Du Ya-Li, Peng Xi, Liu Yang, Wang Jia-Song, Ye You-Fan, Xu Kang-Kang, Qu Jing-Yu, Chen Hua, Xie Hua-Tao, Zhang Ming-Chang
Department of Ophthalmology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Department of Ophthalmology, Zhongnan Hospital of Wuhan University, Wuhan 430071, China.
Curr Issues Mol Biol. 2023 Feb 27;45(3):1889-1901. doi: 10.3390/cimb45030122.
Meibomian gland dysfunction (MGD) is a functional and morphological disorder of the meibomian glands which results in qualitative or quantitative alteration in meibum secretion and is the major cause of evaporative dry eye (EDE). EDE is often characterized by tear film instability, increased evaporation, hyperosmolarity, inflammation, and ocular surface disorder. The precise pathogenesis of MGD remains elusive. It has been widely considered that MGD develops as a result of ductal epithelial hyperkeratinization, which obstructs the meibomian orifice, halts meibum secretion, and causes secondary acinar atrophy and gland dropout. Abnormal self-renewal and differentiation of the acinar cells also play a significant role in MGD. This review summarizes the latest research findings regarding the possible pathogenesis of MGD and provides further treatment strategies for MGD-EDE patients.
睑板腺功能障碍(MGD)是睑板腺的一种功能和形态紊乱,导致睑脂分泌在质或量上发生改变,是蒸发过强型干眼(EDE)的主要原因。EDE通常表现为泪膜不稳定、蒸发增加、高渗、炎症和眼表紊乱。MGD的确切发病机制仍不清楚。人们普遍认为,MGD是由于导管上皮过度角化,阻塞睑板腺开口,停止睑脂分泌,并导致继发性腺泡萎缩和腺体缺失而发展的。腺泡细胞的异常自我更新和分化在MGD中也起重要作用。本综述总结了关于MGD可能发病机制的最新研究结果,并为MGD-EDE患者提供了进一步的治疗策略。