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Cerebrospinal fluid Alzheimer's disease biomarkers across the spectrum of lewy body diseases : Results from a large multicenter cohort

Van Steenoven, Inger (författare)
Amsterdam UMC - Vrije Universiteit Amsterdam
Aarsland, Dag (författare)
Karolinska Institutet
Weintraub, Daniel (författare)
University of Pennsylvania
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Londos, Elisabet (författare)
Lund University,Lunds universitet,Klinisk minnesforskning,Forskargrupper vid Lunds universitet,Clinical Memory Research,Lund University Research Groups
Blanc, Frederic (författare)
University Hospital Of Strasbourg
Van Der Flier, Wiesje M. (författare)
Amsterdam UMC - Vrije Universiteit Amsterdam
Teunissen, Charlotte E. (författare)
Amsterdam UMC - Vrije Universiteit Amsterdam
Mollenhauer, Brit (författare)
University of Göttingen
Fladby, Tormod (författare)
Akershus University Hospital
Kramberger, Milica G. (författare)
University Medical Centre Ljubljana
Bonanni, Laura (författare)
University G.d'Annunzio of Chieti-Pescara
Lemstra, Afina W. (författare)
Amsterdam UMC - Vrije Universiteit Amsterdam
Blanc, 'E (författare)
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 (creator_code:org_t)
2016
2016
Engelska 9 s.
Ingår i: Journal of Alzheimer's Disease. - 1387-2877 .- 1875-8908. ; 54:1, s. 287-295
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: Concomitant Alzheimer's disease (AD) pathology is observed in Lewy body diseases (LBD), but the clinical impact is unknown. Only a few biomarker studies in LBD exist and have included small cohorts from single centers. Objective: We aimed to evaluate the prevalence of abnormal cerebrospinal fluid (CSF) AD biomarkers across the spectrum of LBD in a large multicenter cohort and to assess whether an AD biomarker profile was associated with demographic and clinical differences in dementia with Lewy bodies (DLB). Methods:We included 375 DLB patients, 164 Parkinson's disease (PD) patients without dementia, and 55 PD patients with dementia (PDD) from 10 centers. CSF amyloid-beta42 (Aβ42), total tau (t-tau), and phosphorylated tau (p-tau) values were dichotomized as abnormal or normal according to locally available cut-off values. A CSF AD profile was defined as abnormal Aβ42 combined with abnormal t-tau and/or p-tau. Results: A substantial proportion of DLB patients had abnormal values for CSF Aβ42, t-tau, and p-tau, while abnormal values were uncommon in PD without dementia. Patients with PDD had values in between. A CSF AD profile was observed in 25% of DLB patients, compared with only 9% of PDD and 3% of PD without dementia.Within DLB, patients with a CSF AD profile were older, more often female, performed worse on the Mini-Mental State Examination, and had shorter disease duration compared with patients with normal CSF. Conclusion: A CSF AD profile is more common in DLB compared with PDD and PD, and is associated with more severe cognitive impairment in DLB.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Nyckelord

Amyloid beta-protein (1-42)
Biomarkers
Cerebrospinal fluid
Dementia with Lewy bodies
Lewy body disease
Tau protein

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art (ämneskategori)
ref (ämneskategori)

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