Changes in the composition of the human intestinal microbiome in alcohol use disorder: a systematic review

微生物群 某种肠道细菌 普氏粪杆菌 失调 双歧杆菌 酒精使用障碍 梭杆菌门 拟杆菌 生物 专性厌氧菌 医学 生物信息学 乳酸菌 肠道菌群 免疫学 细菌 遗传学 生物化学 16S核糖体RNA
作者
Kamil Litwinowicz,Marcin Choroszy,Ewa Waszczuk
出处
期刊:American Journal of Drug and Alcohol Abuse [Informa]
卷期号:46 (1): 4-12 被引量:46
标识
DOI:10.1080/00952990.2019.1669629
摘要

Background: A growing body of evidence highlights the role of the intestine in the development of various alcohol use disorder (AUD) complications. The intestinal microbiome has been proposed as an essential factor in mediating the development of AUD complications such as alcoholic liver disease.Objectives: To provide a comprehensive description of alcohol-induced intestinal microbiome alterations.Methods: We conducted a systematic review of studies investigating the effect of alcohol on the intestinal microbiome using the PRISMA checklist. We searched the Medline database on the PubMed platform for studies determining the effect of alcohol on microbiota in individuals with AUD. The manual search included references of retrieved articles. Only human studies examining the intestinal bacterial microbiome using 16S ribosomal RNA sequencing were included. Data comparing relative abundances of bacteria comprising intestinal microbiota was extracted.Results: We retrieved 17 studies investigating intestinal microbiome alterations in individuals with AUD. Intestinal microbiome alterations in individuals with AUD included depletion of Akkermansia muciniphila and Faecalibacterium prausnitzii and an increase of Enterobacteriaceae. At the phylum level, a higher abundance of Proteobacteria and lower of Bacteroidetes were found. Mixed results regarding Bifidobacterium were obtained. Several species of short-chain fatty acids producing bacteria had a lower abundance in individuals with alcohol use disorder.Conclusion: Intestinal microbiome alterations associated with dysbiosis in individuals with AUD are generally consistent across studies, making it a promising target in potential AUD complications treatment.
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