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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorFrick, Marie Antoinette
dc.contributor.authorBarba Vert, Ignasi
dc.contributor.authorFenoy-Alejandre, Marina
dc.contributor.authorLópez López, Paula
dc.contributor.authorRodríguez-Molino, Paula
dc.contributor.authorCodina Grau, Gema
dc.contributor.authorEsperalba Esquerra, Juliana
dc.contributor.authorLinde Sillo, Mª Angeles
dc.contributor.authorSoler Palacín, Pere
dc.contributor.authorBaquero-Artigao, Fernando
dc.date.accessioned2021-04-14T07:58:11Z
dc.date.available2021-04-14T07:58:11Z
dc.date.issued2019-11-25
dc.identifier.citationFrick MA, Barba I, Fenoy-Alejandre M, López-López P, Baquero-Artigao F, Rodríguez-Molino P, et al. 1H-NMR Urinary Metabolic Profile, A Promising Tool for the Management of Infants with Human Cytomegalovirus-Infection. Metabolites. 2019 Nov 25;9(12):288.
dc.identifier.issn2218-1989
dc.identifier.urihttps://hdl.handle.net/11351/5850
dc.description1H-NMR; Congenital infection; Human cytomegalovirus
dc.description.abstractCongenital human cytomegalovirus (HCMV) infection is the most common mother-to-child transmitted infection in the developed world. Certain aspects of its management remain a challenge. Urinary metabolic profiling is a promising tool for use in pediatric conditions. The aim of this study was to investigate the urinary metabolic profile in HCMV-infected infants and controls during acute care hospitalization. Urine samples were collected from 53 patients at five hospitals participating in the Spanish congenital HCMV registry. Thirty-one cases of HCMV infection and 22 uninfected controls were included. Proton nuclear magnetic resonance (1H-NMR) spectra were obtained using NOESYPR1D pulse sequence. The dataset underwent orthogonal projection on latent structures discriminant analysis to identify candidate variables affecting the urinary metabolome: HCMV infection, type of infection, sex, chronological age, gestational age, type of delivery, twins, and diet. Statistically significant discriminative models were obtained only for HCMV infection (p = 0.03) and chronological age (p < 0.01). No significant differences in the metabolomic profile were found between congenital and postnatal HCMV infection. When the HCMV-infected group was analyzed according to chronological age, a statistically significant model was obtained only in the neonatal group (p = 0.01), with the differentiating metabolites being betaine, glycine, alanine, and dimethylamine. Despite the considerable variation in urinary metabolic profiles in a real-life setting, clinical application of metabolomics to the study of HCMV infection seems feasible.
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofseriesMetabolites;9(12)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectInfeccions per citomegalovirus
dc.subjectNodrissons
dc.subjectMalalties congènites
dc.subject.meshCytomegalovirus Infections
dc.subject.mesh/congenital
dc.subject.meshInfant, Newborn
dc.title1H-NMR Urinary Metabolic Profile, A Promising Tool for the Management of Infants with Human Cytomegalovirus-Infection
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3390/metabo9120288
dc.subject.decsinfecciones por Citomegalovirus
dc.subject.decs/congénito
dc.subject.decsrecién nacido
dc.relation.publishversionhttps://www.mdpi.com/2218-1989/9/12/288
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Frick MA, Soler-Palacín P] Malalties infeccioses i immunologia pediàtrica, Servei de Pediatria, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Red de Investigación Translacional en Infectología Pediátrica (RITIP), 28046 Madrid, Spain. [Barba I] Malalties Cardiovasculars, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Centro de Investigación Biomédica en Red sobre Enfermedades Cardiovasculares (CIBER-CV), 28029 Madrid, Spain. [Fenoy-Alejandre M] Malalties Infeccioses i Immunologia Pediàtrica, Servei de Pediatria, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [López-López P] Malalties Cardiovasculars, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. [Baquero-Artigao F] Red de Investigación Translacional en Infectología Pediátrica (RITIP), 28046 Madrid, Spain. Pediatrics Infectious Diseases Unit, Pediatrics Department, Hospital University La Paz, 28046 Madrid. [Rodríguez-Molino P] Pediatrics Infectious Diseases Unit, Pediatrics Department, Hospital University La Paz, 28046 Madrid. [Codina-Grau MG, Esperalba Esquerra J] Servei de Microbiologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Linde-Sillo Á] Servei de Neonatologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid31775291
dc.identifier.wos000506676300007
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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