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分析细胞因子作为生物标志物以评估青光眼的严重程度。

Analyzing cytokines as biomarkers to evaluate severity of glaucoma.

作者信息

Tong Yao, Zhou Ya-Li, Zheng Yan, Biswal Manas, Zhao Pei-Quan, Wang Zhao-Yang

机构信息

Department of Ophthalmology, Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200011, China.

Department of Ophthalmology, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai 200092, China.

出版信息

Int J Ophthalmol. 2017 Jun 18;10(6):925-930. doi: 10.18240/ijo.2017.06.15. eCollection 2017.

Abstract

AIM

To analyze cytokines as biomarkers for evaluation of severity of glaucoma.

METHODS

This was a prospective case-control study including 29 eyes with glaucoma. Besides, 28 eyes with senile cataract were used as control. Patients were classified into four groups: acute angle closure glaucoma (AACG), chronic angle closure glaucoma (CACG), primary open angle glaucoma (POAG) and senile cataract. Undiluted vitreous samples were collected, then vitreous concentrations of 9 types of cytokines were determined by cytometric bead assay system: γ-interferon (IFNg), interleukin (IL)-10, IL-2, IL-4, IL-5, interferon-γ-inducible protein (IP)-10, monocyte chemoattractant protein (MCP)-1, tumor necrosis factor (TNF)-α, and vascular endothelial growth factor (VEGF). We also recorded the intraocular pressure (IOP) of patients in each group and Pearson correlated analysis was performed to analysis the correlation between each type of cytokine with IOP.

RESULTS

Vitreous levels of IL-2, IL-5, MCP-1, TNF-α and IP-10 were significantly higher (<0.05) in AACG group. Patients with AACG, CACG and POAG have higher IOP than senile cataract, but we didn't find any significant correlation between IOP with any type of the cytokines.

CONCLUSION

Inflammation and immune reaction have a strong link with the pathology of glaucoma especially AACG. Some cytokines may act as biomarkers to evaluate the severity of glaucoma. Anti-inflammatory treatments and controlling of IOP are necessary for the therapy of glaucoma.

摘要

目的

分析细胞因子作为评估青光眼严重程度的生物标志物。

方法

这是一项前瞻性病例对照研究,纳入29只青光眼患眼。此外,选取28只老年性白内障患眼作为对照。患者分为四组:急性闭角型青光眼(AACG)、慢性闭角型青光眼(CACG)、原发性开角型青光眼(POAG)和老年性白内障。收集未稀释的玻璃体样本,然后通过细胞计数珠分析系统测定9种细胞因子的玻璃体浓度:γ-干扰素(IFNg)、白细胞介素(IL)-10、IL-2、IL-4、IL-5、γ-干扰素诱导蛋白(IP)-10、单核细胞趋化蛋白(MCP)-1、肿瘤坏死因子(TNF)-α和血管内皮生长因子(VEGF)。我们还记录了每组患者的眼压(IOP),并进行Pearson相关性分析以分析每种细胞因子与IOP之间的相关性。

结果

AACG组中IL-2、IL-5、MCP-1、TNF-α和IP-10的玻璃体水平显著更高(<0.05)。AACG、CACG和POAG患者的IOP高于老年性白内障患者,但我们未发现IOP与任何类型的细胞因子之间存在显著相关性。

结论

炎症和免疫反应与青光眼尤其是AACG的病理密切相关。一些细胞因子可能作为评估青光眼严重程度的生物标志物。抗炎治疗和控制眼压对于青光眼治疗是必要的。

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