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Sputum bacterial microbiota signature as a surrogate for predicting disease progression of nontuberculous mycobacterial lung disease.
Huang, Hung-Ling; Lin, Chieh-Hua; Lee, Meng-Rui; Huang, Wei-Chang; Sheu, Chau-Chyun; Cheng, Meng-Hsuan; Lu, Po-Liang; Huang, Cheng-Hsieh; Yeh, Yao-Tsung; Yang, Jinn-Moon; Chong, Inn-Wen; Liao, Yu-Chieh; Wang, Jann-Yuan.
Afiliação
  • Huang HL; Division of Pulmonary and Critical Care Medicine, Kaohsiung, Taiwan; Department of Internal Medicine, Kaohsiung, Taiwan; Department of Internal Medicine, Kaohsiung Municipal Ta-Tung Hospital, Kaohsiung, Taiwan; Graduate Institute of Medicine, College of Medicine, Kaohsiung, Taiwan; Center for Liquid
  • Lin CH; Institute of Population Health Sciences, National Health Research Institutes, Zhunan, Miaoli, Taiwan; Big Data Center, China Medical University Hospital, Taichung 404, Taiwan.
  • Lee MR; Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Huang WC; Division of Chest Medicine, Department of Internal Medicine, Taichung, 407, Taiwan; Mycobacterial Center, Taichung Veterans General Hospital, Taichung, 407, Taiwan; Department of Post-Baccalaureate Medicine, College of Medicine, National Chung Hsing University, Taichung, 402, Taiwan; School of Medic
  • Sheu CC; Division of Pulmonary and Critical Care Medicine, Kaohsiung, Taiwan; Department of Internal Medicine, Kaohsiung, Taiwan.
  • Cheng MH; Division of Pulmonary and Critical Care Medicine, Kaohsiung, Taiwan; Department of Internal Medicine, Kaohsiung, Taiwan; Graduate Institute of Medicine, College of Medicine, Kaohsiung, Taiwan; Department of Respiratory Therapy, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
  • Lu PL; Department of Internal Medicine, Kaohsiung, Taiwan; Graduate Institute of Medicine, College of Medicine, Kaohsiung, Taiwan; Center for Liquid Biopsy and Cohort, Kaohsiung Medical University, Kaohsiung, Taiwan.
  • Huang CH; Aging and Disease Prevention Research Center, Kaohsiung, Taiwan; Department of Medical Laboratory Science and Biotechnology, Fooyin University, Kaohsiung, Taiwan.
  • Yeh YT; Aging and Disease Prevention Research Center, Kaohsiung, Taiwan; Department of Medical Laboratory Science and Biotechnology, Fooyin University, Kaohsiung, Taiwan.
  • Yang JM; Institute of Bioinformatics and Systems Biology, National Yang Ming Chiao Tung University, Hsinchu, Taiwan; Department of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu, Taiwan.
  • Chong IW; Division of Pulmonary and Critical Care Medicine, Kaohsiung, Taiwan; Department of Internal Medicine, Kaohsiung, Taiwan; Graduate Institute of Medicine, College of Medicine, Kaohsiung, Taiwan; Department of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu, Taiwan.
  • Liao YC; Institute of Population Health Sciences, National Health Research Institutes, Zhunan, Miaoli, Taiwan.
  • Wang JY; Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan. Electronic address: jywang@ntu.edu.tw.
Int J Infect Dis ; : 107085, 2024 May 11.
Article em En | MEDLINE | ID: mdl-38740280
ABSTRACT

OBJECTIVES:

Predicting progression of nontuberculous mycobacterial lung disease (NTM-LD) remains challenging. This study evaluated whether sputum bacterial microbiome diversity can be the biomarker and provide novel insights into related phenotypes and treatment timing.

METHODS:

We analyzed 126 sputum microbiomes of 126 patients with newly diagnosed NTM-LD due to Mycobacterium avium complex, M. abscessus complex, and M. kansasii between May 2020 and December 2021. Patients were followed for 2 years to determine their disease progression status. We identified consistently representative genera that differentiated the progressor and nonprogressor by using six methodologies. These genera were used to construct a prediction model using random forest with 5-fold cross validation.

RESULTS:

Disease progression occurred in 49 (38.6%) patients. Compared with nonprogressors, α-diversity was lower in the progressors. Significant compositional differences existed in the ß-diversity between groups (p=0.001). The prediction model for NTM-LD progression constructed using seven genera (Burkholderia, Pseudomonas, Sphingomonas, Candidatus Saccharibacteria, Phocaeicola, Pelomonas, and Phascolarctobacterium) with significantly differential abundance achieved an area under curve of 0.871.

CONCLUSIONS:

Identification of the composition of sputum bacterial microbiome facilitates prediction of the course of NTM-LD, and maybe used to develop precision treatment involving modulating the respiratory microbiome composition to ameliorate NTM-LD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Infect Dis Assunto da revista: DOENCAS TRANSMISSIVEIS Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Infect Dis Assunto da revista: DOENCAS TRANSMISSIVEIS Ano de publicação: 2024 Tipo de documento: Article