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肠道微生物群、炎性细胞因子、外周免疫细胞、血浆代谢组与帕金森病之间的因果关系:一项中介孟德尔随机化研究

Causal Relationship Between Intestinal Microbiota, Inflammatory Cytokines, Peripheral Immune Cells, Plasma Metabolome and Parkinson's Disease: A Mediation Mendelian Randomization Study.

作者信息

Wang Chengcheng, Tang Yuhang, Yang Tao, Wang Yuhao, Niu Zihui, Zhang Kang, Lin Ning, Li Qun

机构信息

Department of Neurosurgery, Affiliated Chuzhou Hospital of Anhui Medical University, First People's Hospital of Chuzhou, Chuzhou, China.

Health Examination Center, Affiliated Chuzhou Hospital of Anhui Medical University, First People's Hospital of Chuzhou, Chuzhou, China.

出版信息

Eur J Neurosci. 2025 Jan;61(2):e16665. doi: 10.1111/ejn.16665.

Abstract

Parkinson's disease (PD) is a neurodegenerative disease involving multiple factors. We explored the connection between intestinal microbiome levels and PD by examining inflammatory cytokines, peripheral immune cell counts and plasma metabolomics as potential factors. By obtaining the Genome-Wide Association Study (GWAS) data needed for this study from GWAS Catalog, including summary data for 473 intestinal microbiota traits (N = 5959), 91 inflammatory cytokine traits (N = 14,824), 118 peripheral immune cell count traits (N = 3757), 1400 plasma metabolite traits (N = 8299) and PD traits (N = 482,730). We used two-step Mendelian randomization (MR) mediated analysis to investigate possible pathways from intestinal microbiota to PD mediated by inflammatory cytokines, peripheral immune cells and plasma metabolites. MR has revealed the causal effects of 19 intestinal microbiota, 1 inflammatory cytokine and 12 plasma metabolites on PD, whereas there is no significant causal relationship between immune cell count characteristics and the occurrence of PD. Mediation analysis showed that the associations between the genus Demequina and PD were mediated by tryptophan with mediated proportions of 17.51% (p = 0.0393). Our study demonstrates that genus Demequina may promote the occurrence of PD by reducing the levels of tryptophan.

摘要

帕金森病(PD)是一种涉及多种因素的神经退行性疾病。我们通过检测炎症细胞因子、外周免疫细胞计数和血浆代谢组学作为潜在因素,探讨肠道微生物群水平与PD之间的联系。通过从GWAS Catalog获取本研究所需的全基因组关联研究(GWAS)数据,包括473个肠道微生物群特征(N = 5959)、91个炎症细胞因子特征(N = 14824)、118个外周免疫细胞计数特征(N = 3757)、1400个血浆代谢物特征(N = 8299)和PD特征(N = 482730)的汇总数据。我们使用两步孟德尔随机化(MR)介导分析来研究从肠道微生物群到由炎症细胞因子、外周免疫细胞和血浆代谢物介导的PD的可能途径。MR揭示了19种肠道微生物群、1种炎症细胞因子和12种血浆代谢物对PD的因果效应,而免疫细胞计数特征与PD的发生之间没有显著的因果关系。中介分析表明,德氏菌属与PD之间的关联由色氨酸介导,介导比例为17.51%(p = 0.0393)。我们的研究表明,德氏菌属可能通过降低色氨酸水平促进PD的发生。

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