Publication:
New candidate blood biomarkers potentially associated with white matter hyperintensities progression.

dc.contributor.authorJiménez-Balado, Joan
dc.contributor.authorPizarro, Jesús
dc.contributor.authorRiba-Llena, Iolanda
dc.contributor.authorPenalba, Anna
dc.contributor.authorFaura, Júlia
dc.contributor.authorPalà, Elena
dc.contributor.authorMontaner, Joan
dc.contributor.authorHernández-Guillamon, Mar
dc.contributor.authorDelgado, Pilar
dc.date.accessioned2023-02-09T11:43:14Z
dc.date.available2023-02-09T11:43:14Z
dc.date.issued2021-07-12
dc.description.abstractWe aimed to discover blood biomarkers associated with longitudinal changes in white matter hyperintensities (WMH). This study was divided into a discovery phase and a replication phase. Subjects in both studies were patients with hypertension, aged 50-70, who underwent two magnetic resonance imaging (MRI) sessions and blood extractions over a 4-year follow-up period. In the discovery phase, we screened 1305 proteins in 12 subjects with WMH progression and in 12 matched control subjects. We found that 41 proteins were differentially expressed: 13 were upregulated and 28 were downregulated. We subsequently selected three biomarkers for replication in baseline and follow-up samples in 80 subjects with WMH progression and in 80 control subjects. The selected protein candidates for the replication were MMP9 (matrix metalloproteinase-9), which was higher in cases, MET (hepatocyte growth factor receptor) and ASAH2 (neutral ceramidase), which were both lower in cases of WMH progression. Baseline biomarker concentrations did not predict WMH progression. In contrast, patients with WMH progression presented a steeper decline in MET over time. Furthermore, cases showed higher MMP9 and lower ASAH2 levels than controls at the follow-up. These results indicate that MMP9, MET, and ASAH2 are potentially associated with the progression of WMH, and could therefore be interesting candidates to validate in future studies.
dc.identifier.doi10.1038/s41598-021-93498-w
dc.identifier.essn2045-2322
dc.identifier.pmcPMC8275657
dc.identifier.pmid34253757
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275657/pdf
dc.identifier.unpaywallURLhttps://www.nature.com/articles/s41598-021-93498-w.pdf
dc.identifier.urihttp://hdl.handle.net/10668/18193
dc.issue.number1
dc.journal.titleScientific reports
dc.journal.titleabbreviationSci Rep
dc.language.isoen
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationHospital Universitario Virgen del Rocío
dc.organizationHospital Universitario Virgen Macarena
dc.page.number14324
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshAged
dc.subject.meshBiomarkers
dc.subject.meshBlood-Brain Barrier
dc.subject.meshHumans
dc.subject.meshHypertension
dc.subject.meshMagnetic Resonance Imaging
dc.subject.meshMatrix Metalloproteinase 9
dc.subject.meshMiddle Aged
dc.subject.meshNeutral Ceramidase
dc.subject.meshProto-Oncogene Proteins c-met
dc.subject.meshWhite Matter
dc.titleNew candidate blood biomarkers potentially associated with white matter hyperintensities progression.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number11
dspace.entity.typePublication

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