Comparing 2-dimensional macular pigment optical density with objective and subjective perimetry and visual acuity in age-related macular degeneration
Purpose To compare diagnostic power for different severities of age-related macular degeneration (AMD) of two-dimensional macular pigment optical densities (2D-MPOD) and spatially matched objective perimetry, with standard perimetry and best-corrected visual acuity (BCVA). Methods The ObjectiveField...
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creator | Rai, Bhim B. Sabeti, Faran van Kleef, Joshua P. Carle, Corinne F. Rohan, Emilie M. F. Essex, Rohan W. Barry, Richard C. Maddess, Ted |
description | Purpose
To compare diagnostic power for different severities of age-related macular degeneration (AMD) of two-dimensional macular pigment optical densities (2D-MPOD) and spatially matched objective perimetry, with standard perimetry and best-corrected visual acuity (BCVA).
Methods
The ObjectiveField Analyser (OFA) provided objective perimetry, and a Heidelberg Spectralis optical coherence tomography (OCT) measured 2D-MPOD in AMD patients, both completed twice over 0.99 ± 0.16 years. From each 2D-MPOD image, we extracted 20 regions/macula, matched to the 20 OFA stimuli/macula. For each region, we calculated 7 measures from the 2D-MPOD pixel values and correlated those with OFA sensitivities and delays. We quantified 2D-MPOD changes, the ability of 2D-MPOD and OFA to discriminate AMD stages, and the discriminatory power of Matrix perimetry and BCVA using percentage area under receiver operator characteristic plots (%AUROC).
Results
In 58 eyes of 29 subjects (71.6 ± 6.3 years, 22 females), we found significant correlations between 2D-MPOD and OFA sensitivities for Age-Related Eye Disease Studies (AREDS)-3 and AREDS-4 severities. Delays showed significant correlations with AREDS-2. For AREDS-4, correlations extended across all eccentricities. Regression associated with the Bland–Altman plots showed significant changes in 2D-MPOD over the study period,
especially variability measures
. MPOD per-region medians discriminated AREDS-1 from AREDS-3 eyes at a %AUROC of 80.0 ± 6.3%, outperforming OFA, Matrix perimetry, and BCVA.
Conclusions
MPOD changes correlated with central functional changes and significant correlations extended peripherally in later-stage AMD. Good diagnostic power for earlier-stage AMD and significant change over the study suggest that 2D-MPOD and OFA may provide effective biomarkers. |
doi_str_mv | 10.1007/s00417-024-06437-6 |
format | Article |
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To compare diagnostic power for different severities of age-related macular degeneration (AMD) of two-dimensional macular pigment optical densities (2D-MPOD) and spatially matched objective perimetry, with standard perimetry and best-corrected visual acuity (BCVA).
Methods
The ObjectiveField Analyser (OFA) provided objective perimetry, and a Heidelberg Spectralis optical coherence tomography (OCT) measured 2D-MPOD in AMD patients, both completed twice over 0.99 ± 0.16 years. From each 2D-MPOD image, we extracted 20 regions/macula, matched to the 20 OFA stimuli/macula. For each region, we calculated 7 measures from the 2D-MPOD pixel values and correlated those with OFA sensitivities and delays. We quantified 2D-MPOD changes, the ability of 2D-MPOD and OFA to discriminate AMD stages, and the discriminatory power of Matrix perimetry and BCVA using percentage area under receiver operator characteristic plots (%AUROC).
Results
In 58 eyes of 29 subjects (71.6 ± 6.3 years, 22 females), we found significant correlations between 2D-MPOD and OFA sensitivities for Age-Related Eye Disease Studies (AREDS)-3 and AREDS-4 severities. Delays showed significant correlations with AREDS-2. For AREDS-4, correlations extended across all eccentricities. Regression associated with the Bland–Altman plots showed significant changes in 2D-MPOD over the study period,
especially variability measures
. MPOD per-region medians discriminated AREDS-1 from AREDS-3 eyes at a %AUROC of 80.0 ± 6.3%, outperforming OFA, Matrix perimetry, and BCVA.
