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酒精使用障碍和酒精性肝病中的微生物组改变。

Microbiome Alterations in Alcohol Use Disorder and Alcoholic Liver Disease.

机构信息

Department of Biochemistry and Immunochemistry, Wroclaw Medical University, 50-368 Wroclaw, Poland.

Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, 53-114 Wrocław, Poland.

出版信息

Int J Mol Sci. 2023 Jan 27;24(3):2461. doi: 10.3390/ijms24032461.

Abstract

Microbiome alterations are emerging as one of the most important factors that influence the course of alcohol use disorder (AUD). Recent advances in bioinformatics enable more robust and accurate characterization of changes in the composition of the microbiome. In this study, our objective was to provide the most comprehensive and up-to-date evaluation of microbiome alterations associated with AUD and alcoholic liver disease (ALD). To achieve it, we have applied consistent, state of art bioinformatic workflow to raw reads from multiple 16S rRNA sequencing datasets. The study population consisted of 122 patients with AUD, 75 with ALD, 54 with non-alcoholic liver diseases, and 260 healthy controls. We have found several microbiome alterations that were consistent across multiple datasets. The most consistent changes included a significantly lower abundance of multiple butyrate-producing families, including , , and in AUD compared to HC and further reduction of these families in ALD compared with AUD. Other important results include an increase in endotoxin-producing in AUD, with the ALD group having the largest increase. All of these alterations can potentially contribute to increased intestinal permeability and inflammation associated with AUD and ALD.

摘要

微生物组的改变正在成为影响酒精使用障碍(AUD)病程的最重要因素之一。生物信息学的最新进展使我们能够更准确地描述微生物组组成的变化。在这项研究中,我们的目的是提供与 AUD 和酒精性肝病(ALD)相关的微生物组改变的最全面和最新的评估。为了实现这一目标,我们应用了一致的、最先进的生物信息学工作流程来处理来自多个 16S rRNA 测序数据集的原始读数。研究人群包括 122 名 AUD 患者、75 名 ALD 患者、54 名非酒精性肝病患者和 260 名健康对照者。我们发现了多个在多个数据集之间一致的微生物组改变。最一致的变化包括与 HC 相比,AUD 中多种产生丁酸盐的家族的丰度显著降低,包括 、 和 ,而与 AUD 相比,ALD 中的这些家族进一步减少。其他重要结果包括 AUD 中内毒素产生菌 的增加,ALD 组的增加最大。所有这些改变都可能导致 AUD 和 ALD 相关的肠道通透性增加和炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47b5/9916746/0bb667ba28ba/ijms-24-02461-g001.jpg

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