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肠道微生物群落失调通过炎症蛋白与消化性溃疡疾病的发病机制相关:一项基于孟德尔随机化的研究。

Dysbiosis of gut microbiota is associated with pathogenesis of peptic ulcer diseases through inflammatory proteins: A Mendelian randomization study.

机构信息

Heilongjiang University of Chinese Medicine, Harbin, China.

First Affiliated Hospital, Heilongjiang University of Chinese Medicine, Harbin, China.

出版信息

Medicine (Baltimore). 2024 Sep 27;103(39):e39814. doi: 10.1097/MD.0000000000039814.

DOI:10.1097/MD.0000000000039814
PMID:39331926
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11441939/
Abstract

The gut microbiota and inflammatory proteins may affect the development of peptic ulcer disease. However, this association remains unclear. We analyzed genome-wide association study data of gut microbiota, inflammatory proteins, and peptic ulcer disease using Mendelian randomization with instrumental variables to assess causal relationships. Various statistical methods, including inverse variance weighting, Mendelian randomization Egger regression, and sensitivity analysis were employed to evaluate the data and calculate mediation ratios. Our findings reveal that the genus Butyriciccus plays a role in mitigating the adverse effects of gastric ulcers by 7.9%, primarily through reducing beta-negative growth factor levels. Additionally, the genus Lachnospiraceae UCG004 can significantly alleviate the negative outcomes of gastric ulcers and reduces hepatocyte growth factor and beta-reserve growth factor levels by 6.39% and 7.45%, respectively. This study highlights the independent and mediating effects of the gut microbiota and inflammatory proteins on peptic ulcers, offering insights on potential pathways and targets for future preventive interventions.

摘要

肠道微生物群和炎症蛋白可能会影响消化性溃疡的发展。然而,这种关联尚不清楚。我们使用基于工具变量的孟德尔随机化分析了肠道微生物群、炎症蛋白和消化性溃疡的全基因组关联研究数据,以评估因果关系。采用了多种统计方法,包括逆方差加权、孟德尔随机化 Egger 回归和敏感性分析来评估数据并计算中介比率。我们的研究结果表明,丁酸杆菌属通过降低β-阴性生长因子水平,对胃溃疡的不良影响减轻 7.9%。此外,毛螺菌科 UCG004 可以显著减轻胃溃疡的不良后果,分别降低肝细胞生长因子和β-储备生长因子水平 6.39%和 7.45%。本研究强调了肠道微生物群和炎症蛋白对消化性溃疡的独立和中介作用,为未来的预防干预提供了潜在的途径和靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca37/11441939/f0ef79740e6c/medi-103-e39814-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca37/11441939/65c244c06602/medi-103-e39814-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca37/11441939/a0b425730bb7/medi-103-e39814-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca37/11441939/a68f7e601d4d/medi-103-e39814-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca37/11441939/a55f47b38799/medi-103-e39814-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca37/11441939/cf7a506fc545/medi-103-e39814-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca37/11441939/f0ef79740e6c/medi-103-e39814-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca37/11441939/65c244c06602/medi-103-e39814-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca37/11441939/ca958a39c359/medi-103-e39814-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca37/11441939/a0b425730bb7/medi-103-e39814-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca37/11441939/a68f7e601d4d/medi-103-e39814-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca37/11441939/a55f47b38799/medi-103-e39814-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca37/11441939/cf7a506fc545/medi-103-e39814-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca37/11441939/f0ef79740e6c/medi-103-e39814-g007.jpg

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本文引用的文献

1
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Dig Dis Sci. 2024 Jun;69(6):1963-1971. doi: 10.1007/s10620-024-08322-y. Epub 2024 Mar 6.
2
Associations between Serum Mineral Nutrients, Gut Microbiota, and Risk of Neurological, Psychiatric, and Metabolic Diseases: A Comprehensive Mendelian Randomization Study.血清矿物质营养物、肠道微生物群与神经、精神和代谢性疾病风险之间的关联:一项综合的孟德尔随机化研究。
Nutrients. 2024 Jan 12;16(2):244. doi: 10.3390/nu16020244.
3
East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease.
基于2011 - 2018年美国国家健康与营养检查调查(NHANES)数据的胃肠道疾病与骨关节炎风险之间的关联
PLoS One. 2025 Aug 13;20(8):e0330064. doi: 10.1371/journal.pone.0330064. eCollection 2025.
4
LN33 fermented feed improves growth performance in Cherry Valley ducks by enhancing immune function and intestinal barrier integrity.LN33发酵饲料通过增强免疫功能和肠道屏障完整性来提高樱桃谷鸭的生长性能。
Front Vet Sci. 2025 Jul 23;12:1619287. doi: 10.3389/fvets.2025.1619287. eCollection 2025.
5
Gut microbiota and stress ulcers: unraveling the neurotransmitter connection.肠道微生物群与应激性溃疡:揭示神经递质联系
Front Neurosci. 2025 Jul 10;19:1594179. doi: 10.3389/fnins.2025.1594179. eCollection 2025.
6
Fatty acid traits mediate the effects of uric acid on cancers: a Mendelian randomization study.脂肪酸特征介导尿酸对癌症的影响:一项孟德尔随机化研究。
Front Genet. 2024 Dec 2;15:1449205. doi: 10.3389/fgene.2024.1449205. eCollection 2024.
东亚人群特异性及跨种族全基因组荟萃分析为消化性溃疡病提供了机制见解。
Nat Genet. 2023 Dec;55(12):2129-2138. doi: 10.1038/s41588-023-01569-7. Epub 2023 Nov 30.
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5
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6
Early-life exposure to the Great Chinese Famine and gut microbiome disruption across adulthood for type 2 diabetes: three population-based cohort studies.中国“大饥荒”时期的早期生活暴露与成年后患 2 型糖尿病的肠道微生物组紊乱:三项基于人群的队列研究。
BMC Med. 2023 Nov 1;21(1):414. doi: 10.1186/s12916-023-03123-y.
7
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8
Integration of gut microbiome and serum metabolome revealed the effect of Qing-Wei-Zhi-Tong Micro-pills on gastric ulcer in rats.肠道微生物组和血清代谢组的整合揭示了清胃止痛微丸对大鼠胃溃疡的作用。
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9
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Front Med (Lausanne). 2023 Jul 31;10:1200317. doi: 10.3389/fmed.2023.1200317. eCollection 2023.
10
Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets.循环炎症蛋白的遗传学鉴定出了免疫介导疾病风险的驱动因素和治疗靶点。
Nat Immunol. 2023 Sep;24(9):1540-1551. doi: 10.1038/s41590-023-01588-w. Epub 2023 Aug 10.