Spatial Functional Characteristics of East Asian Patients With Occult Macular Dystrophy (Miyake Disease); EAOMD Report No. 2.
Adolescent
Adult
Aged
Aged, 80 and over
Asian People
/ genetics
Child
Electroretinography
Eye Proteins
/ genetics
Female
Fluorescein Angiography
Humans
Macular Degeneration
/ genetics
Male
Middle Aged
Phenotype
Retina
/ physiopathology
Retrospective Studies
Spatial Navigation
/ physiology
Tomography, Optical Coherence
Visual Acuity
/ physiology
Exome Sequencing
Young Adult
Journal
American journal of ophthalmology
ISSN: 1879-1891
Titre abrégé: Am J Ophthalmol
Pays: United States
ID NLM: 0370500
Informations de publication
Date de publication:
01 2021
01 2021
Historique:
received:
18
05
2020
revised:
11
07
2020
accepted:
14
07
2020
pubmed:
25
7
2020
medline:
30
1
2021
entrez:
25
7
2020
Statut:
ppublish
Résumé
To describe the functional phenotypic features of East Asian patients with RP1L1-associated occult macular dystrophy (ie, Miyake disease). An international multicenter retrospective cohort study. Twenty-eight participants (53 eyes) with Miyake disease were enrolled at 3 centers (in Japan, China, and South Korea). Ophthalmologic examinations including spectral-domain optical coherence tomography (SDOCT) and multifocal electroretinogram (mfERG) were performed. Patients were classified into 3 functional groups based on mfERG: Group 1, paracentral dysfunction with relatively preserved central/peripheral function; Group 2, homogeneous central dysfunction with preserved peripheral function; and Group 3, widespread dysfunction over the recorded area. Three functional phenotypes were compared in clinical parameters and SDOCT morphologic classification (severe phenotype, blurred/flat ellipsoid zone and absence of the interdigitation zone; mild phenotype, preserved ellipsoid zone). There were 8 eyes in Group 1, 40 eyes in Group 2, and 5 eyes in Group 3. The patients in Group 1 showed significantly later onset (P = .005) and shorter disease duration (P = .002), compared with those in Group 2. All 8 eyes in Group 1 showed the mild morphologic phenotype, while 43 of 45 eyes in Groups 2 and 3 presented the severe phenotype, which identified a significant association between the functional grouping and the morphologic classification (P < .001). A spectrum of functional phenotypes of Miyake disease was first documented with identification of 3 functional subtypes. Patients with paracentral dysfunction had the mildest phenotype, and those with homogeneous central or widespread dysfunction showed overlapping clinical findings with severe photoreceptor changes, suggesting various extents of visual impairment.
Identifiants
pubmed: 32707201
pii: S0002-9394(20)30382-2
doi: 10.1016/j.ajo.2020.07.025
pii:
doi:
Substances chimiques
Eye Proteins
0
RP1L1 protein, human
0
Types de publication
Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
169-180Informations de copyright
Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.