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Bacterial Signatures of Paediatric Respiratory Disease: An Individual Participant Data Meta-Analysis.
Broderick, David T J; Waite, David W; Marsh, Robyn L; Camargo, Carlos A; Cardenas, Paul; Chang, Anne B; Cookson, William O C; Cuthbertson, Leah; Dai, Wenkui; Everard, Mark L; Gervaix, Alain; Harris, J Kirk; Hasegawa, Kohei; Hoffman, Lucas R; Hong, Soo-Jong; Josset, Laurence; Kelly, Matthew S; Kim, Bong-Soo; Kong, Yong; Li, Shuai C; Mansbach, Jonathan M; Mejias, Asuncion; O'Toole, George A; Paalanen, Laura; Pérez-Losada, Marcos; Pettigrew, Melinda M; Pichon, Maxime; Ramilo, Octavio; Ruokolainen, Lasse; Sakwinska, Olga; Seed, Patrick C; van der Gast, Christopher J; Wagner, Brandie D; Yi, Hana; Zemanick, Edith T; Zheng, Yuejie; Pillarisetti, Naveen; Taylor, Michael W.
Afiliação
  • Broderick DTJ; School of Biological Sciences, University of Auckland, Auckland, New Zealand.
  • Waite DW; School of Biological Sciences, University of Auckland, Auckland, New Zealand.
  • Marsh RL; Child Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, NT, Australia.
  • Camargo CA; Department of Emergency Medicine, Massachusetts General Hospital, Boston, MA, United States.
  • Cardenas P; Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, United States.
  • Chang AB; Harvard Medical School, Boston, MA, United States.
  • Cookson WOC; Colegio de Ciencias Biológicas y Ambientales, Instituto de Microbiología, Universidad San Francisco de Quito, Quito, Ecuador.
  • Cuthbertson L; Child Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, NT, Australia.
  • Dai W; Department of Respiratory and Sleep Medicine, Queensland Children's Hospital, Brisbane, QLD, Australia.
  • Everard ML; Australian Centre for Health Services Innovation, Queensland University of Technology, Brisbane, QLD, Australia.
  • Gervaix A; National Heart and Lung Institute, Imperial College London, London, United Kingdom.
  • Harris JK; Royal Brompton and Harefield NHS Foundation Trust, London, United Kingdom.
  • Hasegawa K; Royal Brompton and Harefield NHS Foundation Trust, London, United Kingdom.
  • Hoffman LR; Department of Obstetrics and Gynecology, Peking University Shenzhen Hospital, Shenzhen, China.
  • Hong SJ; School of Medicine, University of Western Australia, Perth, WA, Australia.
  • Josset L; Department of Pediatrics, Gynecology and Obstetrics, Faculty of Medicine, University Hospitals of Geneva, Geneva, Switzerland.
  • Kelly MS; Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO, United States.
  • Kim BS; Department of Emergency Medicine, Massachusetts General Hospital, Boston, MA, United States.
  • Kong Y; Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, United States.
  • Li SC; Harvard Medical School, Boston, MA, United States.
  • Mansbach JM; Seattle Children's Hospital, Seattle, WA, United States.
  • Mejias A; Department of Pediatrics and Microbiology, University of Washington, Seattle, WA, United States.
  • O'Toole GA; Department of Pediatrics, Childhood Asthma Atopy Center, Humidifier Disinfectant Health Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
  • Paalanen L; Hospices Civils de Lyon, Lyon, France.
  • Pérez-Losada M; Division of Pediatric Infectious Diseases, Duke University, Durham, NC, United States.
  • Pettigrew MM; Department of Life Science, Multidisciplinary Genome Institute, Hallym University, Chuncheon, South Korea.
  • Pichon M; Department of Biostatistics, Yale School of Public Health, Yale University, New Haven, CT, United States.
  • Ramilo O; Department of Computer Science, City University of Hong Kong, Kowloon, Hong Kong SAR, China.
  • Ruokolainen L; Department of Biomedical Engineering, City University of Hong Kong, Kowloon, Hong Kong SAR, China.
  • Sakwinska O; Harvard Medical School, Boston, MA, United States.
  • Seed PC; Department of Pediatrics, Boston Children's Hospital, Boston, MA, United States.
  • van der Gast CJ; Division of Pediatric Infectious Diseases, Department of Pediatrics, Center for Vaccines and Immunity, Abigail Wexner Research Institute at Nationwide Children's Hospital, The Ohio State University College of Medicine, Columbus, OH, United States.
  • Wagner BD; Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Hanover, NH, United States.
  • Yi H; Finnish Institute for Health and Welfare (THL), Helsinki, Finland.
  • Zemanick ET; Department of Biostatistics and Bioinformatics, Computational Biology Institute, Milken Institute School of Public Health, George Washington University, Washington, DC, United States.
  • Zheng Y; CIBIO-InBIO, Centro de Investigação em Biodiversidade e Recursos Genéticos, Universidade do Porto, Campus Agrário de Vairão, Vairão, Portugal.
  • Pillarisetti N; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, United States.
  • Taylor MW; CHU Poitiers, Infectious Agents Department, Poitiers, France.
Front Microbiol ; 12: 711134, 2021.
Article em En | MEDLINE | ID: mdl-35002989
ABSTRACT

Introduction:

The airway microbiota has been linked to specific paediatric respiratory diseases, but studies are often small. It remains unclear whether particular bacteria are associated with a given disease, or if a more general, non-specific microbiota association with disease exists, as suggested for the gut. We investigated overarching patterns of bacterial association with acute and chronic paediatric respiratory disease in an individual participant data (IPD) meta-analysis of 16S rRNA gene sequences from published respiratory microbiota studies.

Methods:

We obtained raw microbiota data from public repositories or via communication with corresponding authors. Cross-sectional analyses of the paediatric (<18 years) microbiota in acute and chronic respiratory conditions, with >10 case subjects were included. Sequence data were processed using a uniform bioinformatics pipeline, removing a potentially substantial source of variation. Microbiota differences across diagnoses were assessed using alpha- and beta-diversity approaches, machine learning, and biomarker analyses.

Results:

We ultimately included 20 studies containing individual data from 2624 children. Disease was associated with lower bacterial diversity in nasal and lower airway samples and higher relative abundances of specific nasal taxa including Streptococcus and Haemophilus. Machine learning success in assigning samples to diagnostic groupings varied with anatomical site, with positive predictive value and sensitivity ranging from 43 to 100 and 8 to 99%, respectively.

Conclusion:

IPD meta-analysis of the respiratory microbiota across multiple diseases allowed identification of a non-specific disease association which cannot be recognised by studying a single disease. Whilst imperfect, machine learning offers promise as a potential additional tool to aid clinical diagnosis.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies / Systematic_reviews Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies / Systematic_reviews Idioma: En Ano de publicação: 2021 Tipo de documento: Article