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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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Dry Eye Disease: What Is the Role of Vitamin D?

TL;DR: A review of the literature reporting on the pathogenesis and treatment of dry eye disease with a special emphasis on the potential role of the systemic administration of vitamin D as a therapeutic approach in the management of such condition is presented in this paper .
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A retrospective study of the efficacy of intense pulsed light delivered by the Lacrystim® for meibomian gland dysfunction therapy

TL;DR: In this paper , the first study on Lacrystim® with an objective assessment of its efficacy and an extended follow-up over 6 months was presented, where patients presenting with a dry eye disease (DED) with stable mild to moderate MGD and having received Lacry Stimulation® treatment between june 2019 and june 2020 were included.
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The Correlation between Matrix Metalloproteinase-9 Point-of-Care Immunoassay, Tear Film Osmolarity, and Ocular Surface Parameters

TL;DR: Tear film MMP-9 may be an indicator for tear film osmolarity, or vice-versa, and osmolarship may have a correlation with corneal staining in patients with dry eye.
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A Practical Approach to Severity Classification and Treatment of Dry Eye Disease: A Proposal from the Mexican Dry Eye Disease Expert Panel

TL;DR: In this paper , the authors proposed a DED classification system based on disease severity to help clinicians discriminate cases needing referral to subspecialty clinics from those they could attend, and also proposed a systematic management approach and general management considerations to improve patients' therapeutic outcomes according to disease severity.
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A novel osmoprotective liposomal formulation from synthetic phospholipids to reduce in vitro hyperosmolar stress in dry eye treatments

TL;DR: The liposomal formulations developed were well-tolerated in cell cultures and showed osmoprotective activity in a hyperosmolar model, and are promising candidates for the treatment of DED.
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