Quantitative Fundus Autofluorescence in Rhesus Macaques in Aging and Age-Related Drusen.


Journal

Investigative ophthalmology & visual science
ISSN: 1552-5783
Titre abrégé: Invest Ophthalmol Vis Sci
Pays: United States
ID NLM: 7703701

Informations de publication

Date de publication:
01 07 2020
Historique:
entrez: 15 7 2020
pubmed: 15 7 2020
medline: 8 1 2021
Statut: ppublish

Résumé

To employ quantitative fundus autofluorescence (qAF) imaging in rhesus macaques to noninvasively assess retinal pigment epithelial (RPE) lipofuscin in nonhuman primates (NHPs) as a model of aging and age-related macular degeneration (AMD). The qAF imaging was performed on eyes of 26 rhesus macaques (mean age 18.8 ± 8.2 years, range 4-27 years) with normal-appearing fundus or with age-related soft drusen using a confocal scanning laser ophthalmoscope with 488 nm excitation and an internal fluorescence reference. Eyes with soft drusen also underwent spectral-domain optical coherence tomography imaging to measure drusen volume and height of individual drusen lesions. The qAF levels were measured from the perifoveal annular ring (quantitative autofluorescence 8 [qAF8]) using the Delori grid, as well as focally over individual drusen lesions in this region. The association between qAF levels and age, sex, and drusen presence and volume were determined using multivariable regression analysis. Mean qAF levels increased with age (P < 0.001) and were higher in females (P = 0.047). Eyes with soft drusen exhibited reduced mean qAF compared with age-matched normal eyes (P = 0.003), with greater drusen volume showing a trend toward decreased qAF levels. However, qAF levels are focally increased over most individual drusen (P < 0.001), with larger drusen appearing more hyperautofluorescent (R2 = 0.391, P < 0.001). In rhesus macaques, qAF levels are increased with age and female sex, but decreased in eyes with soft drusen, similar to human AMD. However, drusen lesions appear hyperautofluorescent unlike those in humans, suggesting similarities and differences in RPE lipofuscin between humans and NHPs that may provide insight into drusen biogenesis and AMD pathogenesis.

Identifiants

pubmed: 32663290
pii: 2770312
doi: 10.1167/iovs.61.8.16
pmc: PMC7425688
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

16

Subventions

Organisme : NEI NIH HHS
ID : K08 EY027463
Pays : United States
Organisme : NEI NIH HHS
ID : P30 EY005722
Pays : United States
Organisme : NEI NIH HHS
ID : R21 EY031108
Pays : United States
Organisme : NEI NIH HHS
ID : K08 EY026101
Pays : United States
Organisme : NIH HHS
ID : P51 OD011107
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY032238
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY016134
Pays : United States
Organisme : NIEHS NIH HHS
ID : U01 ES027288
Pays : United States
Organisme : NEI NIH HHS
ID : U24 EY029904
Pays : United States

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