• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

使用年龄和视网膜位点特异性参考阈值解读MAIA微视野计检查结果

Interpreting MAIA Microperimetry Using Age- and Retinal Loci-Specific Reference Thresholds.

作者信息

Charng Jason, Sanfilippo Paul G, Attia Mary S, Dolliver Monika, Arunachalam Sukanya, Chew Avenell L, Wong Evan N, Mackey David A, Chen Fred K

机构信息

Centre of Ophthalmology and Visual Science (incorporating Lions Eye Institute), The University of Western Australia, Perth, Western Australia.

Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, University of Melbourne, Melbourne, Victoria, Australia.

出版信息

Transl Vis Sci Technol. 2020 Jun 18;9(7):19. doi: 10.1167/tvst.9.7.19. eCollection 2020 Jun.

DOI:10.1167/tvst.9.7.19
PMID:32832226
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7414638/
Abstract

PURPOSE

Macular Integrity Assessment (MAIA) microperimetry is used widely in clinical trials and routine practice to assess paracentral scotoma. Current interpretation of MAIA is based on an assumed uniform 25 decibel (dB) cutoff for normal function irrespective of subject age and retinal location. We examined this convention by establishing an age- and loci-specific reference in healthy eyes and comparing this to the <25 dB cutoff.

METHODS

Retrospective MAIA results from healthy eyes were analyzed for prevalence of loci with <25 dB. At each locus, a new reference cutoff was derived from quantile regression of sensitivity against age at the 2.5th percentile. Two clinical cases of serial MAIA testing were analyzed using the new approach and compared to the <25 dB cutoff.

RESULTS

Fifty-four and 56 age-matched (range: 16-75 years) healthy eyes underwent small (37 loci) and large (68 loci) grid testing, respectively. Retinal sensitivity <25 dB was found in 5% of the small grid (1998 data points) and 10% of the large grid (3808 data points). These were found predominantly in older subjects and at the central point or in the perifoveal region. Quantile regression at each individual locus showed age-related decline with a median gradient of 0.6 dB/decade.

CONCLUSIONS

We caution against using <25 dB cutoff in MAIA interpretation and advocate an age- and loci-specific cutoff criterion.

TRANSLATIONAL RELEVANCE

Our study suggests that MAIA interpretation is influenced by the criterion used for defining abnormal pointwise measurement.

摘要

目的

黄斑完整性评估(MAIA)微视野检查在临床试验和常规实践中被广泛用于评估旁中心暗点。目前对MAIA的解读基于一个假定的正常功能统一25分贝(dB)阈值,而不考虑受试者年龄和视网膜位置。我们通过在健康眼中建立年龄和位置特异性参考值并将其与<25 dB阈值进行比较,来检验这一惯例。

方法

分析健康眼的回顾性MAIA结果中<25 dB位置的患病率。在每个位置,从第2.5百分位数的敏感度对年龄的分位数回归中得出一个新的参考阈值。使用新方法分析了两个连续进行MAIA检测的临床病例,并与<25 dB阈值进行比较。

结果

分别对54只和56只年龄匹配(范围:16 - 75岁)的健康眼进行了小网格(37个位置)和大网格(68个位置)测试。在小网格(1998个数据点)的5%和大网格(3808个数据点)的10%中发现视网膜敏感度<25 dB。这些主要出现在老年受试者以及中心点或黄斑周围区域。每个单独位置的分位数回归显示与年龄相关的下降,中位数梯度为0.6 dB/十年。

结论

我们提醒在MAIA解读中不要使用<25 dB阈值,并提倡采用年龄和位置特异性的阈值标准。

转化相关性

我们的研究表明,MAIA解读受到用于定义异常逐点测量的标准的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/7414638/de6ca0938393/tvst-9-7-19-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/7414638/eefe700f19f9/tvst-9-7-19-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/7414638/8d079a160d24/tvst-9-7-19-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/7414638/527120d14c38/tvst-9-7-19-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/7414638/a8702be5c62e/tvst-9-7-19-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/7414638/de6ca0938393/tvst-9-7-19-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/7414638/eefe700f19f9/tvst-9-7-19-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/7414638/8d079a160d24/tvst-9-7-19-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/7414638/527120d14c38/tvst-9-7-19-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/7414638/a8702be5c62e/tvst-9-7-19-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/7414638/de6ca0938393/tvst-9-7-19-f005.jpg

