Department of Ophthalmology, Hospital de Braga, Braga, Portugal.
Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus Gualtar, Braga, Portugal.
Retina. 2021 Feb 1;41(2):345-354. doi: 10.1097/IAE.0000000000002852.
To study the role of serum biomarkers as prognostic factors for qualitative and quantitative response to anti-vascular endothelial growth factor injections for diabetic macular edema (DME).
Sixty-seven eyes with DME were treated with intravitreal bevacizumab during a 12-month follow-up period. All cases underwent a baseline workup consisting of 12 inflammatory, metabolic and prothrombotic factors. The following outcomes were evaluated at 3-month intervals until 1 year of follow-up: visual acuity, central subfield thickness (CST), macular volume (MV), % of change from baseline in CST, occurrence of a CST change < 10%, a CST change >20%, and a CST <330 µm, achieving an improvement ≥2 lines of visual acuity, achieving visual acuity ≥20/40.
A significant improvement in CST and visual acuity was seen from third month onwards. Twenty-eight (48.1%) cases were classified as "early responders," 24 (35.8%) as "late responders", and 15 (22.4%) as "poor responders." Serum vascular endothelial growth factor-A levels were significantly lower in "poor responders" (P = 0.006). C-reactive protein (hsCRP) was associated with a limited anatomic response (<10% CST change) (P = 0.002, OR = 1.845, cutoff value of hsCRP = 1.84 mg/L). hsCRP was also negatively associated with obtaining a final CST <330 µm (P = 0.04, r2 = 0.112, OR = 0.643). Baseline visual acuity was significantly associated with 12th month visual acuity (P < 0.001, r2 = 0.602) and also with an improvement ≥2 visual acuity lines (P = 0.009, OR = 20.54).
Increased high-sensitivity C-reactive protein was associated with limited anatomic response to anti-vascular endothelial growth factor treatment and persistent DME. Poor responders had significantly lower values of serum vascular endothelial growth factor-A, suggesting an alternative pathogenic pathway for persisting DME.
研究血清生物标志物作为抗血管内皮生长因子注射治疗糖尿病黄斑水肿(DME)的定性和定量反应的预后因素的作用。
67 只患有 DME 的眼睛在 12 个月的随访期间接受了玻璃体内贝伐单抗治疗。所有病例均进行了基线检查,包括 12 种炎症、代谢和促血栓形成因子。在 3 个月的间隔内评估以下结果,直到 1 年的随访期:视力、中央视网膜厚度(CST)、黄斑体积(MV)、CST 从基线的变化百分比、CST 变化<10%、CST 变化>20%和 CST<330μm,视力提高≥2 行,视力≥20/40。
从第三个月开始,CST 和视力均有显著改善。28 例(48.1%)病例被归类为“早期反应者”,24 例(35.8%)为“晚期反应者”,15 例(22.4%)为“反应不佳者”。“反应不佳者”血清血管内皮生长因子-A 水平显著降低(P=0.006)。C 反应蛋白(hsCRP)与有限的解剖反应(<10%的 CST 变化)相关(P=0.002,OR=1.845,hsCRP 的临界值=1.84mg/L)。hsCRP 也与最终 CST<330μm 呈负相关(P=0.04,r2=0.112,OR=0.643)。基线视力与 12 个月视力显著相关(P<0.001,r2=0.602),也与视力提高≥2 行相关(P=0.009,OR=20.54)。
高敏 C 反应蛋白增加与抗血管内皮生长因子治疗的解剖反应有限和持续的 DME 相关。“反应不佳者”血清血管内皮生长因子-A 值显著降低,提示持续 DME 的另一种致病途径。