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肠道微生物群和代谢产物对近视和病理性近视的因果影响:一项中介孟德尔随机化研究。

The causal impact of gut microbiota and metabolites on myopia and pathological myopia: a mediation Mendelian randomization study.

作者信息

Hui Jingwen, Tang Kexin, Zhou Yuejun, Cui Xuehao, Han Quanhong

机构信息

Tianjin Eye Hospital, No.4 Gansu Road, Heping District, Tianjin, 300020, China.

Tianjin Key Lab of Ophthalmology and Visual Science, Tianjin, China.

出版信息

Sci Rep. 2025 Apr 15;15(1):12928. doi: 10.1038/s41598-025-97722-9.

Abstract

Myopia, a major cause of irreversible visual impairment globally, is projected to affect about 25% of the world's population by 2025. Myopia progresses through childhood and adolescence, necessitating frequent prescription updates. While genetic and environmental factors are well-established contributors to myopia, emerging evidence suggests a significant role of the gut microbiota (GM) in its development, mainly through metabolic interactions. This study utilized a Mendelian Randomization (MR) approach to investigate the causal relationships between GM, metabolites, and myopia and pathological myopia (PM) progression. Using genetic variants as instrumental variables, we analyzed data from extensive genome-wide association studies (GWAS) to assess the impacts of 473 GM taxa and 233 metabolites on myopia risks. Our MR analysis identified specific GM taxa and metabolites with significant causal relationship to myopia and PM. Notably, lipid metabolites were found to mediate the effects of GM on myopia, suggesting a biochemical pathway that could influence ocular development and myopia progression. We also observed significant mediation effects, indicating that specific metabolites might serve as therapeutic targets to modulate myopia progression. The findings highlight the potential of GM and metabolites as novel targets for preventing or managing myopia. This study underscores the importance of further research into the gut-metabolite-eye axis to develop targeted interventions for myopia based on modifying the GM through diet, probiotics, or other means. Future studies should aim to elucidate the specific metabolites involved and their roles in ocular health, potentially offering new avenues for treatment.

摘要

近视是全球不可逆视力损害的主要原因,预计到2025年将影响全球约25%的人口。近视在儿童和青少年时期发展,需要频繁更新处方。虽然遗传和环境因素是公认的近视成因,但新出现的证据表明肠道微生物群(GM)在其发展中起重要作用,主要通过代谢相互作用。本研究采用孟德尔随机化(MR)方法来研究GM、代谢物与近视及病理性近视(PM)进展之间的因果关系。我们使用基因变异作为工具变量,分析了来自广泛全基因组关联研究(GWAS)的数据,以评估473种GM分类群和233种代谢物对近视风险的影响。我们的MR分析确定了与近视和PM有显著因果关系的特定GM分类群和代谢物。值得注意的是,发现脂质代谢物介导了GM对近视的影响,这表明了一条可能影响眼部发育和近视进展的生化途径。我们还观察到显著的中介效应,表明特定代谢物可能作为调节近视进展的治疗靶点。这些发现突出了GM和代谢物作为预防或控制近视新靶点的潜力。本研究强调了进一步研究肠道-代谢物-眼轴的重要性,以便通过饮食、益生菌或其他手段改变GM来开发针对近视的靶向干预措施。未来的研究应旨在阐明所涉及的特定代谢物及其在眼部健康中的作用,可能为治疗提供新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3804/12000407/f7a33c827c5f/41598_2025_97722_Fig1_HTML.jpg

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