Background More than 1500 variants in the ATP-binding cassette, sub-family A, member 4 (ABCA4), locus underlie a heterogeneous spectrum of retinal disorders ranging from aggressive childhood-onset chorioretinopathy to milder late-onset macular disease. Genotype-phenotype correlation studies have been limited in clinical applicability as patient cohorts are typically small and seldom capture the full natural history of individual genotypes. To overcome these limitations, we constructed a genotype-phenotype correlation matrix that provides quantifiable probabilities of long-term disease outcomes associated with specific ABCA4 genotypes from a large, age-restricted patient cohort.Methods The study included 112 unrelated patients at least 50 years of age in whom 2 pathogenic variants were identified after sequencing of the ABCA4 locus. Clinical characterization was performed using the results of best corrected visual acuity, retinal imaging, and full-field electroretinogram testing.Results Four distinct prognostic groups were defined according to the spatial severity of disease features across the fundus. Recurring genotypes were observed in milder prognoses, including a newly defined class of rare hypomorphic alleles. PVS1 (predicted null) variants were enriched in the most severe prognoses; however, missense variants were present in a larger-than-expected fraction of these patients. Analysis of allele combinations and their respective prognostic severity showed that certain variants, such as p.(Gly1961Glu), and both rare and frequent hypomorphic alleles, were “clinically dominant” with respect to patient phenotypes irrespective of the allele in trans.Conclusion These results provide much-needed structure to the complex genetic and clinical landscape of ABCA4 disease and add a tool to the clinical repertoire to quantitatively assess individual genotype-specific prognoses in patients.FUNDING National Eye Institute, NIH, grants R01 EY028203, R01 EY028954, R01 EY029315, P30 19007 (Core Grant for Vision Research); the Foundation Fighting Blindness USA, grant no. PPA-1218-0751-COLU; and Research to Prevent Blindness.
Winston Lee, Jana Zernant, Pei-Yin Su, Takayuki Nagasaki, Stephen H. Tsang, Rando Allikmets
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ABCA4 Deep Intronic Variants Contributed to Nearly Half of Unsolved Stargardt Cases With a Milder Phenotype
Wang Y, Wang P, Yi Z, Ouyang J, Jiang Y, Li S, Jia X, Xiao X, Hejtmancik JF, Sun W, Zhang Q |
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Unravelling genotype-phenotype correlations in Stargardt disease using patient-derived retinal organoids
Watson A, Queen R, Ferrández-Peral L, Dorgau B, Collin J, Nelson A, Hussain R, Coxhead J, McCorkindale M, Atkinson R, Zerti D, Chichagova V, Conesa A, Armstrong L, Cremers FP, Lako M |
Cell Death & Disease | 2025 |
ABCA4-related retinopathies in Lebanon
Ibrahim M, Jaffal L, Assi A, Helou C, El Shamieh S |
Heliyon | 2024 |
Retinoid Synthesis Regulation by Retinal Cells in Health and Disease.
Andreazzoli M, Longoni B, Angeloni D, Demontis GC |
Cells | 2024 |
Functional Characterization of ABCA4 Missense Variants Aids Variant Interpretation and Phenotype Prediction in Patients With ABCA4-Retinal Dystrophies
Aslaksen S, Aukrust I, Molday L, Holtan JP, Jansson RW, Berland S, Rødahl E, Bredrup C, Bragadóttir R, Bratland E, Molday RS, Knappskog PM |
Investigative ophthalmology & visual science | 2024 |
Late-Onset Slowly Progressing Cone/Macular Dystrophy in Patients With the Biallelic Hypomorphic Variant p.Arg1933Ter in RP1
Choi SW, Woo SJ, Kim M, Lee S, Joo K |
Translational Vision Science & Technology | 2024 |
Genotype–Phenotype Correlation Model for the Spectrum of TYR-Associated Albinism
Bjeloš M, Ćurić A, Bušić M, Rak B, Kuzmanović Elabjer B |
Diagnostics | 2024 |
Targeted long-read sequencing enriches disease-relevant genomic regions of interest to provide complete Mendelian disease diagnostics
Kenji Nakamichi, Jennifer Huey, Riccardo Sangermano, Emily M. Place, Kinga M Bujakowska, Molly Marra, Lesley A. Everett, Paul Yang, Jennifer R Chao, Russell N. Van Gelder, Debarshi Mustafi |
JCI Insight | 2024 |
