Institut Clínic d'Oftalmologia (ICOF), Hospital Clínic, Barcelona, Spain.
August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
Invest Ophthalmol Vis Sci. 2019 Apr 1;60(5):1336-1343. doi: 10.1167/iovs.18-26215.
To determine whether baseline cytokine aqueous humor (AH) levels are associated with diabetic macular edema (DME) anatomic response to dexamethasone intravitreal implant (DEX) injection.
This was a prospective cohort study of DME cases receiving DEX treatment. Seventy patients were recruited with center-involving DME with spectral-domain (SD) optical coherence tomography (OCT) detection of central macular thickness (CMT) ≥300 μm on macular cube 518 × 128-μm scan protocol (Cirrus SD-OCT). DEX injection and anterior chamber tap to obtain an AH sample were performed at the same time. Multiplex immunoassay was carried out for interleukin (IL)-1β, IL-3, IL-6, IL-8, IL-10; monocyte chemoattractant protein (MCP)-1; interferon gamma-induced protein (IP)-10; tumor necrosis factor (TNF)-α; and vascular endothelial growth factor (VEGF). A follow-up visit and OCT exam were undertaken 6 to 8 weeks afterward. The association between AH cytokine baseline levels and change in CMT and macular volume (MV) was defined as main outcome measure.
Multivariate linear regression analysis showed a higher decrease in MV to be associated (Rs of 0.512) with four baseline items: higher MCP-1 (β = -0.4; P = 0.028), higher CMT (β = -0.003; P = 0.024), decreased visual acuity (β = -0.7; P = 0.040), and a diffuse retinal thickening (DRT) OCT pattern (β = -1.3; P < 0.001). Logistic regression found DRT also to be associated with higher odds of a good MV response (odds ratio, 31.96; 95% confidence interval [CI] 7.11-143.72; P < 0.001).
Even though visual acuity response and anatomic effect are not always correlated in DME, we found that baseline elevated MCP-1 AH levels and DRT pattern were biomarkers that predicted a future favorable anatomic response to DEX.
确定基线细胞因子房水(AH)水平是否与糖尿病黄斑水肿(DME)对地塞米松玻璃体内植入物(DEX)注射的解剖学反应有关。
这是一项接受 DEX 治疗的 DME 病例的前瞻性队列研究。共招募了 70 名中心性 DME 患者,采用频域(SD)光学相干断层扫描(OCT)检测黄斑中心厚度(CMT)≥300μm,采用黄斑立方 518×128μm 扫描方案(Cirrus SD-OCT)。DEX 注射和前房穿刺以获取 AH 样本同时进行。采用多重免疫分析法检测白细胞介素(IL)-1β、IL-3、IL-6、IL-8、IL-10;单核细胞趋化蛋白(MCP)-1;干扰素γ诱导蛋白(IP)-10;肿瘤坏死因子(TNF)-α;和血管内皮生长因子(VEGF)。6 至 8 周后进行随访和 OCT 检查。将 AH 细胞因子基线水平与 CMT 和黄斑体积(MV)变化之间的关系定义为主要观察指标。
多元线性回归分析显示,MV 下降幅度较大与四项基线指标相关(Rs 为 0.512):较高的 MCP-1(β=-0.4;P=0.028)、较高的 CMT(β=-0.003;P=0.024)、视力下降(β=-0.7;P=0.040)和弥漫性视网膜增厚(DRT)OCT 模式(β=-1.3;P<0.001)。Logistic 回归发现 DRT 也与 MV 反应良好的几率较高相关(比值比,31.96;95%置信区间[CI]7.11-143.72;P<0.001)。
尽管在 DME 中视力恢复和解剖效果并不总是相关,但我们发现基线时 AH 中升高的 MCP-1 水平和 DRT 模式是预测 DEX 未来良好解剖反应的生物标志物。