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dc.contributor.authorFernandes, AG
dc.contributor.authorAlexopoulos, P
dc.contributor.authorBurgos-Rodriguez, A
dc.contributor.authorMartinez, MI
dc.contributor.authorGhassibi, M
dc.contributor.authorLeskov, I
dc.contributor.authorBrent, LJN
dc.contributor.authorSnyder-Mackler, N
dc.contributor.authorDanias, J
dc.contributor.authorWollstein, G
dc.contributor.authorHigham, JP
dc.contributor.authorMelin, AD
dc.date.accessioned2023-06-05T10:57:14Z
dc.date.issued2023-06-01
dc.date.updated2023-06-05T10:12:50Z
dc.description.abstractPURPOSE: Rhesus macaques (Macaca mulatta) are the premier nonhuman primate model for studying human health and disease. We investigated if age was associated with clinically relevant ocular features in a large cohort of free-ranging rhesus macaques from Cayo Santiago, Puerto Rico. METHODS: We evaluated 120 rhesus macaques (73 males, 47 females) from 0 to 29 years old (mean ± SD: 12.6 ± 6.4) from September to December 2021. The ophthalmic evaluation included intraocular pressure (IOP) assessment, corneal pachymetry, biomicroscopy, A-scan biometry, automated refraction, and fundus photography after pupil dilation. The associations of age with the outcomes were investigated through multilevel mixed-effects models adjusted for sex and weight. RESULTS: On average, IOP, pachymetry, axial length, and automated refraction spherical equivalent were 18.37 ± 4.68 mmHg, 474.43 ± 32.21 µm, 19.49 ± 1.24 mm, and 0.30 ± 1.70 diopters (D), respectively. Age was significantly associated with pachymetry (β coefficient = -1.20; 95% confidence interval [CI], -2.27 to -0.14; P = 0.026), axial length (β coefficient = 0.03; 95% CI, 0.01 to 0.05; P = 0.002), and spherical equivalent (β coefficient = -0.12; 95% CI, -0.22 to -0.02; P = 0.015). No association was detected between age and IOP. The prevalence of cataracts in either eye was 10.83% (95% CI, 6.34-17.89) and was significantly associated with age (odds ratio [OR] = 1.20; 95% CI, 1.06-1.36; P = 0.004). Retinal drusen in either eye was observed in 15.00% (95% CI, 9.60-22.68) of animals, which was also significantly associated with age (OR = 1.14; 95% CI, 1.02-1.27; P = 0.020). CONCLUSIONS: Rhesus macaques exhibit age-related ocular associations similar to those observed in human aging, including decreased corneal thickness, increased axial length, myopic shift, and higher prevalence of cataract and retinal drusen.en_GB
dc.description.sponsorshipNew Frontiers in Research Foundationen_GB
dc.description.sponsorshipNatural Sciences and Engineering Research Councilen_GB
dc.description.sponsorshipCanada Research Chairs Programen_GB
dc.description.sponsorshipNational Aging Instituteen_GB
dc.description.sponsorshipBrightFocus Foundationen_GB
dc.description.sponsorshipNational Institutes of Health (NIH)en_GB
dc.description.sponsorshipUniversity of Calgaryen_GB
dc.format.extent3-
dc.identifier.citationVol. 64(7), article 3en_GB
dc.identifier.doihttps://doi.org/10.1167/iovs.64.7.3
dc.identifier.grantnumberNFRFE-2018-02159en_GB
dc.identifier.grantnumberRGPIN-2017-03782en_GB
dc.identifier.grantnumber950-231257en_GB
dc.identifier.grantnumber1R56AG071023en_GB
dc.identifier.grantnumberR01AG060931en_GB
dc.identifier.grantnumberG2020047en_GB
dc.identifier.grantnumberNIH R01-EY030770en_GB
dc.identifier.urihttp://hdl.handle.net/10871/133293
dc.identifierORCID: 0000-0002-1202-1939 (Brent, Lauren JN)
dc.language.isoenen_GB
dc.publisherAssociation for Research in Vision and Ophthalmology (ARVO)en_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/37261386en_GB
dc.rights© 2023 The Authors. Open access. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.en_GB
dc.subjectagingen_GB
dc.subjectanimal modelsen_GB
dc.subjectnonhuman primateen_GB
dc.subjectrhesus macaqueen_GB
dc.titleAge-Related Differences in Ocular Features of a Naturalistic Free-Ranging Population of Rhesus Macaquesen_GB
dc.typeArticleen_GB
dc.date.available2023-06-05T10:57:14Z
dc.identifier.issn0146-0404
exeter.place-of-publicationUnited States
dc.descriptionThis is the final version. Available on open access from the Association for Research in Vision and Ophthalmology via the DOI in this recorden_GB
dc.identifier.eissn1552-5783
dc.identifier.journalInvestigative Ophthalmology & Visual Scienceen_GB
dc.relation.ispartofInvest Ophthalmol Vis Sci, 64(7)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/en_GB
dcterms.dateAccepted2023-02-28
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2023-06-01
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2023-06-05T10:53:10Z
refterms.versionFCDVoR
refterms.dateFOA2023-06-05T10:57:19Z
refterms.panelAen_GB


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© 2023 The Authors. Open access. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Except where otherwise noted, this item's licence is described as © 2023 The Authors. Open access. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.