Literature DB >> 27820952

The Effect on Retinal Structure and Function of 15 Specific ABCA4 Mutations: A Detailed Examination of 82 Hemizygous Patients.

Ana Fakin1, Anthony G Robson1, John Pei-Wen Chiang2, Kaoru Fujinami3, Anthony T Moore4, Michel Michaelides1, Graham E Holder1, Andrew R Webster1.   

Abstract

PURPOSE: To determine the effect of 15 individual ABCA4 mutations on disease severity.
METHODS: Eighty-two patients harboring 15 distinct ABCA4 mutations in trans with null (hemizygous), 10 homozygous, and 20 nullizygous patients were recruited. Age of onset was determined from medical histories. Electroretinography (ERG) responses were classified into three groups (normal; cone dysfunction; cone and rod dysfunction). The dark-adapted bright-flash (DA 10.0) a-wave amplitudes and the light-adapted flicker ERG (LA 3.0 30 Hz) amplitudes were plotted against age and compared with the nullizygous patients. Fundus autofluorescence imaging (FAF) was assessed when available.
RESULTS: Patients hemizygous for p.G1961E and p.R2030Q had normal ERGs. Patients harboring p.R24H, p.R212C, p.G863A/delG, p.R1108C, p.P1380L, p.L2027F, and c.5714+5G>A had abnormal ERGs (ERG group 2 or 3) at older ages, in most cases with significantly higher amplitudes than nullizygous patients. Mutations p.L541P+A1038V, p.E1022K, p.C1490Y, p.E1087K, p.T1526M, and p.C2150Y were associated with abnormal ERGs (group 2 or 3) and amplitudes comparable to those of nullizygous patients. The majority of patients, including those harboring p.G1961E, had foveal atrophy; while both patients harboring p.R2030Q had foveal sparing. Most patients harboring intermediate and null-like mutations displayed FAF abnormalities extending beyond the vascular arcades.
CONCLUSIONS: In the hemizygous state, 2/15 ABCA4 alleles retain preserved peripheral retinal function; 7/15 are associated with either preserved or only mildly abnormal retinal function, worse in older patients; 6/15 behave like null mutations. These data help characterize the degree of dysfunction conferred by specific mutant ABCA4 proteins in the human retina.

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Year:  2016        PMID: 27820952     DOI: 10.1167/iovs.16-20446

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


  16 in total

1.  The Clinical Spectrum and Disease Course of DRAM2 Retinopathy.

Authors:  Tjaša Krašovec; Marija Volk; Maja Šuštar Habjan; Marko Hawlina; Nataša Vidović Valentinčič; Ana Fakin
Journal:  Int J Mol Sci       Date:  2022-07-02       Impact factor: 6.208

2.  Stargardt disease: monitoring incidence and diagnostic trends in the Netherlands using a nationwide disease registry.

Authors:  Esmee H Runhart; Patty Dhooge; Magda Meester-Smoor; Jeroen Pas; Jan Willem R Pott; Redmer van Leeuwen; Hester Y Kroes; Arthur A Bergen; Yvonne de Jong-Hesse; Alberta A Thiadens; Mary J van Schooneveld; Maria van Genderen; Camiel Boon; Caroline Klaver; L Ingeborg van den Born; Frans P M Cremers; Carel B Hoyng
Journal:  Acta Ophthalmol       Date:  2021-08-25       Impact factor: 3.988

3.  Functional analysis and classification of homozygous and hypomorphic ABCA4 variants associated with Stargardt macular degeneration.

Authors:  Susan B Curtis; Laurie L Molday; Fabian A Garces; Robert S Molday
Journal:  Hum Mutat       Date:  2020-09-09       Impact factor: 4.878

4.  Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New ABCA4 Mutations.

Authors:  Yousra Falfoul; Imen Habibi; Ahmed Turki; Ahmed Chebil; Asma Hassairi; Daniel F Schorderet; Leila El Matri
Journal:  J Ophthalmol       Date:  2018-03-15       Impact factor: 1.909

5.  Retinal phenotypic characterization of patients with ABCA4 retinopathydue to the homozygous p.Ala1773Val mutation.

Authors:  Salvador López-Rubio; Oscar F Chacon-Camacho; Rodrigo Matsui; Dalia Guadarrama-Vallejo; Mirena C Astiazarán; Juan C Zenteno
Journal:  Mol Vis       Date:  2018-02-01       Impact factor: 2.367

6.  Detailed Phenotyping and Therapeutic Strategies for Intronic ABCA4 Variants in Stargardt Disease.

Authors:  Mubeen Khan; Gavin Arno; Ana Fakin; David A Parfitt; Patty P A Dhooge; Silvia Albert; Nathalie M Bax; Lonneke Duijkers; Michael Niblock; Kwan L Hau; Edward Bloch; Elena R Schiff; Davide Piccolo; Michael C Hogden; Carel B Hoyng; Andrew R Webster; Frans P M Cremers; Michael E Cheetham; Alejandro Garanto; Rob W J Collin
Journal:  Mol Ther Nucleic Acids       Date:  2020-06-12       Impact factor: 8.886

7.  Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8.

Authors:  Kaoru Fujinami; Rupert W Strauss; John Pei-Wen Chiang; Isabelle S Audo; Paul S Bernstein; David G Birch; Samantha M Bomotti; Artur V Cideciyan; Ann-Margret Ervin; Meghan J Marino; José-Alain Sahel; Saddek Mohand-Said; Janet S Sunness; Elias I Traboulsi; Sheila West; Robert Wojciechowski; Eberhart Zrenner; Michel Michaelides; Hendrik P N Scholl
Journal:  Br J Ophthalmol       Date:  2018-06-20       Impact factor: 4.638

8.  Prospective Cohort Study of Childhood-Onset Stargardt Disease: Fundus Autofluorescence Imaging, Progression, Comparison with Adult-Onset Disease, and Disease Symmetry.

Authors:  Michalis Georgiou; Thomas Kane; Preena Tanna; Zaina Bouzia; Navjit Singh; Angelos Kalitzeos; Rupert W Strauss; Kaoru Fujinami; Michel Michaelides
Journal:  Am J Ophthalmol       Date:  2019-12-06       Impact factor: 5.258

9.  Functional Characterization of ABCA4 Missense Variants Linked to Stargardt Macular Degeneration.

Authors:  Fabian A Garces; Jessica F Scortecci; Robert S Molday
Journal:  Int J Mol Sci       Date:  2020-12-27       Impact factor: 5.923

10.  Full-field ERG as a predictor of the natural course of ABCA4-associated retinal degenerations.

Authors:  Marion Schroeder; Ulrika Kjellström
Journal:  Mol Vis       Date:  2018-01-04       Impact factor: 2.367

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