Literature DB >> 24148654

Retinal structure and function in achromatopsia: implications for gene therapy.

Venki Sundaram1, Caroline Wilde2, Jonathan Aboshiha1, Jill Cowing2, Colin Han3, Christopher S Langlo4, Ravinder Chana1, Alice E Davidson1, Panagiotis I Sergouniotis2, James W Bainbridge1, Robin R Ali2, Alfredo Dubra5, Gary Rubin2, Andrew R Webster1, Anthony T Moore1, Marko Nardini2, Joseph Carroll6, Michel Michaelides7.   

Abstract

PURPOSE: To characterize retinal structure and function in achromatopsia (ACHM) in preparation for clinical trials of gene therapy.
DESIGN: Cross-sectional study. PARTICIPANTS: Forty subjects with ACHM.
METHODS: All subjects underwent spectral domain optical coherence tomography (SD-OCT), microperimetry, and molecular genetic testing. Foveal structure on SD-OCT was graded into 5 distinct categories: (1) continuous inner segment ellipsoid (ISe), (2) ISe disruption, (3) ISe absence, (4) presence of a hyporeflective zone (HRZ), and (5) outer retinal atrophy including retinal pigment epithelial loss. Foveal and outer nuclear layer (ONL) thickness was measured and presence of hypoplasia determined. MAIN OUTCOME MEASURES: Photoreceptor appearance on SD-OCT imaging, foveal and ONL thickness, presence of foveal hypoplasia, retinal sensitivity and fixation stability, and association of these parameters with age and genotype.
RESULTS: Forty subjects with a mean age of 24.9 years (range, 6-52 years) were included. Disease-causing variants were found in CNGA3 (n = 18), CNGB3 (n = 15), GNAT2 (n = 4), and PDE6C (n = 1). No variants were found in 2 individuals. In all, 22.5% of subjects had a continuous ISe layer at the fovea, 27.5% had ISe disruption, 20% had an absent ISe layer, 22.5% had an HRZ, and 7.5% had outer retinal atrophy. No significant differences in age (P = 0.77), mean retinal sensitivity (P = 0.21), or fixation stability (P = 0.34) across the 5 SD-OCT categories were evident. No correlation was found between age and foveal thickness (P = 0.84) or between age and foveal ONL thickness (P = 0.12).
CONCLUSIONS: The lack of a clear association of disruption of retinal structure or function in ACHM with age suggests that the window of opportunity for intervention by gene therapy is wider in some individuals than previously indicated. Therefore, the potential benefit for a given subject is likely to be better predicted by specific measurement of photoreceptor structure rather than simply by age. The ability to directly assess cone photoreceptor preservation with SD-OCT and/or adaptive optics imaging is likely to prove invaluable in selecting subjects for future trials and measuring the trials' impact.
Copyright © 2014 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 24148654      PMCID: PMC3895408          DOI: 10.1016/j.ophtha.2013.08.017

Source DB:  PubMed          Journal:  Ophthalmology        ISSN: 0161-6420            Impact factor:   12.079


  31 in total

1.  Achromatopsia caused by novel mutations in both CNGA3 and CNGB3.

Authors:  S Johnson; M Michaelides; I A Aligianis; J R Ainsworth; J D Mollon; E R Maher; A T Moore; D M Hunt
Journal:  J Med Genet       Date:  2004-02       Impact factor: 6.318

Review 2.  Anatomical correlates to the bands seen in the outer retina by optical coherence tomography: literature review and model.

Authors:  Richard F Spaide; Christine A Curcio
Journal:  Retina       Date:  2011-09       Impact factor: 4.256

3.  Photoreceptor structure and function in patients with congenital achromatopsia.

Authors:  Mohamed A Genead; Gerald A Fishman; Jungtae Rha; Adam M Dubis; Daniela Maria O Bonci; Alfredo Dubra; Edwin M Stone; Maureen Neitz; Joseph Carroll
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-09-21       Impact factor: 4.799

4.  Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2).

