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中年相关性黄斑变性的异质性视觉功能缺陷:MACUSTAR报告

Heterogeneous Visual Function Deficits in Intermediate Age-Related Macular Degeneration: A MACUSTAR Report.

作者信息

Dunbar Hannah M P, Crabb David P, Behning Charlotte, Binns Alison M, Abdirahman Amina, Terheyden Jan H, Poor Stephen, Finger Robert P, Leal Sergio, Tufail Adnan, Holz Frank G, Schmid Matthias, Luhmann Ulrich F O

机构信息

Institute of Ophthalmology, London, UK.

Moorfields Eye Hospital NHS Foundation Trust, London, UK.

出版信息

Ophthalmol Sci. 2025 Jan 13;5(4):100708. doi: 10.1016/j.xops.2025.100708. eCollection 2025 Jul-Aug.

Abstract

OBJECTIVE

To examine the extent to which visual function in Beckman age-related macular degeneration (AMD) disease stages differs from age-similar peers with no AMD and, using reference limits derived from those with no AMD, test the hypothesis that people with intermediate AMD (iAMD) have heterogeneous visual function deficits.

DESIGN

Cross-sectional analyses of a range of baseline visual function measures from the MACUSTAR study-an international, multicenter (n = 20), noninterventional clinical trial.

PARTICIPANTS

Five hundred eighty-five participants with iAMD (67% female, mean [standard deviation] age 72 [7] years) were recruited alongside 56 with no AMD (59% female, 68 [6]), 34 with early AMD (79% female, 72 [6]), and 43 with late AMD (49% female, 75 [6]).

METHODS

Participants performed best-corrected visual acuity (BCVA), low luminance visual acuity (LLVA), Moorfields acuity test (MAT), Pelli-Robson contrast sensitivity (PR-CS), small print standardized International reading speed test (SPS), mesopic and scotopic average threshold (MesAT and ScoAT; macular integrity assessment, iCare), and rod intercept time (RIT; AdaptDx, Lumithera).

MAIN OUTCOME MEASURES

Relationship between each visual function measure and disease classification was examined by linear regression adjusted for age, sex, and phakic status. No AMD data were used to estimate normal reference limits for each visual function test. Intermediate AMD scores were dichotomized against reference limits, and the proportion worse than each limit was calculated.

RESULTS

Relative to no AMD, SPS was significantly worse in early AMD ( = 0.001); all measures except SPS were significantly reduced in iAMD ( < 0.02), and all measures were markedly reduced in late AMD ( < 0.0001). Thirty-one point three percent of iAMD participants breached reference limits for PR-CS, 29.4% for RIT, 24.1% for LLVA, 23.2% for MAT, 20.5% for BCVA, 19.8% for MesAT, 17.9% for ScoAT, and 12.6% for SPS. Of the iAMD participants, 69.6% and 42.7% breached ≥1 and ≥2 reference limits, respectively, whereas 33.6% and 5.7% would be expected by chance.

CONCLUSIONS

A large proportion of people with structurally defined iAMD exhibit heterogeneous visual function deficits outside normal reference limits. This observation may be relevant for the design and inclusion criteria of future interventional trials.

FINANCIAL DISCLOSURES

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

摘要

目的

研究贝克曼年龄相关性黄斑变性(AMD)疾病各阶段的视觉功能与无AMD的年龄相仿同龄人相比的差异程度,并利用无AMD者得出的参考值范围,检验中度AMD(iAMD)患者存在异质性视觉功能缺陷的假设。

设计

对MACUSTAR研究中一系列基线视觉功能指标进行横断面分析,该研究是一项国际多中心(n = 20)非干预性临床试验。

参与者

招募了585例iAMD患者(67%为女性,平均[标准差]年龄72[7]岁),同时招募了56例无AMD者(59%为女性,68[6]岁)、34例早期AMD患者(79%为女性,72[6]岁)和43例晚期AMD患者(49%为女性,75[6]岁)。

方法

参与者进行最佳矫正视力(BCVA)、低亮度视力(LLVA)、摩尔菲尔德视力测试(MAT)、佩利-罗布森对比敏感度(PR-CS)、小字体标准化国际阅读速度测试(SPS)、中间视觉和暗视觉平均阈值(MesAT和ScoAT;黄斑完整性评估,iCare)以及视杆细胞截距时间(RIT;AdaptDx,Lumithera)测试。

主要观察指标

通过对年龄、性别和晶状体状态进行校正的线性回归分析,研究每项视觉功能指标与疾病分类之间的关系。使用无AMD者的数据来估计每项视觉功能测试的正常参考值范围。将iAMD患者的得分与参考值范围进行二分法划分,并计算出比每个限值差的比例。

结果

与无AMD者相比,早期AMD患者的SPS显著更差(P = 0.001);iAMD患者中除SPS外的所有指标均显著降低(P < 0.02),晚期AMD患者的所有指标均显著降低(P < 0.0001)。31.3%的iAMD参与者PR-CS超出参考值范围,29.4%的RIT超出,24.1%的LLVA超出,23.2%的MAT超出,20.5%的BCVA超出,19.8%的MesAT超出,17.9%的ScoAT超出,12.6%的SPS超出。在iAMD参与者中,分别有69.6%和42.7%超出≥1个和≥2个参考值范围,而随机情况下预期分别为33.6%和5.7%。

结论

很大一部分结构上定义为iAMD的患者表现出超出正常参考值范围的异质性视觉功能缺陷。这一观察结果可能与未来干预试验的设计和纳入标准相关。

财务披露

本文末尾的脚注和披露中可能会有专有或商业披露信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb64/11985047/3a1c133e612a/gr1.jpg

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