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Segmentation of the foveal and parafoveal retinal architecture using handheld spectral-domain optical coherence tomography in children with Down syndrome

Segmentation of the foveal and parafoveal retinal architecture using handheld spectral-domain optical coherence tomography in children with Down syndrome
Segmentation of the foveal and parafoveal retinal architecture using handheld spectral-domain optical coherence tomography in children with Down syndrome

Background: Down syndrome is a common multigene, multisystem disorder associated with abnormalities of visual function and characteristic changes in the majority of tissues in the eye. Historic descriptions of macular structure in Down syndrome have been variable, but optical coherence tomography allows increasingly detailed characterization of retinal architecture in vivo. We demonstrate the feasibility of retinal imaging in children with Down syndrome using handheld OCT in an outpatient clinical setting, and describe the foveal and parafoveal retinal architecture in this group. Methods: Fourteen White British children aged between 4 and 11 with Down syndrome were recruited to have handheld SD-OCT retinal imaging performed at a single centre in an outpatient clinical setting. The thickness of the retinal layers at the fovea and parafovea was analysed using segmentation software, and compared with age-matched controls from a previously published normative UK dataset. Results: Sixty-seven percent of the children studied had grade 1 foveal hypoplasia. At the fovea, the ganglion cell layer (p = 0.002) and inner nuclear layer (p < 0.001) were thickened relative to the control group. At the parafovea, there was thickening of the retina attributable to numerous layers in both the inner and outer retina, which remained significant after Bonferroni correction. Conclusion: OCT imaging of children with Down syndrome in an outpatient setting is feasible. There is a high incidence of foveal hypoplasia in this group, associated with thickening of the ganglion cell and inner nuclear layers at the fovea.

0950-222X
963-968
Nicholson, Rory
3bcab9e8-9929-432a-823c-04b159d6f9b9
Osborne, Daniel
d42306f4-65ba-4e3f-8402-6663f3963ee7
Fairhead, Lisa
2eb1454d-efd5-4dfc-8e70-f7ca65bf8c54
Beed, Leonora
03e3d2b5-a5b6-4968-a73a-e0fab7ce3cf0
Hill, Catherine M
867cd0a0-dabc-4152-b4bf-8e9fbc0edf8d
Lee, Helena
5d36fd1e-9334-4db5-b201-034d147133fb
Nicholson, Rory
3bcab9e8-9929-432a-823c-04b159d6f9b9
Osborne, Daniel
d42306f4-65ba-4e3f-8402-6663f3963ee7
Fairhead, Lisa
2eb1454d-efd5-4dfc-8e70-f7ca65bf8c54
Beed, Leonora
03e3d2b5-a5b6-4968-a73a-e0fab7ce3cf0
Hill, Catherine M
867cd0a0-dabc-4152-b4bf-8e9fbc0edf8d
Lee, Helena
5d36fd1e-9334-4db5-b201-034d147133fb

Nicholson, Rory, Osborne, Daniel, Fairhead, Lisa, Beed, Leonora, Hill, Catherine M and Lee, Helena (2022) Segmentation of the foveal and parafoveal retinal architecture using handheld spectral-domain optical coherence tomography in children with Down syndrome. Eye, 36 (5), 963-968. (doi:10.1038/s41433-021-01883-6).

Record type: Article

Abstract

Background: Down syndrome is a common multigene, multisystem disorder associated with abnormalities of visual function and characteristic changes in the majority of tissues in the eye. Historic descriptions of macular structure in Down syndrome have been variable, but optical coherence tomography allows increasingly detailed characterization of retinal architecture in vivo. We demonstrate the feasibility of retinal imaging in children with Down syndrome using handheld OCT in an outpatient clinical setting, and describe the foveal and parafoveal retinal architecture in this group. Methods: Fourteen White British children aged between 4 and 11 with Down syndrome were recruited to have handheld SD-OCT retinal imaging performed at a single centre in an outpatient clinical setting. The thickness of the retinal layers at the fovea and parafovea was analysed using segmentation software, and compared with age-matched controls from a previously published normative UK dataset. Results: Sixty-seven percent of the children studied had grade 1 foveal hypoplasia. At the fovea, the ganglion cell layer (p = 0.002) and inner nuclear layer (p < 0.001) were thickened relative to the control group. At the parafovea, there was thickening of the retina attributable to numerous layers in both the inner and outer retina, which remained significant after Bonferroni correction. Conclusion: OCT imaging of children with Down syndrome in an outpatient setting is feasible. There is a high incidence of foveal hypoplasia in this group, associated with thickening of the ganglion cell and inner nuclear layers at the fovea.

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More information

Accepted/In Press date: 29 November 2021
e-pub ahead of print date: 10 January 2022
Published date: May 2022
Additional Information: Funding Information: We thank Jan Sniatecki for his contribution to data collection, and Gift of Sight for providing funding for the handheld OCT. Publisher Copyright: © 2021, The Author(s), under exclusive licence to The Royal College of Ophthalmologists.

Identifiers

Local EPrints ID: 454436
URI: http://eprints.soton.ac.uk/id/eprint/454436
ISSN: 0950-222X
PURE UUID: a1884183-d7ef-47b7-aa51-8ff200b9e303
ORCID for Catherine M Hill: ORCID iD orcid.org/0000-0003-2372-5904
ORCID for Helena Lee: ORCID iD orcid.org/0000-0002-2573-9536

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Date deposited: 09 Feb 2022 17:38
Last modified: 17 Mar 2024 03:38

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Contributors

Author: Rory Nicholson
Author: Daniel Osborne
Author: Lisa Fairhead
Author: Leonora Beed
Author: Helena Lee ORCID iD

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