Metabolomics in pediatric lower respiratory tract infections and sepsis: a literature review.


Journal

Pediatric research
ISSN: 1530-0447
Titre abrégé: Pediatr Res
Pays: United States
ID NLM: 0100714

Informations de publication

Date de publication:
02 2023
Historique:
received: 05 01 2022
accepted: 23 05 2022
revised: 19 04 2022
pubmed: 2 7 2022
medline: 9 3 2023
entrez: 1 7 2022
Statut: ppublish

Résumé

Lower respiratory tract infections (LRTIs) are a leading cause of morbidity and mortality in children. The ability of healthcare providers to diagnose and prognose LRTIs in the pediatric population remains a challenge, as children can present with similar clinical features regardless of the underlying pathogen or ultimate severity. Metabolomics, the large-scale analysis of metabolites and metabolic pathways offers new tools and insights that may aid in diagnosing and predicting the outcomes of LRTIs in children. This review highlights the latest literature on the clinical utility of metabolomics in providing care for children with bronchiolitis, pneumonia, COVID-19, and sepsis. IMPACT: This article summarizes current metabolomics approaches to diagnosing and predicting the course of pediatric lower respiratory infections. This article highlights the limitations to current metabolomics research and highlights future directions for the field.

Identifiants

pubmed: 35778499
doi: 10.1038/s41390-022-02162-0
pii: 10.1038/s41390-022-02162-0
pmc: PMC9247944
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

492-502

Informations de copyright

© 2022. The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc.

