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Central macular morphology and optic nerve fibre layer thickness in young adults born premature and screened for retinopathy of prematurity

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dc.contributor Landspitali - The National University Hospital of Iceland
dc.contributor.author Pétursdóttir, Dýrleif
dc.contributor.author Åkerblom, Hanna
dc.contributor.author Holmström, Gerd
dc.contributor.author Larsson, Eva
dc.date.accessioned 2024-01-13T01:06:18Z
dc.date.available 2024-01-13T01:06:18Z
dc.date.issued 2023-11-22
dc.identifier.citation Pétursdóttir , D , Åkerblom , H , Holmström , G & Larsson , E 2023 , ' Central macular morphology and optic nerve fibre layer thickness in young adults born premature and screened for retinopathy of prematurity ' , Acta Ophthalmologica . https://doi.org/10.1111/aos.15814
dc.identifier.issn 1755-375X
dc.identifier.other 215151170
dc.identifier.other 2b82f033-211e-49dd-b0e8-33dafe9d5e53
dc.identifier.other 85177548640
dc.identifier.uri https://hdl.handle.net/20.500.11815/4647
dc.description Publisher Copyright: © 2023 The Authors. Acta Ophthalmologica published by John Wiley & Sons Ltd on behalf of Acta Ophthalmologica Scandinavica Foundation.
dc.description.abstract Purpose: To investigate central retinal morphology and optic retinal nerve fibre layer (RNFL) in prematurely born young adults and compare to term born controls. Materials and Methods: The participants were 59 prematurely born individuals, with a birthweight ≤1.500 g, and 44 term born controls, all 25–29 years of age. Visual acuity (VA) and contrast sensitivity (CS) were assessed. The retinal macular thickness, ganglion cell-inner plexiform layer (GC-IPL) thickness and RNFL thickness were assessed with Cirrus optical coherence tomography (OCT). Results: Central macular thickness was increased (mean 26.7 μm) in prematurely born individuals compared to controls. The macular GC-IPL was thinner (mean 3.84 μm), also when excluding those with previous retinopathy of prematurity (ROP) and those with neurological complications. Gestational age at birth and previous treatment of ROP were risk factors for a thicker macula, however, not for reduced GC-IPL. The average peripapillary RNFL was thinner (mean 4.61 μm) in the prematurely born individuals, also when excluding those with previous ROP and/or neurological complications. Within the prematurely born group, treated ROP was correlated with increased average RNFL. Further, both better VA and CS were associated with thinner optic nerve RNFL and thicker average GC-IPL. Conclusion: Macular and optic nerve morphology were influenced by premature birth as assessed with OCT in adult individuals. Gestational age at birth and treatment for ROP seemed to affect central macular thickness, and treated ROP affected the peripapillary RNFL. Thus, retinal sequelae remained in adulthood.
dc.format.extent 5565837
dc.format.extent
dc.language.iso en
dc.relation.ispartofseries Acta Ophthalmologica; ()
dc.rights info:eu-repo/semantics/openAccess
dc.subject Augnlæknisfræði
dc.subject ganglion cell-inner plexiform layer (GC-IPL)
dc.subject macular thickness
dc.subject optical coherence tomography (OCT)
dc.subject prematurity
dc.subject retinal nerve fibre layer (RNFL)
dc.subject retinopathy of prematurity (ROP)
dc.subject Ophthalmology
dc.title Central macular morphology and optic nerve fibre layer thickness in young adults born premature and screened for retinopathy of prematurity
dc.type /dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article
dc.description.version Peer reviewed
dc.identifier.doi 10.1111/aos.15814
dc.relation.url http://www.scopus.com/inward/record.url?scp=85177548640&partnerID=8YFLogxK


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