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

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 retros...

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Autores principales: Zeng, Qiang, Li, Dongfang, He, Yuan, Li, Yinhu, Yang, Zhenyu, Zhao, Xiaolan, Liu, Yanhong, Wang, Yu, Sun, Jing, Feng, Xin, Wang, Fei, Chen, Jiaxing, Zheng, Yuejie, Yang, Yonghong, Sun, Xuelin, Xu, Ximing, Wang, Daxi, Kenney, Toby, Jiang, Yiqi, Gu, Hong, Li, Yongli, Zhou, Ke, Li, Shuaicheng, Dai, Wenkui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6748942/
https://www.ncbi.nlm.nih.gov/pubmed/31530820
http://dx.doi.org/10.1038/s41598-019-49462-w
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author Zeng, Qiang
Li, Dongfang
He, Yuan
Li, Yinhu
Yang, Zhenyu
Zhao, Xiaolan
Liu, Yanhong
Wang, Yu
Sun, Jing
Feng, Xin
Wang, Fei
Chen, Jiaxing
Zheng, Yuejie
Yang, Yonghong
Sun, Xuelin
Xu, Ximing
Wang, Daxi
Kenney, Toby
Jiang, Yiqi
Gu, Hong
Li, Yongli
Zhou, Ke
Li, Shuaicheng
Dai, Wenkui
author_facet Zeng, Qiang
Li, Dongfang
He, Yuan
Li, Yinhu
Yang, Zhenyu
Zhao, Xiaolan
Liu, Yanhong
Wang, Yu
Sun, Jing
Feng, Xin
Wang, Fei
Chen, Jiaxing
Zheng, Yuejie
Yang, Yonghong
Sun, Xuelin
Xu, Ximing
Wang, Daxi
Kenney, Toby
Jiang, Yiqi
Gu, Hong
Li, Yongli
Zhou, Ke
Li, Shuaicheng
Dai, Wenkui
author_sort Zeng, Qiang
collection PubMed
description 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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spelling pubmed-67489422019-09-27 Discrepant gut microbiota markers for the classification of obesity-related metabolic abnormalities Zeng, Qiang Li, Dongfang He, Yuan Li, Yinhu Yang, Zhenyu Zhao, Xiaolan Liu, Yanhong Wang, Yu Sun, Jing Feng, Xin Wang, Fei Chen, Jiaxing Zheng, Yuejie Yang, Yonghong Sun, Xuelin Xu, Ximing Wang, Daxi Kenney, Toby Jiang, Yiqi Gu, Hong Li, Yongli Zhou, Ke Li, Shuaicheng Dai, Wenkui Sci Rep Article 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. Nature Publishing Group UK 2019-09-17 /pmc/articles/PMC6748942/ /pubmed/31530820 http://dx.doi.org/10.1038/s41598-019-49462-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zeng, Qiang
Li, Dongfang
He, Yuan
Li, Yinhu
Yang, Zhenyu
Zhao, Xiaolan
Liu, Yanhong
Wang, Yu
Sun, Jing
Feng, Xin
Wang, Fei
Chen, Jiaxing
Zheng, Yuejie
Yang, Yonghong
Sun, Xuelin
Xu, Ximing
Wang, Daxi
Kenney, Toby
Jiang, Yiqi
Gu, Hong
Li, Yongli
Zhou, Ke
Li, Shuaicheng
Dai, Wenkui
Discrepant gut microbiota markers for the classification of obesity-related metabolic abnormalities
title Discrepant gut microbiota markers for the classification of obesity-related metabolic abnormalities
title_full Discrepant gut microbiota markers for the classification of obesity-related metabolic abnormalities
title_fullStr Discrepant gut microbiota markers for the classification of obesity-related metabolic abnormalities
title_full_unstemmed Discrepant gut microbiota markers for the classification of obesity-related metabolic abnormalities
title_short Discrepant gut microbiota markers for the classification of obesity-related metabolic abnormalities
title_sort discrepant gut microbiota markers for the classification of obesity-related metabolic abnormalities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6748942/
https://www.ncbi.nlm.nih.gov/pubmed/31530820
http://dx.doi.org/10.1038/s41598-019-49462-w
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