Non-allergic eye rubbing is a major behavioral risk factor for keratoconus

PLoS One. 2023 Apr 13;18(4):e0284454. doi: 10.1371/journal.pone.0284454. eCollection 2023.

Abstract

Since the environmental, behavioral, and socioeconomic factors in the etiology of keratoconus (KTCN) remain poorly understood, we characterized them as features influencing KTCN phenotype, and especially affecting the corneal epithelium (CE). In this case-control study, 118 KTCN patients and 73 controls were clinically examined and the Questionnaire covering the aforementioned aspects was completed and then statistically elaborated. Selected KTCN-specific findings were correlated with the outcomes of the RNA-seq assessment of the CE samples. Male sex, eye rubbing, time of using a computer after work, and dust in the working environment, were the substantial KTCN risk factors identified in multivariate analysis, with ORs of 8.66, 7.36, 2.35, and 5.25, respectively. Analyses for genes whose expression in the CE was correlated with the eye rubbing manner showed the enrichment in apoptosis (TP53, BCL2L1), chaperon-related (TLN1, CTDSP2, SRPRA), unfolded protein response (NFYA, TLN1, CTDSP2, SRPRA), cell adhesion (TGFBI, PTPN1, PDPK1), and cellular stress (TFDP1, SRPRA, CAPZB) pathways. Genes whose expression was extrapolated to the allergy status didn't contribute to IgE-related or other inflammatory pathways. Presented findings support the hypothesis of chronic mechanical corneal trauma in KTCN. Eye-rubbing causes CE damage and triggers cellular stress which through its influence on cell apoptosis, migration, and adhesion affects the KTCN phenotype.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3-Phosphoinositide-Dependent Protein Kinases / genetics
  • Case-Control Studies
  • Epithelium, Corneal* / metabolism
  • Humans
  • Keratoconus* / genetics
  • Keratoconus* / metabolism
  • Male
  • Phenotype
  • Risk Factors

Substances

  • PDPK1 protein, human
  • 3-Phosphoinositide-Dependent Protein Kinases

Grants and funding

Supported by National Science Centre in Poland (https://www.ncn.gov.pl/en), Grants 2018/31/B/NZ5/03280 (to MG) and 2021/41/B/NZ5/02245 (to MG). Next-generation sequencing was performed thanks to Genomics Core Facility CeNT UW using the NovaSeq 6000 platform financed by the Polish Ministry of Science and Higher Education (decision no. 6817/IA/SP/2018 of 2018-04-10). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.