Censoring the Floor Effect in Long-Term Stargardt Disease Microperimetry Data Produces a Faster Rate of Decline

IF 3.2 Q1 OPHTHALMOLOGY Ophthalmology science Pub Date : 2024-07-20 DOI:10.1016/j.xops.2024.100581
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Abstract

Purpose

To evaluate progression rate estimation in long-term Stargardt disease microperimetry data by accounting for floor effect.

Design

Cohort study.

Subjects

Thirty-seven subjects (23 females, 14 males) with biallelic ABCA4 pathogenic or likely pathogenic variants and more than >2 years of longitudinal microperimetry data.

Methods

Cross-sectional and longitudinal microperimetry data (Grid A: 18° diameter, Grid B: 6° diameter; Macular Integrity Assessment microperimeter, dynamic range 0–36 decibels [dB]) was extracted from patients with biallelic mutation in the adenosine triphosphate-binding cassette subfamily A member 4 (ABCA4) gene. For each eye, mean sensitivity (MS) and responding point sensitivity (RPS) rates were extracted. Floor censored sensitivity (FCS) progression rate, which accounts for the floor effect at each locus by terminating calculation when scotoma was observed in 2 consecutive visits, was also calculated. In a subset of eyes with ≥1 scotomatous locus at baseline (Grid A), sensitivity progression of loci around the scotoma (edge of scotoma sensitivity [ESS]) was examined against other progression parameters. Paired t test compared progression rate parameters across the same eyes.

Main Outcome Measures

Microperimetry grid parameters at baseline and progression rates.

Results

A total of 37 subjects with biallelic ABCA4 mutations and >2 years of longitudinal microperimetry data were included in the study. In Grid A, at baseline, the average MS and RPS were 16.5 ± 7.9 and 19.1 ± 5.7 dB, respectively. Similar MS (18.4 ± 7.6 dB) and RPS (20.0 ± 5.5 dB) values were found at baseline for Grid B. In Grid A, overall, MS, RPS, and FCS progression rates were −0.57 ± 1.05, −0.74 ± 1.24, and −1.26 ± 1.65 (all dB/year), respectively. Floor censored sensitivity progression rate was significantly greater than the MS or RPS progression rates. Similar findings were observed in Grid B (MS −1.22 ± 1.42, RPS −1.44 ± 1.44, FCS −2.16 ± 2.24, all dB/year), with paired t test again demonstrated that FCS had a significantly faster rate of decline than MS or RPS. In patients with progression data in both grids, MS, RPS, and FCS progression rates were significantly faster in the smaller Grid B. In 24 eyes with scotoma at baseline, fastest rate of decline was ESS combined with FCS compared with other progression parameters.

Conclusions

Incorporation of FCS can reduce confound of floor effect in perimetry analysis and can in turn detect a faster rate of decline.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

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在长期斯塔加特病显微视力数据中删去底线效应,可加快视力下降速度
设计队列研究对象37名受试者(23名女性,14名男性)患有双叶ABCA4致病变异或可能致病变异,并有超过>2年的纵向微观视力数据。方法从三磷酸腺苷结合盒A亚家族成员4(ABCA4)基因双倍拷贝突变患者中提取横向和纵向微观视力数据(A栅:18°直径,B栅:6°直径;黄斑完整性评估微压计,动态范围0-36分贝[dB])。提取了每只眼睛的平均灵敏度 (MS) 和反应点灵敏度 (RPS) 率。此外,还计算了底限删减灵敏度(FCS)进展率,该进展率考虑了每个位点的底限效应,即在连续两次观察中观察到黑影时终止计算。在基线(网格 A)上有≥1 个焦斑的眼球子集中,对照其他进展参数检查焦斑周围的灵敏度进展(焦斑边缘灵敏度 [ESS])。主要结果测量基线时的微观视力栅参数和进展率。结果研究共纳入 37 名双侧 ABCA4 突变的受试者和 >2年的纵向微观视力数据。在网格 A 中,基线平均 MS 和 RPS 分别为 16.5 ± 7.9 和 19.1 ± 5.7 dB。在网格 A 中,总体 MS、RPS 和 FCS 的进展率分别为 -0.57±1.05、-0.74±1.24 和 -1.26±1.65(均为 dB/年)。地板删减灵敏度进展率明显高于 MS 或 RPS 进展率。在 B 网格中也观察到类似的结果(MS -1.22 ± 1.42,RPS -1.44 ± 1.44,FCS -2.16 ± 2.24,均为 dB/年),配对 t 检验再次表明 FCS 的下降速度明显快于 MS 或 RPS。在基线存在视网膜朦胧的 24 只眼睛中,与其他视力下降参数相比,ESS 结合 FCS 的视力下降速度最快。结论在近视分析中纳入 FCS 可以减少底线效应的干扰,进而检测出更快的视力下降速度。
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来源期刊
Ophthalmology science
Ophthalmology science Ophthalmology
CiteScore
3.40
自引率
0.00%
发文量
0
审稿时长
89 days
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