Padmanabhan Nair Archana, Machiraju Praveen, Tejwani Sushma, Dinakaran Shoruba, A V Sathi Devi, Shetty Naren, Shetty Rohit, Ghosh Arkasubhra, Sethu Swaminathan
GROW Research Lab, Narayana Netralaya Foundation, Bangalore, India.
Manipal Academy of Higher Education, Manipal, India.
J Ocul Pharmacol Ther. 2025 Sep;41(7):408-417. doi: 10.1089/jop.2025.0085. Epub 2025 Jun 9.
Glaucoma, a neurodegenerative condition of the optic nerve is driven by increased intraocular pressure (IOP) due to fibrotic changes of the trabecular meshwork (TM). Interferon beta (IFN-β), a pleiotropic cytokine is known for its neuroprotective and antifibrotic potential. Hence, we investigated the intraocular status of IFN-β in patients with primary glaucoma. Aqueous humor (AqH) from patients with primary glaucoma [107 eyes; primary open-angle glaucoma (POAG), 59 eyes; primary angle-closure glaucoma (PACG), 48 eyes] and controls (70 eyes) were collected during cataract surgery and/or trabeculectomy. TM from patients with POAG (20 eyes) and PACG (18 eyes) was collected during trabeculectomy. IFN-β in AqH was measured using bead-based Enzyme-Linked Immunosorbent Assay (ELISA), and messenger RNA (mRNA) expression of IFN-β in TM was measured by quantitative PCR. AqH-IFN-β levels were significantly ( < 0.05) lower in patients with glaucoma, particularly in patients with POAG compared with controls (area under the receiver operating characteristic curve = 0.723, < 0.001; odds ratio of 5.1, < 0.0001). AqH-IFN-β levels correlated positively with visual field index of both patients with POAG ( = 0.307; = 0.0321) and PACG ( = 0.518; P = 0.0007). Whereas, AqH-IFN-β levels correlated positively with retinal nerve fiber layer thickness in patients with POAG ( = 0.460; = 0.0042) only. TM-IFN-β mRNA expression was significantly lower in glaucoma patients with poor IOP control compared with those with good IOP control by IOP-lowering medications. Lower IFN-β in AqH and TM of patients with glaucoma and its association with clinical indices suggests its neuroprotective and antifibrotic role in glaucoma. The findings highlight the potential for IFN-β-based prognostication and therapy in the management of glaucoma.
青光眼是一种视神经的神经退行性疾病,由小梁网(TM)纤维化改变导致眼内压(IOP)升高引起。干扰素β(IFN-β)是一种多效细胞因子,以其神经保护和抗纤维化潜力而闻名。因此,我们研究了原发性青光眼患者眼内IFN-β的状况。在白内障手术和/或小梁切除术期间,收集了原发性青光眼患者[107只眼;原发性开角型青光眼(POAG),59只眼;原发性闭角型青光眼(PACG),48只眼]和对照组(70只眼)的房水(AqH)。在小梁切除术期间收集了POAG患者(20只眼)和PACG患者(18只眼)的TM。使用基于磁珠的酶联免疫吸附测定(ELISA)测量AqH中的IFN-β,并通过定量PCR测量TM中IFN-β的信使核糖核酸(mRNA)表达。与对照组相比,青光眼患者,特别是POAG患者的AqH-IFN-β水平显著降低(<0.05)(受试者操作特征曲线下面积=0.723,<0.001;优势比为5.1,<0.0001)。POAG患者(=0.307;=0.0321)和PACG患者(=0.518;P=0.0007)的AqH-IFN-β水平与视野指数呈正相关。而仅POAG患者的AqH-IFN-β水平与视网膜神经纤维层厚度呈正相关(=0.460;=0.0042)。与通过降低眼压药物实现良好眼压控制的青光眼患者相比,眼压控制不佳的青光眼患者TM-IFN-β mRNA表达显著降低。青光眼患者AqH和TM中IFN-β水平较低及其与临床指标的关联表明其在青光眼中具有神经保护和抗纤维化作用。这些发现突出了基于IFN-β的预后评估和治疗在青光眼管理中的潜力。