Ma Xiao-Hua, Li Jing-Hai, Bi Hong-Sheng, Zhou Fang, Li Yan
Jinan Shierming Ophthalmology Hospital, Jinan 250001, China.
Zhonghua Yan Ke Za Zhi. 2003 Mar;39(3):140-5.
To compare effects of photorefractive keratectomy (PRK) and laser in situ keratomileusis (LASIK) on the cornea and corneal wound healing and to investigate the possible mechanism of corneal haze and myopic regression histopathologically.
Twenty-four New Zealand white rabbits were allocated randomly to correct -4.00 and -8.00 diopters and were operated with PRK on right eyes and LASIK on left eyes. At 10 days and 1, 3, and 6 months, corneal haze was observed, refraction was evaluated, and 3 rabbits were randomly selected for each time point to be enucleated, and corneas to be bisected. One half of each cornea was evaluated using transmission electron microscopy, and the other half was evaluated using either light microscopy or immunohistochemical staining for collagen type III, IV, fibronectin (FN) and transforming growth factor-beta(1) (TGF-beta(1)).
Different degrees of corneal haze and myopic regression were observed after PRK: the higher the desired myopic correction, the heavier the haze. Corneal wound healing response was greater and lasted longer after PRK than after LASIK. Various pathological findings such as epithelial hyperplasia, basal membrane reforming and extracellular matrix deposits were found in the ablation zone and repair mechanisms were still active at 6 months after PRK. Whereas after LASIK, the interface between the flap and stromal bed was transparent except for growing epithelial plugs and lightly proliferating stroma coinciding with the flap margins. After both PRK and LASIK, all corneal cell types were consistently positive for TGF-beta(1) antibody during the corneal wound healing time. TGF-beta(1) antibody positivity decreased as the wound healing approached completion. The histopathological changes of corneal haze and myopic regression are as follows: epithelial hyperplasia, basal membrane immaturity, anterior stromal keratocyte increase and activity, new collagen III production and irregular arrangement thereof, and FN deposition in the extracellular matrix under the epithelium.
Compared with PRK, LASIK ensures refractive stability with quick wound healing and minimal tissue proliferation resulting in a more promising corneal refractive surgery to correct myopia, especially more severe cases of myopia. The corneal wound healing especially the stromal healing is the key to the cause of haze and myopic regression. TGF-beta(1) may be involved in scar formation during wound healing by stimulating expression of collagen III and FN and is believed to be an important regulating factor.
比较准分子激光角膜切削术(PRK)和准分子激光原位角膜磨镶术(LASIK)对角膜及角膜伤口愈合的影响,并从组织病理学角度研究角膜 haze 和近视回退的可能机制。
将 24 只新西兰白兔随机分为两组,分别矫正 -4.00 和 -8.00 屈光度,右眼行 PRK 手术,左眼行 LASIK 手术。在术后 10 天、1、3 和 6 个月,观察角膜 haze,评估屈光状态,每个时间点随机选取 3 只兔子摘除眼球,将角膜对半切开。一半角膜用透射电子显微镜评估,另一半用光学显微镜或免疫组织化学染色评估Ⅲ型、Ⅳ型胶原、纤连蛋白(FN)和转化生长因子 -β(1)(TGF-β(1))。
PRK 术后观察到不同程度的角膜 haze 和近视回退:预期近视矫正度数越高,haze 越重。PRK 术后角膜伤口愈合反应比 LASIK 更大且持续时间更长。PRK 术后 6 个月,在消融区发现各种病理改变,如上皮增生、基底膜重塑和细胞外基质沉积,修复机制仍活跃。而 LASIK 术后,除了生长的上皮栓和与瓣边缘一致的轻度增生基质外,瓣与基质床之间的界面是透明的。PRK 和 LASIK 术后,在角膜伤口愈合期间,所有角膜细胞类型对 TGF-β(1)抗体均持续呈阳性。随着伤口愈合接近完成,TGF-β(1)抗体阳性率降低。角膜 haze 和近视回退的组织病理学变化如下:上皮增生、基底膜不成熟、前基质角膜细胞增多和活性增强、新的Ⅲ型胶原产生及其排列不规则,以及上皮下细胞外基质中 FN 沉积。
与 PRK 相比,LASIK 确保屈光稳定性,伤口愈合快,组织增殖少,是一种更有前景的矫正近视的角膜屈光手术,尤其适用于更严重的近视病例。角膜伤口愈合尤其是基质愈合是 haze 和近视回退的关键原因。TGF-β(1)可能通过刺激Ⅲ型胶原和 FN 的表达参与伤口愈合过程中的瘢痕形成,被认为是一个重要的调节因子。