TFOS DEWS II pathophysiology report

Anthony J. Bron, Cintia S. de Paiva, Sunil K. Chauhan, Stefano Bonini, Eric E. Gabison, Sandeep Jain, Erich Knop, Maria Markoulli, Yoko Ogawa, Victor Perez, Yuichi Uchino, Norihiko Yokoi, Driss Zoukhri, David A. Sullivan

Research output: Contribution to journalArticle

149 Citations (Scopus)

Abstract

The TFOS DEWS II Pathophysiology Subcommittee reviewed the mechanisms involved in the initiation and perpetuation of dry eye disease. Its central mechanism is evaporative water loss leading to hyperosmolar tissue damage. Research in human disease and in animal models has shown that this, either directly or by inducing inflammation, causes a loss of both epithelial and goblet cells. The consequent decrease in surface wettability leads to early tear film breakup and amplifies hyperosmolarity via the Vicious Circle. Pain in dry eye is caused by tear hyperosmolarity, loss of lubrication, inflammatory mediators and neurosensory factors, while visual symptoms arise from tear and ocular surface irregularity. Increased friction targets damage to the lids and ocular surface, resulting in characteristic punctate epithelial keratitis, superior limbic keratoconjunctivitis, filamentary keratitis, lid parallel conjunctival folds, and lid wiper epitheliopathy. Hybrid dry eye disease, with features of both aqueous deficiency and increased evaporation, is common and efforts should be made to determine the relative contribution of each form to the total picture. To this end, practical methods are needed to measure tear evaporation in the clinic, and similarly, methods are needed to measure osmolarity at the tissue level, to better determine the severity of dry eye. Areas for future research include the role of genetic mechanisms in non-Sjögren syndrome dry eye, the targeting of the terminal duct in meibomian gland disease and the influence of gaze dynamics and the closed eye state on tear stability and ocular surface inflammation.

Original languageEnglish
JournalOcular Surface
DOIs
Publication statusAccepted/In press - 2017

Fingerprint

Tears
Eye Diseases
Keratitis
Dry Eye Syndromes
Meibomian Glands
Keratoconjunctivitis
Inflammation
Wettability
Lubrication
Animal Disease Models
Goblet Cells
Friction
Osmolar Concentration
Epithelial Cells
Pain
Water
Research

Keywords

  • DEWS II
  • Dry eye disease
  • Dry eye workshop
  • Glycocalyx
  • Hyperosmolarity
  • Inflammation
  • Pathophysiology
  • TFOS
  • Vicious circle

ASJC Scopus subject areas

  • Ophthalmology

Cite this

Bron, A. J., de Paiva, C. S., Chauhan, S. K., Bonini, S., Gabison, E. E., Jain, S., ... Sullivan, D. A. (Accepted/In press). TFOS DEWS II pathophysiology report. Ocular Surface. https://doi.org/10.1016/j.jtos.2017.05.011

TFOS DEWS II pathophysiology report. / Bron, Anthony J.; de Paiva, Cintia S.; Chauhan, Sunil K.; Bonini, Stefano; Gabison, Eric E.; Jain, Sandeep; Knop, Erich; Markoulli, Maria; Ogawa, Yoko; Perez, Victor; Uchino, Yuichi; Yokoi, Norihiko; Zoukhri, Driss; Sullivan, David A.

In: Ocular Surface, 2017.

Research output: Contribution to journalArticle

Bron, AJ, de Paiva, CS, Chauhan, SK, Bonini, S, Gabison, EE, Jain, S, Knop, E, Markoulli, M, Ogawa, Y, Perez, V, Uchino, Y, Yokoi, N, Zoukhri, D & Sullivan, DA 2017, 'TFOS DEWS II pathophysiology report', Ocular Surface. https://doi.org/10.1016/j.jtos.2017.05.011
Bron AJ, de Paiva CS, Chauhan SK, Bonini S, Gabison EE, Jain S et al. TFOS DEWS II pathophysiology report. Ocular Surface. 2017. https://doi.org/10.1016/j.jtos.2017.05.011
Bron, Anthony J. ; de Paiva, Cintia S. ; Chauhan, Sunil K. ; Bonini, Stefano ; Gabison, Eric E. ; Jain, Sandeep ; Knop, Erich ; Markoulli, Maria ; Ogawa, Yoko ; Perez, Victor ; Uchino, Yuichi ; Yokoi, Norihiko ; Zoukhri, Driss ; Sullivan, David A. / TFOS DEWS II pathophysiology report. In: Ocular Surface. 2017.
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