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TFOS DEWS II pathophysiology report

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TLDR
The TFOS DEWS II Pathophysiology Subcommittee reviewed the mechanisms involved in the initiation and perpetuation of dry eye disease, finding 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 to be important.
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 a 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 across the ocular surface, to better determine the severity of dry eye. Areas for future research include the role of genetic mechanisms in non-Sjogren 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.

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TFOS DEWS II Definition and Classification Report

TL;DR: The new definition recognizes the multifactorial nature of dry eye as a disease where loss of homeostasis of the tear film is the central pathophysiological concept and central to the scheme is a positive diagnosis of DED with signs and symptoms, and this is directed towards management to restore homeostosis.
References
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Journal Article

The effect of ageing and disease on tear constituents.

TL;DR: Results of tear lysozyme assays from patients on various beta-blockers are discussed with the suggested hypothesis that stimulation of beta-receptors per se in the human lacrimal gland is not required for tear protein secretion.
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Lacrimal function and ocular complications in patients treated with systemic isotretinoin.

TL;DR: Isotretinoin causes signs and symptoms of dry eye, probably by reducing meibomian gland function, but ocular complications are generally not serious when low doses are used for a limited time, and are reversible after discontinuation.
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Isolation and Characterization of Progenitor Cells in Uninjured, Adult Rat Lacrimal Gland

TL;DR: It is concluded that uninjured, adult LG contains progenitor cells that may be MECs, which can be isolated and differentiated into multiple lineages.
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The lid wiper contains goblet cells and goblet cell crypts for ocular surface lubrication during the blink.

TL;DR: Contrary to conventional assumptions, the lid wiper is part of the conjunctiva and contains previously undescribed goblet cell crypts deep in the epithelium, suitable as an internal lubrication system for reduction of friction between the lid margin and the globe.
Journal ArticleDOI

Incidence and risk factors for ocular GVHD after allogeneic hematopoietic stem cell transplantation.

TL;DR: Careful monitoring of ocular GVhd is needed in patients with chronic GVHD in multiple organs and preexisting diabetes mellitus in patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT) in Korea.
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