Conclusions
MPOD changes correlated with central functional changes and significant correlations extended peripherally in later-stage AMD. Good diagnostic power for earlier-stage AMD and significant change over the study suggest that 2D-MPOD and OFA may provide effective biomarkers.</description><identifier>ISSN: 0721-832X</identifier><identifier>ISSN: 1435-702X</identifier><identifier>EISSN: 1435-702X</identifier><identifier>DOI: 10.1007/s00417-024-06437-6</identifier><identifier>PMID: 38483610</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Acuity ; Aged ; Eye diseases ; Female ; Follow-Up Studies ; Humans ; Macula Lutea - diagnostic imaging ; Macular degeneration ; Macular Degeneration - diagnosis ; Macular Degeneration - metabolism ; Macular Degeneration - physiopathology ; Macular Pigment - metabolism ; Male ; Medicine ; Medicine & Public Health ; Ophthalmology ; Optical density ; Photopigments ; Retinal Disorders ; ROC Curve ; Tomography, Optical Coherence - methods ; Visual acuity ; Visual Acuity - physiology ; Visual Field Tests - methods ; Visual Fields - physiology</subject><ispartof>Graefe's archive for clinical and experimental ophthalmology, 2024-08, Vol.262 (8), p.2449-2459</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2024 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c426t-a595c923aad9c5861a06d2dfb06a2d0cb781ef0d144ef9ab525a49cefacd1cf3</cites><orcidid>0000-0003-2167-0348 ; 0000-0003-0748-4581 ; 0000-0002-3309-9073 ; 0000-0001-5323-0334 ; 0000-0003-0402-3296 ; 0000-0003-4591-3658 ; 0000-0001-9187-7569 ; 0000-0002-0566-6667</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00417-024-06437-6$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00417-024-06437-6$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27903,27904,41467,42536,51298</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38483610$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rai, Bhim B.</creatorcontrib><creatorcontrib>Sabeti, Faran</creatorcontrib><creatorcontrib>van Kleef, Joshua P.</creatorcontrib><creatorcontrib>Carle, Corinne F.</creatorcontrib><creatorcontrib>Rohan, Emilie M. F.</creatorcontrib><creatorcontrib>Essex, Rohan W.</creatorcontrib><creatorcontrib>Barry, Richard C.</creatorcontrib><creatorcontrib>Maddess, Ted</creatorcontrib><title>Comparing 2-dimensional macular pigment optical density with objective and subjective perimetry and visual acuity in age-related macular degeneration</title><title>Graefe's archive for clinical and experimental ophthalmology</title><addtitle>Graefes Arch Clin Exp Ophthalmol</addtitle><addtitle>Graefes Arch Clin Exp Ophthalmol</addtitle><description>Purpose
To compare diagnostic power for different severities of age-related macular degeneration (AMD) of two-dimensional macular pigment optical densities (2D-MPOD) and spatially matched objective perimetry, with standard perimetry and best-corrected visual acuity (BCVA).
Methods
The ObjectiveField Analyser (OFA) provided objective perimetry, and a Heidelberg Spectralis optical coherence tomography (OCT) measured 2D-MPOD in AMD patients, both completed twice over 0.99 ± 0.16 years. From each 2D-MPOD image, we extracted 20 regions/macula, matched to the 20 OFA stimuli/macula. For each region, we calculated 7 measures from the 2D-MPOD pixel values and correlated those with OFA sensitivities and delays. We quantified 2D-MPOD changes, the ability of 2D-MPOD and OFA to discriminate AMD stages, and the discriminatory power of Matrix perimetry and BCVA using percentage area under receiver operator characteristic plots (%AUROC).
Results
In 58 eyes of 29 subjects (71.6 ± 6.3 years, 22 females), we found significant correlations between 2D-MPOD and OFA sensitivities for Age-Related Eye Disease Studies (AREDS)-3 and AREDS-4 severities. Delays showed significant correlations with AREDS-2. For AREDS-4, correlations extended across all eccentricities. Regression associated with the Bland–Altman plots showed significant changes in 2D-MPOD over the study period,
especially variability measures
. MPOD per-region medians discriminated AREDS-1 from AREDS-3 eyes at a %AUROC of 80.0 ± 6.3%, outperforming OFA, Matrix perimetry, and BCVA.
