Takeyama Masayuki, Takeuchi Fumio, Gosho Masahiko, Sugita Keijiro, Zako Masahiro, Iwaki Masayoshi, Kamei Motohiro
Department of Ophthalmology, Aichi Medical University, Nagakute.
Department of Biochemistry, Aichi Medical University, Nagakute.
Clin Ophthalmol. 2017 Dec 20;12:35-41. doi: 10.2147/OPTH.S149935. eCollection 2018.
Tranexamic acid (TXA) is a widely used antifibrinolytic agent that can also cause a decrease in vascular permeability. We hypothesized that TXA could improve macular edema (ME) that is caused by an increase in retinal vascular permeability. The aim of this study is to evaluate the efficacy of oral TXA for ME associated with retinal vein occlusion (RVO) or diabetic ME (DME).
Oral TXA (1,500 mg daily for 2 weeks) was administered to patients with persistent ME secondary to RVO (7 eyes) and DME (7 eyes). After 2 weeks (ie, the final day of administration) and 6 weeks (ie, 4 weeks after the final administration), best-corrected visual acuity and central macular thickness (CMT) were measured and compared with baseline. Analyses were performed for RVO and DME cases. No other treatment was performed during the study period.
In RVO cases, significant improvement in CMT was found between baseline (467.7±121.4 μm) and 2-week measurements after treatment (428.7±110.5 μm, =0.024). No significant change was found in CMT between measurements taken at baseline and 6 weeks after treatment. In DME cases, no significant change was found in CMT between measurements taken at baseline and 2 or 6 weeks after treatment. In all analyses of best-corrected visual acuity, no significant change was observed.
The results support the hypothesis that plasmin plays a role in the development of ME associated with RVO, and oral TXA administration may be useful as an adjuvant treatment when combined with other agents such as anti-vascular endothelial growth factor.
氨甲环酸(TXA)是一种广泛使用的抗纤溶药物,它也可导致血管通透性降低。我们推测TXA可以改善由视网膜血管通透性增加引起的黄斑水肿(ME)。本研究的目的是评估口服TXA治疗与视网膜静脉阻塞(RVO)或糖尿病性黄斑水肿(DME)相关的ME的疗效。
对继发于RVO(7只眼)和DME(7只眼)的持续性ME患者给予口服TXA(每日1500mg,共2周)。在2周(即给药最后一天)和6周(即最后一次给药后4周)时,测量最佳矫正视力和中心黄斑厚度(CMT),并与基线进行比较。对RVO和DME病例进行分析。研究期间未进行其他治疗。
在RVO病例中,治疗后2周测量时CMT较基线(467.7±121.4μm)有显著改善(428.7±110.5μm,P = 0.024)。治疗后基线和6周测量时CMT无显著变化。在DME病例中,治疗后基线与2周或6周测量时CMT无显著变化。在所有最佳矫正视力分析中,未观察到显著变化。
结果支持纤溶酶在与RVO相关的ME发生中起作用的假设,口服TXA联合抗血管内皮生长因子等其他药物作为辅助治疗可能有用。