The association between mucin balls and corneal infiltrative events during extended contact lens wear

Loretta Szczotka-Flynn, Beth Ann Benetz, Jonathan Lass, Matthew Albright, Beth Gillespie, Jana Kuo, Desmond Fonn, Ajay Sethi, Alfred Rimm, Loretta Szczotka-Flynn, Beth Ann Benetz, Jonathan Lass, Matthew Albright, Beth Gillespie, Jana Kuo, Desmond Fonn, Ajay Sethi, Alfred Rimm

Abstract

Purpose: To determine the association between mucin ball formation and corneal infiltrative events (CIEs) during continuous wear with lotrafilcon A silicone hydrogel contact lenses.

Methods: Subjects (n = 205) in the Longitudinal Analysis of Silicone Hydrogel Contact Lens Study wore lotrafilcon A contact lenses for 12 months of continuous wear. The primary outcome was a CIE. Kaplan-Meier methods were used to estimate the unadjusted cumulative incidence of remaining CIE free stratified by mucin ball presence. Cox proportional hazards regression was used to model the hazard of developing a CIE as a function of mucin ball formation and other covariates.

Results: Over half (54.2%) of the subjects displayed some presence of mucin balls during at least 1 visit and about one third (32.8%) displayed repeated episodes. Mucin ball scores were correlated between the 2 eyes and weakly correlated with corneal curvature (P ≤ 0.005). Univariate analyses revealed that the relative hazard for a CIE was 0.35 [95% confidence interval (CI), 0.19-0.68] if a single episode of mucin balls was detected and 0.17 (95% CI, 0.06-0.43) if repeated episodes were detected. Upon multivariate analysis, repeated presence of mucin balls was associated with an 84% decreased hazard of experiencing a CIE (hazard ratio: 0.16; 95% CI, 0.06-0.44).

Conclusions: The presence of mucin balls is significantly associated with a decreased incidence of CIEs, and the effect is greatest when they are repeatedly present over time. We hypothesize that the mucin ball presence represents a more concentrated or viscous mucus layer, which prevents upregulation of the immune response against bacterial ligands.

Trial registration: ClinicalTrials.gov NCT00727402.

Figures

Figure 1
Figure 1
Conceptual model for CIE development.
Figure 2
Figure 2
Example of photographic mucin ball fluorescein depression grading. Each of the 5 corneal zones was graded for surface area and density of mucin ball depressions. On this subject-visit this eye was classified with substantial mucin ball presence.
Figure 3
Figure 3
Example of photographic differences between corneal staining and mucin ball fluorescein pooling depressions: a) arrow points to center of corneal fluorescein staining area displaying small and irregularly bordered dots of stain; b) arrow points to one of many mucin ball depressions pooling with fluorescein which are brighter, rounder, and larger than that noted in 2a.
Figure 3
Figure 3
Example of photographic differences between corneal staining and mucin ball fluorescein pooling depressions: a) arrow points to center of corneal fluorescein staining area displaying small and irregularly bordered dots of stain; b) arrow points to one of many mucin ball depressions pooling with fluorescein which are brighter, rounder, and larger than that noted in 2a.
Figure 4
Figure 4
Unadjusted cumulative probability of remaining CIE free stratified by presence or absence of at least one episode of mucin ball formation.
Figure 5
Figure 5
Unadjusted cumulative probability of remaining CIE free stratified by presence or absence of repeated episodes of mucin ball formation.

Source: PubMed

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