炎症介质(白细胞介素和皮质醇浓度)与角膜上皮量化指标的关系

IF 3.2 Q1 OPHTHALMOLOGY
Marcony R. Santhiago MD, PhD , Larissa R. Stival MD, PhD , Daniella C. Araujo PhD , Rosalia Antunes-Foschini MD, PhD , Marcia C. Toledo MD , Ianne L.S. Nunes MS , Claudia R. Morgado MD , Newton Kara-Junior MD, PhD
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引用次数: 0

摘要

目的研究角膜炎患者和健康眼的炎症生物标志物与角膜上皮量化指标的关系:方法对两组患者的泪液细胞因子浓度进行调查:白细胞介素(IL)1B、IL6、IL8、IL10、IL12p70和肿瘤坏死因子α(TNFα)通过毛细管流动获得,并使用流式细胞仪进行测量。通过液相色谱质谱法测定两组毛发的皮质醇浓度,作为累积分泌的指标。上皮变量通过 OCT 获得。皮尔逊相关性(r)用于测量两个不同变量之间的线性关系。主要结果测量调查炎症生物标记物(IL1B、IL6、IL8、IL10、IL12p70、TNFα和毛发皮质醇浓度)与 OCT 角膜上皮量化变量(如地图的最小和最大上皮厚度)之间是否存在相关性、相关性的强度和意义、上皮厚度最小值和最大值之差(Epithelial Min-Max)和上皮厚度标准偏差(Epithelial Std Dev),以及上、下角膜上皮厚度的平均值。结果与健康对照组相比,角膜炎患者的 IL1b (P = 0.02)、IL6 (P < 0.0001)、IL8 (P < 0.0001)、TNFα (P < 0.0001) 和毛发皮质醇浓度(P = 0.与健康对照组相比,IL6与测量上皮最小值-最大值(Pearson = -0.59 (-0.69, -0.47);P <;0.0001)和上皮标准偏差(Pearson = +0.56 [0.44, 0.67];P <;0.0001)之间存在显著相关性。)毛发皮质醇浓度与上皮最小值组(Pearson = -0.27 [-0.42, -0.1];P <;0.0001])和上皮标准差组(Pearson = +0.2 [0.03, 0.36];P = 0.021)之间存在明显相关性。TNFα 与上皮最大值之间也存在明显的相关性(Pearson = -0.37 [-0.55, 0.17];P < 0.0001)。结论 角膜炎患者眼部炎症标志物(IL6 和毛发皮质醇)浓度较高,与识别上皮变异性的 OCT 指标(如上皮最小值-最大值和 Std Dev)存在明显相关性。这些研究结果表明了慢性炎症在角膜炎患者眼中的作用,而且用 OCT 检测到的这些上皮变化对这一炎症过程非常敏感。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Relationship of Inflammatory Mediators (Interleukin and Cortisol Concentrations) with Corneal Epithelial Quantifiable Metrics

Purpose

To investigate the relationship of inflammatory biomarkers with corneal epithelial quantifiable metrics in patients with keratoconus and in healthy eyes.

Design

Prospective observational comparative study.

Participants

This study included 100 eyes of 100 patients: 48 eyes of 48 patients with keratoconus and 52 healthy eyes of 52 healthy controls.

Methods

The concentrations of tear cytokines were investigated in both groups: interleukin (IL) 1B, IL6, IL8, IL10, IL12p70, and tumor necrosis factor α (TNFα) were obtained by capillary flow and measured using flow cytometer. Cortisol concentrations were determined in both groups from the most proximal hair segment as an index of cumulative secretion and measured by liquid chromatography mass spectrometry. Epithelial variables were obtained with OCT. Pearson correlation (r) was used to measure linear dependence between 2 different variables.

Main Outcome Measures

Investigating the existence, strength, and significance of any correlation between inflammatory biomarkers (IL1B, IL6, IL8, IL10, IL12p70, TNFα, and hair cortisol concentration) and OCT corneal epithelial quantifiable variables such as minimum and maximum epithelial thickness of the map, difference between the minimum and maximum (Epithelial Min-Max) and standard deviation of the epithelial thickness of the map (Epithelial Std Dev), and average epithelial thickness of the superior and inferior regions of the map.

Results

Eyes with keratoconus presented statistically significantly higher levels of IL1b (P = 0.02), IL6 (P < 0.0001), IL8 (P < 0.0001), and TNFα (P < 0.0001) and hair cortisol concentration (P = 0.01) compared with healthy controls.
There was a significant correlation between IL6 and measurement Epithelium Min-Max [Pearson = −0.59 (−0.69, −0.47); P < 0.0001] and Epithelial Std Dev (Pearson = +0.56 [0.44, 0.67]; P < 0.0001). There was a significant correlation between hair cortisol concentration and Epithelium Min-Max (Pearson = −0.27 [−0.42, −0.1]; P < 0.0001]) and Epithelium Std Dev groups (Pearson = +0.2 [0.03, 0.36]; P = 0.021). There was also a significant correlation between TNFα and Epithelial Max (Pearson = −0.37 [−0.55, 0.17]; P < 0.0001). We found no significant correlation between the concentration of IL1b, IL8, IL10, and IL2p70 with any epithelium parameters.

Conclusions

The higher concentration of inflammatory markers (IL6 and hair cortisol) in eyes with keratoconus present a significant correlation with OCT metrics identifying epithelial variability, such as Epithelial Min-Max and Std Dev. These findings demonstrate the role of chronic inflammation in eyes with keratoconus, and that these epithelial changes detectable with OCT are sensitive to this inflammatory process.

Financial Disclosure(s)

The author(s) have no proprietary or commercial interest in any materials discussed in this article.
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来源期刊
Ophthalmology science
Ophthalmology science Ophthalmology
CiteScore
3.40
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