• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

抗血管内皮生长因子治疗对 nAMD 患者血清代谢组学的影响研究。

A serum metabolomics study of patients with nAMD in response to anti-VEGF therapy.

机构信息

Singapore Eye Research Institute, Singapore, Singapore.

Singapore National Eye Centre, Singapore, Singapore.

出版信息

Sci Rep. 2020 Jan 28;10(1):1341. doi: 10.1038/s41598-020-58346-3.

DOI:10.1038/s41598-020-58346-3
PMID:31992792
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6987119/
Abstract

Intravitreal injection of anti-vascular endothelial growth factor (anti-VEGF) is the current standard of treatment for choroidal neovascularization (CNV) secondary to neovascular age-related macular degeneration (nAMD), but there are no diagnostic tools to predict response of these therapies. We hypothesize that differences in baseline metabolic profiles of patients with nAMD may influence responsiveness to anti-VEGF therapy, and thus provide prognosticating information for these patients. A prospective study was performed on 100 patients with nAMD treated with anti-VEGF therapy. We classified patients into two groups: responders (n = 54) and non-responders (n = 46). The expression levels of glycerophosphocholine,LysoPC (18:2) and PS (18:0/20:4) were higher in non-responders and these findings were verified in the validation cohort, implicating that reductions in these three metabolites can be used as predictors for responsiveness to anti-VEGF therapy during the initial loading phase for patients with nAMD. Our study also provided new insights into the pathophysiological changes and molecular mechanism of anti- VEGF therapy for nAMD patients.

摘要

玻璃体内注射抗血管内皮生长因子(anti-VEGF)是治疗新生血管性年龄相关性黄斑变性(nAMD)继发脉络膜新生血管(CNV)的目前标准治疗方法,但目前还没有诊断工具来预测这些治疗的反应。我们假设 nAMD 患者的基线代谢特征的差异可能会影响对抗 VEGF 治疗的反应,从而为这些患者提供预后信息。我们对 100 名接受抗 VEGF 治疗的 nAMD 患者进行了前瞻性研究。我们将患者分为两组:应答者(n=54)和无应答者(n=46)。无应答者的甘油磷酸胆碱、溶血磷脂酰胆碱(18:2)和 PS(18:0/20:4)的表达水平较高,这些发现在验证队列中得到了验证,表明在 nAMD 患者的初始负荷期,这三种代谢物的减少可以用作对抗 VEGF 治疗反应的预测因子。我们的研究还为 nAMD 患者抗 VEGF 治疗的病理生理变化和分子机制提供了新的见解。

