• 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

孟德尔随机化研究为原发性膜性肾病与肠道微生物群之间的多种因果关系提供了证据。

Evidence from mendelian randomization identifies several causal relationships between primary membranous nephropathy and gut microbiota.

机构信息

Department of Medical Technology, Gannan Healthcare Vocational College, Ganzhou, China.

Department of Laboratory, GanZhou Cancer Hospital, Ganzhou, China.

出版信息

Ren Fail. 2024 Dec;46(1):2349136. doi: 10.1080/0886022X.2024.2349136. Epub 2024 May 21.

DOI:10.1080/0886022X.2024.2349136
PMID:38770992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11110878/
Abstract

BACKGROUND

Research has showcased a correlation between disruptions in gut microbiota and primary membranous nephropathy (pMN), giving rise to the concept of the 'gut-kidney axis'. However, the precise relationship between gut microbiota and pMN remains elusive. Hence, this study endeavors to investigate whether a causal relationship exists between gut microbiota and pMN utilizing Mendelian randomization (MR) analysis.

METHODS

The primary method employed for MR analysis is the inverse variance weighting method, supplemented by MR-Egger and the weighted median method, to infer causality. This approach was validated within the pMN cohort across two distinct populations.

RESULTS

At the species level, the abundance of and was negatively correlated with the risk of pMN. Conversely, pMN was positively associated with abundance at the class level, abundance at the family level, and abundance at the genus level. Specifically, at the species level, pMN was positively correlated with the abundance of , , and

CONCLUSION

These findings lay the groundwork for future research exploring the interplay between pMN and the gut microbiota, with substantial implications for the prevention and treatment of pMN and its associated complications.

摘要

背景

研究表明,肠道微生物群的紊乱与原发性膜性肾病(pMN)之间存在关联,从而产生了“肠-肾轴”的概念。然而,肠道微生物群与 pMN 的确切关系仍难以捉摸。因此,本研究利用孟德尔随机化(MR)分析来研究肠道微生物群与 pMN 之间是否存在因果关系。

方法

MR 分析的主要方法是逆方差加权法,辅以 MR-Egger 和加权中位数法来推断因果关系。该方法在两个不同人群的 pMN 队列中进行了验证。

结果

在物种水平上, 和 的丰度与 pMN 的风险呈负相关。相反,pMN 与类水平的 丰度、科水平的 丰度和属水平的 丰度呈正相关。具体而言,在物种水平上,pMN 与 、 和 的丰度呈正相关。

结论

这些发现为未来探索 pMN 与肠道微生物群之间相互作用的研究奠定了基础,对 pMN 及其相关并发症的预防和治疗具有重要意义。

相似文献

1
Evidence from mendelian randomization identifies several causal relationships between primary membranous nephropathy and gut microbiota.孟德尔随机化研究为原发性膜性肾病与肠道微生物群之间的多种因果关系提供了证据。
Ren Fail. 2024 Dec;46(1):2349136. doi: 10.1080/0886022X.2024.2349136. Epub 2024 May 21.
2
The causal association of specific gut microbiota on the risk of membranous nephropathy: a Mendelian randomization study.特定肠道微生物群与膜性肾病风险的因果关联:一项孟德尔随机化研究。
Int Urol Nephrol. 2024 Jun;56(6):2021-2030. doi: 10.1007/s11255-023-03926-1. Epub 2024 Jan 5.
3
Causal relationship between gut microbiota and kidney diseases: a two-sample Mendelian randomization study.肠道微生物群与肾脏疾病之间的因果关系:两样本孟德尔随机化研究。
Front Immunol. 2024 Jan 12;14:1277554. doi: 10.3389/fimmu.2023.1277554. eCollection 2023.
4
The causal relationship between gut microbiota and neuroblastoma: a bidirectional Mendelian randomization analysis and meta-analysis.肠道微生物群与神经母细胞瘤的因果关系:双向孟德尔随机化分析和荟萃分析。
Microbiol Spectr. 2024 Apr 2;12(4):e0365623. doi: 10.1128/spectrum.03656-23. Epub 2024 Feb 27.
5
The influence of gut microbiota on membranous nephropathy: A two-sample Mendelian randomization study.肠道微生物群对膜性肾病的影响:一项两样本孟德尔随机化研究。
Clin Nephrol. 2024 Sep;102(3):134-143. doi: 10.5414/CN111346.
6
Causal association between gut microbiota and intrahepatic cholestasis of pregnancy: mendelian randomization study.肠道微生物群与妊娠肝内胆汁淤积症的因果关联:孟德尔随机化研究。
BMC Pregnancy Childbirth. 2023 Aug 5;23(1):568. doi: 10.1186/s12884-023-05889-8.
7
The Effects of Specific Gut Microbiota and Metabolites on IgA Nephropathy-Based on Mendelian Randomization and Clinical Validation.特定肠道菌群及其代谢物对 IgA 肾病的影响——基于孟德尔随机化和临床验证。
Nutrients. 2023 May 22;15(10):2407. doi: 10.3390/nu15102407.
8
Genetic evidence supporting the causal role of gut microbiota in chronic kidney disease and chronic systemic inflammation in CKD: a bilateral two-sample Mendelian randomization study.支持肠道微生物群在慢性肾脏病和慢性肾脏病系统性炎症中起因果作用的遗传证据:一项双侧双样本孟德尔随机研究。
Front Immunol. 2023 Nov 2;14:1287698. doi: 10.3389/fimmu.2023.1287698. eCollection 2023.
9
Causal effects of gut microbiota on appendicitis: a two-sample Mendelian randomization study.肠道微生物群对阑尾炎的因果影响:两样本孟德尔随机化研究。
Front Cell Infect Microbiol. 2023 Dec 15;13:1320992. doi: 10.3389/fcimb.2023.1320992. eCollection 2023.
10
Identification of host gene-microbiome associations in colorectal cancer patients using mendelian randomization.利用孟德尔随机化鉴定结直肠癌患者的宿主基因-微生物组关联。
J Transl Med. 2023 Aug 10;21(1):535. doi: 10.1186/s12967-023-04335-9.

