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Distinct enterotypes and dysbiosis: unraveling gut microbiota in pulmonary and critical care medicine inpatients.
Li, Naijian; Tan, Guiyan; Xie, Zhiling; Chen, Weixin; Yang, Zhaowei; Wang, Zhang; Liu, Sha; He, Mengzhang.
Afiliação
  • Li N; Department of Allergy and Clinical Immunology, State Key Laboratory of Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital, Guangzhou Medical University, Guangzhou, People's Republic of China.
  • Tan G; Johns Hopkins Asthma & Allergy Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Xie Z; Department of Respiratory and Critical Care Medicine, The First People's Hospital of Foshan, Foshan, People's Republic of China.
  • Chen W; Department of Pulmonary and Critical Care Medicine, Zhongshan City People's Hospital, Zhongshan, People's Republic of China.
  • Yang Z; Department of Chinese and Western Medicine in Clinical Medicine, The Clinical School of Chinese and Western Medicine, Guangzhou Medical University, Guangzhou, People's Republic of China.
  • Wang Z; Department of Allergy and Clinical Immunology, State Key Laboratory of Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital, Guangzhou Medical University, Guangzhou, People's Republic of China.
  • Liu S; Biomedical Research Center, Institute of Ecological Sciences, School of Life Sciences, State Key Laboratory of Respiratory Disease, South China Normal University, Guangzhou, People's Republic of China.
  • He M; Department of Pulmonary and Critical Care Medicine, The Second Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, People's Republic of China. 2018020001@usc.edu.cn.
Respir Res ; 25(1): 304, 2024 Aug 10.
Article em En | MEDLINE | ID: mdl-39127664
ABSTRACT

BACKGROUND:

The gut-lung axis, pivotal for respiratory health, is inadequately explored in pulmonary and critical care medicine (PCCM) inpatients.

METHODS:

Examining PCCM inpatients from three medical university-affiliated hospitals, we conducted 16S ribosomal RNA sequencing on stool samples (inpatients, n = 374; healthy controls, n = 105). We conducted statistical analyses to examine the gut microbiota composition in PCCM inpatients, comparing it to that of healthy controls. Additionally, we explored the associations between gut microbiota composition and various clinical factors, including age, white blood cell count, neutrophil count, platelet count, albumin level, hemoglobin level, length of hospital stay, and medical costs.

RESULTS:

PCCM inpatients exhibited lower gut microbiota diversity than healthy controls. Principal Coordinates Analysis revealed marked overall microbiota structure differences. Four enterotypes, including the exclusive Enterococcaceae enterotype in inpatients, were identified. Although no distinctions were found at the phylum level, 15 bacterial families exhibited varying abundances. Specifically, the inpatient population from PCCM showed a significantly higher abundance of Enterococcaceae, Lactobacillaceae, Erysipelatoclostridiaceae, Clostridiaceae, and Tannerellaceae. Using random forest analyses, we calculated the areas under the receiver operating characteristic curves (AUCs) to be 0.75 (95% CIs 0.69-0.80) for distinguishing healthy individuals from inpatients. The four most abundant genera retained in the classifier were Blautia, Subdoligranulum, Enterococcus, and Klebsiella.

CONCLUSIONS:

Evidence of gut microbiota dysbiosis in PCCM inpatients underscores the gut-lung axis's significance, promising further avenues in respiratory health research.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Disbiose / Microbioma Gastrointestinal Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Disbiose / Microbioma Gastrointestinal Idioma: En Ano de publicação: 2024 Tipo de documento: Article