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TFOS DEWS III: Digest

  • Fiona Stapleton
  • , Pablo Argüeso
  • , Penny Asbell
  • , Dimitri Azar
  • , Charles Bosworth
  • , Wei Chen
  • , Joseph Ciolino
  • , Jennifer P Craig
  • , Juana Gallar
  • , Anat Galor
  • , José A P Gomes
  • , Isabelle Jalbert
  • , Ying Jie
  • , Lyndon Jones
  • , Kenji Konomi
  • , Yang Liu
  • , Jesus Merayo-Lloves
  • , Fabiola R Oliveira
  • , Victor A Perez Quinones
  • , Eduardo M Rocha
  • Benjamin D Sullivan, David A Sullivan, Jelle Vehof, Susan Vitale, Mark Willcox, James Wolffsohn, Murat Dogru
  • University of Waterloo, School of Optometry and Vision Science
  • Tufts University School of Medicine
  • University of Memphis
  • University of Illinois System
  • Azura Ophthalmics
  • Eye Hospital of Wenzhou Medical University
  • Harvard University
  • University of Auckland
  • Ocular Neurobiology Group
  • University of Miami
  • Paulista School of Medicine / Federal University of São Paulo
  • Capital Medical University
  • University of Waterloo
  • Keio University Hospital
  • Zhongnan Hospital of Wuhan University
  • Instituto Universitario Fernandez-Vega, Universidad de Oviedo, Principality of Asturias, Spain.
  • Universidade de São Paulo
  • University of Miami Leonard M. Miller School of Medicine
  • Lµbris BioPharma
  • Schepens Eye Research Institute of Massachusetts Eye and Ear
  • University of Groningen
  • National Eye Institute
  • Ichikawa General Hospital Tokyo Dental College Dept of Ophthalmology Ichikawa

Research output: Contribution to journalReview articlepeer-review

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Abstract

This digest summarizes the interdisciplinary research in dry eye disease (DED) published since the 2017 TFOS DEWS II reports. It comprises 7 topics including Sex, Gender, and Hormones; Epidemiology; Pathophysiology; Tear Film; Pain and Sensation; Iatrogenic Dry Eye; and Clinical Trial Design and explores how each of these inform diagnostic methodology, disease subtype, and management of DED. Sex- and gender-related differences significantly influence the ocular surface due to hormones, sex chromosomes, sex-specific autosomal factors, epigenetics, care-seeking behaviors, and service use. Epidemiologic data reveal that DED prevalence varies by age and sex, influenced by diagnostic criteria and the multifactorial nature of the disease. New risk factors for DED include environmental, iatrogenicity, systemic diseases, and lifestyle domains. Pathophysiological distinctions between aqueous deficient and more evaporative forms of DED have been clarified, with the latter most commonly characterized by a muted inflammatory response at the ocular surface, meibomian gland dysfunction, and conceivably phenotypic changes in corneal epithelial cells. There is an expanding role for metabolic, hormonal, physical, neural and cellular stresses, including hyperosmolarity, mitochondrial stress, and neurogenic inflammation. Advancements in tear film research recommend new approaches to understanding DED pathogenesis and identifying biomarkers, such as microRNAs. Ocular pain perception is linked to structural integrity of corneal nerves, functional capacities of neurons, and activity of the central and peripheral nervous systems. Iatrogenic DED can result from medications, contact lenses, and surgical procedures. Clinical trials now emphasize aligning design and end points with DED subtypes and therapeutic mechanisms, with new therapeutics and trial designs under consideration.

Original languageEnglish
Pages (from-to)451-553
Number of pages103
JournalAmerican Journal of Ophthalmology
Volume279
Early online date4 Jun 2025
DOIs
Publication statusPublished - Nov 2025

Bibliographical note

Copyright © 2025 The Author(s). Published by Elsevier Inc.
This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/)

Funding

The TFOS DEWS III effort was supported by unrestricted donations from Alcon, Bausch + Lomb, Azura, AbbVie, CooperVision, Dompé, Espansione Group, Harrow, Laboratoire Théa, SIFI, SINQI, Tarsus, Topcon and Trukera.

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