Deparment of Genetics and Development.
Department of Ophthalmology, and.
JCI Insight. 2022 Jan 25;7(2):e156154. doi: 10.1172/jci.insight.156154.
BackgroundMore 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.MethodsThe 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.ResultsFour 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.ConclusionThese 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.FUNDINGNational 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.
ATP 结合盒,亚家族 A,成员 4(ABCA4)基因座中的超过 1500 种变体导致了从侵袭性儿童期发病的脉络膜视网膜病变到较轻的晚发性黄斑疾病等不同谱的视网膜疾病。由于患者队列通常较小且很少捕获个体基因型的完整自然史,因此基因型-表型相关性研究在临床适用性方面受到限制。为了克服这些限制,我们构建了一个基因型-表型相关性矩阵,该矩阵提供了来自大型年龄受限患者队列的特定 ABCA4 基因型与长期疾病结局相关的可量化概率。
该研究纳入了 112 名年龄至少 50 岁的无血缘关系的患者,这些患者在 ABCA4 基因座测序后发现了 2 种致病性变异。临床特征分析使用最佳矫正视力、视网膜成像和全视野视网膜电图检查的结果进行。
根据眼底疾病特征的空间严重程度,定义了四个不同的预后组。在较轻的预后中观察到反复出现的基因型,包括一种新定义的罕见低功能等位基因类。PVS1(预测无效)变体在最严重的预后中富集;然而,错义变体在这些患者中所占比例高于预期。对等位基因组合及其各自的预后严重程度的分析表明,某些变体,如 p.(Gly1961Glu),以及罕见和常见的低功能等位基因,在患者表型方面相对于等位基因在反式中具有“临床优势”。
这些结果为 ABCA4 疾病复杂的遗传和临床景观提供了急需的结构,并为临床提供了一种工具,以定量评估患者个体基因型特异性的预后。
美国国立卫生研究院国家眼科研究所,资助 R01 EY028203、R01 EY028954、R01 EY029315、P30 19007(视觉研究核心赠款);美国基金会抗击失明,无编号 PPA-1218-0751-COLU;以及预防失明研究。