蠕形螨定植与睑板腺功能障碍表现的关系

Shorouk Mohammed, T. Mostafa, Rehab M. Kamel, Walaa A El Kholy
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引用次数: 0

摘要

背景与目的睑板腺功能障碍(MGD)是临床上常见的疾病。它是导致蒸发性干眼症的根本原因。它是一种慢性弥漫性睑板腺疾病,以末端导管阻塞和/或腺体分泌的定性/定量变化为特征。它可能导致泪膜的改变、眼睛刺激的表现、临床上明显的炎症,以及眼表疾病(OSD)。本研究的目的是将Demodex定殖与MGD联系起来。患者和方法本研究包括76眼,分为两组,A组(患者组)包括38眼MGD,B组(对照组)包括38眼正常眼睑边缘。两组均接受病史采集、MGD分级评估、荧光素裂解时间、OSD指数、Schirmer-1试验和睫毛取样。通过光学显微镜检查取样的睫毛的Demodex定植情况。结果患者组16眼(42.1%)和对照组4眼(10.5%)的蠕形螨定植率有统计学意义。MGD患者组以女性为主(84.2%),Schirmer-1检验P值小于0.001。结论蠕形螨定植是引起MGD和OSD的重要原因。我们的研究表明,治疗蠕形螨对MGD患者至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The relation between Demodex colonization and manifestations of meibomian-gland dysfunction
Background and aim Meibomian-gland dysfunction (MGD) is a very common disease we face every day in the clinic. It is the essential cause of evaporative dry eye. It is a chronic, diffuse disorder of the meibomian glands, distinguished by terminal-duct obstruction and/or qualitative/quantitative variations in glandular secretion. It may result in alteration of the tear film, manifestations of eye irritation, clinically evident inflammation, and also ocular-surface disease (OSD). The aim of the study was to relate Demodex colonization to MGD. Patients and methods This study included 76 eyes divided into two groups, group A (patients’ group) included 38 eyes with MGD, group B (control group) included 38 eyes with normal lid margin. Both groups were subjected to history taking, MGD evaluation by MGD grading, fluorescein breakup time, OSD index, Schirmer-1 test, and lash sampling. The lashes sampled were examined for Demodex colonization by light microscopy. Results There was a statistically significant difference in Demodex colonization between the patients’ group 16 (42.1%) eyes and the control group four (10.5%)eyes. We noticed predominance of female sex in the MGD patients’ group (84.2%). There was a statistically significant difference between the two groups regarding fluorescein breakup time, OSD index, and Schirmer-1 test with P value less than 0.001. Conclusion Demodex colonization is incriminated as an important cause of MGD and OSD. Our study suggests that treating Demodex is crucial in MGD patients.
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