小切口晶状体摘除(SMILE)与微角膜切除术获得角膜晶状体的组织病理学比较。

IF 1.6 Q3 OPHTHALMOLOGY Journal of Ophthalmic & Vision Research Pub Date : 2023-01-01 DOI:10.18502/jovr.v18i1.12722
Salwa Abdelkawi Ahmed, Ibrahim Mohi Eldin Taher, Dina Fouad Ghoneim, Mohammed Ahmed Elnaggar, Aziza Ahmed Hassan
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引用次数: 0

摘要

目的:研究飞秒(Femto)小切口晶状体摘除术(SMILE)与微角膜刀摘除角膜游离帽术后晶状体的差异。方法:visuMax (500 kHz;激光能量:180 nJ)用于小切口晶状体提取。用微角刀切除人尸体角膜游离帽。采用光镜和透射电子显微镜(TEM)对采集的角膜小透镜进行组织学分析,琼脂糖凝胶电泳评估DNA片段,彗星法评估DNA损伤,傅里叶变换红外光谱(FTIR)评估角膜蛋白二级结构。结果:光镜检查显示,Femto SMILE下比自由帽下有更多的水肿间质,变化率为101.6%。在Femto SMILE组中,TEM检查显示Femto SMILE下的角质细胞固缩,胶原阵列间质区破裂和空化。Femto SMILE组的DNA片段显示一个大小为1.1 Kbp的未定义条带。彗星分析显示,free cap组和Femto SMILE组的尾细胞分别为3%和8.0%。自由帽组和Femto SMILE组尾长分别为1.33±0.16和1.67±0.13µm (P < 0.01),尾DNA百分比分别为1.41±0.18% (P < 0.01)和1.72±0.15%,尾瞬间分别为1.88±0.12 AU和2.87±0.14 AU (P < 0.001)。Femto smile组的FTIR光谱显示蛋白质的二级和三级结构紊乱。结论:Femto SMILE技术诱导的角膜结构改变、DNA断裂、DNA损伤和角膜蛋白二级结构改变明显高于微角膜切割。这些变化可能归因于高能级对角膜层的深穿透。这些发现可能会突出Femto SMILE对角膜的潜在影响以及管理使用的激光参数的必要性。
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Histopathology of Corneal Lenticules Obtained from Small Incision Lenticule Extraction (SMILE) versus Microkeratome Excision.

Purpose: To study the alterations on the lenticules extracted after femtosecond (Femto) small incision lenticule extraction (SMILE) versus the corneal free cap removed using a microkeratome.

Methods: The visuMax (500 kHz; laser energy: 180 nJ) was used for small-incision lenticule extraction. Free caps from human cadaveric corneas were excised by microkeratome. The collected lenticules were examined with the light and transmission electron microscope (TEM) for histological analysis, DNA fragmentation was assessed by agarose gel electrophoresis, DNA damage was evaluated using comet assay, and corneal proteins secondary structure was assessed by Fourier transform infrared spectroscopy (FTIR).

Results: Light microscopic examination showed the presence of more edematous stroma under Femto SMILE than under free cap with a percentage change of 101.6%. In the Femto SMILE group, TEM examination showed pyknotic keratocytes, disruption, and cavitation of the collagen arrays stromal area under Femto SMILE. The DNA fragmentation for the Femto SMILE group revealed one undefined band with a size of 1.1 Kbp. The comet assay analysis indicated the presence of 3% and 8.0% tailed cells for the free cap and Femto SMILE groups, respectively. The tail lengths were 1.33 ± 0.16 and 1.67 ± 0.13 µm (P < 0.01), the percentage of tail DNA was 1.41 ± 0.18% (P < 0.01) and 1.72 ± 0.15%, and the tail moments were 1.88 ± 0.12 AU and 2.87 ± 0.14 AU (P < 0.001) for the free cap and Femto SMILE groups, respectively. FTIR spectroscopy of the Femto smile group revealed disorders in the secondary and tertiary structure of the proteins.

Conclusion: Femto SMILE technique induced more structural changes, DNA fragmentation, DNA damage, and corneal proteins secondary structure alteration than those induced by a microkeratome cutting. These changes may be attributed to the deep penetration of high energy levels to the corneal layer. These findings may highlight the potential impact of the Femto SMILE on the cornea and the necessity for managing the laser parameters used.

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