Composition of gut microbiota and non-alcoholic fatty liver disease: A systematic review and meta-analysis

被引:32
作者
Su, Xin [1 ]
Chen, Shiyun [1 ]
Liu, Jiazi [1 ]
Feng, Yonghui [1 ]
Han, Eerdun [2 ]
Hao, Xiaolei [2 ]
Liao, Minqi [3 ]
Cai, Jun [1 ]
Zhang, Shiwen [1 ]
Niu, Jianxiang [4 ]
He, Shihua [5 ]
Huang, Shaofen [6 ]
Lo, Kenneth [7 ,8 ]
Zeng, Fangfang [1 ]
机构
[1] Jinan Univ, Sch Med, Dept Publ Hlth & Prevent Med, 601 Huangpu Rd West, Guangzhou 510632, Guangdong, Peoples R China
[2] Inner Mongolia Med Univ, Dept Hepatobiliary Surg, Affiliated Hosp, Hohhot, Inner Mongolia, Peoples R China
[3] Helmholtz Zentrum Munchen, Inst Epidemiol, German Res Ctr Environm Hlth, Neuherberg, Germany
[4] Inner Mongolia Med Univ, Affiliated Hosp, Gen Surg, Hohhot, Inner Mongolia, Peoples R China
[5] Shenzhen Qianhai Shekou Free Trade Zone Hosp, Dept Infect Dis, Shenzhen, Peoples R China
[6] Shenzhen Qianhai Shekou Free Zone Hosp, Shenzhen, Peoples R China
[7] Hong Kong Polytech Univ, Dept Food Sci & Nutr, Kowloon, Hong Kong 999077, Peoples R China
[8] Hong Kong Polytech Univ, Res Inst Future Food, Kowloon, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
gut microbiota; meta-analysis; non-alcoholic fatty liver; systematic review; FUSOBACTERIUM-NUCLEATUM; FECAL MICROBIOTA; RECEPTOR; STEATOHEPATITIS; INFLAMMATION; DYSBIOSIS; BUTYRATE; ETHANOL; OBESITY; IL-17;
D O I
10.1111/obr.13646
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The present systematic review and meta-analysis aimed to summarize the associations between gut microbiota composition and non-alcoholic fatty liver disease. To compare the differences between individuals with or without NAFLD, the standardized mean difference and 95% confidence interval were computed for each alpha-diversity index and relative abundance of gut microbes. The beta-diversity indices were summarized in a qualitative manner. A total of 54 studies with 8894 participants were included. Overall, patients with NAFLD had moderate reduction in alpha-diversity indices including Shannon (SMD = -0.36, 95% CI = [-0.53, -0.19], p < 0.001) and Chao 1 (SMD = -0.42, 95% CI = [-0.68, -0.17], p = 0.001), but no significant differences were found for Simpson, observed species, phylogenetic diversity, richness, abundance-based coverage estimator, and evenness (p ranged from 0.081 to 0.953). Over 75% of the included studies reported significant differences in beta-diversity. Although there was substantial interstudy heterogeneity, especially for analyses at the phylum, class, and family levels, the majority of the included studies showed alterations in the depletion of anti-inflammatory microbes (i.e., Ruminococcaceae and Coprococcus) and the enrichment of proinflammatory microbes (i.e., Fusobacterium and Escherichia) in patients with NAFLD. Perturbations in gut microbiota were associated with NAFLD, commonly reflected by a reduction in beneficial species and an increase in the pathogenic species.
引用
收藏
页数:20
相关论文
共 117 条
[1]  
Anderson JW, 2001, AM J CLIN NUTR, V74, P579
[2]  
Appleton KM, 2021, COCHRANE DB SYST REV, DOI [10.1002/14651858.CD004692.pub5, 10.1002/14651858.00004692.pub5]
[3]   Gut microbiota and human NAFLD: disentangling microbial signatures from metabolic disorders [J].
Aron-Wisnewsky, Judith ;
Vigliotti, Chloe ;
Witjes, Julia ;
Le, Phuong ;
Holleboom, Adriaan G. ;
Verheij, Joanne ;
Nieuwdorp, Max ;
Clement, Karine .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2020, 17 (05) :279-297
[4]   Constitution of mucosa-associated microbiota in the lower digestive tract does not change in early stage of non-alcoholic fatty liver disease with fecal dysbiosis [J].