相似文献

1
Interpreting MAIA Microperimetry Using Age- and Retinal Loci-Specific Reference Thresholds.使用年龄和视网膜位点特异性参考阈值解读MAIA微视野计检查结果
Transl Vis Sci Technol. 2020 Jun 18;9(7):19. doi: 10.1167/tvst.9.7.19. eCollection 2020 Jun.
2
MP1 AND MAIA FUNDUS PERIMETRY IN HEALTHY SUBJECTS AND PATIENTS AFFECTED BY RETINAL DYSTROPHIES.健康受试者及视网膜营养不良患者的MP1和MAIA眼底周边视野检查
Retina. 2015 Aug;35(8):1662-9. doi: 10.1097/IAE.0000000000000504.
3
Interdevice comparison of retinal sensitivity assessments in a healthy population: the CenterVue MAIA and the Nidek MP-3 microperimeters.健康人群中视网膜敏感度评估的设备间比较:CenterVue MAIA和尼德克MP-3微视野计
Br J Ophthalmol. 2018 Jan;102(1):109-113. doi: 10.1136/bjophthalmol-2017-310258. Epub 2017 May 11.
4
Edge of Scotoma Sensitivity as a Microperimetry Clinical Trial End Point in Retinopathy.视网膜病变中作为微视野临床试验终点的暗点边缘敏感度
Transl Vis Sci Technol. 2020 Sep 9;9(10):9. doi: 10.1167/tvst.9.10.9. eCollection 2020 Sep.
5
Inter-device comparison of retinal sensitivity measurements: the CenterVue MAIA and the Nidek MP-1.视网膜敏感度测量的设备间比较:CenterVue MAIA和尼德克MP-1
Clin Exp Ophthalmol. 2016 Jan-Feb;44(1):15-23. doi: 10.1111/ceo.12629.
6
Normal values for microperimetry with the MAIA microperimeter: sensitivity and fixation analysis in healthy adults and children.MAIA微视野计微视野检查的正常数值:健康成人和儿童的敏感度及固视分析
Eur J Ophthalmol. 2017 Aug 30;27(5):607-613. doi: 10.5301/ejo.5000930. Epub 2017 Jan 23.
7
Microperimetry as an Outcome Measure in Choroideremia Trials: Reproducibility and Beyond.微视野检查作为无脉络膜症试验的一项结果指标:可重复性及其他。
Invest Ophthalmol Vis Sci. 2016 Aug 1;57(10):4151-61. doi: 10.1167/iovs.16-19338.
8
Optimisation of dark adaptation time required for mesopic microperimetry.优化暗适应时间对中间视觉微视野计的要求。
Br J Ophthalmol. 2019 Aug;103(8):1092-1098. doi: 10.1136/bjophthalmol-2018-312253. Epub 2018 Sep 29.
9
Test-Retest Reliability of Scotopic and Mesopic Fundus-Controlled Perimetry Using a Modified MAIA (Macular Integrity Assessment) in Normal Eyes.正常眼使用改良MAIA(黄斑完整性评估)进行暗适应和中间视觉眼底控制视野检查的重测信度
Ophthalmologica. 2017;237(1):42-54. doi: 10.1159/000453079. Epub 2016 Dec 21.
10
Investigating the discrepancy between MAIA and MP-1 microperimetry results.研究 MAIA 和 MP-1 微视野计结果之间的差异。
Ophthalmic Physiol Opt. 2021 Nov;41(6):1231-1240. doi: 10.1111/opo.12877. Epub 2021 Aug 29.

引用本文的文献

1
Optical influence of myopia control spectacles at the retinal level: Effect of local light modulation.近视控制眼镜在视网膜层面的光学影响:局部光调制的作用。
Ophthalmic Physiol Opt. 2025 Jun;45(4):995-1003. doi: 10.1111/opo.13515. Epub 2025 Apr 12.
2
Assessing structure - Function relationships in non-neovascular age-related macular degeneration.评估非新生血管性年龄相关性黄斑变性中的结构-功能关系。
Exp Eye Res. 2025 Jun;255:110349. doi: 10.1016/j.exer.2025.110349. Epub 2025 Mar 22.
3
Multicenter Normative Data for Mesopic Microperimetry.