相似文献

1
A serum metabolomics study of patients with nAMD in response to anti-VEGF therapy.抗血管内皮生长因子治疗对 nAMD 患者血清代谢组学的影响研究。
Sci Rep. 2020 Jan 28;10(1):1341. doi: 10.1038/s41598-020-58346-3.
2
Peripheral blood mononuclear cells from neovascular age-related macular degeneration patients produce higher levels of chemokines CCL2 (MCP-1) and CXCL8 (IL-8).来自新生血管性年龄相关性黄斑变性患者的外周血单个核细胞产生更高水平的趋化因子CCL2(MCP-1)和CXCL8(IL-8)。
J Neuroinflammation. 2017 Feb 23;14(1):42. doi: 10.1186/s12974-017-0820-y.
3
Optimizing Anti-VEGF Treatment Outcomes for Patients with Neovascular Age-Related Macular Degeneration.优化新生血管性年龄相关性黄斑变性患者的抗 VEGF 治疗效果。
J Manag Care Spec Pharm. 2018 Feb;24(2-a Suppl):S3-S15. doi: 10.18553/jmcp.2018.24.2-a.s3.
4
Inflammatory Factors of Macular Atrophy in Eyes With Neovascular Age-Related Macular Degeneration Treated With Aflibercept.抗血管内皮生长因子药物治疗新生血管性年龄相关性黄斑变性脉络膜新生血管后黄斑萎缩的炎症因子分析。
Front Immunol. 2021 Oct 13;12:738521. doi: 10.3389/fimmu.2021.738521. eCollection 2021.
5
Real-life management of neovascular age-related macular degeneration (nAMD) in France: a nationwide observational study using retrospective claims data.法国新生血管性年龄相关性黄斑变性(nAMD)的真实世界管理:使用回顾性索赔数据的全国性观察性研究。
J Med Econ. 2021 Jan-Dec;24(1):1087-1097. doi: 10.1080/13696998.2021.1971416.
6
Profiling neovascular age-related macular degeneration choroidal neovascularization lesion response to anti-vascular endothelial growth factor therapy using SSOCTA.应用 SSOCTA 对新生血管性年龄相关性黄斑变性脉络膜新生血管病变对抗血管内皮生长因子治疗的反应进行分析。
Acta Ophthalmol. 2021 Mar;99(2):e240-e246. doi: 10.1111/aos.14554. Epub 2020 Jul 24.
7
Metabolomics study of treatment response to conbercept of patients with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.新生血管性年龄相关性黄斑变性和息肉状脉络膜血管病变患者对康柏西普治疗反应的代谢组学研究
Front Pharmacol. 2022 Sep 19;13:991879. doi: 10.3389/fphar.2022.991879. eCollection 2022.
8
Multimodal imaging based biomarkers predictive of early and late response to anti-VEGFs during the first year of treatment for neovascular age-related macular degeneration.基于多模态成像的生物标志物预测新生血管性年龄相关性黄斑变性治疗第一年对抗血管内皮生长因子(anti-VEGFs)的早期和晚期反应
J Fr Ophtalmol. 2019 Jan;42(1):22-31. doi: 10.1016/j.jfo.2018.06.005. Epub 2018 Dec 19.
9
Enhanced depth imaging of the choroid in patients with neovascular age-related macular degeneration treated with anti-VEGF therapy versus untreated patients.抗血管内皮生长因子治疗与未治疗的新生血管性年龄相关性黄斑变性患者脉络膜的增强深度成像。
Graefes Arch Clin Exp Ophthalmol. 2013 Jun;251(6):1483-8. doi: 10.1007/s00417-012-2199-x. Epub 2012 Nov 17.
10
Pharmacogenetic associations with vascular endothelial growth factor inhibition in participants with neovascular age-related macular degeneration in the IVAN Study.在 IVAN 研究中,血管内皮生长因子抑制与新生血管性年龄相关性黄斑变性患者的遗传关联性。
Ophthalmology. 2013 Dec;120(12):2637-2643. doi: 10.1016/j.ophtha.2013.07.046. Epub 2013 Sep 23.

引用本文的文献

1
Systematic review of clinical practice guidelines for the management of neovascular age-related macular degeneration.新生血管性年龄相关性黄斑变性管理临床实践指南的系统评价
Eye (Lond). 2025 May 15. doi: 10.1038/s41433-025-03829-8.
2
Association of plasma metabolites with treatment response after intravitreal anti-vascular endothelial growth factor injections in treatment-naïve neovascular age-related macular degeneration.初治新生血管性年龄相关性黄斑变性患者玻璃体内注射抗血管内皮生长因子后血浆代谢物与治疗反应的关联
BMJ Open Ophthalmol. 2025 Mar 15;10(1):e002149. doi: 10.1136/bmjophth-2025-002149.
3
Metabolomics facilitates differential diagnosis in common inherited retinal degenerations by exploring their profiles of serum metabolites.