Authors:  I A Aligianis; T Forshew; S Johnson; M Michaelides; C A Johnson; R C Trembath; D M Hunt; A T Moore; E R Maher
Journal:  J Med Genet       Date:  2002-09       Impact factor: 6.318

5.  Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders.

Authors:  Alberta A H J Thiadens; Anneke I den Hollander; Susanne Roosing; Sander B Nabuurs; Renate C Zekveld-Vroon; Rob W J Collin; Elfride De Baere; Robert K Koenekoop; Mary J van Schooneveld; Tim M Strom; Janneke J C van Lith-Verhoeven; Andrew J Lotery; Norka van Moll-Ramirez; Bart P Leroy; L Ingeborgh van den Born; Carel B Hoyng; Frans P M Cremers; Caroline C W Klaver
Journal:  Am J Hum Genet       Date:  2009-07-16       Impact factor: 11.025

6.  Relation of optical coherence tomography to microanatomy in normal and rd chickens.

Authors:  Y Huang; A V Cideciyan; G I Papastergiou; E Banin; S L Semple-Rowland; A H Milam; S G Jacobson
Journal:  Invest Ophthalmol Vis Sci       Date:  1998-11       Impact factor: 4.799

7.  Fixation stability measurement using the MP1 microperimeter.

Authors:  Michael D Crossland; Hannah M P Dunbar; Gary S Rubin
Journal:  Retina       Date:  2009-05       Impact factor: 4.256

8.  Early signs of longitudinal progressive cone photoreceptor degeneration in achromatopsia.

Authors:  Mervyn George Thomas; Rebecca Jane McLean; Susanne Kohl; Viral Sheth; Irene Gottlob
Journal:  Br J Ophthalmol       Date:  2012-07-11       Impact factor: 4.638

9.  Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel.

Authors:  S Kohl; T Marx; I Giddings; H Jägle; S G Jacobson; E Apfelstedt-Sylla; E Zrenner; L T Sharpe; B Wissinger
Journal:  Nat Genet       Date:  1998-07       Impact factor: 38.330

10.  Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy.

Authors:  Livia S Carvalho; Jianhua Xu; Rachael A Pearson; Alexander J Smith; James W Bainbridge; Lynsie M Morris; Steven J Fliesler; Xi-Qin Ding; Robin R Ali
Journal:  Hum Mol Genet       Date:  2011-05-15       Impact factor: 6.150

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Authors:  Shu Feng; Michael J Gale; Jonathan D Fay; Ambar Faridi; Hope E Titus; Anupam K Garg; Keith V Michaels; Laura R Erker; Dawn Peters; Travis B Smith; Mark E Pennesi
Journal:  Invest Ophthalmol Vis Sci       Date:  2015-09       Impact factor: 4.799

2.  Differences in ocular findings in two siblings: one with complete and other with incomplete achromatopsia.

Authors:  Shinji Ueno; Ayami Nakanishi; Akira Sayo; Taro Kominami; Yasuki Ito; Takaaki Hayashi; Kazushige Tsunoda; Takeshi Iwata; Hiroko Terasaki
Journal:  Doc Ophthalmol       Date:  2017-02-14       Impact factor: 2.379

3.  SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder.

Authors:  Valentina Del Dotto; Farid Ullah; Ivano Di Meo; Pamela Magini; Mirjana Gusic; Alessandra Maresca; Leonardo Caporali; Flavia Palombo; Francesca Tagliavini; Evan Harris Baugh; Bertil Macao; Zsolt Szilagyi; Camille Peron; Margaret A Gustafson; Kamal Khan; Chiara La Morgia; Piero Barboni; Michele Carbonelli; Maria Lucia Valentino; Rocco Liguori; Vandana Shashi; Jennifer Sullivan; Shashi Nagaraj; Mays El-Dairi; Alessandro Iannaccone; Ioana Cutcutache; Enrico Bertini; Rosalba Carrozzo; Francesco Emma; Francesca Diomedi-Camassei; Claudia Zanna; Martin Armstrong; Matthew Page; Nicholas Stong; Sylvia Boesch; Robert Kopajtich; Saskia Wortmann; Wolfgang Sperl; Erica E Davis; William C Copeland; Marco Seri; Maria Falkenberg; Holger Prokisch; Nicholas Katsanis; Valeria Tiranti; Tommaso Pippucci; Valerio Carelli
Journal:  J Clin Invest       Date:  2020-01-02       Impact factor: 14.808

