Evidence map›Paper›PMID 42053839›Full record

ArticleInternational ophthalmology2026

Epithelial thickness gradients as a diagnostic biomarker for early-stage keratoconus.

Zane Jansone-Langina, Jana Gertnere, Viktorija Kezika, Carlos Rocha-de-Lossada, José-María Sánchez-González

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Article in International ophthalmology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Zane Jansone-LanginaDepartment of Optometry and Vision Science, University of Latvia, Riga, Latvia.
Jana GertnereDr. Solomatin Eye Center, Riga, Latvia.
Viktorija KezikaDr. Solomatin Eye Center, Riga, Latvia.
Carlos Rocha-de-LossadaQvision, Ophthalmology Department, Vithas Almeria Hospital, 04120, Almeria, Spain.
José-María Sánchez-GonzálezDepartament of Physics of Condensed Matter, Optics Area, Pharmacy Faculty, University of Seville, Seville, Spain. jsanchez80@us.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo evaluate peripheral-central epithelial thickness (ET) gradients in eyes with keratoconus and regular astigmatism, and to determine their potential utility as a non-invasive biomarker for disease detection in early-stage keratoconus.

methodsThis retrospective cross-sectional analyzed ET with spectral-domain OCT at the cone apex and at 3 mm in the superior, temporal, nasal, and inferior directions. Epithelial thickness gradients (ΔET) were calculated as the difference between peripheral and central ET. Statistical comparisons were performed using non-parametric tests, with significance set at p < 0.05.

resultsA total of 396 eyes (208 keratoconus, 188 regular astigmatism) were analyzed. Central ET was significantly reduced in KC (38.55 ± 5.42 µm) vs controls (48.78 ± 3.94 µm; p < 0.001). While peripheral thickness showed minor differences, the ET gradients (ΔET) were markedly steeper in KC across all quadrants (temporal, superior, nasal, inferior, p < 0.001). Within Stage I KC, eyes with more advanced disease exhibited steeper ΔET values, particularly in the nasal and temporal directions. Mean ΔET, demonstrated significant differences between KC (8.43 ± 4.97 µm) and controls (- 1.55 ± 1.77 µm; p < 0.001), and correlated positively with steep keratometry (r = 0.521, p < 0.001) and negatively with thinnest corneal thickness (TCT) (r =  - 0.641, p < 0.001).

conclusionΔET is markedly steeper in keratoconus than in regular astigmatism-even in Stage I-and correlates with steep keratometry and TCT. With areas under the curves (AUCs) up to 0.976, ΔET provides a rapid, non-invasive epithelial-based biomarker for early detection and staging of keratoconus. Its utility for monitoring progression remains to be established in prospective longitudinal studies.

Indexed as

Epithelium, CornealKeratoconusTomography, Optical CoherenceAdultBiomarkersCorneal TopographyCross-Sectional StudiesEarly DiagnosisFemaleHumansMaleRetrospective StudiesROC CurveYoung AdultBiomarkersDiagnostic biomarkerEarly diagnosisEpithelial thicknessKeratoconus

Identifiers

PMID42053839
PMCPMC13128721

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.