Discrepant gut microbiota markers for the classification of obesity-related metabolic abnormalities

Qiang Zeng(People's Liberation Army No. 150 Hospital), Dongfang Li(Wuhan National Laboratory for Optoelectronics), Yuan He, Yinhu Li(City University of Hong Kong), Zhenyu Yang(Nankai University), Xiaolan Zhao(Army Medical University), Yanhong Liu(Shenzhen Children's Hospital), Yu Wang(The 180th Hospital of PLA), Jing Sun(Jilin University), Xin Feng(Shenzhen Children's Hospital), Fei Wang(People's Liberation Army No. 150 Hospital), Jiaxing Chen(City University of Hong Kong), Yuejie Zheng(Shenzhen Children's Hospital), Yonghong Yang(Shenzhen Children's Hospital), Xuelin Sun(Haikou City People's Hospital), Ximing Xu(Nankai University), Daxi Wang(Shenzhen Children's Hospital), Toby Kenney(Dalhousie University), Yiqi Jiang(City University of Hong Kong), Hong Gu(Dalhousie University), Yongli Li(City University of Hong Kong), Ke Zhou(Wuhan National Laboratory for Optoelectronics), Shuai Cheng Li(City University of Hong Kong), Wenkui Dai(City University of Hong Kong)
Scientific Reports
September 17, 2019
Cited by 418Open Access
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Abstract

The gut microbiota (GM) is related to obesity and other metabolic diseases. To detect GM markers for obesity in patients with different metabolic abnormalities and investigate their relationships with clinical indicators, 1,914 Chinese adults were enrolled for 16S rRNA gene sequencing in this retrospective study. Based on GM composition, Random forest classifiers were constructed to screen the obesity patients with (Group OA) or without metabolic diseases (Group O) from healthy individuals (Group H), and high accuracies were observed for the discrimination of Group O and Group OA (areas under the receiver operating curve (AUC) equal to 0.68 and 0.76, respectively). Furthermore, six GM markers were shared by obesity patients with various metabolic disorders (Bacteroides, Parabacteroides, Blautia, Alistipes, Romboutsia and Roseburia). As for the discrimination with Group O, Group OA exhibited low accuracy (AUC = 0.57). Nonetheless, GM classifications to distinguish between Group O and the obese patients with specific metabolic abnormalities were not accurate (AUC values from 0.59 to 0.66). Common biomarkers were identified for the obesity patients with high uric acid, high serum lipids and high blood pressure, such as Clostridium XIVa, Bacteroides and Roseburia. A total of 20 genera were associated with multiple significant clinical indicators. For example, Blautia, Romboutsia, Ruminococcus2, Clostridium sensu stricto and Dorea were positively correlated with indicators of bodyweight (including waistline and body mass index) and serum lipids (including low density lipoprotein, triglyceride and total cholesterol). In contrast, the aforementioned clinical indicators were negatively associated with Bacteroides, Roseburia, Butyricicoccus, Alistipes, Parasutterella, Parabacteroides and Clostridium IV. Generally, these biomarkers hold the potential to predict obesity-related metabolic abnormalities, and interventions based on these biomarkers might be beneficial to weight loss and metabolic risk improvement.


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