Literature DB >> 27491512

Multimodal imaging of foveal cavitation in retinal dystrophies.

Maurizio Battaglia Parodi1, Maria Vittoria Cicinelli2, Pierluigi Iacono3, Gianluigi Bolognesi1, Francesco Bandello1.   

Abstract

PURPOSE: Inherited retinal dystrophies and cone dysfunction syndromes may show a sharp hyporeflective interruption in the outermost retinal layers on optical coherence tomography (OCT), known as foveal cavitation (FC). The aim of the study was to describe the morpho-functional features of FC in patients affected by retinal dystrophies by means of multimodal imaging.
METHODS: A consecutive series of patients affected by FC were prospectively recruited for the study. Patients underwent short-wavelength (SW) and near-infraRed (NIR) fundus autofluorescence (FAF), spectral domain OCT (SD-OCT), microperimetry (MP), and multifocal electroretinogram (mfERG). Mean size of FC on OCT was correlated with best-corrected visual acuity (BCVA).
RESULTS: Overall, 15 patients (30 eyes) were enrolled. Mean age was 38.2 ± 14.5 years (range: 10-60), with nine females (60 %). Mean BCVA was 0.5 ± 0.4 LogMAR. SD-OCT revealed focal loss of outer retinal layers and disruption of inner segment ellipsoid zone. Vertical height of FC (mean 27.77 ± 18.77 μm) was indirectly related to BCVA; complete forms of FC, with total loss of outer OCT bands, showed a poorer visual outcome. The FC size on NIR-FAF turned out to be larger with respect to SD-OCT and SW-FAF.
CONCLUSION: Our data indicate that the presence of FC worsens functional outcome in patients affected by retinal disorders; complete and higher lesions are associated with a worse morpho-functional prognosis in these eyes.

Entities:  

Keywords:  Foveal Cavitation; Genetics; Inherited retinal dystrophy; Microperimetry; Optical coherence tomography

Mesh:

Year:  2016        PMID: 27491512     DOI: 10.1007/s00417-016-3450-7

Source DB:  PubMed          Journal:  Graefes Arch Clin Exp Ophthalmol        ISSN: 0721-832X            Impact factor:   3.117


  35 in total

1.  Rod sensitivity, cone sensitivity, and photoreceptor layer thickness in retinal degenerative diseases.

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2.  Foveal cavitation as an optical coherence tomography finding in central cone dysfunction.

Authors:  Theodore Leng; Michael F Marmor; Ulrich Kellner; Dorothy A Thompson; Agnes B Renner; William Moore; Jane C Sowden
Journal:  Retina       Date:  2012-07       Impact factor: 4.256

3.  Pseudocystic foveal cavitation in tamoxifen retinopathy.

Authors:  Rishi R Doshi; Jorge A Fortun; Brian T Kim; Sander R Dubovy; Philip J Rosenfeld
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5.  Morphologic characteristics of the outer retina in cone dystrophy on spectral-domain optical coherence tomography.

Authors:  Soo Chang Cho; Se Joon Woo; Kyu Hyung Park; Jeong-Min Hwang
Journal:  Korean J Ophthalmol       Date:  2013-01-15

6.  Multimodal imaging and multifocal electroretinography demonstrate autosomal recessive Stargardt disease may present like occult macular dystrophy.

Authors:  Robert A Sisk; Theodore Leng
Journal:  Retina       Date:  2014-08       Impact factor: 4.256

7.  A pilot study of Fourier-domain optical coherence tomography of retinal dystrophy patients.

Authors:  Jennifer I Lim; Ou Tan; Amani A Fawzi; J Jill Hopkins; John H Gil-Flamer; David Huang
Journal:  Am J Ophthalmol       Date:  2008-07-17       Impact factor: 5.258

Review 8.  Gene therapy for Stargardt disease associated with ABCA4 gene.

Authors:  Zongchao Han; Shannon M Conley; Muna I Naash
Journal:  Adv Exp Med Biol       Date:  2014       Impact factor: 2.622

Review 9.  [Clinical findings and diagnostics of cone dystrophy].

Authors:  U Kellner; S Kellner
Journal:  Ophthalmologe       Date:  2009-02       Impact factor: 1.059

10.  Diagnostic fundus autofluorescence patterns in achromatopsia.

Authors:  Abigail T Fahim; Naheed W Khan; Sarwar Zahid; Ira H Schachar; Kari Branham; Susanne Kohl; Bernd Wissinger; Victor M Elner; John R Heckenlively; Thiran Jayasundera
Journal:  Am J Ophthalmol       Date:  2013-08-20       Impact factor: 5.258

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  4 in total

1.  Widefield Optical Coherence Tomography in Pediatric Retina: A Case Series of Intraoperative Applications Using a Prototype Handheld Device.

Authors:  Thanh-Tin P Nguyen; Shuibin Ni; Guangru Liang; Shanjida Khan; Xiang Wei; Alison Skalet; Susan Ostmo; Michael F Chiang; Yali Jia; David Huang; Yifan Jian; J Peter Campbell
Journal:  Front Med (Lausanne)       Date:  2022-07-04

2.  Phenotypic Differences in a PRPH2 Mutation in Members of the Same Family Assessed with OCT and OCTA.

Authors:  Henar Albertos-Arranz; Xavier Sánchez-Sáez; Natalia Martínez-Gil; Isabel Pinilla; Rosa M Coco-Martin; Jesús Delgado; Nicolás Cuenca
Journal:  Diagnostics (Basel)       Date:  2021-04-26

3.  Comparing Retinal Structure in Patients with Achromatopsia and Blue Cone Monochromacy Using OCT.

Authors:  Emily J Patterson; Christopher S Langlo; Michalis Georgiou; Angelos Kalitzeos; Mark E Pennesi; Jay Neitz; Alison J Hardcastle; Maureen Neitz; Michel Michaelides; Joseph Carroll
Journal:  Ophthalmol Sci       Date:  2021-07-28

Review 4.  Reviewing the Role of Ultra-Widefield Imaging in Inherited Retinal Dystrophies.

Authors:  Maria Vittoria Cicinelli; Alessandro Marchese; Alessandro Bordato; Maria Pia Manitto; Francesco Bandello; Maurizio Battaglia Parodi
Journal:  Ophthalmol Ther       Date:  2020-03-05
  4 in total

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