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慢性酒精过度摄入患者肠道微生物组成和功能的特征。

Characterization of gut microbiota composition and functions in patients with chronic alcohol overconsumption.

机构信息

Unger-Vetlesen Institute, Lovisenberg Diaconal Hospital, Oslo, Norway.

PatoGen AS, Ålesund, Norway.

出版信息

Gut Microbes. 2019;10(6):663-675. doi: 10.1080/19490976.2019.1580097. Epub 2019 Mar 20.

DOI:10.1080/19490976.2019.1580097
PMID:30894059
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6866679/
Abstract

Excessive alcohol intake can alter the gut microbiota, which may underlie the pathophysiology of alcohol-related diseases. We examined gut microbiota composition and functions in patients with alcohol overconsumption for >10 years, compared to a control group of patients with a history of no or low alcohol intake. Faecal microbiota composition was assessed by 16S rRNA sequencing. Gut microbiota functions were evaluated by quantification of short-chain fatty acids (SCFAs) and predictive metagenome profiling (PICRUSt). Twenty-four patients, mean age 64.8 years (19 males), with alcohol overconsumption, and 18 control patients, mean age 58.2 years (14 males) were included. The two groups were comparable regarding basic clinical variables. Nutritional assessment revealed lower total score on the screening tool Mini Nutritional Assessment, lower muscle mass as assessed by handgrip strength, and lower plasma vitamin C levels in the alcohol overconsumption group. Bacteria from phylum were found in higher relative abundance, while bacteria from genus were found in lower relative abundance in the group of alcohol overconsumers. The group also had higher levels of the genera and , and lower concentration and percentage of butyric acid. When applying PICRUSt to predict the metagenomic composition, we found that genes related to invasion of epithelial cells were more common in the group of alcohol overconsumers. We conclude that gut microbiota composition and functions in patients with alcohol overconsumption differ from patients with low consumption of alcohol, and seem to be skewed into a putative pro-inflammatory direction.

摘要

过量饮酒会改变肠道微生物群,这可能是酒精相关疾病的病理生理学基础。我们研究了超过 10 年过量饮酒的患者与低饮酒或无饮酒史的对照组患者的肠道微生物群组成和功能。通过 16S rRNA 测序评估粪便微生物群组成。通过短链脂肪酸 (SCFA) 的定量和预测宏基因组分析 (PICRUSt) 评估肠道微生物群功能。纳入 24 名平均年龄 64.8 岁(19 名男性)的过量饮酒患者和 18 名平均年龄 58.2 岁(14 名男性)的对照组患者。两组基本临床变量相当。营养评估显示,酒精过量组的筛选工具 Mini Nutritional Assessment 总评分较低,握力评估的肌肉量较低,血浆维生素 C 水平较低。厚壁菌门的细菌相对丰度较高,而拟杆菌属的细菌相对丰度较低。该组还具有较高的属 和 的丰度,丁酸的浓度和百分比较低。当应用 PICRUSt 预测宏基因组组成时,我们发现酒精过量组中与上皮细胞入侵相关的基因更为常见。我们得出结论,过量饮酒患者的肠道微生物群组成和功能与低饮酒量患者不同,并且似乎偏向于一种潜在的促炎方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1c0/6866679/1d60df2461c3/kgmi-10-06-1580097-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1c0/6866679/7460285ebe2b/kgmi-10-06-1580097-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1c0/6866679/273c65f65ff7/kgmi-10-06-1580097-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1c0/6866679/11642910dd10/kgmi-10-06-1580097-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1c0/6866679/1d60df2461c3/kgmi-10-06-1580097-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1c0/6866679/7460285ebe2b/kgmi-10-06-1580097-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1c0/6866679/273c65f65ff7/kgmi-10-06-1580097-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1c0/6866679/11642910dd10/kgmi-10-06-1580097-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1c0/6866679/1d60df2461c3/kgmi-10-06-1580097-g004.jpg

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