Références

Troeger, C. et al. Estimates of the global, regional, and national morbidity, mortality, and aetiologies of lower respiratory tract infections in 195 countries: a systematic analysis for the global burden of disease study 2015. Lancet Infect. Dis. 17, 1133–1161 (2017).
doi: 10.1016/S1473-3099(17)30396-1
Boloursaz, M. R. et al. Epidemiology of lower respiratory tract infections in children. J. Compr. Pediatr. 4, 93–98 (2013).
doi: 10.17795/compreped-10273
Elliott, S. P. & Ray, C. G. Viral infections of the lower respiratory tract. Pediatr. Respir. Med. 481–489 (2008).
Elemraid, M. A. et al. Accuracy of the interpretation of chest radiographs for the diagnosis of paediatric pneumonia. PLoS ONE 9, e106051 (2014).
pubmed: 25148361 pmcid: 4141860 doi: 10.1371/journal.pone.0106051
Edwards, G. et al. Predicting poor outcomes in children aged 1–12 with respiratory tract infections: a systematic review. PLoS ONE 16, e0249533 (2021).
pubmed: 33872323 pmcid: 8055026 doi: 10.1371/journal.pone.0249533
Emwas, A.-H. M. The strengths and weaknesses in NMR spectroscopy and mass spectrometry with particular focus on metabolomics research. Metabonomics Methods Mol. Biol. 1277, 161–193 (2015).
pubmed: 25677154 doi: 10.1007/978-1-4939-2377-9_13
Dieterle, F. et al. NMR and MS methods for metabonomics. Methods Mol. Biol. 691, 385–415 (2011).
pubmed: 20972767 doi: 10.1007/978-1-60761-849-2_24
Dunn, W. B., Broadhurst, D. I., Atherton, H. J., Goodacre, R. & Griffin, J. L. Systems level studies of mammalian metabolomes: the roles of mass spectrometry and nuclear magnetic resonance spectroscopy. Chem. Soc. Rev. 40, 387–426 (2011).
pubmed: 20717559 doi: 10.1039/B906712B
Gowda, G. A. & Djukovic, D. Overview of mass spectrometry-based metabolomics: opportunities and challenges. Methods Mol. Biol. 1198, 3–12 (2014).
pubmed: 25270919 pmcid: 4336784 doi: 10.1007/978-1-4939-1258-2_1
Nakayama, Y., Tamada, Y., Tsugawa, H., Bamba, T. & Fukusaki, E. Novel strategy for non-targeted isotope-assisted metabolomics by means of metabolic turnover and multivariate analysis. Metabolites 4, 722–739 (2014).
pubmed: 25257997 pmcid: 4192689 doi: 10.3390/metabo4030722
Courant, F., Antignac, J. P., Dervilly-Pinel, G., & Le Bizec, B. Basics of mass spectrometry based metabolomics. Proteomics 14, 21–22 (2014).
doi: 10.1002/pmic.201400255
Slupsky, C. M. et al. Streptococcus pneumoniae and Staphylococcus aureus pneumonia induce distinct metabolic responses. J. Proteome Res. 8, 3029–3036 (2009).
pubmed: 19368345 doi: 10.1021/pr900103y
Kaddurah-Daouk, R., Kristal, B. S. & Weinshilboum, R. M. Metabolomics: a global biochemical approach to drug response and disease. Annu. Rev. Pharmacol. Toxicol. 48, 653–683 (2008).
pubmed: 18184107 doi: 10.1146/annurev.pharmtox.48.113006.094715
Atzei, A. et al. Metabolomics in paediatric respiratory diseases and bronchiolitis. J. Matern. Fetal Neonatal Med. 24(Suppl 2), 59–62 (2011).
pubmed: 21966897 doi: 10.3109/14767058.2011.607012
Han, Y. Y. et al. Early reversal of pediatric-neonatal septic shock by community physicians is associated with improved outcome. Pediatrics 112, 793–799 (2003).
pubmed: 14523168 doi: 10.1542/peds.112.4.793
Dessi, A. et al. New diagnostic possibilities in systemic neonatal infections: metabolomics. Early Hum. Dev. 90(Suppl 1), S19–S21 (2014).
pubmed: 24709449 doi: 10.1016/S0378-3782(14)70007-6
Delanghe, J. R. & Speeckaert, M. M. Translational research and biomarkers in neonatal sepsis. Clin. Chim. Acta 451, 46–64 (2015).
pubmed: 25661089 doi: 10.1016/j.cca.2015.01.031
Ng, S. et al. Precision medicine for neonatal sepsis. Front. Mol. Biosci. 5, 70 (2018).
pubmed: 30094238 pmcid: 6070631 doi: 10.3389/fmolb.2018.00070
