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Purpose: To determine the proximity between the thinnest corneal point (TCP) and focal corneal weakening in normal, subclinical keratoconus (SKC), and manifest keratoconus (KC) eyes using motion-tracking Brillouin microscopy.
Design: Prospective cross-sectional study.
Participants: Ninety-five eyes from 95 patients were evaluated: 40 from bilaterally normal patients (controls), 40 from patients with SKC, and 15 from patients with manifest KC.
Methods: All patients underwent Scheimpflug tomography, anterior segment OCT (AS-OCT), and custom-built motion-tracking Brillouin (MTB) imaging. Mean and minimum MTB shift values were calculated within the anterior plateau region. Euclidean distances between the TCP (identified by AS-OCT) and the minimum Brillouin shift (MTB-Min) were determined. Motion-tracking Brillouin minimum values within 10 MHz of the absolute minimum were considered equivalent (MTB-Min(e)). Receiver operating characteristic curves were generated for both metrics to determine the area under the curve (AUC), sensitivity, and specificity.
Main Outcome Measures: Distance between MTB-Min and TCP; group discrimination based on area under the receiver operating characteristic curve, sensitivity, and specificity.
Results: No significant differences were found between groups for age, sex, KMean, or KMax. Subclinical keratoconus and KC eyes were significantly thinner than controls. Motion-tracking Brillouin minimum values were significantly lower in SKC and KC eyes compared with controls. Average distances between MTB-Min and TCP were 0.31 ± 0.16 mm (0.04-0.69 mm) in controls, 0.53 ± 0.28 mm (0.11-1.19 mm) in SKC, and 0.54 ± 0.35 mm (0.10-1.36 mm) for KC ( < 0.001). Motion-tracking Brillouin minimum (e) values were within 1 mm of the TCP in 100% of control eyes, 92.5% of SKC eyes, and 86.7% of KC eyes ( = 0.1). Motion-tracking Brillouin minimum values (e) performed nearly equivalently (AUC = 0.999) to the absolute MTB-Min shift (AUC = 1.0) in differentiating SKC from controls.
Conclusions: Focal corneal weakening occurs in close proximity to the thinnest corneal point in SKC. This study provides the first experimental confirmation of this relationship and demonstrates focal mechanical localization in subclinical and early KC.
Financial Disclosures: Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
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http://dx.doi.org/10.1016/j.xops.2025.100882 | DOI Listing |
Ophthalmol Sci
July 2025
Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio.
Purpose: To determine the proximity between the thinnest corneal point (TCP) and focal corneal weakening in normal, subclinical keratoconus (SKC), and manifest keratoconus (KC) eyes using motion-tracking Brillouin microscopy.
Design: Prospective cross-sectional study.
Participants: Ninety-five eyes from 95 patients were evaluated: 40 from bilaterally normal patients (controls), 40 from patients with SKC, and 15 from patients with manifest KC.
Am J Ophthalmol
June 2025
Fischell Department of Bioengineering (G.S.), University of Maryland, Maryland, USA.
Purpose: To characterize the 3-dimensional (3-D) mechanical differences between normal corneas and those with subclinical keratoconus (SKC) or clinical keratoconus (KC) using motion-tacking (MT) Brillouin microscopy.
Design: Prospective cross-sectional study.
Methods: There were 50 eyes from 50 patients evaluated, including 20 Control eyes from 20 patients, 20 SKC eyes from 20 patients, and 10 stage I or II KC eyes from 10 patients.
Surv Ophthalmol
June 2025
Cole Eye Institute, Cleveland Clinic, Cleveland, OH, USA; Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, OH, USA. Electronic address:
Corneal mechanical weakness is widely recognized as the root cause of keratoconus and a primary driver for undesirable refractive surgery outcomes. Theory, finite element modeling, and initial data predict that focal rather than generalized weakening precipitates corneal mechanical decompensation. Direct, 3-dimensionally (3-D) localized in vivo corneal mechanical measurements thus have the potential to revolutionize keratoconus management and the surgical correction of myopia.
View Article and Find Full Text PDFOphthalmology
May 2024
Narayana Nethralaya Foundation Bangalore, India. Electronic address:
Ophthalmology
March 2024
Fischell Department of Bioengineering, University of Maryland, College Park, Maryland.
Purpose: To characterize focal biomechanical alterations in subclinical keratoconus (SKC) using motion-tracking (MT) Brillouin microscopy and evaluate the ability of MT Brillouin metrics to differentiate eyes with SKC from normal control eyes.
Design: Prospective cross-sectional study.
Participants: Thirty eyes from 30 patients were evaluated, including 15 eyes from 15 bilaterally normal patients and 15 eyes with SKC from 15 patients.