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新的药物使用与多种药物治疗与肠道微生物群落组成和功能潜力在一个大的人群中的联系。

New connections of medication use and polypharmacy with the gut microbiota composition and functional potential in a large population.

机构信息

Department of Clinical Sciences in Malmö, Lund University Diabetes Center, Lund University, Malmö, Sweden.

Public Dental Service of Skåne, Lund, Sweden.

出版信息

Sci Rep. 2024 Oct 10;14(1):23723. doi: 10.1038/s41598-024-71571-4.

Abstract

Medication can affect the gut microbiota composition and function. The aim of this study was to investigate connections between use of common non-antibiotic medicines and the gut microbiota composition and function in a large Swedish cohort (N = 2223). Use of 67 medications and polypharmacy (≥ 5 medications), based on self-reported and prescription registry data, were associated with the relative abundance of 881 gut metagenomic species (> 5% prevalence) and 103 gut metabolic modules (GMMs). Altogether, 97 associations of 26 medications with 40 species and of four medications with five GMMs were observed (false discovery rate < 5%). Several earlier findings were replicated like the positive associations of proton pump inhibitors (PPIs) with numerous oral species, and those of metformin with Escherichia species and with lactate consumption I and arginine degradation II. Several new associations were observed between, among others, use of antidepressants, beta-blockers, nonsteroidal anti-inflammatory drugs and calcium channel blockers, and specific species. Polypharmacy was positively associated with Enterococcus faecalis, Bacteroides uniformis, Rothia mucilaginosa, Escherichia coli and Limosilactobacillus vaginalis, and with 13 GMMs. We confirmed several previous findings and identified numerous new associations between use of medications/polypharmacy and the gut microbiota composition and functional potential. Further studies are needed to confirm the new findings.

摘要

药物可以影响肠道微生物群落的组成和功能。本研究旨在调查在一个大型瑞典队列(N=2223)中,常见非抗生素药物的使用与肠道微生物群落组成和功能之间的联系。基于自我报告和处方登记数据,使用 67 种药物和多种药物(≥5 种药物)与 881 种肠道宏基因组物种(>5%的流行率)和 103 种肠道代谢模块(GMMs)的相对丰度有关。总共观察到 26 种药物与 40 种物种和 4 种药物与 5 种 GMMs 的 97 种关联(错误发现率<5%)。一些先前的发现得到了复制,如质子泵抑制剂(PPIs)与许多口腔物种的正相关,以及二甲双胍与大肠杆菌和乳酸消耗 I 和精氨酸降解 II 的正相关。观察到了几种新的关联,包括使用抗抑郁药、β-受体阻滞剂、非甾体抗炎药和钙通道阻滞剂与特定物种之间的关联。多种药物治疗与粪肠球菌、均匀拟杆菌、粘罗氏菌、大肠杆菌和阴道乳杆菌以及 13 个 GMMs 呈正相关。我们证实了一些先前的发现,并确定了药物/多种药物使用与肠道微生物群落组成和功能潜力之间的许多新关联。需要进一步的研究来证实新的发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac98/11467196/7a4416b8cec6/41598_2024_71571_Fig1_HTML.jpg

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