Hasegawa, K., Tsugawa, Y., Brown, D. F., Mansbach, J. M. & Camargo, C. A. Jr Trends in bronchiolitis hospitalizations in the United States, 2000-2009. Pediatrics 132, 28–36 (2013).
pubmed: 23733801 pmcid: 3691534 doi: 10.1542/peds.2012-3877
Mansbach, J. M. et al. Prospective multicenter study of viral etiology and hospital length of stay in children with severe bronchiolitis. Arch. Pediatr. Adolesc. Med. 166, 700–706 (2012).
pubmed: 22473882 pmcid: 3394902 doi: 10.1001/archpediatrics.2011.1669
Calvo, C. et al. Detection of new respiratory viruses in hospitalized infants with bronchiolitis: a three-year prospective study. Acta Paediatr. 99, 883–887 (2010).
pubmed: 20163373 pmcid: 7159545 doi: 10.1111/j.1651-2227.2010.01714.x
Voets, S., van Berlaer, G. & Hachimi-Idrissi, S. Clinical predictors of the severity of bronchiolitis. Eur. J. Emerg. Med. 13, 134–138 (2006).
pubmed: 16679876 doi: 10.1097/01.mej.0000206194.85072.33
Sigurs, N., Bjarnason, R., Sigurbergsson, F., Kjellman, B. & Björkstén, B. Asthma and immunoglobulin E antibodies after respiratory syncytial virus bronchiolitis: a prospective cohort study with matched controls. Pediatrics 95, 500–505 (1995).
pubmed: 7700748 doi: 10.1542/peds.95.4.500
Sigurs, N. et al. Asthma and allergy patterns over 18 years after severe RSV bronchiolitis in the first year of life. Thorax 65, 1045–1052 (2010).
pubmed: 20581410 doi: 10.1136/thx.2009.121582
Adamko, D. J., Saude, E., Bear, M., Regush, S. & Robinson, J. L. Urine metabolomic profiling of children with respiratory tract infections in the emergency department: a pilot study. BMC Infect. Dis. 16, 439 (2016).
pubmed: 27549246 pmcid: 4994221 doi: 10.1186/s12879-016-1709-6
Jackson, D. J. et al. Wheezing rhinovirus illnesses in early life predict asthma development in high-risk children. Am. J. Respir. Crit. Care Med. 178, 667–672 (2008).
pubmed: 18565953 pmcid: 2556448 doi: 10.1164/rccm.200802-309OC
Turi, K. N. et al. Using urine metabolomics to understand the pathogenesis of infant respiratory syncytial virus (RSV) infection and its role in childhood wheezing. Metabolomics 14, 135 (2018).
pubmed: 30830453 pmcid: 6557166 doi: 10.1007/s11306-018-1431-z
Stewart, C. J. et al. Respiratory syncytial virus and rhinovirus bronchiolitis are associated with distinct metabolic pathways. J. Infect. Dis. 217, 1160–1169 (2018).
pubmed: 29293990 doi: 10.1093/infdis/jix680
Stewart, C. J. et al. Associations of nasopharyngeal metabolome and microbiome with severity among infants with bronchiolitis. A multiomic analysis. Am. J. Respir. Crit. Care Med. 196, 882–891 (2017).
pubmed: 28530140 pmcid: 5649976 doi: 10.1164/rccm.201701-0071OC
Stewart, C. J. et al. Serum metabolome is associated with the nasopharyngeal microbiota and disease severity among infants with bronchiolitis. J. Infect. Dis. 219, 2005–2014 (2019).
pubmed: 30629185 pmcid: 6534192 doi: 10.1093/infdis/jiz021
Golan-Tripto, I. et al. Vitamin D deficiency in children with acute bronchiolitis: a prospective cross-sectional case- control study. BMC Pediatr. 21, 211 (2021).
pubmed: 33931018 pmcid: 8085105 doi: 10.1186/s12887-021-02666-4
Alakaş, Y., Celiloğlu, C., Tolunay, O. & Matyar, S. The relationship between bronchiolitis severity and vitamin D status. J. Trop. Pediatr. 67, fmab081 (2021).
pubmed: 34580716 doi: 10.1093/tropej/fmab081
Hasegawa, K. et al. Circulating 25-hydroxyvitamin D, nasopharyngeal airway metabolome, and bronchiolitis severity. Allergy 73, 1135–1140 (2018).
pubmed: 29315663 doi: 10.1111/all.13379
Hasegawa, K. et al. Serum 25-hydroxyvitamin D, metabolome, and bronchiolitis severity among infants-a multicenter cohort study. Pediatr. Allergy Immunol. 29, 441–445 (2018).
pubmed: 29512857 pmcid: 5992049 doi: 10.1111/pai.12880
