Feasibility of lumbar puncture in the study of cerebrospinal fluid biomarkers for Alzheimer disease in subjects with Down syndrome

dc.contributor.authorCarmona-Iragui, Maria
dc.contributor.authorSantos, Telma
dc.contributor.authorVidela, Sebastià
dc.contributor.authorFernández, Susana
dc.contributor.authorBenejam, Bessy
dc.contributor.authorVidela, Laura
dc.contributor.authorAlcolea, Daniel
dc.contributor.authorBlennow, Kaj
dc.contributor.authorBlesa González, Rafael
dc.contributor.authorLleo, Alberto
dc.contributor.authorFortea Ormaechea, Juan
dc.date.accessioned2020-12-18T16:51:47Z
dc.date.available2020-12-18T16:51:47Z
dc.date.issued2017-10-01
dc.date.updated2020-12-18T16:51:47Z
dc.description.abstractBackground: Alzheimer's disease (AD) is the main medical problem in older adults with Down syndrome (DS). Studies of cerebrospinal fluid (CSF) AD biomarkers are limited and the feasibility of lumbar puncture (LP) is controversial in this population. Objective: to analyze the frequency of complications after a LP in DS. Methods: we collected data from 80 adults with DS that underwent a LP within the Down Alzheimer Barcelona Neuroimaging Initiative. Demographics, cognitive status, headache history, and presence of complications after the LP were recorded in every subject. In 53 of them (active group), this information was collected following a semi-structured and validated protocol that actively looks for complications. Other variables related to the LP procedure were also recorded. A telephone interview to the caregiver was performed 5-7 days after the procedure to ask about complications. Data from 27 subjects (clinical practice group), from whom the presence of complications was obtained in a medical follow-up visit within the three months after the LP, were also included. Results: there were no adverse events in 90% of our participants. The most frequent complication was headache (6.25%); only one subject reported a typical post-lumbar puncture headache with moderate severity that required analgesic treatment. Dizziness (3.75%) and back pain (1.25%) were also reported. All the participants that reported complications belonged to the active group. Conclusion: LP can be safely performed to study CSF biomarkers in DS. The reported complications are qualitatively similar to the general population, but are less frequently reported, even when actively searched for.
dc.format.extent8 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec697988
dc.identifier.issn1387-2877
dc.identifier.pmid27858714
dc.identifier.urihttps://hdl.handle.net/2445/172764
dc.language.isoeng
dc.publisherIOS Press
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3233/JAD-160827
dc.relation.ispartofJournal of Alzheimer's Disease, 2017, vol. 55, num. 4, p. 1489-1496
dc.relation.urihttps://doi.org/10.3233/JAD-160827
dc.rights(c) Carmona-Iragui, Maria et al., 2017
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Patologia i Terapèutica Experimental)
dc.subject.classificationLíquid cefalorraquidi
dc.subject.classificationMalaltia d'Alzheimer
dc.subject.classificationSíndrome de Down
dc.subject.classificationPunció lumbar
dc.subject.otherCerebrospinal fluid
dc.subject.otherAlzheimer's disease
dc.subject.otherDown syndrome
dc.subject.otherSpinal puncture
dc.titleFeasibility of lumbar puncture in the study of cerebrospinal fluid biomarkers for Alzheimer disease in subjects with Down syndrome
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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