Asaji, Naoki ;
Inoue, Jun ;
Hayashi, Hiroki ;
Tokunaga, Eri ;
Shimamoto, Yusaku ;
Kinoshita, Masato ;
Tanaka, Takeshi ;
Sakai, Arata ;
Yano, Yoshihiko ;
Ueda, Yoshihide ;
Kodama, Yuzo .
JGH OPEN, 2022, 6 (10) :677-684
[5]   Lower gut microbiome diversity and higher abundance of proinflammatory genus Collinsella are associated with biopsy-proven nonalcoholic steatohepatitis [J].
Astbury, Stuart ;
Atallah, Edmond ;
Vijay, Amrita ;
Aithal, Guruprasad P. ;
Grove, Jane, I ;
Valdes, Ana M. .
GUT MICROBES, 2020, 11 (03) :569-580
[6]   Toll-like receptor 1 as a possible target in non-alcoholic fatty liver disease [J].
Baumann, Anja ;
Nier, Anika ;
Hernandez-Arriaga, Angelica ;
Brandt, Annette ;
Pisarello, Maria J. Lorenzo ;
Jin, Cheng J. ;
Pilar, Esther ;
Camarinha-Silva, Amelia ;
Schattenberg, Joern M. ;
Bergheim, Ina .
SCIENTIFIC REPORTS, 2021, 11 (01)
[7]   Gut microbiota impact on the peripheral immune response in non-alcoholic fatty liver disease related hepatocellular carcinoma [J].
Behary, Jason ;
Amorim, Nadia ;
Jiang, Xiao-Tao ;
Raposo, Anita ;
Gong, Lan ;
McGovern, Emily ;
Ibrahim, Ragy ;
Chu, Francis ;
Stephens, Carlie ;
Jebeili, Hazem ;
Fragomeli, Vincenzo ;
Koay, Yen Chin ;
Jackson, Miriam ;
O'Sullivan, John ;
Weltman, Martin ;
McCaughan, Geoffrey ;
El-Omar, Emad ;
Zekry, Amany .
NATURE COMMUNICATIONS, 2021, 12 (01)
[8]   Gut microbial metabolites in obesity, NAFLD and T2DM [J].
Canfora, Emanuel E. ;
Meex, Ruth C. R. ;
Venema, Koen ;
Blaak, Ellen E. .
NATURE REVIEWS ENDOCRINOLOGY, 2019, 15 (05) :261-273
[9]   Metabolic endotoxemia initiates obesity and insulin resistance [J].
Cani, Patrice D. ;
Amar, Jacques ;
Iglesias, Miguel Angel ;
Poggi, Marjorie ;
Knauf, Claude ;
Bastelica, Delphine ;
Neyrinck, Audrey M. ;
Fava, Francesca ;
Tuohy, Kieran M. ;
Chabo, Chantal ;
Waget, Aurelie ;
Delmee, Evelyne ;
Cousin, Beatrice ;
Sulpice, Thierry ;
Chamontin, Bernard ;
Ferrieres, Jean ;
Tanti, Jean-Francois ;
Gibson, Glenn R. ;
Casteilla, Louis ;
Delzenne, Nathalie M. ;
Alessi, Marie Christine ;
Burcelin, Remy .
DIABETES, 2007, 56 (07) :1761-1772
[10]   A gut microbiome signature for cirrhosis due to nonalcoholic fatty liver disease [J].
Caussy, Cyrielle ;
Tripathi, Anupriya ;
Humphrey, Greg ;
Bassirian, Shirin ;
Singh, Seema ;
Faulkner, Claire ;
Bettencourt, Ricki ;
Rizo, Emily ;
Richards, Lisa ;
Xu, Zhenjiang Z. ;
Downes, Michael R. ;
Evans, Ronald M. ;
Brenner, David A. ;
Sirlin, Claude B. ;
Knight, Rob ;
Loomba, Rohit .
NATURE COMMUNICATIONS, 2019, 10 (1)