Zhang, X. et al. Serum metabolomic profiling reveals important difference between infants with and without subsequent recurrent wheezing in later childhood after RSV bronchiolitis. APMIS 129, 128–137 (2021).
pubmed: 33155332 doi: 10.1111/apm.13095
Barlotta, A. et al. Metabolomic profiling of infants with recurrent wheezing after bronchiolitis. J. Infect. Dis. 219, 1216–1223 (2019).
pubmed: 30445537 doi: 10.1093/infdis/jiy659
Zhu, Z. et al. Metabolome subtyping of severe bronchiolitis in infancy and risk of childhood asthma. J. Allergy Clin. Immunol. 149, 102–112 (2021).
Castro-Rodriguez, J. A., Cifuentes, L. & Martinez, F. D. Predicting asthma using clinical indexes. Front. Pediatr. 7, 320–320 (2019).
pubmed: 31463300 pmcid: 6707805 doi: 10.3389/fped.2019.00320
Fujiogi, M. et al. Respiratory viruses are associated with serum metabolome among infants hospitalized for bronchiolitis: a multicenter study. Pediatr. Allergy Immunol. 31, 755–766 (2020).
pubmed: 32460384 pmcid: 7704725 doi: 10.1111/pai.13296
Fujiogi, M. et al. Integrated associations of nasopharyngeal and serum metabolome with bronchiolitis severity and asthma: a multicenter prospective cohort study. Pediatr. Allergy Immunol. 32, 905–916 (2021).
pubmed: 33559342 pmcid: 8269431 doi: 10.1111/pai.13466
Ghidoni, R., Caretti, A. & Signorelli, P. Role of sphingolipids in the pathobiology of lung inflammation. Mediators Inflamm. 2015, 487508–487508 (2015).
pubmed: 26770018 pmcid: 4681829 doi: 10.1155/2015/487508
North, M. L., Khanna, N., Marsden, P. A., Grasemann, H. & Scott, J. A. Functionally important role for arginase 1 in the airway hyperresponsiveness of asthma. Am. J. Physiol. Lung Cell Mol. Physiol. 296, L911–L920 (2009).
pubmed: 19286931 doi: 10.1152/ajplung.00025.2009
Lara, A. et al. Alterations of the arginine metabolome in asthma. Am. J. Respir. Crit. Care Med. 178, 673–681 (2008).
pubmed: 18635886 pmcid: 2556449 doi: 10.1164/rccm.200710-1542OC
Liu, L. et al. Global, regional, and national causes of child mortality in 2000-13, with projections to inform post-2015 priorities: an updated systematic analysis. Lancet 385, 430–440 (2015).
pubmed: 25280870 doi: 10.1016/S0140-6736(14)61698-6
Torres, A. et al. Pneumonia. Nat. Rev. Dis. Prim. 7, 25 (2021).
pubmed: 33833230 doi: 10.1038/s41572-021-00259-0
Shah, S. N., Bachur, R. G., Simel, D. L. & Neuman, M. I. Does this child have pneumonia?: the rational clinical examination systematic review. JAMA 318, 462–471 (2017).
pubmed: 28763554 doi: 10.1001/jama.2017.9039
Florin, T. A. et al. Biomarkers and disease severity in children with community-acquired pneumonia. Pediatrics 145, e20193728 (2020).
pubmed: 32404432 doi: 10.1542/peds.2019-3728
Thomas, J., Pociute, A., Kevalas, R., Malinauskas, M. & Jankauskaite, L. Blood biomarkers differentiating viral versus bacterial pneumonia aetiology: a literature review. Ital. J. Pediatr. 46, 4 (2020).
pubmed: 31918745 pmcid: 6953310 doi: 10.1186/s13052-020-0770-3
Laiakis, E. C., Morris, G. A., Fornace, A. J. & Howie, S. R. Metabolomic analysis in severe childhood pneumonia in the Gambia, West Africa: findings from a pilot study. PLoS ONE 5, e12655 (2010).
pubmed: 20844590 pmcid: 2936566 doi: 10.1371/journal.pone.0012655
Hersh, A. L., Shapiro, D. J., Pavia, A. T. & Shah, S. S. Antibiotic prescribing in ambulatory pediatrics in the United States. Pediatrics 128, 1053–1061 (2011).
pubmed: 22065263 doi: 10.1542/peds.2011-1337
Del Borrello, G. et al. New insights into pediatric community-acquired pneumonia gained from untargeted metabolomics: a preliminary study. Pediatr. Pulmonol. 55, 418–425 (2020).
pubmed: 31821737 doi: 10.1002/ppul.24602
