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角膜胶原交联术后圆锥角膜患者泪液生物标志物水平的变化

Changes in tear biomarker levels in keratoconus after corneal collagen crosslinking.

作者信息

Recalde Jose Ignacio, Duran Juan Antonio, Rodriguez-Agirretxe Iñaki, Soria Javier, Sanchez-Tena Miguel Angel, Pereiro Xandra, Suarez Tatiana, Acera Arantxa

机构信息

Instituto Clínico-Quirúrgico de Oftalmología, Bilbao, Bizkaia, Spain.

Department of Ophthalmology, University of the Basque Country, Experimental Ophtalmo-Biology Group UPV/EHU, Leioa, Bizkaia, Spain.

出版信息

Mol Vis. 2019 Jan 20;25:12-21. eCollection 2019.

Abstract

PURPOSE

The purpose of this work was to analyze the expressions of matrix metalloproteinase 9 (MMP-9), calcyclin (S100A6), and cystatin S (CST4) in the tears of keratoconus (KC) patients. The correlations between the expressions of these proteins and the values of various ocular surface parameters were examined after accelerated corneal crosslinking (A-CXL) with pulsed ultraviolet light.

METHODS

This prospective, observational study enrolled patients with different grades of KC, scheduled to undergo the A-CXL procedure, as well as healthy subjects. Tear samples were analyzed by employing customized antibody microarray assays for MMP-9, S100A6, and CST4 proteins. The keratometry readings at the maximum keratometry (Kmax) and the simulated keratometry (SimK) values were obtained for examining the postoperative evolution of corneal topography. The state of the ocular surface was evaluated using the results of the Ocular Surface Disease Index (OSDI) questionnaire, tear osmolarity (OSM) test, Schirmer test (SCH), Tear Break Up Time (TBUT), tear clearance (CLR), and fluorescein (FLUO) and lissamine green (LG) corneal staining.

RESULTS

A total of 18 patients (22 eyes) and 10 healthy subjects were studied. The concentrations of MMP-9 and S100A6 decreased in tears, from 104.5 ± 78.98 ng/ml and 350.20 ± 478.08 ng/ml before the surgery to 48.7 ± 24.20 ng/ml and 55.70 ± 103.62 ng/ml, respectively, after 12 months of follow up. There were no changes in the CST4 concentration after 12 months of follow up (2202.75 ± 2863.70 versus 2139.68 ±2719.89 ng/ml). When the patients were divided into three groups according to the evolutive stage of KC, the trends for the three biomarkers in each group were the same as in the general group. Basal concentrations of MMP-9 and S100A6 from healthy subjects and KC patients were compared. The levels of MMP-9 and S100A6 in tears were (9.8 ± 5.11 and 104.55 ± 78.98 ng/ml, <0.01; and 11.35 ± 3.18 and 350.26 ± 478.06 ng/ml, respectively, <0.01). This was not the case for CST4, which did not exhibit statistically significant differences between the two groups (2261.94 ± 510.65 and 2176.73 ± 2916.27 ng/ml respectively, p=0.07).

CONCLUSIONS

A-CXL promoted a decrease in the concentrations of MMP-9 and S100A6 in the tear film. This effect may be related to the restoration of corneal homeostasis and the consequent repair of the tissue damage caused by KC. Moreover, the A-CXL treatment did not produce lasting alterations in the ocular surface, and the values of the evaluated clinical parameters did not change significantly.

摘要

目的

本研究旨在分析圆锥角膜(KC)患者泪液中基质金属蛋白酶9(MMP - 9)、钙周期蛋白(S100A6)和胱抑素S(CST4)的表达情况。在脉冲紫外光加速角膜交联(A - CXL)后,检测这些蛋白质表达与各种眼表参数值之间的相关性。

方法

这项前瞻性观察性研究纳入了计划接受A - CXL手术的不同等级KC患者以及健康受试者。通过定制的抗体微阵列分析法对MMP - 9、S100A6和CST4蛋白进行泪液样本分析。获取最大角膜曲率(Kmax)和模拟角膜曲率(SimK)值的角膜曲率测量读数,以检查角膜地形图的术后演变情况。使用眼表疾病指数(OSDI)问卷、泪液渗透压(OSM)测试、泪液分泌试验(SCH)、泪膜破裂时间(TBUT)、泪液清除率(CLR)以及荧光素(FLUO)和丽丝胺绿(LG)角膜染色结果评估眼表状态。

结果

共研究了18例患者(22只眼)和10名健康受试者。泪液中MMP - 9和S100A6的浓度降低,术前分别为104.5±78.98 ng/ml和350.20±478.08 ng/ml,随访12个月后分别降至48.7±24.20 ng/ml和55.70±103.62 ng/ml。随访12个月后CST4浓度无变化(分别为2202.75±2863.70与2139.68±2719.89 ng/ml)。根据KC的演变阶段将患者分为三组时,每组中三种生物标志物的变化趋势与总体组相同。比较了健康受试者和KC患者MMP - 9和S100A6的基础浓度。泪液中MMP - 9和S100A6的水平分别为(9.8±5.11和104.55±78.98 ng/ml,<0.01;以及11.35±3.18和350.26±478.06 ng/ml,均<0.01)。CST4并非如此,两组之间未显示出统计学上的显著差异(分别为2261.94±510.65和2176.73±2916.27 ng/ml,p = 0.07)。

结论

A - CXL促使泪膜中MMP - 9和S100A6的浓度降低。这种作用可能与角膜内环境稳态的恢复以及KC所致组织损伤的后续修复有关。此外,A - CXL治疗未对眼表产生持久改变,所评估的临床参数值未发生显著变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05f3/6363636/54d4513b8b25/mv-v25-12-f1.jpg

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