Toris Carol B, Zhan Guilin, Camras Carl B
Department of Ophthalmology, University of Nebraska Medical Center, Omaha 68198-5840, USA.
Arch Ophthalmol. 2004 Dec;122(12):1782-7. doi: 10.1001/archopht.122.12.1782.
To determine the mechanism by which 0.15% unoprostone isopropyl reduces intraocular pressure (IOP) by studying 33 patients with ocular hypertension or primary open-angle glaucoma.
At baseline, IOP was determined by pneumatonometry, aqueous flow and outflow facility by fluorophotometry, episcleral venous pressure by venomanometry, and uveoscleral outflow by mathematical calculation. Unoprostone was administered to one eye and placebo to the fellow eye of each patient twice daily in a randomized masked fashion. In patients who demonstrated an IOP reduction of 3 mm Hg or more in either eye on day 5 +/- 1 (n = 29), determinations were repeated on that day and on day 28 +/- 2. Treated eyes were compared with control eyes, and treatment days were compared with baseline by paired t tests.
Compared with baseline, unoprostone significantly (P<.001) reduced IOP by a mean +/- SEM of 5.6 +/- 0.4 mm Hg and 4.8 +/- 0.6 mm Hg on days 5 and 28, respectively. The change from baseline with unoprostone was significantly (P<.001) greater than with placebo by 2.8 +/- 0.4 mm Hg on day 5 and by 3.2 +/- 0.5 mm Hg on day 28. Compared with baseline, unoprostone significantly (P</=.001) increased outflow facility by 0.05 +/- 0.01 and 0.08 +/- 0.02 microL.min(-1).mm Hg(-1) on days 5 and 28, respectively. The baseline-adjusted between-treatment differences were significant (P</=.04) on day 28 (0.06 +/- 0.02 microL.min(-1).mm Hg(-1)). Other measures were not different from placebo.
In responsive patients, unoprostone decreased IOP by increasing outflow facility.
通过研究33例高眼压症或原发性开角型青光眼患者,确定0.15%异丙前列素降低眼压(IOP)的机制。
在基线时,通过眼压计测量眼压,荧光光度法测量房水流量和流出易度,静脉压力计测量巩膜静脉压,并通过数学计算测量葡萄膜巩膜流出量。以随机双盲方式,给每位患者的一只眼每日两次滴用异丙前列素,另一只眼滴用安慰剂。在第5±1天,若任一眼中眼压降低3 mmHg或更多的患者(n = 29),在当天及第28±2天重复测量。将治疗眼与对照眼进行比较,并通过配对t检验将治疗日与基线进行比较。
与基线相比,异丙前列素在第5天和第28天分别显著(P<.001)降低眼压,平均±标准误分别为5.6±0.4 mmHg和4.8±0.6 mmHg。在第5天,异丙前列素与基线相比的变化比安慰剂显著(P<.001)大2.8±0.4 mmHg,在第28天大3.2±0.5 mmHg。与基线相比,异丙前列素在第5天和第28天分别显著(P≤.001)增加流出易度,分别为0.05±0.01和0.08±0.02 μL·min⁻¹·mmHg⁻¹。在第28天,基线调整后的治疗组间差异显著(P≤.04)(0.06±0.02 μL·min⁻¹·mmHg⁻¹)。其他指标与安慰剂无差异。
在有反应的患者中,异丙前列素通过增加流出易度降低眼压。