Conclusions
MPOD changes correlated with central functional changes and significant correlations extended peripherally in later-stage AMD. Good diagnostic power for earlier-stage AMD and significant change over the study suggest that 2D-MPOD and OFA may provide effective biomarkers.</description><subject>Acuity</subject><subject>Aged</subject><subject>Eye diseases</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Macula Lutea - diagnostic imaging</subject><subject>Macular degeneration</subject><subject>Macular Degeneration - diagnosis</subject><subject>Macular Degeneration - metabolism</subject><subject>Macular Degeneration - physiopathology</subject><subject>Macular Pigment - metabolism</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Ophthalmology</subject><subject>Optical density</subject><subject>Photopigments</subject><subject>Retinal Disorders</subject><subject>ROC Curve</subject><subject>Tomography, Optical Coherence - methods</subject><subject>Visual acuity</subject><subject>Visual Acuity - physiology</subject><subject>Visual Field Tests - methods</subject><subject>Visual Fields - physiology</subject><issn>0721-832X</issn><issn>1435-702X</issn><issn>1435-702X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><recordid>eNp9UcmO1DAQtRCIaQZ-gAOKxIWLwVu2E0ItNmkkLnOYm1WxKxm30nGwnR71h_C_ONNDsxw4WJar3lLlR8hLzt5yxup3kTHFa8qEoqxSsqbVI7LhSpa0ZuLmMdmwWnDaSHFzQZ7FuGMZL0v-lFzIRjWy4mxDfmz9fobgpqEQ1Lo9TtH5CcZiD2YZIRSzG3IxFX5OzuS6XRHpWNy5dFv4bocmuQMWMNkiLufnjCFrpXC8bxxcXDI1K65MNxUwIA04QkJ7NrI44IQBUvZ_Tp70MEZ88XBfkutPH6-3X-jVt89ftx-uqFGiShTKtjStkAC2NWVTcWCVFbbvWAXCMtPVDceeWa4U9i10pShBtQZ7MJabXl6S9yfZeen2aE3eM8Co5zw7hKP24PTfncnd6sEfNOei5nmErPDmQSH47wvGpPcuGhxHmNAvUYu2bPJpW5Whr_-B7vwS8ldHLVkjcmR1tQqKE8oEH2PA_jwNZ3pNXZ9S1zl1fZ-6Xkmv_tzjTPkVcwbIEyDOa9QYfnv_R_YnvXS9tQ</recordid><startdate>20240801</startdate><enddate>20240801</enddate><creator>Rai, Bhim B.</creator><creator>Sabeti, Faran</creator><creator>van Kleef, Joshua P.</creator><creator>Carle, Corinne F.</creator><creator>Rohan, Emilie M. F.</creator><creator>Essex, Rohan W.</creator><creator>Barry, Richard C.</creator><creator>Maddess, Ted</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2167-0348</orcidid><orcidid>https://orcid.org/0000-0003-0748-4581</orcidid><orcidid>https://orcid.org/0000-0002-3309-9073</orcidid><orcidid>https://orcid.org/0000-0001-5323-0334</orcidid><orcidid>https://orcid.org/0000-0003-0402-3296</orcidid><orcidid>https://orcid.org/0000-0003-4591-3658</orcidid><orcidid>https://orcid.org/0000-0001-9187-7569</orcidid><orcidid>https://orcid.org/0000-0002-0566-6667</orcidid></search><sort><creationdate>20240801</creationdate><title>Comparing 2-dimensional macular pigment optical density with objective and subjective perimetry and visual acuity in age-related macular degeneration</title><author>Rai, Bhim B. ; Sabeti, Faran ; van Kleef, Joshua P. ; Carle, Corinne F. ; Rohan, Emilie M. F. ; Essex, Rohan W. ; Barry, Richard C. ; Maddess, Ted</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-a595c923aad9c5861a06d2dfb06a2d0cb781ef0d144ef9ab525a49cefacd1cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Acuity</topic><topic>Aged</topic><topic>Eye diseases</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Macula Lutea - diagnostic imaging</topic><topic>Macular degeneration</topic><topic>Macular Degeneration - diagnosis</topic><topic>Macular Degeneration - metabolism</topic><topic>Macular Degeneration - physiopathology</topic><topic>Macular Pigment - metabolism</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Ophthalmology</topic><topic>Optical density</topic><topic>Photopigments</topic><topic>Retinal Disorders</topic><topic>ROC Curve</topic><topic>Tomography, Optical Coherence - methods</topic><topic>Visual acuity</topic><topic>Visual Acuity - physiology</topic><topic>Visual Field Tests - methods</topic><topic>Visual Fields - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rai, Bhim B.</creatorcontrib><creatorcontrib>Sabeti, Faran</creatorcontrib><creatorcontrib>van Kleef, Joshua P.</creatorcontrib><creatorcontrib>Carle, Corinne F.</creatorcontrib><creatorcontrib>Rohan, Emilie M. F.</creatorcontrib><creatorcontrib>Essex, Rohan W.