Paiva Alexandre de Carvalho Mendes, da Fonseca Adenilson de Souza
Departamento de Ciências Fisiológicas, Instituto Biomédico, Universidade Federal do Estado do Rio de Janeiro, Rua Frei Caneca, 94, Centro, Rio de Janeiro, 20211040, Brazil.
Departamento de Biofísica e Biometria, Instituto de Biologia Roberto Alcantara Gomes, Universidade do Estado do Rio de Janeiro, Boulevard Vinte e Oito de Setembro, 87 fundos, 4º andar, Vila Isabel, Rio de Janeiro, 20551030, Brazil.
Int Ophthalmol. 2019 Jan;39(1):243-257. doi: 10.1007/s10792-017-0775-0. Epub 2017 Nov 30.
Selective laser trabeculoplasty (SLT) has been used for treatment of primary open-angle glaucoma, ocular hypertension, pigmenter and pseudoexfoliative glaucoma being considered a low-risk procedure. Therefore, transitory and permanent adverse effects have been reported, including corneal changes, subclinical edema, and reduction in endothelial cells and in central corneal thickness. Despite rarer, serious corneal complications after SLT can be permanent and lead to visual impairment, central corneal haze, opacity and narrowing. The mechanism involves increase of vasoactive and chemotactic cytokines causing inflammatory infiltrate, destruction of stromal collagen by fibroblasts and increase of matrix metalloproteinases type 2, which impair reepithelization. SLT also increases free radical production and reduces antioxidant enzymes, resulting in endothelium damages. Low-power laser therapy (LPLT) has been used in regenerative medicine based on its biostimulatory and anti-inflammatory effects. Biostimulation occurs through the interaction of laser photons with cytochrome C oxidase enzyme, which activates intracellular biochemical cascades causing synthesis of a number of molecules related to anti-inflammatory, regenerative effects, pain relief and reduction in edema. It has been showed that LPLT reduces gene expression related to pro-inflammatory cytokines and matrix metalloproteinases, and it increases expression of growth factors related to its proliferative and healing actions. Although radiations emitted by low-power lasers are considered safe and able to induce therapeutic effects, researches based on experimental models for glaucoma could bring important data if LPLT could be an alternative approach to improve acceptation for patients undergoing SLT.
选择性激光小梁成形术(SLT)已被用于治疗原发性开角型青光眼、高眼压症、色素性青光眼和假性剥脱性青光眼,被认为是一种低风险手术。因此,已报道了短暂和永久性的不良反应,包括角膜变化、亚临床水肿以及内皮细胞和中央角膜厚度的减少。尽管较少见,但SLT术后严重的角膜并发症可能是永久性的,并导致视力损害、中央角膜混浊、opacity和狭窄。其机制包括血管活性和趋化细胞因子增加导致炎症浸润、成纤维细胞破坏基质胶原蛋白以及2型基质金属蛋白酶增加,从而损害上皮再形成。SLT还会增加自由基产生并减少抗氧化酶,导致内皮损伤。低功率激光疗法(LPLT)基于其生物刺激和抗炎作用已被用于再生医学。生物刺激通过激光光子与细胞色素C氧化酶的相互作用发生,激活细胞内生化级联反应,导致合成许多与抗炎、再生作用、疼痛缓解和水肿减轻相关的分子。研究表明,LPLT可降低与促炎细胞因子和基质金属蛋白酶相关的基因表达,并增加与其增殖和愈合作用相关的生长因子的表达。尽管低功率激光发出的辐射被认为是安全的且能够诱导治疗效果,但如果LPLT可以作为一种替代方法来提高接受SLT治疗患者的接受度,基于青光眼实验模型的研究可能会带来重要数据。