Navigation überspringen
Universitätsbibliothek Heidelberg
Status: Bibliographieeintrag

Verfügbarkeit
Standort: ---
Exemplare: ---
heiBIB
 Online-Ressource
Verfasst von:Jonas, Jost B. [VerfasserIn]   i
 Jonas, Rahul A. [VerfasserIn]   i
 Xu, Jie [VerfasserIn]   i
 Wang, Ya Xing [VerfasserIn]   i
Titel:Prevalence and cause of loss of visual acuity and visual field in highly myopic eyes
Titelzusatz:the Beijing eye study
Verf.angabe:Jost B. Jonas, MD, Rahul A. Jonas, MD, Jie Xu, MD, Ya Xing Wang, MD
E-Jahr:2024
Jahr:January 2024
Umfang:8 S.
Illustrationen:Illustrationen
Fussnoten:Online verfügbar: 9. September 2023, Artikelversion: 19. Dezember 2023 ; Gesehen am 05.03.2025
Titel Quelle:Enthalten in: Ophthalmology
Ort Quelle:Amsterdam [u.a.] : Elsevier, 1978
Jahr Quelle:2024
Band/Heft Quelle:131(2024), 1, Seite 58-65
ISSN Quelle:1549-4713
Abstract:Purpose - To explore the prevalence and causes of loss of visual acuity and visual field in highly myopic eyes. - Design - Population-based study. - Participants - 4439 subjects of the Beijing Eye Study underwent ophthalmological and systemic examinations including frequency doubling technology perimetry. - Methods - High myopia was defined by a refractive error of ≤-6 diopters (D) or axial length >26.0 mm. - Main Outcome Measures - Prevalence of vision impairment causes. - Results - 212 highly myopic eyes from 154 participants were included with a mean age of 56.2 ± 9.6 years, a mean refractive error of -9.87 ± 3.70 D and a mean axial length of 27.2 ± 1.3 mm. We observed moderate/severe vision impairment (MSVI) in 40 eyes (18.9%; 95% confidence interval [CI], 13.6-24.2) and blindness in 10 eyes (4.7%; 95% CI, 1.8-7.6). Primary causes for MSVI and blindness were myopic macular degeneration (MMD) (29/50; 58%), age-related macular degeneration (1/50; 2%), and branch macular retinal vein occlusion (1/50; 2%). Secondary causes were MMD (4/50; 8%) and optic nerve atrophy (14/50, 28%), further differentiated into non-glaucomatous optic atrophy (NGOA) (9/50; 18%) and glaucomatous optic atrophy (GOA) (5/50; 10%). Prevalence of MMD as vision impairment cause increased significantly from 1/61 (1.6%) in the refractive error group of -6.00 to ≥-7.00 D, to 16/25 (64%) in the group of <-15.0 D. Higher MMD prevalence correlated with higher myopic refractive error (P < 0.001) and increased likelihood of concomitant optic neuropathy (P < 0.001). Similarly, prevalence of optic neuropathy as vision impairment cause increased from 0/61 (0%) in the refractive error group of -6.00 D to ≥-7.00 D, to 9/25 (36%) in the group of <-15.0 D. Higher optic neuropathy prevalence correlated with more myopic refraction (P < 0.001) and older age (P = 0.02). - Conclusions - In this population-based recruited cohort of highly myopic patients, optic neuropathy accounted for vision impairment in 9.0% eyes, which was lower than the prevalence of MMD as vision impairment cause (18.9%). Notably, optic neuropathy became a significant contributor to vision impairment in more advanced high myopia, reaching 36% in the group with refractive error of <-15.0 D. - Financial Disclosure(s) - Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
DOI:doi:10.1016/j.ophtha.2023.08.026
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

kostenfrei: Volltext: https://doi.org/10.1016/j.ophtha.2023.08.026
 kostenfrei: Volltext: https://www.sciencedirect.com/science/article/pii/S0161642023006255
 DOI: https://doi.org/10.1016/j.ophtha.2023.08.026
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Beijing Eye Study
 Blindness
 High myopia
 Myopia
 Myopic macular degeneration
 Myopic macular neovascularization
 Vision loss
K10plus-PPN:1919126538
Verknüpfungen:→ Zeitschrift

Permanenter Link auf diesen Titel (bookmarkfähig):  https://katalog.ub.uni-heidelberg.de/titel/69314898   QR-Code
zum Seitenanfang