</creatorcontrib><creatorcontrib>Barry, Richard C.</creatorcontrib><creatorcontrib>Maddess, Ted</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Graefe's archive for clinical and experimental ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rai, Bhim B.</au><au>Sabeti, Faran</au><au>van Kleef, Joshua P.</au><au>Carle, Corinne F.</au><au>Rohan, Emilie M. F.</au><au>Essex, Rohan W.</au><au>Barry, Richard C.</au><au>Maddess, Ted</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparing 2-dimensional macular pigment optical density with objective and subjective perimetry and visual acuity in age-related macular degeneration</atitle><jtitle>Graefe's archive for clinical and experimental ophthalmology</jtitle><stitle>Graefes Arch Clin Exp Ophthalmol</stitle><addtitle>Graefes Arch Clin Exp Ophthalmol</addtitle><date>2024-08-01</date><risdate>2024</risdate><volume>262</volume><issue>8</issue><spage>2449</spage><epage>2459</epage><pages>2449-2459</pages><issn>0721-832X</issn><issn>1435-702X</issn><eissn>1435-702X</eissn><abstract>Purpose
To compare diagnostic power for different severities of age-related macular degeneration (AMD) of two-dimensional macular pigment optical densities (2D-MPOD) and spatially matched objective perimetry, with standard perimetry and best-corrected visual acuity (BCVA).
Methods
The ObjectiveField Analyser (OFA) provided objective perimetry, and a Heidelberg Spectralis optical coherence tomography (OCT) measured 2D-MPOD in AMD patients, both completed twice over 0.99 ± 0.16 years. From each 2D-MPOD image, we extracted 20 regions/macula, matched to the 20 OFA stimuli/macula. For each region, we calculated 7 measures from the 2D-MPOD pixel values and correlated those with OFA sensitivities and delays. We quantified 2D-MPOD changes, the ability of 2D-MPOD and OFA to discriminate AMD stages, and the discriminatory power of Matrix perimetry and BCVA using percentage area under receiver operator characteristic plots (%AUROC).
Results
In 58 eyes of 29 subjects (71.6 ± 6.3 years, 22 females), we found significant correlations between 2D-MPOD and OFA sensitivities for Age-Related Eye Disease Studies (AREDS)-3 and AREDS-4 severities. Delays showed significant correlations with AREDS-2. For AREDS-4, correlations extended across all eccentricities. Regression associated with the Bland–Altman plots showed significant changes in 2D-MPOD over the study period,
especially variability measures
. MPOD per-region medians discriminated AREDS-1 from AREDS-3 eyes at a %AUROC of 80.0 ± 6.3%, outperforming OFA, Matrix perimetry, and BCVA.
Conclusions
MPOD changes correlated with central functional changes and significant correlations extended peripherally in later-stage AMD. Good diagnostic power for earlier-stage AMD and significant change over the study suggest that 2D-MPOD and OFA may provide effective biomarkers.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>38483610</pmid><doi>10.1007/s00417-024-06437-6</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-2167-0348</orcidid><orcidid>https://orcid.org/0000-0003-0748-4581</orcidid><orcidid>https://orcid.org/0000-0002-3309-9073</orcidid><orcidid>https://orcid.org/0000-0001-5323-0334</orcidid><orcidid>https://orcid.org/0000-0003-0402-3296</orcidid><orcidid>https://orcid.org/0000-0003-4591-3658</orcidid><orcidid>https://orcid.org/0000-0001-9187-7569</orcidid><orcidid>https://orcid.org/0000-0002-0566-6667</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acuity Aged Eye diseases Female Follow-Up Studies Humans Macula Lutea - diagnostic imaging Macular degeneration Macular Degeneration - diagnosis Macular Degeneration - metabolism Macular Degeneration - physiopathology Macular Pigment - metabolism Male Medicine Medicine & Public Health Ophthalmology Optical density Photopigments Retinal Disorders ROC Curve Tomography, Optical Coherence - methods Visual acuity Visual Acuity - physiology Visual Field Tests - methods Visual Fields - physiology |
title | Comparing 2-dimensional macular pigment optical density with objective and subjective perimetry and visual acuity in age-related macular degeneration |
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