本文引用的文献

1
Microperimetry in Age-Related Macular Degeneration: An Evidence-Base for Pattern Deviation Probability Analysis in Microperimetry.年龄相关性黄斑变性中的微视野检查:微视野检查中模式偏差概率分析的循证依据
Transl Vis Sci Technol. 2019 Dec 31;8(6):48. doi: 10.1167/tvst.8.6.48. eCollection 2019 Nov.
2
Characterisation of microvascular abnormalities using OCT angiography in patients with biallelic variants in and .使用 OCT 血管造影术对 和 双等位基因突变患者的微血管异常进行特征描述。
Br J Ophthalmol. 2020 Apr;104(4):480-486. doi: 10.1136/bjophthalmol-2019-314243. Epub 2019 Jul 2.
3
Subthreshold Nanosecond Laser Intervention in Intermediate Age-Related Macular Degeneration: Study Design and Baseline Characteristics of the Laser in Early Stages of Age-Related Macular Degeneration Study (Report Number 1).
多中心中间光微视野正常值。
Invest Ophthalmol Vis Sci. 2024 Oct 1;65(12):27. doi: 10.1167/iovs.65.12.27.
4
Censoring the Floor Effect in Long-Term Stargardt Disease Microperimetry Data Produces a Faster Rate of Decline.对长期Stargardt病微视野检查数据中的下限效应进行审查会导致更快的下降速度。
Ophthalmol Sci. 2024 Jul 20;4(6):100581. doi: 10.1016/j.xops.2024.100581. eCollection 2024 Nov-Dec.
5
Comparison of Microperimetry and Static Perimetry for Evaluating Macular Function and Progression in Retinitis Pigmentosa.微视野检查法与静态视野检查法在评估视网膜色素变性黄斑功能及病情进展中的比较
Ophthalmol Sci. 2024 Jul 20;4(6):100582. doi: 10.1016/j.xops.2024.100582. eCollection 2024 Nov-Dec.
6
The Natural History of Retinal Sensitivity Loss in Diabetic Macular Ischemia over One Year Evaluated by Microperimetry.通过微视野计评估糖尿病性黄斑缺血性视网膜敏感度丧失的一年自然病程。
J Clin Med. 2024 Apr 11;13(8):2219. doi: 10.3390/jcm13082219.
7
Baseline Microperimetry and OCT in the RUSH2A Study: Structure-Function Association and Correlation With Disease Severity.RUSH2A 研究中的基线微视野计和 OCT:结构-功能相关性及其与疾病严重程度的关系。
Am J Ophthalmol. 2022 Dec;244:98-116. doi: 10.1016/j.ajo.2022.08.013. Epub 2022 Aug 22.
8
Localised relative scotoma in cuticular drusen.局限性相对切迹性黄斑部视网膜病变。
Graefes Arch Clin Exp Ophthalmol. 2022 Jul;260(7):2157-2164. doi: 10.1007/s00417-022-05570-4. Epub 2022 Feb 7.
9
Microperimetry Hill of Vision and Volumetric Measures of Retinal Sensitivity.视野 Hill 图和视网膜敏感度的容积测量
Transl Vis Sci Technol. 2021 Jun 1;10(7):12. doi: 10.1167/tvst.10.7.12.
10
Low Luminance Visual Acuity and Low Luminance Deficit in Choroideremia and RPGR-Associated Retinitis Pigmentosa.脉络膜视网膜炎和 RPGR 相关的视网膜色素变性中的低亮度视力和低亮度缺损。
Transl Vis Sci Technol. 2021 Feb 5;10(2):28. doi: 10.1167/tvst.10.2.28.
亚阈值纳秒激光干预中度年龄相关性黄斑变性:年龄相关性黄斑变性研究早期阶段激光的研究设计和基线特征(报告编号1)
Ophthalmol Retina. 2017 May-Jun;1(3):227-239. doi: 10.1016/j.oret.2016.12.001. Epub 2017 Jan 31.
4
Early detection of cone photoreceptor cell loss in retinitis pigmentosa using adaptive optics scanning laser ophthalmoscopy.使用自适应光学扫描激光检眼镜早期检测色素性视网膜炎中视锥光感受器细胞的丢失
Graefes Arch Clin Exp Ophthalmol. 2019 Jun;257(6):1169-1181. doi: 10.1007/s00417-019-04307-0. Epub 2019 Apr 1.
5
Microperimetry in age-related macular degeneration: association with macular morphology assessed by optical coherence tomography.年龄相关性黄斑变性的微视野检查:与光学相干断层扫描评估的黄斑形态的相关性。
Br J Ophthalmol. 2019 Dec;103(12):1769-1776. doi: 10.1136/bjophthalmol-2018-313316. Epub 2019 Feb 1.
6
Retest Reliability of Mesopic and Dark-Adapted Microperimetry in Patients With Intermediate Age-Related Macular Degeneration and Age-Matched Controls.复测中间型年龄相关性黄斑变性患者与年龄匹配对照者的明适应和暗适应微视野计的复测可靠性。
Invest Ophthalmol Vis Sci. 2018 Mar 20;59(4):AMD152-AMD159. doi: 10.1167/iovs.18-23878.
7
Effect of Ciliary Neurotrophic Factor on Retinal Neurodegeneration in Patients with Macular Telangiectasia Type 2: A Randomized Clinical Trial.睫状神经营养因子对 2 型黄斑毛细血管扩张症患者视网膜神经退行性变的影响:一项随机临床试验。
Ophthalmology. 2019 Apr;126(4):540-549. doi: 10.1016/j.ophtha.2018.09.041. Epub 2018 Oct 4.
8
Choroideremia Gene Therapy Phase 2 Clinical Trial: 24-Month Results.脉络膜黑蒙 2 型基因治疗的 2 期临床试验:24 个月的结果。
Am J Ophthalmol. 2019 Jan;197:65-73. doi: 10.1016/j.ajo.2018.09.012. Epub 2018 Sep 19.
9
Visual Function Metrics in Early and Intermediate Dry Age-related Macular Degeneration for Use as Clinical Trial Endpoints.早期和中期干性年龄相关性黄斑变性的视觉功能指标作为临床试验终点的应用。
Am J Ophthalmol. 2018 May;189:127-138. doi: 10.1016/j.ajo.2018.02.012. Epub 2018 Mar 15.
10
Perifoveal interdigitation zone loss in hydroxychloroquine toxicity leads to subclinical bull's eye lesion appearance on near-infrared reflectance imaging.羟氯喹毒性导致的黄斑周围指状交叉区缺失在近红外反射成像上表现为亚临床靶心病变。
Doc Ophthalmol. 2018 Feb;136(1):57-68. doi: 10.1007/s10633-017-9615-9. Epub 2017 Nov 9.