| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Frick, Marie Antoinette |
| dc.contributor.author | Barba Vert, Ignasi |
| dc.contributor.author | Fenoy-Alejandre, Marina |
| dc.contributor.author | López López, Paula |
| dc.contributor.author | Rodríguez-Molino, Paula |
| dc.contributor.author | Codina Grau, Gema |
| dc.contributor.author | Esperalba Esquerra, Juliana |
| dc.contributor.author | Linde Sillo, Mª Angeles |
| dc.contributor.author | Soler Palacín, Pere |
| dc.contributor.author | Baquero-Artigao, Fernando |
| dc.date.accessioned | 2021-04-14T07:58:11Z |
| dc.date.available | 2021-04-14T07:58:11Z |
| dc.date.issued | 2019-11-25 |
| dc.identifier.citation | Frick 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.issn | 2218-1989 |
| dc.identifier.uri | https://hdl.handle.net/11351/5850 |
| dc.description | 1H-NMR; Congenital infection; Human cytomegalovirus |
| dc.description.abstract | 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.language.iso | eng |
| dc.publisher | MDPI |
| dc.relation.ispartofseries | Metabolites;9(12) |
| dc.rights | Attribution 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ |
| dc.source | Scientia |
| dc.subject | Infeccions per citomegalovirus |
| dc.subject | Nodrissons |
| dc.subject | Malalties congènites |
| dc.subject.mesh | Cytomegalovirus Infections |
| dc.subject.mesh | /congenital |
| dc.subject.mesh | Infant, Newborn |
| dc.title | 1H-NMR Urinary Metabolic Profile, A Promising Tool for the Management of Infants with Human Cytomegalovirus-Infection |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.3390/metabo9120288 |
| dc.subject.decs | infecciones por Citomegalovirus |
| dc.subject.decs | /congénito |
| dc.subject.decs | recién nacido |
| dc.relation.publishversion | https://www.mdpi.com/2218-1989/9/12/288 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut 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.pmid | 31775291 |
| dc.identifier.wos | 000506676300007 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |