Age-related differences in corneal nerve regeneration after SMILE and the mechanism revealed by metabolomics

再生(生物学) 机制(生物学) 代谢组学 生物 细胞生物学 生物信息学 物理 量子力学
作者
Min Li,Lin Liu,Yuehui Shi,Lina Sun,Xiaoyun Ma,Jun Zou
出处
期刊:Experimental Eye Research [Elsevier BV]
卷期号:209: 108665-108665 被引量:14
标识
DOI:10.1016/j.exer.2021.108665
摘要

To investigate the effect of age on wound healing after small incision lenticule extraction (SMILE) and the underlying metabolomic mechanisms. This prospective study was conducted on 216 patients in four groups: the 18–20 (n = 38, Group I), 21–30 (n = 84, Group Ⅱ), 31–40 (n = 58, Group Ⅲ), and 41–50 (n = 36, Group IV) age groups. The density of corneal epithelial wing cells, basal cells, corneal stromal cells, endothelial cells and corneal nerves were examined with a laser confocal microscope (HRT III-RCM) before and 1 month, 3 month, 6 month and 1 year after SMILE. The central nerve fiber length (CNFL), the central corneal nerve fibre density (CNFD), and the central corneal nerve branch density (CNBD) were analyzed by Nero J. The corneal stroma lenticules were obtained from SMILE to analyze metabolites by high-performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry (HPLC-QTOF-MS). The density of corneal wing epithelial cells and basal epithelial cells have no significant difference among the four groups. The CNFL was 21.90 ± 1.68 mm/mm2 in Group Ⅰ and 21.63 ± 2.09 mm/mm2 in Group Ⅱ after 1 year of SMILE, which represented a return to the preoperative level, whereas the CNFL of Group Ⅲ (19.40 ± 0.98 mm/mm2) and Group Ⅳ (18.94 ± 0.72 mm/mm2) were lower than that preoperation (P ˂0.01). CNFL repair had a negative correlation with age after surgery (Pearson's R = −0.572, P ˂0.01). The CNFD and the CNBD showed the same trend with the CNFL (Pearson's R = −0.602 and −0.531, P ˂0.05). Through screening the significantly different metabolites between the 18–30 age group (including Group I and Group Ⅱ) and other two groups, 6 common remarkably different metabolites were identified. Meanwhile, 5 unique different metabolites were identified only between the 18–30 age group and the 31–40 age group. Six unique different metabolites were identified only between the 18–30 age group and the 41–50 age group. Corneal nerve repair after SMILE was significantly affected by age. The identified age-associated differences in metabolites were mainly related to inflammation, oxidation, nerve protection and regeneration.
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