Shiley Eye Institute, University of California, San Diego, La Jolla, Caifornia, USA; Beijing Tongren Eye Center, Beijing Institute of Ophthalmology, Beijing Tongren Hospital, Capital Medical University, Beijing, China.
Shiley Eye Institute, University of California, San Diego, La Jolla, Caifornia, USA.
Am J Ophthalmol. 2020 Jul;215:112-117. doi: 10.1016/j.ajo.2020.02.010. Epub 2020 Feb 20.
To test the hypothesis that the correlation between office-hour intraocular pressure (IOP) and peak nocturnal IOP is weakened after using a prostaglandin analog.
Before-and-after study.
Twenty-four-hour IOP data obtained in a sleep laboratory of 51 patients (22 patients with open-angle glaucoma and 29 patients with ocular hypertension) were reviewed. Patients had no IOP-lowering medication upon study entry and were then treated with prostaglandin monotherapy for 4 weeks. Measurements of IOP were taken every 2 hours in the sitting and supine positions during the diurnal/wake period (7:30 AM-9:30 PM) and in the supine position during the nocturnal/sleep period (11:30 PM-5:30 AM). Individual and average IOP readings during office hours (9:30 AM-3:30 PM) and peak IOP during the nocturnal/sleep hours were analyzed using the Pearson correlation coefficient and linear regression.
There were statistically significant correlations for all the paired variables for the analyses. Average office-hour IOP had a higher correlation with peak nocturnal IOP than individual office-hour IOP. After the treatment with prostaglandin analog, the correlation between average office-hour IOP and nocturnal peak IOP in the sitting position (r = 0.373) and the supine position (r = 0.386) were reduced from the sitting baseline (r = 0.517) and the supine baseline (r = 0.573) in right eyes. Similar change patterns appeared in left eyes.
There is a correlation between office-hour IOP reading and peak nocturnal IOP under no IOP-lowering treatment as well as under prostaglandin monotherapy. The strength of correlation was weaker under the treatment compared with baseline.
检验假设,即在使用前列腺素类似物后,诊室眼压(IOP)与夜间眼压峰值之间的相关性会减弱。
前后对照研究。
回顾了 51 例患者(22 例开角型青光眼患者和 29 例高眼压症患者)在睡眠实验室中 24 小时眼压数据。患者在研究开始时未使用任何降低眼压的药物,然后接受前列腺素单一疗法治疗 4 周。在白天/清醒期(7:30 AM-9:30 PM),患者取坐位和仰卧位,每 2 小时测量一次眼压;在夜间/睡眠期(11:30 PM-5:30 AM),患者取仰卧位测量眼压。分析白天(9:30 AM-3:30 PM)诊室眼压的个体和平均读数以及夜间/睡眠期间的眼压峰值,采用 Pearson 相关系数和线性回归分析。
所有配对变量的分析均显示有统计学意义的相关性。平均诊室眼压与夜间眼压峰值的相关性高于个体诊室眼压。在使用前列腺素类似物治疗后,右眼前、后位平均诊室眼压与夜间眼压峰值的相关性(r=0.373 和 r=0.386)较前位(r=0.517 和 r=0.573)有所降低。左眼也出现了类似的变化模式。
在未接受任何降眼压治疗以及接受前列腺素单一疗法的情况下,诊室眼压读数与夜间眼压峰值之间存在相关性。与基线相比,治疗后的相关性较弱。