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dc.contributor.authorPoon, Linda Yi-Chieh
dc.contributor.authorAntar, Hussein
dc.contributor.authorTsikata, Edem
dc.contributor.authorGuo, Rong
dc.contributor.authorPapadogeorgou, Georgia
dc.contributor.authorFreeman, Madeline
dc.contributor.authorKhoueir, Ziad
dc.contributor.authorLee, Ramon
dc.contributor.authorShieh, Eric
dc.contributor.authorSimavli, Huseyin
dc.contributor.authorQue, Christian John
dc.contributor.authorde Boer, Johannes F.
dc.contributor.authorChen, Teresa C.
dc.date2022-08-11T08:09:52.000
dc.date.accessioned2022-08-23T16:46:26Z
dc.date.available2022-08-23T16:46:26Z
dc.date.issued2018-11-27
dc.date.submitted2018-12-21
dc.identifier.citation<p>Transl Vis Sci Technol. 2018 Nov 27;7(6):12. doi: 10.1167/tvst.7.6.12. eCollection 2018 Nov. <a href="https://doi.org/10.1167/tvst.7.6.12">Link to article on publisher's site</a></p>
dc.identifier.issn2164-2591 (Linking)
dc.identifier.doi10.1167/tvst.7.6.12
dc.identifier.pmid30510856
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40881
dc.description.abstractPurpose: To evaluate the effects of age, race, and ethnicity on the optic nerve and peripapillary retina using spectral-domain optical coherence tomography (SD-OCT) three-dimensional (3D) volume scans in normal subjects. Methods: This is a cross-sectional study performed at a single institution in Boston. All patients received retinal nerve fiber layer (RNFL) scans and an optic nerve 3D volume scan. The SD-OCT software calculated peripapillary RNFL thickness, retinal thickness (RT), and retinal volume (RV). Custom-designed software calculated neuroretinal rim minimum distance band (MDB) thickness and area. Results: There were 272 normal subjects, including 175 whites, 40 blacks, 40 Asians, and 17 Hispanics. Rates of age-related decline were 2.3%, 2.0%, 1.7%, 3.3%, and 4.3% per decade for RNFL, RT, RV, MDB neuroretinal rim thickness, and MDB area, respectively. The RNFL was most affected by racial and ethnic variations, with Asians having thicker global, superior, and inferior RNFL, Hispanics having thicker inferior RNFL, and blacks having thinner temporal RNFL, compared to whites. For MDB thickness and area, Asians had smaller nasal values and blacks had smaller temporal values. Peripapillary RT and RV parameters were not influenced by race and ethnicity. Conclusions: All of the parameters exhibited age-related declines. RNFL, MDB thickness, and MDB area demonstrated racial and ethnic variations, while peripapillary RT and RV did not. Translational Relevance: This study demonstrates that both normal aging and ethnicity affect several novel 3D OCT parameters used to diagnose and monitor glaucoma (i.e., RT, RV, and MDB), and this should be factored in when making clinical decisions based on these parameters.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=30510856&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rightsCopyright 2018 The Authors. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectage
dc.subjectaging
dc.subjectoptic nerve
dc.subjectperipapillary retina
dc.subjectrace
dc.subjectspectral-domain OCT
dc.subjectthree-dimensional OCT
dc.subjectEpidemiology
dc.subjectEye Diseases
dc.subjectMusculoskeletal, Neural, and Ocular Physiology
dc.subjectOphthalmology
dc.subjectRace and Ethnicity
dc.subjectVision Science
dc.titleEffects of Age, Race, and Ethnicity on the Optic Nerve and Peripapillary Region Using Spectral-Domain OCT 3D Volume Scans
dc.typeJournal Article
dc.source.journaltitleTranslational vision science and technology
dc.source.volume7
dc.source.issue6
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4696&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3684
dc.identifier.contextkey13525581
refterms.dateFOA2022-08-23T16:46:27Z
html.description.abstract<p>Purpose: To evaluate the effects of age, race, and ethnicity on the optic nerve and peripapillary retina using spectral-domain optical coherence tomography (SD-OCT) three-dimensional (3D) volume scans in normal subjects.</p> <p>Methods: This is a cross-sectional study performed at a single institution in Boston. All patients received retinal nerve fiber layer (RNFL) scans and an optic nerve 3D volume scan. The SD-OCT software calculated peripapillary RNFL thickness, retinal thickness (RT), and retinal volume (RV). Custom-designed software calculated neuroretinal rim minimum distance band (MDB) thickness and area.</p> <p>Results: There were 272 normal subjects, including 175 whites, 40 blacks, 40 Asians, and 17 Hispanics. Rates of age-related decline were 2.3%, 2.0%, 1.7%, 3.3%, and 4.3% per decade for RNFL, RT, RV, MDB neuroretinal rim thickness, and MDB area, respectively. The RNFL was most affected by racial and ethnic variations, with Asians having thicker global, superior, and inferior RNFL, Hispanics having thicker inferior RNFL, and blacks having thinner temporal RNFL, compared to whites. For MDB thickness and area, Asians had smaller nasal values and blacks had smaller temporal values. Peripapillary RT and RV parameters were not influenced by race and ethnicity.</p> <p>Conclusions: All of the parameters exhibited age-related declines. RNFL, MDB thickness, and MDB area demonstrated racial and ethnic variations, while peripapillary RT and RV did not. Translational</p> <p>Relevance: This study demonstrates that both normal aging and ethnicity affect several novel 3D OCT parameters used to diagnose and monitor glaucoma (i.e., RT, RV, and MDB), and this should be factored in when making clinical decisions based on these parameters.</p>
dc.identifier.submissionpathoapubs/3684
dc.contributor.departmentMedical Education
dc.source.pages12


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Copyright 2018 The Authors.  This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Except where otherwise noted, this item's license is described as Copyright 2018 The Authors. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.