Hasegawa, K. et al. Association of nasopharyngeal microbiota profiles with bronchiolitis severity in infants hospitalised for bronchiolitis. Eur. Respir. J. 48, 1329–1339 (2016).
pubmed: 27799386 pmcid: 5459592 doi: 10.1183/13993003.00152-2016
Fletcher, M. A., Schmitt, H. J., Syrochkina, M. & Sylvester, G. Pneumococcal empyema and complicated pneumonias: global trends in incidence, prevalence, and serotype epidemiology. Eur. J. Clin. Microbiol. Infect. Dis. 33, 879–910 (2014).
pubmed: 24563274 pmcid: 4110404 doi: 10.1007/s10096-014-2062-6
Light, R. W. Parapneumonic effusions and empyema. Proc. Am. Thorac. Soc. 3, 75–80 (2006).
pubmed: 16493154 doi: 10.1513/pats.200510-113JH
Chung, C. L., Chen, C. H., Sheu, J. R., Chen, Y. C. & Chang, S. C. Proinflammatory cytokines, transforming growth factor-beta1, and fibrinolytic enzymes in loculated and free-flowing pleural exudates. Chest 128, 690–697 (2005).
pubmed: 16100155 doi: 10.1016/S0012-3692(15)50413-3
Gayretli-Aydın, Z. G. et al. Evaluation of complicated and uncomplicated parapneumonic effusion in children. Turk. J. Pediatr. 58, 623–631 (2016).
pubmed: 29090876 doi: 10.24953/turkjped.2016.06.008
Chiu, C. Y. et al. Metabolomic profiling of infectious parapneumonic effusions reveals biomarkers for guiding management of children with streptococcus pneumoniae pneumonia. Sci. Rep. 6, 24930 (2016).
pubmed: 27103079 pmcid: 4840347 doi: 10.1038/srep24930
Chiu, C. Y. et al. Metabolomics reveals anaerobic bacterial fermentation and hypoxanthine accumulation for fibrinous pleural effusions in children with pneumonia. J. Proteome Res. 18, 1248–1254 (2019).
pubmed: 30757903 doi: 10.1021/acs.jproteome.8b00864
Bridy-Pappas, A. E., Margolis, M. B., Center, K. J. & Isaacman, D. J. Streptococcus pneumoniae: description of the pathogen, disease epidemiology, treatment, and prevention. Pharmacotherapy 25, 1193–1212 (2005).
pubmed: 16164394 doi: 10.1592/phco.2005.25.9.1193
Hartman, M. E., Linde-Zwirble, W. T., Angus, D. C. & Watson, R. S. Trends in the epidemiology of pediatric severe sepsis. Pediatr. Crit. Care Med. 14, 686–693 (2013).
pubmed: 23897242 doi: 10.1097/PCC.0b013e3182917fad
Weiss, S. L. et al. Surviving sepsis campaign international guidelines for the management of septic shock and sepsis-associated organ dysfunction in children. Pediatr. Crit. Care Med. 21, e52–e106 (2020).
pubmed: 32032273 doi: 10.1097/PCC.0000000000002198
Patel, K. & McElvania, E. Diagnostic challenges and laboratory considerations for pediatric sepsis. J. Appl. Lab. Med. 3, 587–600 (2019).
pubmed: 31639728 doi: 10.1373/jalm.2017.025908
Hazwani, T. R. et al. Association between culture-negative versus culture-positive sepsis and outcomes of patients admitted to the pediatric intensive care unit. Cureus 12, e9981 (2020).
pubmed: 32855896 pmcid: 7447147
Mickiewicz, B., Vogel, H. J., Wong, H. R. & Winston, B. W. Metabolomics as a novel approach for early diagnosis of pediatric septic shock and its mortality. Am. J. Respir. Crit. Care Med. 187, 967–976 (2013).
pubmed: 23471468 pmcid: 3707368 doi: 10.1164/rccm.201209-1726OC
Ambroggio, L. et al. Emerging biomarkers of illness severity: urinary metabolites associated with sepsis and necrotizing methicillin-resistant Staphylococcus aureus pneumonia. Pharmacotherapy 37, 1033–1042 (2017).
pubmed: 28632946 pmcid: 5600674 doi: 10.1002/phar.1973
Mickiewicz, B. et al. Development of metabolic and inflammatory mediator biomarker phenotyping for early diagnosis and triage of pediatric sepsis. Crit. Care 19, 320 (2015).
pubmed: 26349677 pmcid: 4563828 doi: 10.1186/s13054-015-1026-2
Mickiewicz, B. et al. Biomarker phenotype for early diagnosis and triage of sepsis to the pediatric intensive care unit. Sci. Rep. 8, 16606 (2018).
pubmed: 30413795 pmcid: 6226431 doi: 10.1038/s41598-018-35000-7