本文引用的文献

1
Moving beyond P values: data analysis with estimation graphics.超越P值:使用估计图进行数据分析。
Nat Methods. 2019 Jul;16(7):565-566. doi: 10.1038/s41592-019-0470-3.
2
HAWK and HARRIER: Phase 3, Multicenter, Randomized, Double-Masked Trials of Brolucizumab for Neovascular Age-Related Macular Degeneration.HAWK 和 HARRIER:贝鲁珠单抗治疗新生血管性年龄相关性黄斑变性的 3 期、多中心、随机、双盲试验。
Ophthalmology. 2020 Jan;127(1):72-84. doi: 10.1016/j.ophtha.2019.04.017. Epub 2019 Apr 12.
3
Macular Morphology and Visual Acuity in Year Five of the Comparison of Age-related Macular Degeneration Treatments Trials.
代谢组学通过探索常见遗传性视网膜变性的血清代谢物特征,有助于其进行鉴别诊断。
Nat Commun. 2024 Apr 26;15(1):3562. doi: 10.1038/s41467-024-47911-3.
4
Applications of artificial intelligence and bioinformatics methodologies in the analysis of ocular biofluid markers: a scoping review.人工智能和生物信息学方法在眼内生物流体标志物分析中的应用:范围综述。
Graefes Arch Clin Exp Ophthalmol. 2024 Apr;262(4):1041-1091. doi: 10.1007/s00417-023-06100-6. Epub 2023 Jul 8.
5
Integrating genetics and metabolomics from multi-ethnic and multi-fluid data reveals putative mechanisms for age-related macular degeneration.整合多民族和多体液数据的遗传学和代谢组学揭示了与年龄相关的黄斑变性的潜在机制。
Cell Rep Med. 2023 Jul 18;4(7):101085. doi: 10.1016/j.xcrm.2023.101085. Epub 2023 Jun 21.
6
The Interplay Between Metabolites and MicroRNAs in Aqueous Humor to Coordinate Corneal Endothelium Integrity.房水中代谢物与微小RNA之间的相互作用以协调角膜内皮完整性
Ophthalmol Sci. 2023 Mar 16;3(3):100299. doi: 10.1016/j.xops.2023.100299. eCollection 2023 Sep.
7
New insight of metabolomics in ocular diseases in the context of 3P medicine.3P医学背景下代谢组学在眼部疾病中的新见解。
EPMA J. 2023 Feb 17;14(1):53-71. doi: 10.1007/s13167-023-00313-9. eCollection 2023 Mar.
8
Metabolomics study of treatment response to conbercept of patients with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.新生血管性年龄相关性黄斑变性和息肉状脉络膜血管病变患者对康柏西普治疗反应的代谢组学研究
Front Pharmacol. 2022 Sep 19;13:991879. doi: 10.3389/fphar.2022.991879. eCollection 2022.
9
Artificial Intelligence Analysis of Biofluid Markers in Age-Related Macular Degeneration: A Systematic Review.年龄相关性黄斑变性中生物流体标志物的人工智能分析:一项系统综述。
Clin Ophthalmol. 2022 Aug 7;16:2463-2476. doi: 10.2147/OPTH.S377262. eCollection 2022.
10
Metabolomics in Retinal Diseases: An Update.视网膜疾病中的代谢组学:最新进展
Biology (Basel). 2021 Sep 22;10(10):944. doi: 10.3390/biology10100944.
五年期年龄相关性黄斑变性治疗试验比较的黄斑形态和视力。
Ophthalmology. 2019 Feb;126(2):252-260. doi: 10.1016/j.ophtha.2018.08.035. Epub 2018 Sep 3.
4
Projection of Long-Term Visual Acuity Outcomes Based on Initial Treatment Response in Neovascular Age-Related Macular Degeneration.基于新生血管性年龄相关性黄斑变性初始治疗反应的长期视力预后预测。
Ophthalmology. 2019 Jan;126(1):64-74. doi: 10.1016/j.ophtha.2018.08.023. Epub 2018 Aug 24.
5
Integrative proteomics in prostate cancer uncovers robustness against genomic and transcriptomic aberrations during disease progression.前列腺癌的整合蛋白质组学揭示了在疾病进展过程中对基因组和转录组异常的稳健性。
Nat Commun. 2018 Mar 21;9(1):1176. doi: 10.1038/s41467-018-03573-6.
6
HDL-cholesterol levels and risk of age-related macular degeneration: a multiethnic genetic study using Mendelian randomization.高密度脂蛋白胆固醇水平与年龄相关性黄斑变性的风险:一项基于孟德尔随机化的多民族遗传研究。
Int J Epidemiol. 2017 Dec 1;46(6):1891-1902. doi: 10.1093/ije/dyx189.
7
Human Plasma Metabolomics Study across All Stages of Age-Related Macular Degeneration Identifies Potential Lipid Biomarkers.人类血浆代谢组学研究贯穿年龄相关性黄斑变性的所有阶段,确定潜在的脂质生物标志物。
Ophthalmology. 2018 Feb;125(2):245-254. doi: 10.1016/j.ophtha.2017.08.008. Epub 2017 Sep 12.
8
Analyzing and Predicting Visual Acuity Outcomes of Anti-VEGF Therapy by a Longitudinal Mixed Effects Model of Imaging and Clinical Data.通过影像和临床数据的纵向混合效应模型分析和预测抗VEGF治疗的视力结果
Invest Ophthalmol Vis Sci. 2017 Aug 1;58(10):4173-4181. doi: 10.1167/iovs.17-21878.
9
Plasma lipoprotein subfraction concentrations are associated with lipid metabolism and age-related macular degeneration.血浆脂蛋白亚组分浓度与脂质代谢及年龄相关性黄斑变性有关。
J Lipid Res. 2017 Sep;58(9):1785-1796. doi: 10.1194/jlr.M073684. Epub 2017 Jul 11.
10
Change in vision-related quality of life and influencing factors in Asians receiving treatment for neovascular age-related macular degeneration.亚洲接受新生血管性年龄相关性黄斑变性治疗的患者的视力相关生活质量变化及其影响因素。
Br J Ophthalmol. 2018 Mar;102(3):377-382. doi: 10.1136/bjophthalmol-2017-310532. Epub 2017 Jun 28.