دورية أكاديمية

Optic Disc and Retinal Architecture Changes in Patients with Spinocerebellar Ataxia Type 2.

التفاصيل البيبلوغرافية
العنوان: Optic Disc and Retinal Architecture Changes in Patients with Spinocerebellar Ataxia Type 2.
المؤلفون: Rezende Filho FM; Division of General Neurology and Ataxia Unit, Department of Neurology, Universidade Federal de São Paulo, Sao Paulo, Brazil., Jurkute N; Moorfields Eye Hospital NHS Foundation Trust, London, United Kingdom.; Institute of Ophthalmology, University College London, London, United Kingdom.; The National Hospital for Neurology and Neurosurgery, University College London Hospitals NHS Foundation Trust, London, United Kingdom., de Andrade JBC; Division of General Neurology and Ataxia Unit, Department of Neurology, Universidade Federal de São Paulo, Sao Paulo, Brazil., Marianelli BF; Department of Ophthalmology, Universidade Federal de São Paulo, Sao Paulo, Brazil., de Lima FD; Department of Neurology, School of Medical Sciences-University of Campinas (UNICAMP), São Paulo, Brazil., França MC Jr; Department of Neurology, School of Medical Sciences-University of Campinas (UNICAMP), São Paulo, Brazil., Sallum JMF; Department of Ophthalmology, Universidade Federal de São Paulo, Sao Paulo, Brazil., Yu-Wai-Man P; Moorfields Eye Hospital NHS Foundation Trust, London, United Kingdom.; Institute of Ophthalmology, University College London, London, United Kingdom.; Department of Clinical Neurosciences, Cambridge Centre for Brain Repair and MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, United Kingdom.; Cambridge Eye Unit, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, United Kingdom., Barsottini OGP; Division of General Neurology and Ataxia Unit, Department of Neurology, Universidade Federal de São Paulo, Sao Paulo, Brazil., Pedroso JL; Division of General Neurology and Ataxia Unit, Department of Neurology, Universidade Federal de São Paulo, Sao Paulo, Brazil.
المصدر: Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2024 Jan; Vol. 39 (1), pp. 203-209. Date of Electronic Publication: 2023 Nov 30.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE
أسماء مطبوعة: Publication: <2001->: New York, NY : Wiley-Liss
Original Publication: [New York, N.Y.] : Raven Press, [c1986-
مواضيع طبية MeSH: Optic Disk*/pathology , Macula Lutea*/pathology, Humans ; Retinal Ganglion Cells/pathology ; Retina/diagnostic imaging ; Retina/pathology ; Tomography, Optical Coherence/methods
مستخلص: Background: ATXN2 is the causative gene of spinocerebellar ataxia type 2 (SCA2) and has been implicated in glaucoma pathogenesis. Therefore, studying ocular changes in SCA2 could uncover clinically relevant changes.
Objective: The aim was to investigate optic disc and retinal architecture in SCA2.
Methods: We evaluated 14 patients with SCA2 and 26 controls who underwent intraocular pressure measurement, fundoscopy, and macular and peripapillary spectral domain optical coherence tomography (SD-OCT). We compared SD-OCT measurements in SCA2 and controls, and the frequency of glaucomatous changes among SCA2, controls, and 76 patients with other SCAs (types 1, 3, 6, and 7).
Results: The macula, peripapillary retinal nerve fiber and inner plexiform layers were thinner in SCA2 than in controls. Increased cup-to-disc ratio was more frequent in SCA2 than in controls and other SCAs.
Conclusions: Ocular changes are part of SCA2 phenotype. Future studies should further investigate retinal and optic nerve architecture in this disorder.
(© 2023 International Parkinson and Movement Disorder Society.)
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فهرسة مساهمة: Keywords: ataxia; biomarkers; optical coherence tomography; retina; spinocerebellar ataxia type 2
تواريخ الأحداث: Date Created: 20231201 Date Completed: 20240201 Latest Revision: 20240201
رمز التحديث: 20240201
DOI: 10.1002/mds.29675
PMID: 38037516
قاعدة البيانات: MEDLINE
الوصف
تدمد:1531-8257
DOI:10.1002/mds.29675