Retina Research Group, School of Optometry and Vision Science, University of Waterloo, Waterloo, Ontario, Canada.
Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, Ontario, Canada.
Acta Ophthalmol. 2019 Aug;97(5):e673-e679. doi: 10.1111/aos.14016. Epub 2019 Jan 28.
The aim of this study was to assess the relationship between retinal blood oxygen saturation (SO ) and specific aqueous humour (AH) concentrations of proangiogenic biomarkers in diabetic patients with nonproliferative diabetic retinopathy (NPDR) and to compare them with those of matched control subjects.
The sample comprised 14 participants with mild-to-moderate NPDR (69.1 ± 6.6 years) and 17 age-matched healthy controls (69.7 ± 6.3 years); all participants were previously scheduled for routine cataract extraction with intraocular lens implantation. Multiplex cytokine analyses of specific biomarkers, including vascular endothelial growth factor A (VEGF-A), angiopoietin2 (Ang2), epidermal growth factor (EGF), hepatocyte growth factor (HGF) and interleukin-8 (IL-8) were performed by BioPlex 200 system. Six non-invasive hyperspectral retinal images were acquired.
Mean SO was significantly higher in both arterioles (94.4 ± 1.9 versus 93.0 ± 1.6) and venules (64.4 ± 5.6 versus 55.9 ± 4.8) of NPDR than in the healthy controls (p < 0.001). AH levels of HGF (p = 0.018), Ang2 (p = 0.005) and IL-8 (p = 0.034) were significantly higher, and EGF (p = 0.030) was significantly lower in NPDR subjects. The study demonstrated a correlation between venular retinal blood oxygen saturation and proangiogenic factors HGF (r = 0.558, p = 0.038), Ang2 (r = 0.556, p = 0.039) and EGF (r = -0.554, p = 0.040), but did not find any correlation for IL-8 (r = 0.330, p = 0.249) even though this biomarker was significantly higher in the diabetic group.
To our knowledge, the present study is the first report considering the association between SO and AH concentrations of protein biomarkers in diabetic retinopathy. The biomarkers of interest have been shown to participate in cell death, which may explain higher oxygen saturation in NPDR.
本研究旨在评估患有非增生性糖尿病视网膜病变(NPDR)的糖尿病患者视网膜血氧饱和度(SO )与特定房水中促血管生成生物标志物浓度之间的关系,并将其与匹配的对照组进行比较。
该样本包括 14 名轻度至中度 NPDR 患者(69.1 ± 6.6 岁)和 17 名年龄匹配的健康对照者(69.7 ± 6.3 岁);所有参与者均计划常规行白内障超声乳化联合人工晶状体植入术。通过 BioPlex 200 系统对包括血管内皮生长因子 A(VEGF-A)、血管生成素 2(Ang2)、表皮生长因子(EGF)、肝细胞生长因子(HGF)和白细胞介素 8(IL-8)在内的特定生物标志物的浓度进行多元细胞因子分析。采集 6 张非侵入性高光谱视网膜图像。
与健康对照组相比,NPDR 患者的动、静脉(分别为 94.4 ± 1.9 和 64.4 ± 5.6)的 SO 均显著升高(p < 0.001)。NPDR 患者的房水中 HGF(p = 0.018)、Ang2(p = 0.005)和 IL-8(p = 0.034)水平显著升高,而 EGF(p = 0.030)水平显著降低。研究表明,静脉 SO 与促血管生成因子 HGF(r = 0.558,p = 0.038)、Ang2(r = 0.556,p = 0.039)和 EGF(r = -0.554,p = 0.040)之间存在相关性,但未发现 IL-8(r = 0.330,p = 0.249)存在相关性,尽管该生物标志物在糖尿病组中显著升高。
据我们所知,本研究首次报告了糖尿病视网膜病变患者 SO 与房水中蛋白质生物标志物浓度之间的相关性。这些感兴趣的生物标志物已被证明参与细胞死亡,这可能解释了 NPDR 中较高的血氧饱和度。