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1.
Int Ophthalmol ; 40(6): 1501-1508, 2020 Jun.
Article in English | MEDLINE | ID: mdl-32130624

ABSTRACT

PURPOSE: Adult vitelliform lesions (AVL) are associated with age related macular degeneration (AMD) and subretinal drusenoid deposits (SRDD). We evaluated the natural course of AVL, assessing the influence of SRDD on disease progression, visual function and incidence of macular atrophy (MA) and choroidal neovascular membranes (CNVM). METHODS: A retrospective cohort study was conducted between January 2011 and March 2016. Demographic, clinical and imaging data from 26 consecutive AVL patients were analysed following case note review. Optical coherence tomography images were graded for SRDD and patients divided into those with/without SRDD. Outcomes included presenting/changes in best corrected visual acuity (BCVA) and incidence of MA/CNVM. RESULTS: Mean age was 78.6 ± 7.6 years. Mean follow-up was 51.5 ± 25.6 months. Twelve patients (46.2%) had SRDD at presentation with 3 more (11.5%) developing them. Subjects with SRDD were older (mean 81.7 ± 6.1 years vs 74.3 ± 7.6 years, p = 0.010). Mean presenting BCVA was worse in SRDD eyes (0.39 ± 0.31 logMAR vs 0.19 ± 0.18 logMAR, p = 0.017). Eight of 15 patients with SRDD (53.3%) developed incident MA or CNVM; higher than those with no SRDD (1/11, 9.1%; p = 0.036). Two patients (7.7%) developed full thickness macular holes. CONCLUSIONS: Patients with AVL and SRDD likely represent an advanced pathological stage or phenotype with worse visual outcome and higher risk of MA/CNVM. Possible overlap with AMD exists. Follow-up, counselling and provisions for early detection/treatment of complications should be made. Better classification including improved understanding of phenotypic and genetic variations with reference to comorbid diseases including AMD is required. Presence of SRDD in AVL offers a dichotomous classification, indicating risk of future MA/CNVM formation.


Subject(s)
Fluorescein Angiography/methods , Macula Lutea/diagnostic imaging , Retinal Drusen/diagnosis , Tomography, Optical Coherence/methods , Visual Acuity , Vitelliform Macular Dystrophy/diagnosis , Aged , Aged, 80 and over , Comorbidity , Female , Fundus Oculi , Humans , Male , Middle Aged , Retinal Drusen/epidemiology , Retrospective Studies , Vitelliform Macular Dystrophy/epidemiology
2.
Arch Ophthalmol ; 126(5): 665-9, 2008 May.
Article in English | MEDLINE | ID: mdl-18474777

ABSTRACT

OBJECTIVE: To determine the distribution of cell membrane proteins and extracellular matrix proteins around the limbal epithelial crypt (LEC) compared with adjacent limbus and corneal epithelium. METHODS: Serial histological sections of human corneoscleral limbus rims were stained with antibodies of interest by standard immunohistochemistry. RESULTS: Superficial cells of the limbus were desmoglein 3 positive, compared with the negative basal cells of the limbus that correspond to cells with more stemlike properties. The LEC had a much lower proportion of desmoglein 3 staining in comparison. Tenascin C staining demonstrated regional variations of the limbus depending on their association with the LEC. Limbus that was associated with or adjacent to the LEC had a greater tenascin C expression compared with normal limbus, whereas the LEC demonstrated the greatest tenascin C expression. CONCLUSIONS: Based on these and similar results previously reported for connexin 43, we propose a novel model on the mechanism of corneal surface epithelium maintenance involving 3 different limbal regions: zone 1, limbus including the LEC; zone 2, limbus associated with the LEC; and zone 3, limbus distant to the LEC. CLINICAL RELEVANCE: The noted limbal variations may influence the selection of the donor site for limbal grafts in the future.


Subject(s)
Epithelial Cells/cytology , Epithelium, Corneal/cytology , Limbus Corneae/cytology , Stem Cells/cytology , Desmoglein 3/metabolism , Epithelial Cells/metabolism , Epithelium, Corneal/physiology , Eye Proteins/metabolism , Fluorescent Antibody Technique, Indirect , Humans , Limbus Corneae/metabolism , Microscopy, Fluorescence , Models, Biological , Regeneration , Stem Cells/metabolism , Tenascin/metabolism
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