Literature DB >> 31618761

Late-Onset Stargardt Disease Due to Mild, Deep-Intronic ABCA4 Alleles.

Esmee H Runhart1,2, Dyon Valkenburg1,2, Stéphanie S Cornelis2,3, Mubeen Khan2,3, Riccardo Sangermano3,4, Silvia Albert2,3, Nathalie M Bax1,2, Galuh D N Astuti3,5, Christian Gilissen2,3, Jan-Willem R Pott6, Joke B G M Verheij7, Ellen A W Blokland3, Frans P M Cremers2,3, L Ingeborgh van den Born8, Carel B Hoyng1,2.   

Abstract

Purpose: To investigate the role of two deep-intronic ABCA4 variants, that showed a mild splice defect in vitro and can occur on the same allele as the low penetrant c.5603A>T, in Stargardt disease (STGD1).
Methods: Ophthalmic data were assessed of 18 STGD1 patients who harbored c.769-784C>T or c.4253+43G>A in combination with a severe ABCA4 variant. Subjects carrying c.[769-784C>T; 5603A>T] were clinically compared with a STGD1 cohort previously published carrying c.5603A>T noncomplex. We calculated the penetrances of the intronic variants using ABCA4 allele frequency data of the general population and investigated the effect of c.769-784C>T on splicing in photoreceptor progenitor cells (PPCs).
Results: Mostly, late-onset, foveal-sparing STGD1 was observed among subjects harboring c.769-784C>T or c.4253+43G>A (median age of onset, 54.5 and 52.0 years, respectively). However, ages of onset, phenotypes in fundo, and visual acuity courses varied widely. No significant clinical differences were observed between the c.[769-784C>T; 5603A>T] cohort and the c.4253+43G>A or the c.5603A>T cohort. The penetrances of c.769-784C>T (20.5%-39.6%) and c.4253+43G>A (35.8%-43.1%) were reduced, when not considering the effect of yet unidentified or known factors in cis, such as c.5603A>T (identified in 7/7 probands with c.769-784C>T; 1/8 probands with c.4253+43G>A). Variant c.769-784C>T resulted in a pseudo-exon insertion in 15% of the total mRNA (i.e., ∼30% of the c.769-784C>T allele alone). Conclusions: Two mild intronic ABCA4 variants could further explain missing heritability in late-onset STGD1, distinguishing it from AMD. The observed clinical variability and calculated reduced penetrance urge research into modifiers within and outside of the ABCA4 gene.

Entities:  

Year:  2019        PMID: 31618761     DOI: 10.1167/iovs.19-27524

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


  11 in total

Review 1.  Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations.

Authors:  Frans P M Cremers; Winston Lee; Rob W J Collin; Rando Allikmets
Journal:  Prog Retin Eye Res       Date:  2020-04-09       Impact factor: 21.198

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.  Personalized genetic counseling for Stargardt disease: Offspring risk estimates based on variant severity.

Authors:  Stéphanie S Cornelis; Esmee H Runhart; Miriam Bauwens; Zelia Corradi; Elfride De Baere; Susanne Roosing; Lonneke Haer-Wigman; Claire-Marie Dhaenens; Anneke T Vulto-van Silfhout; Frans P M Cremers
Journal:  Am J Hum Genet       Date:  2022-02-03       Impact factor: 11.043

Review 4.  An Overview of the Genetics of ABCA4 Retinopathies, an Evolving Story.

Authors:  Saoud Al-Khuzaei; Suzanne Broadgate; Charlotte R Foster; Mital Shah; Jing Yu; Susan M Downes; Stephanie Halford
Journal:  Genes (Basel)       Date:  2021-08-13       Impact factor: 4.096

5.  Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt Disease.

Authors:  Esmee H Runhart; Mubeen Khan; Stéphanie S Cornelis; Susanne Roosing; Marta Del Pozo-Valero; Tina M Lamey; Petra Liskova; Lisa Roberts; Heidi Stöhr; Caroline C W Klaver; Carel B Hoyng; Frans P M Cremers; Claire-Marie Dhaenens
Journal:  JAMA Ophthalmol       Date:  2020-10-01       Impact factor: 7.389

6.  Antisense Oligonucleotide-Based Rescue of Aberrant Splicing Defects Caused by 15 Pathogenic Variants in ABCA4.

Authors:  Tomasz Z Tomkiewicz; Nuria Suárez-Herrera; Frans P M Cremers; Rob W J Collin; Alejandro Garanto
Journal:  Int J Mol Sci       Date:  2021-04-28       Impact factor: 5.923

7.  Cis-acting modifiers in the ABCA4 locus contribute to the penetrance of the major disease-causing variant in Stargardt disease.

Authors:  Winston Lee; Jana Zernant; Takayuki Nagasaki; Laurie L Molday; Pei-Yin Su; Gerald A Fishman; Stephen H Tsang; Robert S Molday; Rando Allikmets
Journal:  Hum Mol Genet       Date:  2021-06-26       Impact factor: 5.121

8.  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

9.  Increasing the Genetic Diagnosis Yield in Inherited Retinal Dystrophies: Assigning Pathogenicity to Novel Non-canonical Splice Site Variants.

Authors:  Vasileios Toulis; Vianney Cortés-González; Marta de Castro-Miró; Juliana Ferraz Sallum; Jaume Català-Mora; Cristina Villanueva-Mendoza; Marcela Ciccioli; Roser Gonzàlez-Duarte; Rebeca Valero; Gemma Marfany
Journal:  Genes (Basel)       Date:  2020-03-31       Impact factor: 4.096

10.  Inherited retinal diseases are the most common cause of blindness in the working-age population in Australia.

Authors:  Rachael C Heath Jeffery; Syed Aqif Mukhtar; Ian L McAllister; William H Morgan; David A Mackey; Fred K Chen
Journal:  Ophthalmic Genet       Date:  2021-05-03       Impact factor: 1.803

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