Hyporeflective Cores within Drusen Association with Progression of Age-Related Macular Degeneration and Impact on Visual Sensitivity

被引:26
作者
Goh, Kai Lyn [1 ,2 ]
Abbott, Carla J. [1 ,2 ]
Hadoux, Xavier [1 ,2 ]
Jannaud, Maxime [1 ]
Hodgson, Lauren A. B. [1 ]
van Wijngaarden, Peter [1 ,2 ]
Guymer, Robyn H. [1 ,2 ]
Wu, Zhichao [1 ,2 ]
机构
[1] Royal Victorian Eye & Ear Hosp, Ctr Eye Res Australia, Level 7,32 Gisborne St, East Melbourne, Vic 3002, Australia
[2] Univ Melbourne, Dept Surg Ophthalmol, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
drusen; optical coherence tomography; age-related macular degeneration; internal reflectivity; progression; microperimetry; risk factors; prognosis; geographic atrophy; visual sensitivity; OPTICAL COHERENCE TOMOGRAPHY; NASCENT GEOGRAPHIC ATROPHY; MODELS;
D O I
10.1016/j.oret.2021.11.004
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To examine the association between hyporeflective cores within drusen (HCD) and disease progression in age-related macular degeneration (AMD) and with visual function. Design: Longitudinal observational study. Participants: Two hundred and eighty eyes from 140 participants with bilateral large drusen, without late AMD. Methods: Multimodal imaging and microperimetry were performed at baseline and subsequently every 6 months for up to 3 years. Baseline OCT scans were graded for the presence of HCD and used to calculate drusen volume. The total area of the drusenoid lesions containing hyporeflective cores (HCD extent) on color fundus photographs (CFPs) was calculated. CFPs were also graded for the presence of pigmentary abnormalities. The association between HCD extent with progression to late AMD (including OCT signs of atrophy) and visual sensitivity measured using microperimetry at baseline and its rate of change over time was evaluated with and without adjustment for confounders of drusen volume, pigmentary abnormalities, and age. Main Outcome Measures: Time to develop late AMD and visual sensitivity. Results: Twenty (7%) eyes from 12 (9%) individuals were found to have HCD at baseline, which was associated with a nonsignificantly increased rate of progression to late AMD (unadjusted P = 0.050). HCD extent was significantly associated with an increased rate of progression to late AMD (unadjusted P = 0.034) and lower visual sensitivity at baseline (unadjusted P < 0.001). However, these associations were no longer significant (P >= 0.264 for both) after adjusting for known risk factors for AMD progression. HCD extent was also not associated with a faster rate of visual sensitivity decline before the development of late AMD, with or without adjustment (P >= 0.674 for both). Increasing age and larger drusen volume were associated with HCD extent (P <= 0.041). Conclusions: In a cohort with bilateral large drusen, HCD presence and extent were not independently associated with an increased rate of progression to late AMD over 3 years, nor with lower visual sensitivity or an increased rate of visual sensitivity decline before the development of late AMD, after adjusting for known risk factors for disease progression. (C) 2021 by the American Academy of Ophthalmology
引用
收藏
页码:284 / 290
页数:7
相关论文
共 27 条
[1]   Understanding age-related macular degeneration (AMD): Relationships between the photoreceptor/retinal pigment epithelium/Bruch's membrane/choriocapillaris complex [J].
Bhutto, Imran ;
Lutty, Gerard .
MOLECULAR ASPECTS OF MEDICINE, 2012, 33 (04) :295-317
[2]  
Ferris FL, 2005, ARCH OPHTHALMOL-CHIC, V123, P1570
[3]   Clinical Classification of Age-related Macular Degeneration [J].
Ferris, Frederick L., III ;
Wilkinson, C. P. ;
Bird, Alan ;
Chakravarthy, Usha ;
Chew, Emily ;
Csaky, Karl ;
Sadda, SriniVas R. .
OPHTHALMOLOGY, 2013, 120 (04) :844-851
[4]   Drusen Volume and Retinal Pigment Epithelium Abnormal Thinning Volume Predict 2-Year Progression of Age-Related Macular Degeneration [J].
Folgar, Francisco A. ;
Yuan, Eric L. ;
Sevilla, Monica B. ;
Chiu, Stephanie J. ;
Farsiu, Sina ;
Chew, Emily Y. ;
Toth, Cynthia A. .
OPHTHALMOLOGY, 2016, 123 (01) :39-+
[5]   Spectral Domain Optical Coherence Tomography Imaging of Drusen in Nonexudative Age-Related Macular Degeneration [J].
Gregori, Giovanni ;
Wang, Fenghua ;
Rosenfeld, Philip J. ;
Yehoshua, Zohar ;
Gregori, Ninel Z. ;
Lujan, Brandon J. ;
Puliafito, Carmen A. ;
Feuer, William J. .
OPHTHALMOLOGY, 2011, 118 (07) :1373-1379
[6]   Subthreshold Nanosecond Laser Intervention in Age-Related Macular Degeneration The LEAD Randomized Controlled Clinical Trial [J].
Guymer, Robyn H. ;
Wu, Zhichao ;
Hodgson, Lauren A. B. ;
Caruso, Emily ;
Brassington, Kate H. ;
Tindill, Nicole ;
Aung, Khin Zaw ;
McGuinness, Myra B. ;
Fletcher, Erica L. ;
Chen, Fred K. ;
Chakravarthy, Usha ;
Arnold, Jennifer J. ;
Heriot, Wilson J. ;
Durkin, Shane R. ;
Lek, Jia Jia ;
Harper, Colin A. ;
Wickremasinghe, Sanjeewa S. ;
Sandhu, Sukhpal S. ;
Baglin, Elizabeth K. ;
Sharangan, Pyrawy ;
Braat, Sabine ;
Luu, Chi D. .
OPHTHALMOLOGY, 2019, 126 (06) :829-838
[7]   Incidence, Progression, and Associated Risk Factors of Medium Drusen in Age-Related Macular Degeneration Findings From the 15-Year Follow-up of an Australian Cohort [J].
Joachim, Nichole D. L. ;
Mitchell, Paul ;
Kifley, Annette ;
Wang, Jie Jin .
JAMA OPHTHALMOLOGY, 2015, 133 (06) :698-705
[8]   Drusen Ultrastructure Imaging with Spectral Domain Optical Coherence Tomography in Age-related Macular Degeneration [J].
Khanifar, Aziz A. ;
Koreishi, Anjum F. ;
Izatt, Joseph A. ;
Toth, Cynthia A. .
OPHTHALMOLOGY, 2008, 115 (11) :1883-1890
[9]   The five-year incidence and progression of age-related maculopathy - The Beaver Dam eye study [J].
Klein, R ;
Klein, BEK ;
Jensen, SC ;
Meuer, SM .
OPHTHALMOLOGY, 1997, 104 (01) :7-21
[10]  
Lek JJ, 2017, OPHTHALMOL RETINA, V1, P227, DOI 10.1016/j.oret.2016.12.001