Wang Yuliang, Liu Fang, Zhu Xingxue, Liu Yujia, He Ji C, Zhou Xingtao, Qu Xiaomei
Department of Ophthalmology and Vision Science, Eye & ENT Hospital, Fudan University, Shanghai, China.
NHC Key Laboratory of Myopia, Fudan University, Shanghai, China.
Acta Ophthalmol. 2024 Feb;102(1):e69-e77. doi: 10.1111/aos.15679. Epub 2023 May 4.
The morphological changes in the cornea and crystalline lens have not been closely evaluated after the administration of atropine 0.01%. This study aims to evaluate the radii of curvature and refractive power of the cornea and lens in myopic eyes during atropine 0.01% treatment.
Children aged 6-14 years with myopia <-6.0 D were randomized to receive atropine 0.01% once nightly with single vision lenses or simply wear single vision lenses. Ocular biometric parameters were measured using the IOLMaster 700 biometry and the radii of corneal and lenticular curvature were simulated using a customized program.
At the 9-month visit, 69 atropine-treated eyes and 50 control eyes were included in the final analyses. In atropine-treated eyes, the posterior corneal surface steepened (-0.05 ± 0.13 mm) and the anterior lenticular surface flattened (0.20 ± 0.69 mm) significantly within 3-6 months, whereas the posterior corneal surface and anterior lenticular surface gradually flattened (0.07 ± 0.23 and 0.32 ± 0.80 mm respectively) in the control eyes over 9 months. The difference in the change of corneal refractive power was significant between groups (-0.03 ± 0.18 D vs. 0.11 ± 0.24 D, p = 0.001), while that in the change of lenticular refractive power was statistically insignificant (0.01 ± 0.92 D vs. -0.22 ± 0.86 D, p = 0.161).
The administration of atropine 0.01% exhibited a clinically short and subtle impact on the cornea and lens, which may shed light on new targets of action for atropine in inhibiting myopia.
0.01%阿托品给药后角膜和晶状体的形态变化尚未得到密切评估。本研究旨在评估0.01%阿托品治疗期间近视眼的角膜和晶状体曲率半径及屈光力。
将6至14岁近视度数<-6.0 D的儿童随机分为两组,一组每晚使用单光镜片并滴用一次0.01%阿托品,另一组仅佩戴单光镜片。使用IOLMaster 700生物测量仪测量眼部生物测量参数,并使用定制程序模拟角膜和晶状体曲率半径。
在9个月的随访中,最终分析纳入了69只阿托品治疗眼和50只对照眼。在阿托品治疗眼中,角膜后表面在3至6个月内显著变陡(-0.05±0.13 mm),晶状体前表面变平(0.20±0.69 mm),而对照眼在9个月内角膜后表面和晶状体前表面逐渐变平(分别为0.07±0.23和0.32±0.80 mm)。两组间角膜屈光力变化的差异有统计学意义(-0.03±0.18 D vs. 0.11±0.24 D,p = 0.001),而晶状体屈光力变化的差异无统计学意义(0.01±0.92 D vs. -0.22±0.86 D,p = 0.161)。
0.01%阿托品给药对角膜和晶状体的临床影响短暂且细微,这可能为阿托品抑制近视的新作用靶点提供线索。