4.  Evaluating outer segment length as a surrogate measure of peak foveal cone density.

Authors:  Melissa A Wilk; Brandon M Wilk; Christopher S Langlo; Robert F Cooper; Joseph Carroll
Journal:  Vision Res       Date:  2016-12-02       Impact factor: 1.886

5.  Genotype-dependent variability in residual cone structure in achromatopsia: toward developing metrics for assessing cone health.

Authors:  Adam M Dubis; Robert F Cooper; Jonathan Aboshiha; Christopher S Langlo; Venki Sundaram; Benjamin Liu; Frederick Collison; Gerald A Fishman; Anthony T Moore; Andrew R Webster; Alfredo Dubra; Joseph Carroll; Michel Michaelides
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-10-02       Impact factor: 4.799

6.  Interocular Symmetry of Foveal Cone Topography in Congenital Achromatopsia.

Authors:  Katie M Litts; Michalis Georgiou; Christopher S Langlo; Emily J Patterson; Rebecca R Mastey; Angelos Kalitzeos; Rachel E Linderman; Byron L Lam; Gerald A Fishman; Mark E Pennesi; Christine N Kay; William W Hauswirth; Michel Michaelides; Joseph Carroll
Journal:  Curr Eye Res       Date:  2020-03-13       Impact factor: 2.424

7.  Autosomal recessive cone-rod dystrophy can be caused by mutations in the ATF6 gene.

Authors:  Anna Skorczyk-Werner; Wei-Chieh Chiang; Anna Wawrocka; Katarzyna Wicher; Małgorzata Jarmuż-Szymczak; Magdalena Kostrzewska-Poczekaj; Aleksander Jamsheer; Rafał Płoski; Małgorzata Rydzanicz; Dorota Pojda-Wilczek; Nicole Weisschuh; Bernd Wissinger; Susanne Kohl; Jonathan H Lin; Maciej R Krawczyński
Journal:  Eur J Hum Genet       Date:  2017-08-16       Impact factor: 4.246

8.  In vivo imaging of human cone photoreceptor inner segments.

Authors:  Drew Scoles; Yusufu N Sulai; Christopher S Langlo; Gerald A Fishman; Christine A Curcio; Joseph Carroll; Alfredo Dubra
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-06-06       Impact factor: 4.799

9.  Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia.

Authors:  Susanne Kohl; Ditta Zobor; Wei-Chieh Chiang; Nicole Weisschuh; Jennifer Staller; Irene Gonzalez Menendez; Stanley Chang; Susanne C Beck; Marina Garcia Garrido; Vithiyanjali Sothilingam; Mathias W Seeliger; Franco Stanzial; Francesco Benedicenti; Francesca Inzana; Elise Héon; Ajoy Vincent; Jill Beis; Tim M Strom; Günther Rudolph; Susanne Roosing; Anneke I den Hollander; Frans P M Cremers; Irma Lopez; Huanan Ren; Anthony T Moore; Andrew R Webster; Michel Michaelides; Robert K Koenekoop; Eberhart Zrenner; Randal J Kaufman; Stephen H Tsang; Bernd Wissinger; Jonathan H Lin
Journal:  Nat Genet       Date:  2015-06-01       Impact factor: 38.330

10.  Adaptive optics ophthalmoscopy.

Authors:  Austin Roorda; Jacque L Duncan
Journal:  Annu Rev Vis Sci       Date:  2015-10-14       Impact factor: 6.422

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