Archetypal Analysis Reveals Quantifiable Patterns of Visual Field Loss in Optic Neuritis

被引:5
作者
Solli, Elena [1 ]
Doshi, Hiten [2 ]
Elze, Tobias [4 ]
Pasquale, Louis [3 ]
Wall, Michael [5 ,6 ,7 ]
Kupersmith, Mark [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Neurol, 17E 102 St 8th Floor, New York, NY 10029 USA
[2] Albert Einstein Coll Med, Montefiore Med Ctr, Bronx, NY USA
[3] Icahn Sch Med Mt Sinai, Dept Ophthalmol, New York, NY USA
[4] Harvard Med Sch, Schepens Eye Res Inst, Boston, MA USA
[5] Univ Iowa, Dept Neurol, Iowa City, IA USA
[6] Univ Iowa, Dept Ophthalmol, Iowa City, IA USA
[7] Univ Iowa, Dept Visual Sci, Iowa City, IA USA
来源
TRANSLATIONAL VISION SCIENCE & TECHNOLOGY | 2022年 / 11卷 / 01期
关键词
archetypal analysis; visual field; optic neuritis; deep learning; GLAUCOMA; PROGRESSION; EXPERIENCE; RECOVERY; PROFILE; TRIAL;
D O I
10.1167/tvst.11.1.27
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: Identifying and monitoring visual field (VF) defects due to optic neuritis (ON) relies on qualitative clinician interpretation. Archetypal analysis (AA), a form of unsupervised machine learning, is used to quantify VF defects in glaucoma. We hypothesized that AA can identify quantifiable, ON-specific patterns (as archetypes [ATs]) of VF loss that resemble known ON VF defects. Methods: We applied AA to a dataset of 3892 VFs prospectively collected from 456 eyes in the Optic Neuritis Treatment Trial (ONTT), and decomposed each VF into component ATs (total weight = 100%). AA of 568 VFs from 61 control eyes was used to define a minimum meaningful (<= 7%) AT weight and weight change. We correlated baseline ON AT weights with global VF indices, visual acuity, and contrast sensitivity. For eyes with a dominant AT (weight >= 50%), we compared the ONTT VF classification with the AT pattern. Results: AA generated a set of 16 ATs containing patterns seen in the ONTT. These were distinct from control ATs. Baseline study eye VFs were decomposed into 2.9 +/- 1.5 ATs. AT2, a global dysfunction pattern, had the highest mean weight at baseline (36%; 95% confidence interval, 33%-40%), and showed the strongest correlation withMD(r= -0.91; P < 0.001), visual acuity (r = 0.70; P < 0.001), and contrast sensitivity (r=-0.77; P< 0.001). Of 191 baseline VFs with a dominant AT, 81% matched the descriptive classifications. Conclusions: AA identifies and quantifies archetypal, ON-specific patterns of VF loss. Translational Relevance: AA is a quantitative, objective method for demonstrating and monitoring change in regional VF deficits in ON.
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页数:11
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