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Improved sensitivity of microperimetric outcomes for clinical studies in age-related macular degeneration

To investigate sensitive outcome measures based exclusively on abnormal points in microperimetry testing of eyes with intermediate age-related macular degeneration (iAMD). 25 eyes of 25 subjects with iAMD had undergone 2 successive tests of mesopic microperimetry with the Macular Integrity Assessmen...

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Autores principales: Barkana, Yaniv, Pondorfer, Susanne G., Schmitz-Valckenberg, Steffen, Russ, Hermann, Finger, Robert P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910434/
https://www.ncbi.nlm.nih.gov/pubmed/33637858
http://dx.doi.org/10.1038/s41598-021-83716-w
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author Barkana, Yaniv
Pondorfer, Susanne G.
Schmitz-Valckenberg, Steffen
Russ, Hermann
Finger, Robert P.
author_facet Barkana, Yaniv
Pondorfer, Susanne G.
Schmitz-Valckenberg, Steffen
Russ, Hermann
Finger, Robert P.
author_sort Barkana, Yaniv
collection PubMed
description To investigate sensitive outcome measures based exclusively on abnormal points in microperimetry testing of eyes with intermediate age-related macular degeneration (iAMD). 25 eyes of 25 subjects with iAMD had undergone 2 successive tests of mesopic microperimetry with the Macular Integrity Assessment Microperimeter (MAIA), using a custom grid of 33 points spanning the central 14 degrees of the macula. Each point was defined as abnormal if its threshold sensitivity was lower than 1.65 standard deviations (SD) (5%) or 2 SD (2.5%) than the expected threshold in healthy eyes according to the MAIA internal database. Among the 25 eyes there were 11.8 ± 9 and 8.4 ± 8.2 abnormal points at < 5% and < 2.5%, with mean deviation of thresholds from normal − 4.9 ± 1.2 dB and − 5.8 ± 1.5 dB, respectively. These deviations were greater, and their SD smaller, compared with the complete microperimetry grid, − 2.3 ± 2.0 dB. The 95% limits of agreement for average threshold between the 2 successive tests were smaller when only abnormal points were included. Analyzing only abnormal grid points yields an outcome parameter with a greater deviation from normal, a more homogenous dataset, and better test–retest variability, compared with analysis of all grid points. This parameter may thus be more sensitive to change, while moderately limiting the number of potential recruits. The proposed outcome measures should be further investigated as potential endpoints in clinical trials in iAMD.
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spelling pubmed-79104342021-03-02 Improved sensitivity of microperimetric outcomes for clinical studies in age-related macular degeneration Barkana, Yaniv Pondorfer, Susanne G. Schmitz-Valckenberg, Steffen Russ, Hermann Finger, Robert P. Sci Rep Article To investigate sensitive outcome measures based exclusively on abnormal points in microperimetry testing of eyes with intermediate age-related macular degeneration (iAMD). 25 eyes of 25 subjects with iAMD had undergone 2 successive tests of mesopic microperimetry with the Macular Integrity Assessment Microperimeter (MAIA), using a custom grid of 33 points spanning the central 14 degrees of the macula. Each point was defined as abnormal if its threshold sensitivity was lower than 1.65 standard deviations (SD) (5%) or 2 SD (2.5%) than the expected threshold in healthy eyes according to the MAIA internal database. Among the 25 eyes there were 11.8 ± 9 and 8.4 ± 8.2 abnormal points at < 5% and < 2.5%, with mean deviation of thresholds from normal − 4.9 ± 1.2 dB and − 5.8 ± 1.5 dB, respectively. These deviations were greater, and their SD smaller, compared with the complete microperimetry grid, − 2.3 ± 2.0 dB. The 95% limits of agreement for average threshold between the 2 successive tests were smaller when only abnormal points were included. Analyzing only abnormal grid points yields an outcome parameter with a greater deviation from normal, a more homogenous dataset, and better test–retest variability, compared with analysis of all grid points. This parameter may thus be more sensitive to change, while moderately limiting the number of potential recruits. The proposed outcome measures should be further investigated as potential endpoints in clinical trials in iAMD. Nature Publishing Group UK 2021-02-26 /pmc/articles/PMC7910434/ /pubmed/33637858 http://dx.doi.org/10.1038/s41598-021-83716-w Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Barkana, Yaniv
Pondorfer, Susanne G.
Schmitz-Valckenberg, Steffen
Russ, Hermann
Finger, Robert P.
Improved sensitivity of microperimetric outcomes for clinical studies in age-related macular degeneration
title Improved sensitivity of microperimetric outcomes for clinical studies in age-related macular degeneration
title_full Improved sensitivity of microperimetric outcomes for clinical studies in age-related macular degeneration
title_fullStr Improved sensitivity of microperimetric outcomes for clinical studies in age-related macular degeneration
title_full_unstemmed Improved sensitivity of microperimetric outcomes for clinical studies in age-related macular degeneration
title_short Improved sensitivity of microperimetric outcomes for clinical studies in age-related macular degeneration
title_sort improved sensitivity of microperimetric outcomes for clinical studies in age-related macular degeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910434/
https://www.ncbi.nlm.nih.gov/pubmed/33637858
http://dx.doi.org/10.1038/s41598-021-83716-w
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