From the Department of Ophthalmology, Mayo Clinic, Rochester, Minnesota, USA.
Department of Ophthalmology, Duke University, Durham, North Carolina, USA.
Am J Ophthalmol. 2021 Jun;226:262-269. doi: 10.1016/j.ajo.2021.01.019. Epub 2021 Jan 29.
Intraocular pressure (IOP) reduction is key to controlling primary open angle glaucoma (POAG). Pharmacotherapies for POAG or ocular hypertension (OHT) commonly lower IOP by increasing uveoscleral outflow or decreasing aqueous humor production. Netarsudil (Rhopressa), a Rho kinase inhibitor, reduces IOP by improving trabecular outflow facility, which is reduced in POAG. We investigated the effects of netarsudil on aqueous humor dynamics in patients with POAG or OHT.
Double-masked, randomized, vehicle-controlled, Phase 2 trial.
Netarsudil 0.02% was instilled in 1 eye and vehicle into the contralateral eye of 20 patients once daily in the morning for 7 days. The primary endpoint was change in mean diurnal outflow facility on day 8 versus that on day 1 (baseline). Outflow facility was measured by using Schiøtz tonography, IOP by pneumotonometry, and episcleral venous pressure (EVP) by automated venomanometry.
Eighteen patients (90%) completed the study. Mean diurnal outflow facility increased 0.039 versus 0.007 µL/min/mm Hg from baseline in the netarsudil- and the vehicle-treated groups, respectively (P < .001 vs. baseline for netarsudil), a treatment difference of 0.03 µL/min/mm Hg (P ≤ .001). Mean diurnal IOP change from baseline at day 8 was -4.52 mm Hg for netarsudil versus -0.98 mm Hg for vehicle, a treatment difference of -3.54 mm Hg (P < .0001). Mean diurnal EVP change from baseline was -0.79 mm Hg in the netarsudil-treated group versus 0.10 mm Hg for vehicle, a treatment difference of -0.89 mm Hg (P < .001). All patients reporting an adverse event reported conjunctival hyperemia of mild or moderate severity.
Netarsudil acts on the conventional outflow pathway, both proximal and distal, to significantly reduce IOP in POAG and OHT by improving trabecular outflow facility and decreasing EVP.
眼压(IOP)降低是控制原发性开角型青光眼(POAG)的关键。用于 POAG 或高眼压(OHT)的药物治疗通常通过增加葡萄膜巩膜流出或减少房水生成来降低 IOP。Rhopressa(奈塔舒地尔)是一种 Rho 激酶抑制剂,通过改善小梁流出道通畅度来降低 IOP,而 POAG 患者的小梁流出道通畅度会降低。我们研究了奈塔舒地尔对 POAG 或 OHT 患者房水动力学的影响。
双盲、随机、对照、2 期试验。
在 7 天的早晨,20 名患者每天将奈塔舒地尔 0.02%滴入一只眼,将载体滴入对侧眼。主要终点是第 8 天与第 1 天(基线)相比平均日间流出道通畅度的变化。通过 Schiøtz 眼压描记法测量流出道通畅度,通过气动眼压测量法测量 IOP,通过自动静脉压测量法测量巩膜静脉压(EVP)。
18 名患者(90%)完成了研究。奈塔舒地尔组和载体组的平均日间流出道通畅度分别增加了 0.039 和 0.007 µL/min/mm Hg(与基线相比,P <.001),治疗差异为 0.03 µL/min/mm Hg(P ≤.001)。奈塔舒地尔组第 8 天与基线相比的平均日间 IOP 变化为-4.52mmHg,而载体组为-0.98mmHg,治疗差异为-3.54mmHg(P <.0001)。奈塔舒地尔组与基线相比的平均日间 EVP 变化为-0.79mmHg,而载体组为 0.10mmHg,治疗差异为-0.89mmHg(P <.001)。所有报告不良反应的患者均报告结膜轻度或中度充血。
奈塔舒地尔作用于传统的流出途径,包括近端和远端,通过改善小梁流出道通畅度和降低 EVP,显著降低 POAG 和 OHT 的眼压。