Department of Ophthalmology, Taipei Veterans General Hospital, Taipei 112, Taiwan.
School of Medicine, National Yang-Ming University, Taipei 112, Taiwan.
Biomolecules. 2020 Oct 6;10(10):1414. doi: 10.3390/biom10101414.
Retinal vein occlusions (RVO) are associated with systemic risk factors. However, the ocular occlusive events might also influence a patient's systemic condition. This study tried to investigate serum biomarkers associated with oxidative stress, before and after intravitreal anti-vascular endothelial growth factor (aVEGF) therapy in patients with RVOs.
Newly-onset RVO patients were categorized into two groups: comorbid with macular edema requiring aVEGF therapy (treatment group) and no edema (observation group). Age and sex-matched patients (who received cataract surgery) were included as the control group. Intravitreal ranibizumab with a pro-re-nata regimen were administered. Serum samples were collected prior to treatment, at 6 and 12 months after therapy/observation and were collected once before controls who received cataract surgery. mRNA expression of sirtuin-1, its downstream genes, anti-oxidative biomarkers, and proinflammatory cytokines were measured.
There were 32, 26, and 34 patients enrolled in the treatment, observation, and control groups, respectively. The expressions of sirtuin-1 and its downstream genes were significantly lower in patients with RVO compared with the control group. Sirtuin-1 gene expression increased after 1 year of aVEGF therapy in the treatment group but remained unchanged in the observation group. Biomarkers of oxidative stress and proinflammatory cytokines were reduced after 1 year of aVEGF therapy. These biomarkers remained with no changes in the observation group.
Our study showed that the systemic oxidative stress increased in RVO patients. The aVEGF therapy could alter the gene expression of anti-oxidative proteins and reduce systemic oxidative stress in these patients.
视网膜静脉阻塞(RVO)与全身危险因素有关。然而,眼部闭塞事件也可能影响患者的全身状况。本研究试图在 RVO 患者中,在接受玻璃体内抗血管内皮生长因子(aVEGF)治疗前后,调查与氧化应激相关的血清生物标志物。
将新发 RVO 患者分为两组:伴有需要 aVEGF 治疗的黄斑水肿(治疗组)和无水肿(观察组)。还纳入了年龄和性别匹配的接受白内障手术的患者作为对照组。给予玻璃体内雷珠单抗,采用 pro-re-nata 方案。在治疗前、治疗/观察后 6 个月和 12 个月采集血清样本,并在接受白内障手术的对照组中采集一次。测量了 SIRT1 及其下游基因、抗氧化生物标志物和促炎细胞因子的 mRNA 表达。
治疗组、观察组和对照组分别纳入 32、26 和 34 例患者。与对照组相比,RVO 患者的 SIRT1 及其下游基因表达明显降低。治疗组接受 aVEGF 治疗 1 年后 Sirtuin-1 基因表达增加,但观察组无变化。接受 aVEGF 治疗 1 年后,氧化应激和促炎细胞因子的生物标志物减少,观察组无变化。
本研究表明,RVO 患者全身氧化应激增加。aVEGF 治疗可以改变抗氧化蛋白的基因表达,减轻这些患者的全身氧化应激。