Gut metabolites and inflammation factors in non-alcoholic fatty liver disease: A systematic review and meta-analysis

被引:62
作者
Pan, Xiongfeng [1 ]
Wen, Shi Wu [2 ,3 ,4 ]
Kaminga, Atipatsa C. [1 ,5 ]
Liu, Aizhong [1 ]
机构
[1] Cent South Univ, Xiangya Sch Publ Hlth, Dept Epidemiol & Hlth Stat, Changsha, Peoples R China
[2] Ottawa Hosp Res Inst, OMNI Res Grp, Ottawa, ON, Canada
[3] Univ Ottawa, Dept Obstet & Gynaecol, Fac Med, Ottawa, ON, Canada
[4] Univ Ottawa, Sch Epidemiol & Publ Hlth, Fac Med, Ottawa, ON, Canada
[5] Mzuzu Univ, Dept Math & Stat, Mzuzu, Malawi
基金
加拿大健康研究院;
关键词
DOUBLE-BLIND; SYNBIOTIC SUPPLEMENTATION; POTENTIAL ROLE; MICROBIOTA; OBESITY; STRESS; PILOT; GENE;
D O I
10.1038/s41598-020-65051-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The interaction of gut microbiota, related metabolites and inflammation factors with nonalcoholic fatty liver disease (NAFLD) remains unclearly defined. The aim of this systematic review and meta-analysis was to synthesize previous study findings to better understand this interaction. Relevant research articles published not later than September, 2019 were searched in the following databases: Web of Science, PubMed, Embase, and Cochrane Library. The search strategy and inclusion criteria for this study yielded a total of 47 studies, of which only 11 were eligible for meta-analysis. The narrative analysis of these articles found that there is interplay between the key gut microbiota, related metabolites and inflammation factors, which modulate the development and progression of NAFLD. In addition, the results of meta-analysis showed that probiotic supplementation significantly decreased tumor necrosis factor-alpha (TNF-alpha) in NAFLD patients (standardized mean difference (SMD) = -0.52, confidence interval (CI): -0.86 to -0.18, and p = 0.003) and C-reactive protein (CRP) (SMD = -0.62, CI: -0.80 to -0.43, and p < 0.001). However, whether therapies can target TNF-alpha and CRP in order treat NAFLD still needs further investigation. Therefore, these results suggest that the interaction of the key gut microbiota, related metabolites and inflammation factors with NAFLD may provide a novel therapeutic target for the clinical and pharmacological treatment of NAFLD.
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收藏
页数:11
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