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用于评估色素性视网膜炎的自动明适应和暗适应视野检查:满足多中心临床试验的需求

Automated Light- and Dark-Adapted Perimetry for Evaluating Retinitis Pigmentosa: Filling a Need to Accommodate Multicenter Clinical Trials.

作者信息

McGuigan David B, Roman Alejandro J, Cideciyan Artur V, Matsui Rodrigo, Gruzensky Michaela L, Sheplock Rebecca, Jacobson Samuel G

出版信息

Invest Ophthalmol Vis Sci. 2016 Jun 1;57(7):3118-28. doi: 10.1167/iovs.16-19302.

Abstract

PURPOSE

The purpose of this study was to develop a convenient means to measure rod (and cone) function by automated perimetry in patients with inherited retinal degenerations (IRDs).

METHODS

A currently available automated perimeter was used to determine sensitivity (in decibels) to a blue target in the dark-adapted (DA) state and a white target in the light-adapted (LA) state. Normal subjects and IRD patients were evaluated with a full-threshold 71-locus strategy (the retinitis pigmentosa [RP] test) and a size III target. Comparisons were made with results from the more commonly used methods of two-color DA perimetry and middle/long-wavelength LA perimetry in the same patients.

RESULTS

Rod function using the blue target and the RP test was determined for normal subjects by measuring DA sensitivities. If patients detected the blue stimulus in the DA state, it was determined whether the value was rod mediated by using normal data acquired during the cone plateau phase of dark adaptation. If rod mediated, rod sensitivity loss (RSL) was calculated and mapped across the visual field. Light-adapted sensitivities in normal subjects were also measured, permitting cone sensitivity losses (CSL) to be calculated for the patients. Multiple methods were used to compare RSL and CSL results with those from two-color DA perimetry and chromatic LA perimetry, and there was close correspondence between the methods.

CONCLUSIONS

The unmodified automated static perimeter used in the DA and LA states presents a practical approach to accomplish current goals of treatment trials in IRDs. This proof-of-principle study is an initial step toward establishing a clinical method to gather reproducible data on photoreceptor-mediated sensitivity.

摘要

目的

本研究的目的是开发一种便捷的方法,通过自动视野计测量遗传性视网膜变性(IRD)患者的视杆(和视锥)功能。

方法

使用一种现有的自动视野计,在暗适应(DA)状态下测定对蓝色目标的敏感度(以分贝为单位),在明适应(LA)状态下测定对白色目标的敏感度。采用全阈值71位点策略(视网膜色素变性[RP]测试)和III号视标对正常受试者和IRD患者进行评估。将结果与同一患者中更常用的双色暗适应视野计和中/长波长明适应视野计的结果进行比较。

结果

通过测量暗适应敏感度,使用蓝色目标和RP测试确定正常受试者的视杆功能。如果患者在暗适应状态下检测到蓝色刺激,则通过使用在暗适应的视锥平台期获取的正常数据来确定该值是否由视杆介导。如果是视杆介导的,则计算视杆敏感度损失(RSL)并在视野中进行映射。还测量了正常受试者的明适应敏感度,从而能够为患者计算视锥敏感度损失(CSL)。使用多种方法将RSL和CSL结果与双色暗适应视野计和彩色明适应视野计的结果进行比较,这些方法之间具有密切的对应关系。

结论

在暗适应和明适应状态下使用未经修改的自动静态视野计,为实现IRD治疗试验的当前目标提供了一种实用的方法。这项原理验证研究是朝着建立一种临床方法以收集关于光感受器介导的敏感度的可重复数据迈出的第一步。

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