explain the variability across all severity groups. The model's predictive accuracy was higher in early glaucoma (R<sup>2</sup>, 0.71) compared to moderate-advanced stages (R<sup>2</sup>, 0.42) for both criteria.</p><p><strong>Conclusions: </strong>The initial 2-year rate of VF MD change predicts subsequent progression events based on FDA-consistent criteria in both early and moderate-to-advanced glaucoma eyes. These findings suggest initial VF MD change rates identify patients at higher risk of future progression, enabling timely management decisions and, also, potentially serving as a progression end point in clinical trials.</p><p><strong>Financial disclosure(s): </strong>Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.</p>","PeriodicalId":56368,"journal":{"name":"Ophthalmology. Glaucoma","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ophthalmology. Glaucoma","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.ogla.2025.05.006","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: To explore the prognostic significance of short-term rates of visual field (VF) mean deviation (MD) change in predicting progression across various levels of glaucoma severity.

Design: Observational cohort.

Participants: A total of 349 eyes from 254 patients followed up to 5 years.

Methods: Primary open-angle glaucoma eyes were included with ≥ 5 24-2 VFs tests during the initial 2 years over a period of up to 5 years. Two assessment methods, Guided Progression Analysis (GPA) and a United States Food and Drug Administration (FDA)-consistent end point, were utilized to identify progression events. Rates of change in VF MD during the initial 2 years were calculated, and survival models were employed to evaluate the risk of faster initial VF MD loss on the development of GPA and FDA-consistent end points.

Main outcomes and measures: Risk of progression based on initial MD change rates.

Results: Over a mean follow-up of 4.3 years, progression was observed in 17.2% (GPA end point) and 24.9% (FDA-consistent end point) of eyes. Faster initial rates of VF MD loss significantly increased the progression risk (hazard ratio [HR] per 0.1 dB/year faster for GPA: 1.16, 95% confidence interval [CI]: 1.12-1.20; HR for FDA: 1.16, 95% confidence interval: 1.12-1.21; both P < 0.001) with survival-adjusted R2 values of 0.67 for GPA and 0.75 for FDA-consistent end points. Global initial 2-year slopes showed the highest predictive accuracy for FDA progression events, with adjusted R2 values of 0.75 overall, 0.71 for early glaucoma, and 0.42 for moderate-to-advanced glaucoma. Superior and inferior sectoral slopes demonstrated lower abilities to explain the variability across all severity groups. The model's predictive accuracy was higher in early glaucoma (R2, 0.71) compared to moderate-advanced stages (R2, 0.42) for both criteria.

Conclusions: The initial 2-year rate of VF MD change predicts subsequent progression events based on FDA-consistent criteria in both early and moderate-to-advanced glaucoma eyes. These findings suggest initial VF MD change rates identify patients at higher risk of future progression, enabling timely management decisions and, also, potentially serving as a progression end point in clinical trials.

Financial disclosure(s): Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

短期视野变化速度预测青光眼进展。
目的:探讨短期视野平均偏差率(VF)变化在预测不同程度青光眼进展中的预后意义。设计:观察队列参与者:来自254例原发性开角型青光眼(POAG)患者的349只眼睛每6个月随访一次,随访时间长达5年。方法:在这项研究中,在最初的2年中,在长达5年的时间里,眼睛被纳入了至少5次24-2 VFs测试。两种评估方法,指导性进展分析(GPA)和美国食品和药物管理局(FDA)一致的终点,用于识别进展事件。计算最初2年VF MD的变化率,并采用生存模型来评估在GPA和fda一致终点发展时初始VF MD更快丧失的风险。主要结局和测量:基于VF MD发病率的初始变化经历疾病进展的风险。结果:在平均4.3年的随访中,17.2% (GPA终点)和24.9% (fda一致终点)的眼睛观察到进展。更快的VF MD初始丧失率显著增加了进展风险(每0.1 dB/年的HR比GPA更快:1.16,95% CI: 1.12-1.20;FDA的HR: 1.16, 95% CI: 1.12-1.21;均P < 0.001), GPA的生存校正R2值为0.67,与fda一致的终点为0.75。全球初始2年斜率对FDA进展事件的预测准确性最高,调整后的R2值为0.75,早期青光眼为0.71,中晚期青光眼为0.42。上级和下级部门斜坡显示较低的能力来解释变异性在所有严重程度组。该模型在早期青光眼的预测准确度(R2: 0.71)高于中晚期青光眼(R2: 0.42)。结论:根据fda一致的标准,在早期和中晚期青光眼中,初始VF MD变化率可以预测随后的进展事件。这些发现表明,最初的VF MD变化率可以识别出未来进展风险较高的患者,从而能够及时做出管理决策,也可能作为临床试验的进展终点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Ophthalmology. Glaucoma
Ophthalmology. Glaucoma Medicine-Medicine (all)
CiteScore
4.20
自引率
0.00%
发文量
140
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信