Current uses of artificial intelligence in the analysis of biofluid markers involved in corneal and ocular surface diseases: a systematic review

Eye (Lond). 2023 Jul;37(10):2007-2019. doi: 10.1038/s41433-022-02307-9. Epub 2022 Nov 15.

Abstract

Corneal and ocular surface diseases (OSDs) carry significant psychosocial and economic burden worldwide. We set out to review the literature on the application of artificial intelligence (AI) and bioinformatics for analysis of biofluid biomarkers in corneal and OSDs and evaluate their utility in clinical decision making. MEDLINE, EMBASE, Cochrane and Web of Science were systematically queried for articles using AI or bioinformatics methodology in corneal and OSDs and examining biofluids from inception to August 2021. In total, 10,264 articles were screened, and 23 articles consisting of 1058 individuals were included. Using various AI/bioinformatics tools, changes in certain tear film cytokines that are proinflammatory such as increased expression of apolipoprotein, haptoglobin, annexin 1, S100A8, S100A9, Glutathione S-transferase, and decreased expression of supportive tear film components such as lipocalin-1, prolactin inducible protein, lysozyme C, lactotransferrin, cystatin S, and mammaglobin-b, proline rich protein, were found to be correlated with pathogenesis and/or treatment outcomes of dry eye, keratoconus, meibomian gland dysfunction, and Sjögren's. Overall, most AI/bioinformatics tools were used to classify biofluids into diseases subgroups, distinguish between OSD, identify risk factors, or make predictions about treatment response, and/or prognosis. To conclude, AI models such as artificial neural networks, hierarchical clustering, random forest, etc., in conjunction with proteomic or metabolomic profiling using bioinformatics tools such as Gene Ontology or Kyoto Encylopedia of Genes and Genomes pathway analysis, were found to inform biomarker discovery, distinguish between OSDs, help define subgroups with OSDs and make predictions about treatment response in a clinical setting.

摘要: 角膜和眼表疾病 (OSDs) 在世界范围内带来了严重的心理和经济负担。我们对人工智能 (AI) 和生物信息学分析角膜和眼表疾病中生物流体标志物的相关文献进行了综述, 评估其在临床决策中的实用性。 本文对MEDLINE、EMBASE、Cochrane和Web of Science数据库进行系统筛选, 找到从建库到2021年8月期间将人工智能或生物信息学方法应用于角膜和眼表疾病并检查了生物体液的文章。共筛选10264篇文献, 纳入23篇, 共1058位受试者。 使用各种人工智能/生物信息学工具发现某些促炎性泪膜细胞因子的表达变化, 例如载脂蛋白、结合珠蛋白、膜联蛋白1、S100A8、S100A9和谷胱甘肽S-转移酶的表达增加, 支持性泪膜成分如脂质运载蛋白-1、催乳素诱导蛋白、溶菌酶C、乳转铁蛋白、胱抑素S的表达减少, 乳球蛋白-B和脯氨酸富集类蛋白等与干眼症、圆锥角膜、睑板腺功能障碍和干燥综合征的发病机制和/或治疗结果相关。总之, 大部分人工智能/生物信息学工具可根据生物液体将疾病亚群进行分类, 从而区分眼表疾病, 识别风险因素或对治疗反应和/或预后进行预测。 总的来说, 人工智能模型如人工神经网络, 分层聚类, 随机森林等, 在进行蛋白质组或代谢组分析中使用的生物信息学工具, 如基因本体论或京都基因和基因组路径分析百科全书, 可以为生物标志物的发现提供信息, 区分眼表疾病, 帮助定义眼表疾病亚群, 并在临床环境中预测治疗反应。.

Publication types

  • Systematic Review
  • Review

MeSH terms

  • Artificial Intelligence*
  • Cornea / metabolism
  • Dry Eye Syndromes* / drug therapy
  • Humans
  • Proteomics
  • Tears / metabolism