IOBA (Institute of Applied Ophthalmobiology), Universidad de Valladolid, Valladolid, Spain.
Department of Vision Sciences, School of Health and Life Sciences, Glasgow Caledonian University, Glasgow G4 0BA, UK.
Cont Lens Anterior Eye. 2022 Dec;45(6):101705. doi: 10.1016/j.clae.2022.101705. Epub 2022 May 11.
To investigate the effect of time of day on tear evaporation rate (TER) and tear break-up time, and its possible relationship with the concentration of inflammatory tear molecules (cytokines) in healthy subjects.
Participants with healthy ocular surfaces attended 3 visits, including the screening visit (V0), the 2nd visit (V1) and the 3rd visit (V2). There were 7-day intervals between visits. Participants with Dry Eye Disease (DED) were excluded by using appropriate clinical tests during V0. Clinical evaluation (TER and Non-Invasive Tear Break-Up Time (NITBUT)) and tear collection were performed during V1 and V2, between 9 and 10AM and 3-4PM. The relative humidity and temperature of the examination room were also measured. The tear fluid concentrations of 15 cytokines were measured by multiplex bead analysis.
Seven men and 10 women (mean age ± S.D; 25.1 ± 6.63 years old) participated in the study. There were no differences in neither the TER and NITBUT outcomes, nor humidity and temperature among times or visits. Eleven out of the 15 cytokines measured were detectable in tear fluids in > 50% of the participants. In the tear levels, no significant (p > 0.05) inter- and/or intra-day differences were detected for EGF, fractalkine, IL-1RA, IL-1β and IP-10. However, significant inter-day differences were found in the tear levels of IL-10 (p = 0.027), IFN-γ (p = 0.035) and TNF-α(p = 0.04) and intra-day differences in the tear levels of IL-8/CXCL8 (p = 0.034) and MCP-1 (p = 0.002). A significant correlation between TER and IL1-β, IL-2, and Fractalkine (p = 0.03, p = 0.03 and p = 0.046, respectively) was found at V1.
NITBUT and TER values had no significant variability over the course of a day (AM versus PM), or on different days in healthy participants when humidity and temperature were constant. However, some tear molecule levels did show inter- and intra-day variability, having an inconsistent and moderate correlation with TER diurnal variation.
研究时间对泪液蒸发率(TER)和泪膜破裂时间的影响,并探讨其与健康受试者炎症性泪液分子(细胞因子)浓度的可能关系。
具有健康眼表面的参与者参加了 3 次访问,包括筛选访问(V0)、第 2 次访问(V1)和第 3 次访问(V2)。每次访问之间间隔 7 天。在 V0 期间通过适当的临床检查排除干眼症(DED)患者。在 V1 和 V2 期间(上午 9 点至 10 点和下午 3 点至 4 点)进行临床评估(TER 和非侵入性泪膜破裂时间(NITBUT))和泪液采集。还测量了检查室的相对湿度和温度。通过多重珠分析测量了 15 种细胞因子的泪液浓度。
7 名男性和 10 名女性(平均年龄±标准差;25.1±6.63 岁)参加了研究。在时间或访问之间,TER 和 NITBUT 结果以及湿度和温度均无差异。在>50%的参与者的泪液中可检测到 15 种细胞因子中的 11 种。在泪液水平中,EGF、 fractalkine、IL-1RA、IL-1β 和 IP-10 未检测到显著的(p>0.05)日内和/或日间差异。然而,在泪液水平上发现了显著的日间差异(p=0.027)、IFN-γ(p=0.035)和 TNF-α(p=0.04),并且在泪液水平上发现了显著的日内差异(p=0.034)和 MCP-1(p=0.002)。在 V1 时,发现 TER 与 IL1-β、IL-2 和 fractalkine 之间存在显著相关性(p=0.03、p=0.03 和 p=0.046)。
当湿度和温度保持不变时,健康参与者在一天中(上午与下午)或不同日子之间,NITBUT 和 TER 值没有明显的变化。然而,一些泪液分子水平确实存在日内和日间变化,与 TER 昼夜变化呈不一致和中度相关。