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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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Journal ArticleDOI

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 ArticleDOI

Mucous Membrane Pemphigoid

TL;DR: The epidemiology, clinical presentation, pathophysiology, diagnosis, and management of MMP are discussed, with mention of related subepithelial bullous dermatoses.
Journal ArticleDOI

Effects of Age and Dysfunction on Human Meibomian Glands

TL;DR: These results indicate that aging human meibomian glands show decreased meibocyte differentiation and cell cycling that is associated with the development of MGD, and suggest that altered PPARγ signaling may lead to acinar atrophy and development of an age-related hyposecretory MGD.
Book ChapterDOI

The meibomian glands and tear film lipids. Structure, function, and control.

TL;DR: This paper reviews current knowledge of the structure and function of the meibomian glands and proposes a new strategy to treat posterior blepharitis with lasers.
Journal Article

The influence of age onthe sensitivity of the cornea

TL;DR: The results are found to be in good accord with those of Boberg-Ans, thus refuting an earlier report asserting that corneal sensitivity (threshold-1) increased up to the fifth decade and declined thereafter.
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