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

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作者
Qiang Zeng
Dongfang Li
Yuan He
Yinhu Li
Zhenyu Yang
Xiaolan Zhao
Yanhong Liu
Yu Wang
Jing Sun
Xin Feng
Fei Wang
Jiaxing Chen
Yuejie Zheng
Yonghong Yang
Xuelin Sun
Ximing Xu
Daxi Wang
Toby Kenney
Yiqi Jiang
Hong Gu
Yongli Li
Ke Zhou
Shuaicheng Li
Wenkui Dai
机构
[1] People’s Liberation Army General Hospital,Health management institute
[2] Huazhong University of Science and Technology,Wuhan National Laboratory for Optoelectronics
[3] WeHealthGene Institute,Department of Microbial Research
[4] Shenzhen Children’s Hospital & Shenzhen WeHealthGene Co. Ltd.,Joint Laboratory of Micro
[5] National Research Institute for Health,ecology and Children’s Health
[6] City University of Hong Kong,Department of Computer Science, College of Science and Engineering
[7] Nankai University,School of Statistics and Data Science
[8] Southwest Hospital of Third Military Medical University,Health management center
[9] The 910th Hospital of People’s Liberation Army,Department of Respiratory
[10] The China-Japan Union Hospital of Jilin University,Department of Cardiology
[11] Shenzhen Children’s Hospital,Department of Mathematics and Statistics
[12] Longkou People’s Hospital,Department of Health Management
[13] Dalhousie University,undefined
[14] Henan Provincial People’s Hospital,undefined
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摘要
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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