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The gut microbiome in atherosclerotic cardiovascular disease

Author

Listed:
  • Zhuye Jie

    (BGI-Shenzhen
    China National Genebank
    Shenzhen Key Laboratory of Human Commensal Microorganisms and Health Research, BGI-Shenzhen)

  • Huihua Xia

    (BGI-Shenzhen
    China National Genebank)

  • Shi-Long Zhong

    (Guangdong Cardiovascular Institute
    Guangdong Academy of Medical Sciences)

  • Qiang Feng

    (BGI-Shenzhen
    China National Genebank
    Shenzhen Engineering Laboratory of Detection and Intervention of Human Intestinal Microbiome
    University of Copenhagen)

  • Shenghui Li

    (BGI-Shenzhen)

  • Suisha Liang

    (BGI-Shenzhen
    China National Genebank)

  • Huanzi Zhong

    (BGI-Shenzhen
    China National Genebank
    Shenzhen Key Laboratory of Human Commensal Microorganisms and Health Research, BGI-Shenzhen
    University of Copenhagen)

  • Zhipeng Liu

    (BGI-Shenzhen
    University of Chinese Academy of Sciences)

  • Yuan Gao

    (BGI-Shenzhen
    China National Genebank)

  • Hui Zhao

    (BGI-Shenzhen)

  • Dongya Zhang

    (BGI-Shenzhen)

  • Zheng Su

    (BGI-Shenzhen)

  • Zhiwei Fang

    (BGI-Shenzhen)

  • Zhou Lan

    (BGI-Shenzhen)

  • Junhua Li

    (BGI-Shenzhen
    China National Genebank
    Shenzhen Key Laboratory of Human Commensal Microorganisms and Health Research, BGI-Shenzhen
    South China University of Technology)

  • Liang Xiao

    (BGI-Shenzhen
    China National Genebank
    Shenzhen Engineering Laboratory of Detection and Intervention of Human Intestinal Microbiome)

  • Jun Li

    (BGI-Shenzhen)

  • Ruijun Li

    (Chinese PLA General Hospital)

  • Xiaoping Li

    (BGI-Shenzhen
    China National Genebank)

  • Fei Li

    (BGI-Shenzhen
    China National Genebank
    University of Chinese Academy of Sciences)

  • Huahui Ren

    (BGI-Shenzhen)

  • Yan Huang

    (BGI-Shenzhen)

  • Yangqing Peng

    (BGI-Shenzhen
    Washington University School of Medicine, St. Louis)

  • Guanglei Li

    (BGI-Shenzhen)

  • Bo Wen

    (BGI-Shenzhen
    China National Genebank)

  • Bo Dong

    (BGI-Shenzhen)

  • Ji-Yan Chen

    (Guangdong Cardiovascular Institute)

  • Qing-Shan Geng

    (Guangdong Cardiovascular Institute)

  • Zhi-Wei Zhang

    (Guangdong Cardiovascular Institute)

  • Huanming Yang

    (BGI-Shenzhen
    China National Genebank
    James D. Watson Institute of Genome Sciences)

  • Jian Wang

    (BGI-Shenzhen
    China National Genebank
    James D. Watson Institute of Genome Sciences)

  • Jun Wang

    (BGI-Shenzhen
    Macau University of Science and Technology
    iCarbonX)

  • Xuan Zhang

    (Chinese Academy of Medical Sciences and Peking Union Medical College)

  • Lise Madsen

    (BGI-Shenzhen
    China National Genebank
    University of Copenhagen
    National Institute of Nutrition and Seafood Research, (NIFES))

  • Susanne Brix

    (Technical University of Denmark (DTU))

  • Guang Ning

    (Shanghai Jiao Tong University School of Medicine)

  • Xun Xu

    (BGI-Shenzhen
    China National Genebank)

  • Xin Liu

    (BGI-Shenzhen
    China National Genebank)

  • Yong Hou

    (BGI-Shenzhen
    China National Genebank)

  • Huijue Jia

    (BGI-Shenzhen
    China National Genebank
    Shenzhen Key Laboratory of Human Commensal Microorganisms and Health Research, BGI-Shenzhen
    Macau University of Science and Technology)

  • Kunlun He

    (Chinese PLA General Hospital)

  • Karsten Kristiansen

    (BGI-Shenzhen
    China National Genebank
    University of Copenhagen)

Abstract

The gut microbiota has been linked to cardiovascular diseases. However, the composition and functional capacity of the gut microbiome in relation to cardiovascular diseases have not been systematically examined. Here, we perform a metagenome-wide association study on stools from 218 individuals with atherosclerotic cardiovascular disease (ACVD) and 187 healthy controls. The ACVD gut microbiome deviates from the healthy status by increased abundance of Enterobacteriaceae and Streptococcus spp. and, functionally, in the potential for metabolism or transport of several molecules important for cardiovascular health. Although drug treatment represents a confounding factor, ACVD status, and not current drug use, is the major distinguishing feature in this cohort. We identify common themes by comparison with gut microbiome data associated with other cardiometabolic diseases (obesity and type 2 diabetes), with liver cirrhosis, and rheumatoid arthritis. Our data represent a comprehensive resource for further investigations on the role of the gut microbiome in promoting or preventing ACVD as well as other related diseases.

Suggested Citation

  • Zhuye Jie & Huihua Xia & Shi-Long Zhong & Qiang Feng & Shenghui Li & Suisha Liang & Huanzi Zhong & Zhipeng Liu & Yuan Gao & Hui Zhao & Dongya Zhang & Zheng Su & Zhiwei Fang & Zhou Lan & Junhua Li & Li, 2017. "The gut microbiome in atherosclerotic cardiovascular disease," Nature Communications, Nature, vol. 8(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-00900-1
    DOI: 10.1038/s41467-017-00900-1
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    Cited by:

    1. Qi Su & Qin Liu & Raphaela Iris Lau & Jingwan Zhang & Zhilu Xu & Yun Kit Yeoh & Thomas W. H. Leung & Whitney Tang & Lin Zhang & Jessie Q. Y. Liang & Yuk Kam Yau & Jiaying Zheng & Chengyu Liu & Mengjin, 2022. "Faecal microbiome-based machine learning for multi-class disease diagnosis," Nature Communications, Nature, vol. 13(1), pages 1-8, December.
    2. Martin Stocker & Claus Klingenberg & Lars Navér & Viveka Nordberg & Alberto Berardi & Salhab el Helou & Gerhard Fusch & Joseph M. Bliss & Dirk Lehnick & Varvara Dimopoulou & Nicholas Guerina & Joanna , 2023. "Less is more: Antibiotics at the beginning of life," Nature Communications, Nature, vol. 14(1), pages 1-9, December.

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