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nSeP: immune and metabolic biomarkers for early detection of neonatal sepsis—protocol for a prospective multicohort study

INTRODUCTION: Diagnosing neonatal sepsis is heavily dependent on clinical phenotyping as culture-positive body fluid has poor sensitivity, and existing blood biomarkers have poor specificity. A combination of machine learning, statistical and deep pathway biology analyses led to the identification o...

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Autores principales: Chakraborty, Mallinath, Rodrigues, Patrícia R S, Watkins, W John, Hayward, Angela, Sharma, Alok, Hayward, Rachel, Smit, Elisa, Jones, Rebekka, Goel, Nitin, Asokkumar, Amar, Calvert, Jennifer, Odd, David, Morris, Ian, Doherty, Cora, Elliott, Sian, Strang, Angela, Andrews, Robert, Zaher, Summia, Sharma, Simran, Bell, Sarah, Oruganti, Siva, Smith, Claire, Orme, Judith, Edkins, Sarah, Craigon, Marie, White, Daniel, Dantoft, Widad, Davies, Luke C, Moet, Linda, McLaren, James E, Clarkstone, Samantha, Watson, Gareth L, Hood, Kerenza, Kotecha, Sailesh, Morgan, B. Paul, O’Donnell, Valerie B, Ghazal, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718461/
https://www.ncbi.nlm.nih.gov/pubmed/37010923
http://dx.doi.org/10.1136/bmjopen-2021-050100
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author Chakraborty, Mallinath
Rodrigues, Patrícia R S
Watkins, W John
Hayward, Angela
Sharma, Alok
Hayward, Rachel
Smit, Elisa
Jones, Rebekka
Goel, Nitin
Asokkumar, Amar
Calvert, Jennifer
Odd, David
Morris, Ian
Doherty, Cora
Elliott, Sian
Strang, Angela
Andrews, Robert
Zaher, Summia
Sharma, Simran
Bell, Sarah
Oruganti, Siva
Smith, Claire
Orme, Judith
Edkins, Sarah
Craigon, Marie
White, Daniel
Dantoft, Widad
Davies, Luke C
Moet, Linda
McLaren, James E
Clarkstone, Samantha
Watson, Gareth L
Hood, Kerenza
Kotecha, Sailesh
Morgan, B. Paul
O’Donnell, Valerie B
Ghazal, Peter
author_facet Chakraborty, Mallinath
Rodrigues, Patrícia R S
Watkins, W John
Hayward, Angela
Sharma, Alok
Hayward, Rachel
Smit, Elisa
Jones, Rebekka
Goel, Nitin
Asokkumar, Amar
Calvert, Jennifer
Odd, David
Morris, Ian
Doherty, Cora
Elliott, Sian
Strang, Angela
Andrews, Robert
Zaher, Summia
Sharma, Simran
Bell, Sarah
Oruganti, Siva
Smith, Claire
Orme, Judith
Edkins, Sarah
Craigon, Marie
White, Daniel
Dantoft, Widad
Davies, Luke C
Moet, Linda
McLaren, James E
Clarkstone, Samantha
Watson, Gareth L
Hood, Kerenza
Kotecha, Sailesh
Morgan, B. Paul
O’Donnell, Valerie B
Ghazal, Peter
author_sort Chakraborty, Mallinath
collection PubMed
description INTRODUCTION: Diagnosing neonatal sepsis is heavily dependent on clinical phenotyping as culture-positive body fluid has poor sensitivity, and existing blood biomarkers have poor specificity. A combination of machine learning, statistical and deep pathway biology analyses led to the identification of a tripartite panel of biologically connected immune and metabolic markers that showed greater than 99% accuracy for detecting bacterial infection with 100% sensitivity. The cohort study described here is designed as a large-scale clinical validation of this previous work. METHODS AND ANALYSIS: This multicentre observational study will prospectively recruit a total of 1445 newborn infants (all gestations)—1084 with suspected early—or late-onset sepsis, and 361 controls—over 4 years. A small volume of whole blood will be collected from infants with suspected sepsis at the time of presentation. This sample will be used for integrated transcriptomic, lipidomic and targeted proteomics profiling. In addition, a subset of samples will be subjected to cellular phenotype and proteomic analyses. A second sample from the same patient will be collected at 24 hours, with an opportunistic sampling for stool culture. For control infants, only one set of blood and stool sample will be collected to coincide with clinical blood sampling. Along with detailed clinical information, blood and stool samples will be analysed and the information will be used to identify and validate the efficacy of immune-metabolic networks in the diagnosis of bacterial neonatal sepsis and to identify new host biomarkers for viral sepsis. ETHICS AND DISSEMINATION: The study has received research ethics committee approval from the Wales Research Ethics Committee 2 (reference 19/WA/0008) and operational approval from Health and Care Research Wales. Submission of study results for publication will involve making available all anonymised primary and processed data on public repository sites. TRIAL REGISTRATION NUMBER: NCT03777670
