Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/165232
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dc.contributor.authorFrick, Marie Antoinette-
dc.contributor.authorBarba, Ignasi-
dc.contributor.authorFenoy-Alejandre, Marina-
dc.contributor.authorLópez-López, Paula-
dc.contributor.authorBaquero Artigao, Fernando-
dc.contributor.authorRodríguez-Molino, Paula-
dc.contributor.authorNoguera Julian, Antoni-
dc.contributor.authorNicolás-López, Marta-
dc.contributor.authorde la Fuente-Juárez, Asunción-
dc.contributor.authorCodina Grau, Maria Gemma-
dc.contributor.authorEsperalba Esquerra, Juliana-
dc.contributor.authorLinde-Sillo, Ángeles-
dc.contributor.authorSoler Palacín, Pere-
dc.date.accessioned2020-06-11T21:32:33Z-
dc.date.available2020-06-11T21:32:33Z-
dc.date.issued2019-11-15-
dc.identifier.issn2218-1989-
dc.identifier.urihttps://hdl.handle.net/2445/165232-
dc.description.abstractAbstract: Congenital 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.format.extent14 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherMDPI-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3390/metabo9120288-
dc.relation.ispartofMetabolites, 2019, vol. 9, p. 288-
dc.relation.urihttps://doi.org/10.3390/metabo9120288-
dc.rightscc-by (c) Frick, Marie Antoinette et al., 2019-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es-
dc.sourceArticles publicats en revistes (Cirurgia i Especialitats Medicoquirúrgiques)-
dc.subject.classificationInfeccions per citomegalovirus-
dc.subject.classificationPediatria-
dc.subject.classificationMetabolòmica-
dc.subject.otherCytomegalovirus infections-
dc.subject.otherPediatrics-
dc.subject.otherMetabolomics-
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.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec693744-
dc.date.updated2020-06-11T21:32:33Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid31775291-
Appears in Collections:Articles publicats en revistes (Cirurgia i Especialitats Medicoquirúrgiques)

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