引用本文的文献

1
A practical guide for nephrologist peer reviewers: understanding and appraising Mendelian randomization studies.肾科同行评审员实用指南:理解和评估孟德尔随机化研究
Ren Fail. 2025 Dec;47(1):2445763. doi: 10.1080/0886022X.2024.2445763. Epub 2025 Jan 13.

本文引用的文献

1
SW207 alleviates enterotoxigenic -induced inflammatory responses in weaned piglets by modulating the intestinal epithelial barrier, the TLR4/MyD88/NF-κB pathway, and intestinal microbiota.SW207 通过调节肠道上皮屏障、TLR4/MyD88/NF-κB 通路和肠道微生物群来减轻肠毒素诱导的断奶仔猪的炎症反应。
Microbiol Spectr. 2024 Apr 2;12(4):e0398823. doi: 10.1128/spectrum.03988-23. Epub 2024 Mar 7.
2
Probiotics M8 and M9 prevent high blood pressure via modulating the gut microbiota composition and host metabolic products.益生菌 M8 和 M9 通过调节肠道微生物群落组成和宿主代谢产物来预防高血压。
mSystems. 2023 Dec 21;8(6):e0033123. doi: 10.1128/msystems.00331-23. Epub 2023 Oct 19.
3
Associations between dietary habits, socio-demographics and gut microbial composition in adolescents.
青少年饮食习惯、社会人口统计学特征与肠道微生物组成的关联。
Br J Nutr. 2024 Mar 14;131(5):809-820. doi: 10.1017/S0007114523002271. Epub 2023 Oct 18.
4
Altered Intestinal Microbial Flora and Metabolism in Patients with Idiopathic Membranous Nephropathy.特发性膜性肾病患者肠道微生物群和代谢的改变
Am J Nephrol. 2023;54(11-12):451-470. doi: 10.1159/000533537. Epub 2023 Oct 4.
5
Select symbionts drive high IgA levels in the mouse intestine.选择共生体驱动小鼠肠道中高 IgA 水平。
Cell Host Microbe. 2023 Oct 11;31(10):1620-1638.e7. doi: 10.1016/j.chom.2023.09.001. Epub 2023 Sep 29.
6
Maternal exposure of mice to glyphosate induces depression- and anxiety-like behavior in the offspring via alterations of the gut-brain axis.母体将小鼠暴露于草甘膦会通过改变肠-脑轴,诱导后代出现类似抑郁和焦虑的行为。
Sci Total Environ. 2023 Dec 20;905:167034. doi: 10.1016/j.scitotenv.2023.167034. Epub 2023 Sep 12.
7
Manipulating the gut and tumor microbiota for immune checkpoint inhibitor therapy: from dream to reality.通过调控肠道和肿瘤微生物群来进行免疫检查点抑制剂治疗:从梦想走向现实。
Trends Mol Med. 2023 Nov;29(11):897-911. doi: 10.1016/j.molmed.2023.08.004. Epub 2023 Sep 11.
8
Fecal microbiota transplantation for the management of autoimmune diseases: Potential mechanisms and challenges.粪便微生物群移植治疗自身免疫性疾病:潜在机制与挑战。
J Autoimmun. 2023 Dec;141:103109. doi: 10.1016/j.jaut.2023.103109. Epub 2023 Sep 9.
9
Lactobacillus species ameliorate membranous nephropathy through inhibiting the aryl hydrocarbon receptor pathway via tryptophan-produced indole metabolites.乳杆菌属通过色氨酸产生的吲哚代谢物抑制芳香烃受体途径来改善膜性肾病。
Br J Pharmacol. 2024 Jan;181(1):162-179. doi: 10.1111/bph.16219. Epub 2023 Sep 19.
10
The Interplay between Gut Microbiota and Oral Medications and Its Impact on Advancing Precision Medicine.肠道微生物群与口服药物之间的相互作用及其对推进精准医学的影响。
Metabolites. 2023 May 21;13(5):674. doi: 10.3390/metabo13050674.