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spelling pubmed-87184612022-01-12 nSeP: immune and metabolic biomarkers for early detection of neonatal sepsis—protocol for a prospective multicohort study Chakraborty, Mallinath Rodrigues, Patrícia R S Watkins, W John Hayward, Angela Sharma, Alok Hayward, Rachel Smit, Elisa Jones, Rebekka Goel, Nitin Asokkumar, Amar Calvert, Jennifer Odd, David Morris, Ian Doherty, Cora Elliott, Sian Strang, Angela Andrews, Robert Zaher, Summia Sharma, Simran Bell, Sarah Oruganti, Siva Smith, Claire Orme, Judith Edkins, Sarah Craigon, Marie White, Daniel Dantoft, Widad Davies, Luke C Moet, Linda McLaren, James E Clarkstone, Samantha Watson, Gareth L Hood, Kerenza Kotecha, Sailesh Morgan, B. Paul O’Donnell, Valerie B Ghazal, Peter BMJ Open Paediatrics INTRODUCTION: Diagnosing neonatal sepsis is heavily dependent on clinical phenotyping as culture-positive body fluid has poor sensitivity, and existing blood biomarkers have poor specificity. A combination of machine learning, statistical and deep pathway biology analyses led to the identification of a tripartite panel of biologically connected immune and metabolic markers that showed greater than 99% accuracy for detecting bacterial infection with 100% sensitivity. The cohort study described here is designed as a large-scale clinical validation of this previous work. METHODS AND ANALYSIS: This multicentre observational study will prospectively recruit a total of 1445 newborn infants (all gestations)—1084 with suspected early—or late-onset sepsis, and 361 controls—over 4 years. A small volume of whole blood will be collected from infants with suspected sepsis at the time of presentation. This sample will be used for integrated transcriptomic, lipidomic and targeted proteomics profiling. In addition, a subset of samples will be subjected to cellular phenotype and proteomic analyses. A second sample from the same patient will be collected at 24 hours, with an opportunistic sampling for stool culture. For control infants, only one set of blood and stool sample will be collected to coincide with clinical blood sampling. Along with detailed clinical information, blood and stool samples will be analysed and the information will be used to identify and validate the efficacy of immune-metabolic networks in the diagnosis of bacterial neonatal sepsis and to identify new host biomarkers for viral sepsis. ETHICS AND DISSEMINATION: The study has received research ethics committee approval from the Wales Research Ethics Committee 2 (reference 19/WA/0008) and operational approval from Health and Care Research Wales. Submission of study results for publication will involve making available all anonymised primary and processed data on public repository sites. TRIAL REGISTRATION NUMBER: NCT03777670 BMJ Publishing Group 2021-12-30 /pmc/articles/PMC8718461/ /pubmed/37010923 http://dx.doi.org/10.1136/bmjopen-2021-050100 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Paediatrics
Chakraborty, Mallinath
Rodrigues, Patrícia R S
Watkins, W John
Hayward, Angela
Sharma, Alok
Hayward, Rachel
Smit, Elisa
Jones, Rebekka
Goel, Nitin
Asokkumar, Amar
Calvert, Jennifer
Odd, David
Morris, Ian
Doherty, Cora
Elliott, Sian
Strang, Angela
Andrews, Robert
Zaher, Summia
Sharma, Simran
Bell, Sarah
Oruganti, Siva
Smith, Claire
Orme, Judith
Edkins, Sarah
Craigon, Marie
White, Daniel
Dantoft, Widad
Davies, Luke C
Moet, Linda
McLaren, James E
Clarkstone, Samantha
Watson, Gareth L
Hood, Kerenza
Kotecha, Sailesh
Morgan, B. Paul
O’Donnell, Valerie B
Ghazal, Peter
nSeP: immune and metabolic biomarkers for early detection of neonatal sepsis—protocol for a prospective multicohort study
title nSeP: immune and metabolic biomarkers for early detection of neonatal sepsis—protocol for a prospective multicohort study
title_full nSeP: immune and metabolic biomarkers for early detection of neonatal sepsis—protocol for a prospective multicohort study
title_fullStr nSeP: immune and metabolic biomarkers for early detection of neonatal sepsis—protocol for a prospective multicohort study
title_full_unstemmed nSeP: immune and metabolic biomarkers for early detection of neonatal sepsis—protocol for a prospective multicohort study
title_short nSeP: immune and metabolic biomarkers for early detection of neonatal sepsis—protocol for a prospective multicohort study
title_sort nsep: immune and metabolic biomarkers for early detection of neonatal sepsis—protocol for a prospective multicohort study
topic Paediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718461/
https://www.ncbi.nlm.nih.gov/pubmed/37010923
http://dx.doi.org/10.1136/bmjopen-2021-050100
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