Literature DB >> 26200501

Characterization of Abnormal Optic Nerve Head Morphology in Albinism Using Optical Coherence Tomography.

Sarim Mohammad, Irene Gottlob, Viral Sheth, Anastasia Pilat, Helena Lee, Ellen Pollheimer, Frank Anthony Proudlock.   

Abstract

PURPOSE: To characterize abnormalities in three-dimensional optic nerve head (ONH) morphology in people with albinism (PWA) using spectral-domain optical coherence tomography (SD-OCT) and to determine whether ONH abnormalities relate to other retinal and clinical abnormalities.
METHODS: Spectral-domain OCT was used to obtain three-dimensional images from 56 PWA and 60 age- and sex-matched control subjects. B-scans were corrected for nystagmus-associated motion artefacts. Disc, cup, and rim ONH dimensions and peripapillary retinal nerve fiber layer (ppRNFL) thickness were calculated using Copernicus and ImageJ software.
RESULTS: Median disc areas were similar in PWA (median = 1.65 mm2) and controls (1.71 mm2, P = 0.128), although discs were significantly elongated horizontally in PWA (P < 0.001). In contrast, median optic cup area in PWA (0.088 mm2) was 23.7% of that in controls (0.373 mm2, P < 0.001), with 39.4% of eyes in PWA not demonstrating a measurable optic cup. This led to significantly smaller cup to disc ratios in PWA (P < 0.001). Median rim volume in PWA (0.273 mm3) was 136.6% of that in controls (0.200 mm3). The ppRNFL was significantly thinner in PWA compared with controls (P < 0.001), especially in the temporal quadrant. In PWA, ppRNFL thickness was correlated to ganglion cell thickness at the central fovea (P = 0.007). Several ONH abnormalities, such as cup to disc ratio, were related to higher refractive errors in PWA.
CONCLUSIONS: In PWA, ocular maldevelopment is not just limited to the retina but also involves the ONH. Reduced ppRNFL thickness is consistent with previous reports of reduced ganglion cell numbers in PWA. The thicker rim volumes may be a result of incomplete maturation of the ONH.

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Year:  2015        PMID: 26200501     DOI: 10.1167/iovs.15-16856

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  8 in total

1.  Aberrant visual pathway development in albinism: From retina to cortex.

Authors:  Sarim Ather; Frank Anthony Proudlock; Thomas Welton; Paul S Morgan; Viral Sheth; Irene Gottlob; Rob A Dineen
Journal:  Hum Brain Mapp       Date:  2018-12-04       Impact factor: 5.038

2.  Altered whole-brain connectivity in albinism.

Authors:  Thomas Welton; Sarim Ather; Frank A Proudlock; Irene Gottlob; Robert A Dineen
Journal:  Hum Brain Mapp       Date:  2016-09-29       Impact factor: 5.038

3.  Abnormal Retinal Vessel Architecture in Albinism and Idiopathic Infantile Nystagmus.

Authors:  Shafak Toufeeq; Irene Gottlob; Zhanhan Tu; Frank A Proudlock; Anastasia Pilat
Journal:  Invest Ophthalmol Vis Sci       Date:  2022-05-02       Impact factor: 4.925

4.  Detection of intracranial hypertension in children using optical coherence tomography: a systematic review protocol.

Authors:  Sohaib R Rufai; Noor Ul Owase Jeelani; Rebecca J McLean
Journal:  BMJ Open       Date:  2020-07-06       Impact factor: 2.692

5.  Multimodal Imaging in a Case of Fovea Plana Associated with Situs Inversus of the Optic Disc

Authors:  Berrak Şekeryapan Gediz; Mehmet Ali Şekeroğlu
Journal:  Turk J Ophthalmol       Date:  2020-06-27

Review 6.  Management of nystagmus in children: a review of the literature and current practice in UK specialist services.

Authors:  J E Self; M J Dunn; J T Erichsen; I Gottlob; H J Griffiths; C Harris; H Lee; J Owen; J Sanders; F Shawkat; M Theodorou; J P Whittle
Journal:  Eye (Lond)       Date:  2020-01-09       Impact factor: 3.775

7.  Recognition of intracranial hypertension using handheld optical coherence tomography in children (RIO Study): a diagnostic accuracy study protocol.

Authors:  Sohaib R Rufai; Noor Ul Owase Jeelani; Richard Bowman; Catey Bunce; Frank A Proudlock; Irene Gottlob
Journal:  BMJ Open       Date:  2022-01-11       Impact factor: 2.692

8.  Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia.

Authors:  Pirro G Hysi; Hélène Choquet; Anthony P Khawaja; Robert Wojciechowski; Milly S Tedja; Jie Yin; Mark J Simcoe; Karina Patasova; Omar A Mahroo; Khanh K Thai; Phillippa M Cumberland; Ronald B Melles; Virginie J M Verhoeven; Veronique Vitart; Ayellet Segre; Richard A Stone; Nick Wareham; Alex W Hewitt; David A Mackey; Caroline C W Klaver; Stuart MacGregor; Peng T Khaw; Paul J Foster; Jeremy A Guggenheim; Jugnoo S Rahi; Eric Jorgenson; Christopher J Hammond
Journal:  Nat Genet       Date:  2020-03-30       Impact factor: 38.330

  8 in total

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