Abstract

PurposeTo evaluate the association between symptoms and signs of dry eye diseases (DED) with corneal biomechanical parameters.MethodsThis cross-sectional study enrolled 81 participants without history of ocular hypertension, glaucoma, keratoconus, corneal edema, contact lens use, diabetes, and ocular surgery. All participants were evaluated for symptoms and signs of DED using OSDI questionnaire, tear film break-up time (TBUT), conjunctival and corneal staining (NEI grading) and Schirmer test. Corneal biomechanical parameters were obtained using Corvis ST. Mixed-effects linear regression analysis was used to determine the association between symptoms and signs of DED with corneal biomechanical parameters. Difference in corneal biomechanical parameter between participants with low (Schirmer value ≤10 mm; LT group) and normal (Schirmer value >10mm; NT group) tear production was analyzed using ANCOVA test.ResultsThe median OSDI scores, TBUT, conjunctival and corneal staining scores as well as Schirmer test were 13±16.5 (range; 0–77), 5.3±4.2 seconds (range; 1.3–11), 0±1 (range; 0–4), 0±2 (ranges; 0–9) and 16±14 mm (range; 0–45) respectively. Regression analysis adjusted with participants’ refraction, intraocular pressure, and central corneal thickness showed that OSDI had a negative association with highest concavity radius (P = 0.02). The association between DED signs and corneal biomechanical parameters were found between conjunctival staining scores with second applanation velocity (A2V, P = 0.04), corneal staining scores with second applanation length (A2L, P = 0.01), Schirmer test with first applanation time (A1T, P = 0.04) and first applanation velocity (P = 0.01). In subgroup analysis, there was no difference in corneal biomechanical parameters between participants with low and normal tear production (P>0.05). The associations were found between OSDI with time to highest concavity (P<0.01) and highest displacement of corneal apex (HC-DA, P = 0.04), conjunctival staining scores with A2L (P = 0.01) and A2V (P<0.01) in LT group, and Schirmer test with A1T (P = 0.02) and HC-DA (P = 0.03), corneal staining scores with A2L (P<0.01) in NT group.ConclusionsAccording to in vivo observation with Corvis ST, patients with DED showed more compliant corneas. The increase in dry eye severity was associated with the worsening of corneal biomechanics in both patients with low and normal tear production.

Highlights

  • Dry eye disease (DED), which is among the most frequently encountered ocular disease, is a multifactorial disease that affects both ocular surface and tear film layer

  • Regression analysis adjusted with participants’ refraction, intraocular pressure, and central corneal thickness showed that Ocular Surface Disease Index (OSDI) had a negative association with highest concavity radius (P = 0.02)

  • There was no difference in corneal biomechanical parameters between participants with low and normal tear production (P>0.05)

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Summary

Introduction

Dry eye disease (DED), which is among the most frequently encountered ocular disease, is a multifactorial disease that affects both ocular surface and tear film layer. Patients with DED usually presented with eye irritation, photosensitivity, and blurred vision which have an impact on both quality of life and quality of vision [1]. The corneal structural change was correlated with dry eye severity [2]. Corneal biomechanics includes elastic and viscoelastic properties, which are the capacity of cornea to reversibly deform under stress [3]. Various alterations of cornea in patients with DED have been demonstrated, including decreased corneal superficial epithelial cell density [5], increased corneal keratocyte density [6], increased inflammatory dendritic cells [7], decreased subbasal nerve plexus number, increased beadings and tortuosity of corneal nerve [8, 9], and decreased endothelial cell density [10, 11]. We hypothesized that DED has an impact on corneal biomechanics and it is interesting to illustrate whether corneal biomechanical alteration associates with the disease severity or not

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