Kass Michael A, Heuer Dale K, Higginbotham Eve J, Parrish Richard K, Khanna Cheryl L, Brandt James D, Soltau Joern B, Johnson Chris A, Keltner John L, Huecker Julia B, Wilson Bradley S, Liu Lei, Miller J Phillip, Quigley Harry A, Gordon Mae O
Washington University School of Medicine in St Louis, St Louis, Missouri.
David Geffen School of Medicine, Los Angeles, California.
JAMA Ophthalmol. 2021 Apr 15;139(5):1-9. doi: 10.1001/jamaophthalmol.2021.0341.
Ocular hypertension is an important risk factor for the development of primary open-angle glaucoma (POAG). Data from long-term follow-up can be used to inform the management of patients with ocular hypertension.
To determine the cumulative incidence and severity of POAG after 20 years of follow-up among participants in the Ocular Hypertension Treatment Study.
DESIGN, SETTING, AND PARTICIPANTS: Participants in the Ocular Hypertension Treatment Study were followed up from February 1994 to December 2008 in 22 clinics. Data were collected after 20 years of follow-up (from January 2016 to April 2019) or within 2 years of death. Analyses were performed from July 2019 to December 2020.
From February 28, 1994, to June 2, 2002 (phase 1), participants were randomized to receive either topical ocular hypotensive medication (medication group) or close observation (observation group). From June 3, 2002, to December 30, 2008 (phase 2), both randomization groups received medication. Beginning in 2009, treatment was no longer determined by study protocol. From January 7, 2016, to April 15, 2019 (phase 3), participants received ophthalmic examinations and visual function assessments.
Twenty-year cumulative incidence and severity of POAG in 1 or both eyes after adjustment for exposure time.
A total of 1636 individuals (mean [SD] age, 55.4 [9.6] years; 931 women [56.9%]; 1138 White participants [69.6%]; 407 Black/African American participants [24.9%]) were randomized in phase 1 of the clinical trial. Of those, 483 participants (29.5%) developed POAG in 1 or both eyes (unadjusted incidence). After adjusting for exposure time, the 20-year cumulative incidence of POAG in 1 or both eyes was 45.6% (95% CI, 42.3%-48.8%) among all participants, 49.3% (95% CI, 44.5%-53.8%) among participants in the observation group, and 41.9% (95% CI, 37.2%-46.3%) among participants in the medication group. The 20-year cumulative incidence of POAG was 55.2% (95% CI, 47.9%-61.5%) among Black/African American participants and 42.7% (95% CI, 38.9%-46.3%) among participants of other races. The 20-year cumulative incidence for visual field loss was 25.2% (95% CI, 22.5%-27.8%). Using a 5-factor baseline model, the cumulative incidence of POAG among participants in the low-, medium-, and high-risk tertiles was 31.7% (95% CI, 26.4%-36.6%), 47.6% (95% CI, 41.6%-53.0%), and 59.8% (95% CI, 53.1%-65.5%), respectively.
In this study, only one-fourth of participants in the Ocular Hypertension Treatment Study developed visual field loss in either eye over long-term follow-up. This information, together with a prediction model, may help clinicians and patients make informed personalized decisions about the management of ocular hypertension.
ClinicalTrials.gov Identifier: NCT00000125.
高眼压症是原发性开角型青光眼(POAG)发生的重要危险因素。长期随访数据可用于指导高眼压症患者的管理。
确定高眼压症治疗研究参与者随访20年后POAG的累积发病率和严重程度。
设计、设置和参与者:高眼压症治疗研究的参与者于1994年2月至2008年12月在22家诊所进行随访。在随访20年后(2016年1月至2019年4月)或死亡前2年内收集数据。分析于2019年7月至2020年12月进行。
从1994年2月28日至2002年6月2日(第1阶段),参与者被随机分为接受局部降眼压药物治疗(药物组)或密切观察(观察组)。从2002年6月3日至2008年12月30日(第2阶段),两个随机分组均接受药物治疗。从2009年开始,治疗不再由研究方案决定。从2016年1月7日至2019年4月15日(第3阶段),参与者接受眼科检查和视觉功能评估。
调整暴露时间后,一只或两只眼睛POAG的20年累积发病率和严重程度。
共有1636名个体(平均[标准差]年龄,55.4[9.6]岁;931名女性[56.9%];1138名白人参与者[69.6%];407名黑人/非裔美国参与者[24.9%])在临床试验的第1阶段被随机分组。其中,483名参与者(29.5%)一只或两只眼睛发生了POAG(未调整发病率)。调整暴露时间后,所有参与者中一只或两只眼睛POAG的20年累积发病率为45.6%(95%CI,42.3%-48.8%),观察组参与者中为49.3%(95%CI,44.5%-53.8%),药物组参与者中为41.9%(95%CI,37.2%-46.3%)。黑人/非裔美国参与者中POAG的20年累积发病率为55.2%(95%CI,47.9%-61.5%),其他种族参与者中为42.7%(95%CI,38.9%-46.3%)。视野缺损的20年累积发病率为25.2%(95%CI,22.5%-27.8%)。使用5因素基线模型,低、中、高风险三分位数参与者中POAG的累积发病率分别为31.7%(95%CI,26.4%-36.6%)、47.6%(95%CI,41.6%-53.0%)和59.8%(95%CI,53.1%-65.5%)。
在本研究中,高眼压症治疗研究中只有四分之一的参与者在长期随访中一只眼睛出现了视野缺损。这些信息,连同预测模型,可能有助于临床医生和患者就高眼压症的管理做出明智的个性化决策。
ClinicalTrials.gov标识符:NCT00000125。