Grauslys, A. et al. Title NMR-based metabolic profiling provides diagnostic and prognostic information in critically ill children with suspected infection. Sci. Rep. 10, 20198 (2020).
pubmed: 33214628 pmcid: 7677384 doi: 10.1038/s41598-020-77319-0
Li, G.-B. et al. Plasma metabolic profiling of pediatric sepsis in a chinese cohort. Front. Cell Dev. Biol. 9, 643979 (2021).
pubmed: 33659257 pmcid: 7917179 doi: 10.3389/fcell.2021.643979
World Health Organization. WHO coronavirus (Covid-19) dashboard. https://covid19.who.int (2022).
de Souza, T. H., Nadal, J. A., Nogueira, R. J. N., Pereira, R. M. & Brandão, M. B. Clinical manifestations of children with COVID-19: a systematic review. Pediatr. Pulmonol. 55, 1892–1899 (2020).
Rabinowicz, S., Leshem, E. & Pessach, I. M. COVID-19 in the pediatric population-review and current evidence. Curr. Infect. Dis. Rep. 22, 29 (2020).
pubmed: 32982599 pmcid: 7501762 doi: 10.1007/s11908-020-00739-6
Wang, C. et al. Multi-omic profiling of plasma reveals molecular alterations in children with COVID-19. Theranostics 11, 8008–8026 (2021).
pubmed: 34335977 pmcid: 8315065 doi: 10.7150/thno.61832
Wu, D. et al. Plasma metabolomic and lipidomic alterations associated with COVID-19. Natl Sci. Rev. 7, 1157–1168 (2020).
pubmed: 34676128 pmcid: 7197563 doi: 10.1093/nsr/nwaa086
Shu, T. et al. Plasma proteomics identify biomarkers and pathogenesis of COVID-19. Immunity 53, 1108.e5–1122.e5 (2020).
doi: 10.1016/j.immuni.2020.10.008
Rist, M. J. et al. Influence of freezing and storage procedure on human urine samples in nmr-based metabolomics. Metabolites 3, 243–258 (2013).
pubmed: 24957990 pmcid: 3901271 doi: 10.3390/metabo3020243
Kamlage, B. et al. Quality markers addressing preanalytical variations of blood and plasma processing identified by broad and targeted metabolite profiling. Clin. Chem. 60, 399–412 (2014).
pubmed: 24305685 doi: 10.1373/clinchem.2013.211979
Ang, J. E. et al. Identification of human plasma metabolites exhibiting time-of-day variation using an untargeted liquid chromatography-mass spectrometry metabolomic approach. Chronobiol. Int. 29, 868–881 (2012).
pubmed: 22823870 pmcid: 3433180 doi: 10.3109/07420528.2012.699122
Kastenmüller, G., Raffler, J., Gieger, C. & Suhre, K. Genetics of human metabolism: an update. Hum. Mol. Genet. 24, R93–R101 (2015).
pubmed: 26160913 pmcid: 4572003 doi: 10.1093/hmg/ddv263
Pinu, F. R., Goldansaz, S. A. & Jaine, J. Translational metabolomics: current challenges and future opportunities. Metabolites 9, 108 (2019).
pubmed: 31174372 pmcid: 6631405 doi: 10.3390/metabo9060108
Annese, V. F. et al. A monolithic single-chip point-of-care platform for metabolomic prostate cancer detection. Microsyst. Nanoeng. 7, 21 (2021).
pubmed: 34567735 pmcid: 8433377 doi: 10.1038/s41378-021-00243-4
McAllister, D. A. et al. Global, regional, and national estimates of pneumonia morbidity and mortality in children younger than 5 years between 2000 and 2015: a systematic analysis. Lancet Glob. Health 7, e47–e57 (2019).
pubmed: 30497986 doi: 10.1016/S2214-109X(18)30408-X

Auteurs

Emily Wildman (E)

Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.

Beata Mickiewicz (B)

Department of Pediatrics, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.

Hans J Vogel (HJ)

Bio-NMR Centre, Department of Biological Sciences, University of Calgary, Calgary, AB, Canada.

Graham C Thompson (GC)

Department of Pediatrics, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada. graham.thompson@albertahealthservices.ca.
Department of Emergency Medicine, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada. graham.thompson@albertahealthservices.ca.

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