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Diversified Shifts in the Cross Talk between Members of the Gut Microbiota and Development of Coronary Artery Diseases

Coronary artery disease (CAD) is one of leading causes of mortality worldwide. Studies on roles that the gut microbiota plays in development of atherosclerosis or acute myocardial infarction (AMI) have been widely reported. However, the gut microbiota is affected by many factors, including age, body...

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Autores principales: Zhang, Tao, Ren, Haiqing, Du, Zhihui, Zou, Tong, Guang, Xuefeng, Zhang, Yanan, Tian, Yuqing, Zhu, Lei, Yu, Jiangkun, Yu, Xue, Zhang, Zhigang, Dai, Hailong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9769841/
https://www.ncbi.nlm.nih.gov/pubmed/36301099
http://dx.doi.org/10.1128/spectrum.02804-22
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author Zhang, Tao
Ren, Haiqing
Du, Zhihui
Zou, Tong
Guang, Xuefeng
Zhang, Yanan
Tian, Yuqing
Zhu, Lei
Yu, Jiangkun
Yu, Xue
Zhang, Zhigang
Dai, Hailong
author_facet Zhang, Tao
Ren, Haiqing
Du, Zhihui
Zou, Tong
Guang, Xuefeng
Zhang, Yanan
Tian, Yuqing
Zhu, Lei
Yu, Jiangkun
Yu, Xue
Zhang, Zhigang
Dai, Hailong
author_sort Zhang, Tao
collection PubMed
description Coronary artery disease (CAD) is one of leading causes of mortality worldwide. Studies on roles that the gut microbiota plays in development of atherosclerosis or acute myocardial infarction (AMI) have been widely reported. However, the gut microbiota is affected by many factors, including age, body mass index (BMI), and hypertension, that lead to high CAD risk. However, the associations between gut microbiota and CAD development or other CAD risk factors remain unexplored. Here, we performed a 16S RNA gene sequencing analysis of 306 fecal samples collected from patients with mild coronary stenosis (MCS; n = 36), stable angina (SA; n = 91), unstable angina (UA; n = 48), and acute myocardial infarction (AMI; n = 66) and 65 non-CAD controls. Using a noise-corrected method based on principal-component analysis (PCA) and the random forest algorithm, we identified the interference with gut microbial profiling of multiple factors (including age, gender, BMI, and hypertension) that potentially contributed significantly to the development of CAD. After correction of noise interference from certain interfering factors, we found consistent indicator microbiota organisms (such as Vampirovibrio, Ruminococcus, and Eisenbergiella) associated with the presence of MCS, SA, and AMI. Establishment of a diagnostic model revealed better performance in early CAD than clinical indexes with indicator microbes. Furthermore, indicator microbes can improve the accuracy of clinical indexes for the diagnosis of AMI. Additionally, we found that the microbial indicators of AMI Sporobacter and Eisenbergiella showed consistent positive and negative correlations to the clinical indexes creatine kinase (CK) and hemoglobin (Hb), respectively. As a control indicator of AMI, Dorea was negatively correlated with CK but positively correlated with Hb. IMPORTANCE Our study discovered the effect of confounding factors on gut microbial variations and identified gut microbial indicators possibly associated with the CAD development after noise correction. Our discovered indicator microbes may have potential for diagnosis or therapy of cardiovascular disorders.
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spelling pubmed-97698412022-12-22 Diversified Shifts in the Cross Talk between Members of the Gut Microbiota and Development of Coronary Artery Diseases Zhang, Tao Ren, Haiqing Du, Zhihui Zou, Tong Guang, Xuefeng Zhang, Yanan Tian, Yuqing Zhu, Lei Yu, Jiangkun Yu, Xue Zhang, Zhigang Dai, Hailong Microbiol Spectr Research Article Coronary artery disease (CAD) is one of leading causes of mortality worldwide. Studies on roles that the gut microbiota plays in development of atherosclerosis or acute myocardial infarction (AMI) have been widely reported. However, the gut microbiota is affected by many factors, including age, body mass index (BMI), and hypertension, that lead to high CAD risk. However, the associations between gut microbiota and CAD development or other CAD risk factors remain unexplored. Here, we performed a 16S RNA gene sequencing analysis of 306 fecal samples collected from patients with mild coronary stenosis (MCS; n = 36), stable angina (SA; n = 91), unstable angina (UA; n = 48), and acute myocardial infarction (AMI; n = 66) and 65 non-CAD controls. Using a noise-corrected method based on principal-component analysis (PCA) and the random forest algorithm, we identified the interference with gut microbial profiling of multiple factors (including age, gender, BMI, and hypertension) that potentially contributed significantly to the development of CAD. After correction of noise interference from certain interfering factors, we found consistent indicator microbiota organisms (such as Vampirovibrio, Ruminococcus, and Eisenbergiella) associated with the presence of MCS, SA, and AMI. Establishment of a diagnostic model revealed better performance in early CAD than clinical indexes with indicator microbes. Furthermore, indicator microbes can improve the accuracy of clinical indexes for the diagnosis of AMI. Additionally, we found that the microbial indicators of AMI Sporobacter and Eisenbergiella showed consistent positive and negative correlations to the clinical indexes creatine kinase (CK) and hemoglobin (Hb), respectively. As a control indicator of AMI, Dorea was negatively correlated with CK but positively correlated with Hb. IMPORTANCE Our study discovered the effect of confounding factors on gut microbial variations and identified gut microbial indicators possibly associated with the CAD development after noise correction. Our discovered indicator microbes may have potential for diagnosis or therapy of cardiovascular disorders. American Society for Microbiology 2022-10-27 /pmc/articles/PMC9769841/ /pubmed/36301099 http://dx.doi.org/10.1128/spectrum.02804-22 Text en Copyright © 2022 Zhang et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Zhang, Tao
Ren, Haiqing
Du, Zhihui
Zou, Tong
Guang, Xuefeng
Zhang, Yanan
Tian, Yuqing
Zhu, Lei
Yu, Jiangkun
Yu, Xue
Zhang, Zhigang
Dai, Hailong
Diversified Shifts in the Cross Talk between Members of the Gut Microbiota and Development of Coronary Artery Diseases
title Diversified Shifts in the Cross Talk between Members of the Gut Microbiota and Development of Coronary Artery Diseases
title_full Diversified Shifts in the Cross Talk between Members of the Gut Microbiota and Development of Coronary Artery Diseases
title_fullStr Diversified Shifts in the Cross Talk between Members of the Gut Microbiota and Development of Coronary Artery Diseases
title_full_unstemmed Diversified Shifts in the Cross Talk between Members of the Gut Microbiota and Development of Coronary Artery Diseases
title_short Diversified Shifts in the Cross Talk between Members of the Gut Microbiota and Development of Coronary Artery Diseases
title_sort diversified shifts in the cross talk between members of the gut microbiota and development of coronary artery diseases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9769841/
https://www.ncbi.nlm.nih.gov/pubmed/36301099
http://dx.doi.org/10.1128/spectrum.02804-22
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