Shahsuvaryan Marianne L
Yerevan State Medical University, Republic of Armenia.
Med Hypothesis Discov Innov Ophthalmol. 2022 Apr 1;11(1):34-41. doi: 10.51329/mehdiophthal1443. eCollection 2022 Spring.
Macular edema (ME) is a vision-threatening condition that commonly develops as a consequence of ocular diseases, including age-related macular degeneration, retinal vaso-occlusion of the central retinal vein and its branches, diabetic retinopathy, central serous chorioretinopathy, uveitis, retinitis pigmentosa, pseudophakia, ocular trauma, and drug toxicity. The treatment of ME remains challenging, although steroids and vascular endothelial growth factor inhibitors are available. Cost-effective therapy using a noninvasive administration route is required. This study aimed at reviewing the role of carbonic anhydrase inhibitors (CAIs) in the management of ME.
A literature search was conducted using PubMed/MEDLINE and Google Scholar for studies from January 2000 to March 2022. The following keywords were used in various combinations: "macular edema", "carbonic anhydrase", "carbonic anhydrase inhibitors", "acetazolamide", "dorzolamide", and "brinzolamide".
Articles with high or medium clinical relevance were selected for this review. We found that multiple studies have demonstrated the relevance and efficacy rates of CAIs in the management of ME. Most published studies focused on acetazolamide and dorzolamide, with nearly all studies reporting therapeutic responses.
ME is the leading cause of vision loss and requires noninvasive and cost-effective pharmacotherapy. With progress in the understanding of ME, particularly the role of carbonic anhydrase as a key driver, CAIs are the focus of research. Further optimization of the choice of CAIs and retinal bioavailability, potentially with nanoparticle formulations, is required to enable the effective management of ME. Further research is warranted to address the therapeutic effects of CAIs in different formulations.
黄斑水肿(ME)是一种威胁视力的疾病,通常由眼部疾病引起,包括年龄相关性黄斑变性、视网膜中央静脉及其分支的视网膜血管阻塞、糖尿病性视网膜病变、中心性浆液性脉络膜视网膜病变、葡萄膜炎、色素性视网膜炎、人工晶状体眼、眼外伤和药物毒性。尽管有类固醇和血管内皮生长因子抑制剂,但ME的治疗仍然具有挑战性。需要一种使用非侵入性给药途径的具有成本效益的治疗方法。本研究旨在综述碳酸酐酶抑制剂(CAIs)在ME治疗中的作用。
使用PubMed/MEDLINE和谷歌学术对2000年1月至2022年3月的研究进行文献检索。以下关键词以各种组合方式使用:“黄斑水肿”、“碳酸酐酶”、“碳酸酐酶抑制剂”、“乙酰唑胺”、“多佐胺”和“布林佐胺”。
选择具有高或中等临床相关性的文章进行本综述。我们发现多项研究已经证明了CAIs在ME治疗中的相关性和有效率。大多数已发表的研究集中在乙酰唑胺和多佐胺上,几乎所有研究都报告了治疗反应。
ME是视力丧失的主要原因,需要非侵入性且具有成本效益的药物治疗。随着对ME认识的进展,特别是碳酸酐酶作为关键驱动因素的作用,CAIs成为研究的焦点。需要进一步优化CAIs的选择和视网膜生物利用度,可能采用纳米颗粒制剂,以实现对ME的有效管理。有必要进行进一步的研究以探讨不同制剂中CAIs的治疗效果。