{"title":"Quantifying ocular microaberration using a high-resolution Shack-Hartmann wavefront sensor.","authors":"Seung Pil Bang, Praveen Kumar, Geunyoung Yoon","doi":"10.1364/BOE.566011","DOIUrl":null,"url":null,"abstract":"<p><p>To quantify high-spatial-frequency wavefront errors caused by microaberration, we developed a high-resolution (20 µm) Shack-Hartmann wavefront sensor (SHWFS). This system was designed using a small lenslet array (100 µm) and a large CMOS sensor (24.6 × 32.8 mm), incorporating 5× pupil magnification. Measurements were performed on 20 normal subjects aged 25 to 60 years, all without clinically evident corneal scars or cataracts. Examinations were performed under cycloplegia with a 4.5-mm pupil diameter. Ocular wavefronts were reconstructed using both modal and zonal methods, derived from the same local wavefront slopes measured by each lenslet. To isolate high-frequency wavefront errors due to microaberration, the modal wavefront was subtracted from the zonal wavefront, and the resulting root mean square (RMS) was calculated as a metric of microaberration-induced wavefront distortions. The mean RMS values increased with age: 13.5 ± 1.1 nm in the 20s, 14.1 ± 0.7 nm in the 30s, 15.9 ± 1.3 nm in the 40s, and 16.3 ± 1.5 nm in the 50s, showing a strong correlation with age (R<sup>2</sup> = 0.73; P < 0.001). This study demonstrates the feasibility of quantifying microaberration using a high-resolution SHWFS combined with zonal reconstruction, confirming an age-related increase in microaberration. This technique offers potential for enhancing optical quality assessment, considering both wavefront aberrations and microaberrations, and could aid in diagnosing age-related ocular disorders such as cataracts and dry eye.</p>","PeriodicalId":8969,"journal":{"name":"Biomedical optics express","volume":"16 8","pages":"3128-3138"},"PeriodicalIF":3.2000,"publicationDate":"2025-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12339307/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedical optics express","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1364/BOE.566011","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
To quantify high-spatial-frequency wavefront errors caused by microaberration, we developed a high-resolution (20 µm) Shack-Hartmann wavefront sensor (SHWFS). This system was designed using a small lenslet array (100 µm) and a large CMOS sensor (24.6 × 32.8 mm), incorporating 5× pupil magnification. Measurements were performed on 20 normal subjects aged 25 to 60 years, all without clinically evident corneal scars or cataracts. Examinations were performed under cycloplegia with a 4.5-mm pupil diameter. Ocular wavefronts were reconstructed using both modal and zonal methods, derived from the same local wavefront slopes measured by each lenslet. To isolate high-frequency wavefront errors due to microaberration, the modal wavefront was subtracted from the zonal wavefront, and the resulting root mean square (RMS) was calculated as a metric of microaberration-induced wavefront distortions. The mean RMS values increased with age: 13.5 ± 1.1 nm in the 20s, 14.1 ± 0.7 nm in the 30s, 15.9 ± 1.3 nm in the 40s, and 16.3 ± 1.5 nm in the 50s, showing a strong correlation with age (R2 = 0.73; P < 0.001). This study demonstrates the feasibility of quantifying microaberration using a high-resolution SHWFS combined with zonal reconstruction, confirming an age-related increase in microaberration. This technique offers potential for enhancing optical quality assessment, considering both wavefront aberrations and microaberrations, and could aid in diagnosing age-related ocular disorders such as cataracts and dry eye.
期刊介绍:
The journal''s scope encompasses fundamental research, technology development, biomedical studies and clinical applications. BOEx focuses on the leading edge topics in the field, including:
Tissue optics and spectroscopy
Novel microscopies
Optical coherence tomography
Diffuse and fluorescence tomography
Photoacoustic and multimodal imaging
Molecular imaging and therapies
Nanophotonic biosensing
Optical biophysics/photobiology
Microfluidic optical devices
Vision research.