Short Chain Fatty Acids and Fecal Microbiota Abundance in Humans with Obesity: A Systematic Review and Meta-Analysis

被引:149
作者
Kim, Kyu Nam [1 ]
Yao, Yao [2 ,3 ]
Ju, Sang Yhun [4 ]
机构
[1] Ajou Univ, Sch Med, Dept Family Practice & Community Hlth, Suwon 16499, Gyeonggi Do, South Korea
[2] Peking Univ, Natl Sch Dev, Ctr Healthy Aging & Dev Studies, Beijing 100871, Peoples R China
[3] Peking Univ, Natl Sch Dev, Raissun Inst Adv Studies, Beijing 100871, Peoples R China
[4] Catholic Univ Korea, Coll Med, Uijeongbu St Marys Hosp, Dept Family Med, 271,Cheonbo Ro, Uijeongbusi 11765, Gyeonggido, South Korea
关键词
obesity; microbiome; feces; colon; humans; systematic review; ALTERED GUT MICROBIOTA; OVERWEIGHT; INFLAMMATION; DIET;
D O I
10.3390/nu11102512
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
There have been mixed results regarding the relationship among short chain fatty acids (SCFAs), microbiota, and obesity in human studies. We selected studies that provided data on SCFA levels or fecal microbiota abundance in obese and nonobese individuals and then combined the published estimates using a random-effects meta-analysis. Obese individuals had significantly higher fecal concentrations of acetate (SMD (standardized mean differences) = 0.87, 95% CI (confidence interva) = 0.24-1.50, I-2 (I-squared) = 88.5), propionate (SMD = 0.86, 95% CI = 0.35-1.36, I-2 = 82.3%), and butyrate (SMD = 0.78, 95% CI = 0.29-1.27, I-2 = 81.7%) than nonobese controls. The subgroup analyses showed no evidence of heterogeneity among obese individuals with a BMI >30 kg/m(2) (I-2 = 0.0%). At the phylum level, the abundance of fecal microbiota was reduced in obese compared to nonobese individuals, but the difference was not statistically significant (Bacteroidetes phylum, SMD = -0.36, 95% CI = -0.73-0.01; Firmicutes phylum, SMD = -0.10, 95% CI = -0.31-0.10). The currently available human case-control studies show that obesity is associated with high levels of SCFA but not gut microbiota richness at the phylum level. Additional well-designed studies with a considerable sample size are needed to clarify whether this association is causal, but it is also necessary to identify additional contributors to SCFA production, absorption, and excretion in humans.
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