Repeatability and Discriminatory Power of Chart-Based Visual Function Tests in Individuals With Age-Related Macular Degeneration
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Published:2022-08-01
Issue:8
Volume:140
Page:780
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ISSN:2168-6165
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Container-title:JAMA Ophthalmology
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language:en
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Short-container-title:JAMA Ophthalmol
Author:
Dunbar Hannah M. P.12, Behning Charlotte3, Abdirahman Amina1, Higgins Bethany E.4, Binns Alison M.4, Terheyden Jan H.5, Zakaria Nadia6, Poor Stephen7, Finger Robert P.5, Leal Sergio8, Holz Frank G.5, Schmid Matthias3, Crabb David P.4, Rubin Gary S.12, Luhmann Ulrich F. O.9, Agostini Hansjürgen10, Bandello Francesco10, Basile Pier, G.10, Berger Moritz10, Boon Camiel, J. F.10, Böttger Michael10, Bouchet Christine10, Brazier John, E.10, Butt Thomas10, Carapezzi Claire10, Carlton Jill10, Carneiro Angela10, Charil Arnaud10, Coimbra Rita10, Cunha-Vaz José10, Dahlke Claudia10, de Sisternes Luis10, Fletcher Emily10, Floyd Heather10, Hogg Ruth10, Hoyng Carel10, Krätzschmar Jörn10, Kühlewein Laura10, Larsen Michael10, Luning Anna10, Martinho Cecília, V.10, Melício Beatriz, A.10, Mohand-Saïd Saddek10, Nunes Sandrina10, Parravano Mariacristina10, Pauleikhoff Daniel10, Pfau Maximilian10, Pondorfer Susanne, G.10, Priglinger Siegfried10, Rowen Donna10, Sahel José A10, Sanches Fernandes Daniel10, Sánchez Clara I.10, Saßmannshausen Marlene10, Schmitz-Valckenberg Steffen10, Schrinner-Fenske Hanna10, Silva Rufino10, Skelly Adrian10, Souied Eric10, Staurenghi Giovanni10, Stöhr Linda10, Tavares Diana10, Taylor Deanna, J.10, Thiele Sarah10, Tufail Adnan10, Wintergerst Ludmila10, Wojek Christian10,
Affiliation:
1. Department of Visual Neuroscience and Function, University College London Institute of Ophthalmology, London, United Kingdom 2. Moorfields Eye Hospital National Health Service Foundation Trust, London, United Kingdom 3. Medical Faculty, Institute of Medical Biometry, Informatics and Epidemiology, University of Bonn, Bonn, Germany 4. Department of Optometry and Visual Sciences, School of Health Sciences, City, University London, London, United Kingdom 5. Department of Ophthalmology, University of Bonn, Bonn, Germany 6. Translational Medicine, Novartis Institute for Biomedical Research, Cambridge, Massachusetts 7. Ophthalmology Research, Novartis Institute for Biomedical Research, Cambridge, Massachusetts 8. Bayer AG, Berlin, Germany 9. Roche Pharmaceutical Research and Early Development, Translational Medicine Ophthalmology, Roche Innovation Center Basel, Switzerland 10. for the MACUSTAR Consortium
Abstract
ImportanceThere is a need for validated clinical end points that are reliably able to quantify potential therapeutic effects of future treatments targeting age-related macular degeneration (AMD) before the onset of serious visual impairment.ObjectiveTo assess the reliability and discriminatory power of 5 simple chart-based visual function (VF) tests as potential measures for clinical trial end points with regulatory and patient-access intention in intermediate AMD (iAMD).Design, Setting, and ParticipantsThis international noninterventional study took place at 18 tertiary ophthalmology departments across Europe. Participants were recruited between April 2018 and March 2020 and were identified during routine clinical review. Participants with no AMD and early AMD were recruited from hospital staff, friends, and family of participants with AMD and via referrals from community ophthalmologists and optometrists. The repeatability and discriminatory power of 5 simple chart-based assessments of VF (best-corrected visual acuity [BCVA], low-luminance visual acuity [LLVA], Moorfields Acuity Test [MAT], Pelli-Robson Contrast Sensitivity [CS], and International Reading Speed Test [IReST]) were assessed in a repeated-measures design. VF assessments were performed on day 0 and day 14. Participants with early AMD, iAMD, late AMD, and no AMD were recruited.Main Outcomes and MeasuresIntraclass correlation coefficients (ICCs) and Bland-Altman 95% limits of agreement (LoA) were computed to assess repeatability. Area under the receiver operating characteristic curves (AUCs) determined the discriminatory ability of all measures to classify individuals as having no AMD or iAMD and to differentiate iAMD from its neighboring disease states.ResultsA total of 301 participants (mean [SD] age, 71 [7] years; 187 female participants [62.1%]) were included in the study. Thirty-four participants (11.3%) had early AMD, 168 (55.8%) had iAMD, 43 (14.3%) had late AMD, and 56 (18.6%) had no AMD. ICCs for all VF measures ranged between 0.88 and 0.96 when all participants were considered, indicating good to excellent repeatability. All measures displayed excellent discrimination between iAMD and late AMD (AUC, 0.92-0.99). Early AMD was indistinguishable from iAMD on all measures (AUC, 0.54-0.64). CS afforded the best discrimination between no AMD and iAMD (AUC, 0.77). Under the same conditions, BCVA, LLVA, and MAT were fair discriminators (AUC, 0.69-0.71), and IReST had poor discrimination (AUC, 0.57-0.61).Conclusions and RelevanceBCVA, LLVA, MAT, CS, and IReST had adequate repeatability in this multicenter, multiexaminer setting but limited power to discriminate between no AMD and iAMD. The prognostic power of these variables to predict conversion from iAMD to late AMD is being examined in the ongoing longitudinal part of the MACUSTAR study.
Publisher
American Medical Association (AMA)
Cited by
6 articles.
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