Evidence map›Paper›PMID 31530820›Full record

Trial reportScientific reports2019

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

Qiang Zeng, Dongfang Li, Yuan He, Yinhu Li, Zhenyu Yang, Xiaolan Zhao, Yanhong Liu, Yu Wang, Jing Sun, Xin Feng and 14 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 218 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
218citing papers in PubMed, 4 pooled it
14.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

218 citing papers in PubMed, 4 syntheses or guidelines pooled it, 413 citations in OpenAlex.

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158 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors at 11 institutions in 3 countries.

Qiang ZengHealth management institute, People's Liberation Army General Hospital, Beijing, China.
Dongfang LiWuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan, Hubei Province, China.
Yuan HeNational Research Institute for Health, Beijing, China.
Yinhu LiDepartment of Computer Science, College of Science and Engineering, City University of Hong Kong, Hong Kong, China.
Zhenyu YangSchool of Statistics and Data Science, Nankai University, Tianjin, China.
Xiaolan ZhaoSouthwest Hospital of Third Military Medical University, Chongqing, China.
Yanhong LiuDepartment of Microbial Research, WeHealthGene Institute, Shenzhen, Guangdong Province, China.
Yu WangHealth management center, The 910th Hospital of People's Liberation Army, Quanzhou, Fujian Province, China.
Jing SunThe China-Japan Union Hospital of Jilin University, Changchun, Jilin Province, China.
Xin FengDepartment of Microbial Research, WeHealthGene Institute, Shenzhen, Guangdong Province, China.
Fei WangHealth management institute, People's Liberation Army General Hospital, Beijing, China.
Jiaxing ChenDepartment of Computer Science, College of Science and Engineering, City University of Hong Kong, Hong Kong, China.
Yuejie ZhengJoint Laboratory of Micro-ecology and Children's Health, Shenzhen Children's Hospital & Shenzhen WeHealthGene Co. Ltd., Shenzhen, Guangdong Province, China.
Yonghong YangJoint Laboratory of Micro-ecology and Children's Health, Shenzhen Children's Hospital & Shenzhen WeHealthGene Co. Ltd., Shenzhen, Guangdong Province, China.
Xuelin SunDepartment of Cardiology, Longkou People's Hospital, Longkou, Shandong Province, China.
Ximing XuSchool of Statistics and Data Science, Nankai University, Tianjin, China.
Daxi WangDepartment of Microbial Research, WeHealthGene Institute, Shenzhen, Guangdong Province, China.
Toby KenneyDepartment of Mathematics and Statistics, Dalhousie University, Halifax, Nova Scotia, Canada.
Yiqi JiangDepartment of Computer Science, College of Science and Engineering, City University of Hong Kong, Hong Kong, China.
Hong GuDepartment of Mathematics and Statistics, Dalhousie University, Halifax, Nova Scotia, Canada.
Yongli LiDepartment of Health Management, Henan Provincial People's Hospital, Zhengzhou, Henan Province, China.
Ke ZhouWuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan, Hubei Province, China. k.zhou@hust.edu.cn.
Shuaicheng LiDepartment of Computer Science, College of Science and Engineering, City University of Hong Kong, Hong Kong, China. shuaicli@cityu.edu.hk.
Wenkui DaiDepartment of Computer Science, College of Science and Engineering, City University of Hong Kong, Hong Kong, China. wenkuidai2-c@my.cityu.edu.hk.
City University of Hong Kong · HKShenzhen Children's Hospital · CNDalhousie University · CANankai University · CNHaikou City People's Hospital · CNHenan Provincial People's Hospital · CNHuazhong University of Science and Technology · CNSouthwest Hospital · CNThe 180th Hospital of PLA · CNUnion Hospital · CNWuhan National Laboratory for Optoelectronics · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AdultBiomarkersBody Mass IndexFecesFemaleGastrointestinal MicrobiomeHumansMaleMiddle AgedObesityBiomarkers

Identifiers

PMID31530820
PMCPMC6748942
OpenAlexW2974432944

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.