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dc.contributor.authorOlivas Martínez, Alicia 
dc.contributor.authorSuárez, Beatriz
dc.contributor.authorSalamanca Fernández, Elena 
dc.contributor.authorReina Pérez, Iris 
dc.contributor.authorRodríguez Carrillo, Andrea 
dc.contributor.authorMustieles Miralles, Vicente 
dc.contributor.authorOlea Serrano, Nicolás 
dc.contributor.authorFreire, Carmen
dc.contributor.authorFernández Cabrera, Mariana Fátima 
dc.date.accessioned2023-03-10T11:52:50Z
dc.date.available2023-03-10T11:52:50Z
dc.date.issued2023-01-12
dc.identifier.citationOlivas-Martinez A... [et al.] (2023) Development and validation of brainderived neurotrophic factor measurement in human urine samples as a non-invasive effect biomarker. Front. Mol. Neurosci. 15:1075613. doi: [10.3389/fnmol.2022.1075613]es_ES
dc.identifier.urihttps://hdl.handle.net/10481/80524
dc.description.abstractBackground: Brain-derived neurotrophic factor (BDNF), a neurotrophic growth factor mainly expressed in the brain, has been proposed as a potential effect biomarker; that is, as a measurable biomarker whose values could be associated with several diseases, including neurological impairments. The European Human Biomonitoring Initiative (HBM4EU) has also recognized effect biomarkers as a useful tool for establishing link between exposure to environmental pollutants and human health. Despite the well-establish protocol for measuring serum BDNF, there is a need to validate its assessment in urine, a non-invasive sample that can be easily repeated over time. The aim of this study was to develop, standardize and validate a methodology to quantify BDNF protein levels in urine samples before its implementation in biomonitoring studies. Methods: Different experimental conditions and non-competitive commercial enzyme-linked immunosorbent assay (ELISA) kits were tested to determine the optimal analytical procedure, trying to minimize the shortcomings of ELISA kits. The fine-tune protocol was validated in a pilot study using both upon awakening (n = 150) and prior to sleeping (n = 106) urine samples from the same Spanish adolescent males in a well-characterized study population (the Spanish INMA-Granada cohort). Results: The best results were obtained in 0.6 ml of urine after the acidification and extraction (pre-concentration) of samples. The highest reproducibility was obtained with the ELISA kit from Raybiotech. Urinary BDNF concentrations of adolescent males were within the previously reported range (morning = 0.047– 6.801 ng/ml and night = 0.047–7.404 ng/ml). Urinary BDNF levels in the awakening and pre-sleep samples did not follow a normal distribution and were not correlated. Conclusion: The developed methodology offers good sensitivity and reproducibility. Having reliable markers in urine may facilitate both diagnosis and monitoring possible diseases (and treatment). Further studies are needed to implement urinary BDNF in biomonitoring studies to further elucidate its usefulness and biological significance for neurological impairments.es_ES
dc.description.sponsorshipEuropean Commission 733032es_ES
dc.description.sponsorshipBiomedical Research Networking Center-CIBER de Epidemiologia y Salud Publica (CIBERESP) of the Institute of Health Carlos IIIes_ES
dc.description.sponsorshipInstitute of Health Carlos III (SCIII) - European Regional Development Fund/FEDER FIS-PI17/01526 FIS-PI20/01656es_ES
dc.description.sponsorshipInstituto de Salud Carlos III FI21/00236es_ES
dc.description.sponsorshipMiguel Servet Type II Program CP1121/00014es_ES
dc.description.sponsorshipSpanish Government FPU17/01848es_ES
dc.description.sponsorshipJunta de Andalucia-PAIDI (Spain)es_ES
dc.language.isoenges_ES
dc.publisherFrontierses_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectBDNFes_ES
dc.subjectValidationes_ES
dc.subjectUrine es_ES
dc.subjectEffect biomarkeres_ES
dc.subjectHuman healthes_ES
dc.titleDevelopment and validation of brain-derived neurotrophic factor measurement in human urine samples as a non-invasive effect biomarkeres_ES
dc.typejournal articlees_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/733032es_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.3389/fnmol.2022.1075613
dc.type.hasVersionVoRes_ES


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