A Retrospective Longitudinal Study of 460 Patients with ABCA4-Associated Retinal Disease
Fenner BJ, Whitmore SS, DeLuca AP, Andorf JL, Daggett HT, Luse MA, Haefeli LM, Riley JB, Critser DB, Wilkinson ME, Dumitrescu AV, Drack AV, Boyce TM, Russell JF, Binkley EM, Sohn EH, Russell SR, Boldt CH, Mullins RF, Tucker BA, Scheetz TE, Han IC, Stone EM |
Ophthalmology | 2024 |
Characterization of the Subclinical Perilesional Zone in the Macula of Early-Stage ABCA4 Disease
Zee A, Lee W, Su PY, Zernant J, Tsang SH, Allikmets R |
medRxiv | 2024 |
Cross-sectional Analysis of Outer Retinal Tubulation in Inherited Retinal Diseases: A Multicenter Study
Liu PK, Lee W, Su PY, Kim AH, Kang EY, Levi SR, Jenny LA, Lin PH, Chi YC, Wu PL, Wang EH, Chang YC, Liu L, Chen KJ, Hwang YS, Wu WC, Lai CC, Tsang SH, Allikmets R, Wang NK |
American journal of ophthalmology | 2024 |
Quantitative natural history modeling of HPDL-related disease based on cross-sectional data reveals genotype-phenotype correlations
Alecu JE, Tam A, Richter S, Quiroz V, Schierbaum L, Saffari A, Ebrahimi-Fakhari D |
Genetics in medicine : official journal of the American College of Medical Genetics | 2024 |
Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis
Panneman DM, Hitti-Malin RJ, Holtes LK, de Bruijn SE, Reurink J, Boonen EG, Khan MI, Ali M, Andréasson S, De Baere E, Banfi S, Bauwens M, Ben-Yosef T, Bocquet B, De Bruyne M, de la Cerda B, Coppieters F, Farinelli P, Guignard T, Inglehearn CF, Karali M, Kjellström U, Koenekoop R, de Koning B, Leroy BP, McKibbin M, Meunier I, Nikopoulos K, Nishiguchi KM, Poulter JA, Rivolta C, Rodríguez de la Rúa E, Saunders P, Simonelli F, Tatour Y, Testa F, Thiadens AA, Toomes C, Tracewska AM, Tran HV, Ushida H, Vaclavik V, Verhoeven VJ, van de Vorst M, Gilissen C, Hoischen A, Cremers FP, Roosing S |
Frontiers in Cell and Developmental Biology | 2023 |
Association Between Genotype and Phenotype Severity in ABCA4-Associated Retinopathy
Bianco L, Arrigo A, Antropoli A, Manitto MP, Martina E, Aragona E, Bandello F, Battaglia Parodi M |
JAMA Ophthalmology | 2023 |
Familial co-segregation and the emerging role of long-read sequencing to re-classify variants of uncertain significance in inherited retinal diseases.
Gupta P, Nakamichi K, Bonnell AC, Yanagihara R, Radulovich N, Hisama FM, Chao JR, Mustafi D |
npj Genomic Medicine | 2023 |
ABCA4 Variant c.5714+5G>A in Trans With Null Alleles Results in Primary RPE Damage
Sajovic J, Meglič A, Corradi Z, Khan M, Maver A, Vidmar MJ, Hawlina M, Cremers FP, Fakin A |
Investigative ophthalmology & visual science | 2023 |
Natural-History of Visual Dysfunction in ABCA4-retinopathy and its Genetic Correlates
Pfau M, Huryn LA, Boyle MP, Cukras CA, Zein WM, Turriff A, Ullah E, Hufnagel RB, Jeffrey BG, Brooks BP |
American Journal of Ophthalmology | 2023 |
Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability
Corradi Z, Khan M, Hitti-Malin R, Mishra K, Whelan L, Cornelis SS, Hoyng CB, Kämpjärvi K, Klaver CC, Liskova P, Stöhr H, Weber BH, Banfi S, Farrar GJ, Sharon D, Zernant J, Allikmets R, Dhaenens CM, Cremers FP |
2023 | |
Stargardt macular dystrophy and therapeutic approaches
Fujinami K, Waheed N, Laich Y, Yang P, Fujinami-Yokokawa Y, Higgins JJ, Lu JT, Curtiss D, Clary C, Michaelides M |
The British journal of ophthalmology | 2023 |
Longitudinal Analysis of a Resolving Foveomacular Vitelliform Lesion in ABCA4 Disease.
Lee W, Su PY, Zernant J, Nagasaki T, Tsang SH, Allikmets R |
Ophthalmology Retina | 2022 |
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy
Karali M, Testa F, Di Iorio V, Torella A, Zeuli R, Scarpato M, Romano F, Onore ME, Pizzo M, Melillo P, Brunetti-Pierri R, Passerini I, Pelo E, Cremers FP, Esposito G, Nigro V, Simonelli F, Banfi S |
Scientific Reports | 2022 |
Stargardt Disease Due to an Intronic Mutation in the ABCA4: A Case Report
Lugo-Merly A, Molina Thurin LJ, Izquierdo-Encarnacion NJ, Casillas-Murphy SM, Oliver-Cruz A |
International Medical Case Reports Journal | 2022 |
Establishment of the iPSC line CUIMCi005-A from a patient with Stargardt disease for retinal organoid culture
Su PY, Lee W, Zernant J, Tsang SH, Nagasaki T, Corneo B, Allikmets R |
Stem Cell Research | 2022 |