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Gut microbiota induced abnormal amino acids and their correlation with diabetic retinopathy.肠道微生物群诱导的异常氨基酸及其与糖尿病视网膜病变的相关性。
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From theory to therapy: a bibliometric and visual study of stem cell advancements in age-related macular degeneration.从理论到治疗:年龄相关性黄斑变性中干细胞进展的文献计量和可视化研究。
Cytotherapy. 2024 Jun;26(6):616-631. doi: 10.1016/j.jcyt.2024.02.022. Epub 2024 Mar 2.
3
Retinal pigment epithelium-Bruch's membrane volume in grading of age-related macular degeneration.视网膜色素上皮- Bruch膜体积在年龄相关性黄斑变性分级中的应用
Int J Ophthalmol. 2023 Nov 18;16(11):1827-1831. doi: 10.18240/ijo.2023.11.14. eCollection 2023.
4
Association of Gut Microbiota with Age-Related Macular Degeneration and Glaucoma: A Bidirectional Mendelian Randomization Study.肠道微生物群与年龄相关性黄斑变性和青光眼的关联:一项双向孟德尔随机研究。
Nutrients. 2023 Nov 2;15(21):4646. doi: 10.3390/nu15214646.
5
Causal Effects of Gut Microbiota on Age-Related Macular Degeneration: A Mendelian Randomization Study.肠道微生物群对年龄相关性黄斑变性的因果影响:一项孟德尔随机化研究。
Invest Ophthalmol Vis Sci. 2023 Sep 1;64(12):32. doi: 10.1167/iovs.64.12.32.
6
Gut microbiota and eye diseases: a bibliometric study and visualization analysis.肠道微生物群与眼部疾病:文献计量学研究与可视化分析。
Front Cell Infect Microbiol. 2023 Aug 9;13:1225859. doi: 10.3389/fcimb.2023.1225859. eCollection 2023.
7
Single-cell RNA sequencing in dissecting microenvironment of age-related macular degeneration: Challenges and perspectives.单细胞 RNA 测序在解析年龄相关性黄斑变性微环境中的应用:挑战与展望。
Ageing Res Rev. 2023 Sep;90:102030. doi: 10.1016/j.arr.2023.102030. Epub 2023 Aug 5.
8
FinnGen provides genetic insights from a well-phenotyped isolated population.FinnGen 为一个表型良好的隔离人群提供了遗传学方面的见解。
Nature. 2023 Jan;613(7944):508-518. doi: 10.1038/s41586-022-05473-8. Epub 2023 Jan 18.
9
Microbiome-based interventions to modulate gut ecology and the immune system.基于微生物组的干预措施来调节肠道生态和免疫系统。
Mucosal Immunol. 2022 Jun;15(6):1095-1113. doi: 10.1038/s41385-022-00564-1. Epub 2022 Sep 30.
10
Causal effects of gut microbiota on diabetic retinopathy: A Mendelian randomization study.肠道微生物群对糖尿病视网膜病变的因果影响:一项孟德尔随机化研究。
Front Immunol. 2022 Sep 8;13:930318. doi: 10.3389/fimmu.2022.930318. eCollection 2022.

探究肠道微生物群与干性年龄相关性黄斑变性之间的因果关系:一项双向孟德尔随机化研究。

Investigating the causal link between gut microbiota and dry age-related macular degeneration: a bidirectional Mendelian randomization study.

作者信息

Huang Hai-Yan, Wang Jing, Qin Bo, Tan Yao

机构信息

Clinical Medical College of Guizhou Medical University, Guiyang 550004, Guizhou Province, China.

Postdoctoral Station of Clinical Medicine, The Third Xiangya Hospital, Central South University, Changsha 410000, Hunan Province, China.

出版信息

Int J Ophthalmol. 2024 Sep 18;17(9):1723-1730. doi: 10.18240/ijo.2024.09.21. eCollection 2024.

DOI:10.18240/ijo.2024.09.21
PMID:39296574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11367437/
Abstract

AIM

To assess the causal link between 211 gut microbiota (GM) taxa and dry age-related macular degeneration (dAMD) risk.

METHODS

Mendelian randomization using instrumental factors taken from a genome-wide association study (GWAS) were used. Inverse variance weighted (IVW) analysis and sensitivity analysis were performed on the FinnGen project, which included 5095 cases and 222 590 controls.

RESULTS

The IVW analysis showed substantial genus- and family-level relationships between GM taxa and dAMD risk. Specifically, the family (=0.03), genus (=3.91×10), genus (=6.55×10), and genus (=0.04) were linked to a higher risk of developing dAMD, while the genus (=7.75×10), genus (=0.04) and genus (=0.04) exhibited a protective effect against dAMD. No significant causal relationships were observed at higher taxonomic levels. Additionally, in the reverse IVW analysis, no meaningful causal effects of the 7 GM taxa.

CONCLUSION

These findings give support for the gut-retina axis participation in dAMD and shed light on putative underlying processes. Investigations on the connection between GM and dAMD have not yet revealed the underlying mechanism.

摘要

目的

评估211种肠道微生物群(GM)分类群与干性年龄相关性黄斑变性(dAMD)风险之间的因果关系。

方法

使用来自全基因组关联研究(GWAS)的工具因素进行孟德尔随机化。对芬兰基因组计划进行逆方差加权(IVW)分析和敏感性分析,该计划包括5095例病例和222590例对照。

结果

IVW分析显示GM分类群与dAMD风险之间存在显著的属和科级关系。具体而言,[具体科名1](=0.03)、[具体属名1](=3.91×10)、[具体属名2](=6.55×10)和[具体属名3](=0.04)与发生dAMD的较高风险相关,而[具体属名4](=7.75×10)、[具体属名5](=0.04)和[具体属名6](=0.04)对dAMD具有保护作用。在较高分类水平上未观察到显著的因果关系。此外,在反向IVW分析中,7种GM分类群没有有意义的因果效应。

结论

这些发现支持肠道 - 视网膜轴参与dAMD,并揭示了潜在的过程。关于GM与dAMD之间联系的研究尚未揭示其潜在机制。