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ABCA4 相关性视网膜病变的基因型与表型严重程度的相关性。

Association Between Genotype and Phenotype Severity in ABCA4-Associated Retinopathy.

机构信息

Department of Ophthalmology, IRCCS San Raffaele Scientific Institute, Milan, Italy.

出版信息

JAMA Ophthalmol. 2023 Sep 1;141(9):826-833. doi: 10.1001/jamaophthalmol.2023.3188.

Abstract

IMPORTANCE

ABCA4-associated retinopathy is a common inherited retinal disease, and its phenotype spans from late-onset macular dystrophy to extensive cone-rod degeneration. Over 2000 disease-causing variants in the ABCA4 gene have been identified.

OBJECTIVE

To investigate genotype-phenotype correlations in ABCA4-associated retinopathy.

DESIGN, SETTING, AND PARTICIPANTS: This cohort study took place at a single referral center for inherited retinal diseases in Italy. Data were prospectively acquired from January 2015 to June 2022. Patients diagnosed with an inherited retinal disease related to biallelic ABCA4 variants were included for analysis.

EXPOSURE

Genotype, classified into 4 groups according to the presence of the (1) p.Gly1961Glu allele, (2) a hypomorphic allele, (3) at least 1 moderate variant (moderate genotypes), or (4) 2 biallelic severe variants (severe genotypes).

MAIN OUTCOMES AND MEASURES

Total decreased autofluorescence (TDAF) and definitely decreased autofluorescence (DDAF) areas, inner and outer retinal volumes, and the respective progression rate.

RESULTS

A total of 71 patients (median [IQR] age, 34 [22.4-47.2] years; 40 [56%] female) were included in the study, and 54 (76%) were followed up for a median (IQR) of 3.5 (1.6-4.7) years. Compared with moderate genotypes, those with the p.Gly1961Glu allele had smaller TDAF lesions by 61% (95% CI, -78% to -33%; P < .001) and DDAF lesions by 77% (95% CI, -93% to -18%; P = .02), along with slower growth rates for both TDAF (0.05 mm/y; 95% CI, 0.01-0.07; P < .001) and DDAF (0.06 mm/y; 95% CI, 0-0.12; P = .004). Hypomorphic alleles were associated with a thicker inner (+0.19 mm3; 95% CI, +0.02 to +0.36; P = .03) and outer retinal volume (+0.16 mm3; 95% CI, +0.03 to +0.28; P = .01) compared with moderate genotypes as well as a slower TDAF growth rate (0.05 mm/y; 95% CI, 0.01-0.08; P = .007). Severe genotypes had a 7-fold larger TDAF area (95% CI, 3.4-14.7; P < .001) and 11-fold larger DDAF area (95% CI, 2.9-42.1; P < .001) compared with moderate genotypes, along with faster growth rates estimated at 0.16 mm/y for TDAF (95% CI, 0.12-0.20; P < .001) and 0.17 mm/y for DDAF (95% CI, 0.12-0.23; P < .001).

CONCLUSIONS AND RELEVANCE

In this study of ABCA4-associated retinopathy, a 4-tier classification of genotypes was found to capture substantial variation in disease phenotype severity. These findings could prove beneficial for the prognostication of patients and warrant consideration of genotype in the design of future clinical trials.

摘要

重要性

ABCA4 相关的视网膜病变是一种常见的遗传性视网膜疾病,其表型从晚期黄斑营养不良到广泛的圆锥-杆状细胞变性不等。在 ABCA4 基因中已经发现了超过 2000 种致病变异。

目的

研究 ABCA4 相关视网膜病变的基因型-表型相关性。

设计、地点和参与者:本队列研究在意大利一家遗传性视网膜疾病的转诊中心进行。数据从 2015 年 1 月至 2022 年 6 月期间前瞻性采集。纳入分析的患者均被诊断为与双等位基因 ABCA4 变异相关的遗传性视网膜疾病。

暴露

基因型,根据存在(1)p.Gly1961Glu 等位基因、(2)低功能等位基因、(3)至少 1 个中度变异(中度基因型)或(4)2 个双等位基因严重变异(严重基因型),分为 4 组。

主要结果和测量

总减荧光(TDAF)和确定减荧光(DDAF)区域、内和外视网膜体积以及各自的进展率。

结果

共纳入 71 名患者(中位数[IQR]年龄,34[22.4-47.2]岁;40[56%]为女性),其中 54 名(76%)患者接受了中位数(IQR)为 3.5(1.6-4.7)年的随访。与中度基因型相比,p.Gly1961Glu 等位基因患者的 TDAF 病变小 61%(95%CI,-78%至-33%;P<0.001),DDAF 病变小 77%(95%CI,-93%至-18%;P=0.02),TDAF(0.05mm/y;95%CI,0.01-0.07;P<0.001)和 DDAF(0.06mm/y;95%CI,0-0.12;P=0.004)的生长速度也较慢。低功能等位基因与较厚的内(+0.19mm3;95%CI,+0.02 至 +0.36;P=0.03)和外视网膜体积(+0.16mm3;95%CI,+0.03 至 +0.28;P=0.01)以及较慢的 TDAF 生长速度(0.05mm/y;95%CI,0.01-0.08;P=0.007)相关。严重基因型患者的 TDAF 面积大 7 倍(95%CI,3.4-14.7;P<0.001),DDAF 面积大 11 倍(95%CI,2.9-42.1;P<0.001),生长速度估计为 0.16mm/y 用于 TDAF(95%CI,0.12-0.20;P<0.001)和 0.17mm/y 用于 DDAF(95%CI,0.12-0.23;P<0.001)。

结论和相关性

在这项 ABCA4 相关视网膜病变的研究中,发现了一种 4 级基因型分类方法,该方法可以捕捉疾病表型严重程度的显著变化。这些发现可能有助于对患者的预后预测,并证明在未来的临床试验设计中考虑基因型是合理的。

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