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Prevalence and prognostic value of CSF markers of Alzheimer's disease pathology in patients with subjective cognitive impairment or mild cognitive impairment in the DESCRIPA study: a prospective cohort study

Visser, Pieter Jelle ; Verhey, Frans ; Knol, Dirk L. ; Scheltens, Philip ; Wahlund, Lars-Olof ; Freund-Levi, Yvonne ; Tsolaki, Magda ; Minthon, Lennart LU ; Wallin, Åsa LU and Hampel, Harald , et al. (2009) In Lancet Neurology 8(7). p.619-627
Abstract
Background Alzheimer's disease (AD) pathology is common in patients with amnestic mild cognitive impairment (aMCI) without dementia, but the prevalence of AD pathology in patients with subjective cognitive impairment (SCI) and non-amnestic mild cognitive impairment (naMCI) is unknown. AD is characterised by decreased CSF concentrations of A beta(42) and increased concentrations of tau. We investigated the prevalence of a CSF AD profile in patients with SCI, naMCI, or aMCI and the association of this profile with cognitive outcome in each group. Methods Patients with SCI, naMCI, aMCI, and neurologically healthy controls were recruited from 20 memory clinics across Europe, between January, 2003, and June, 2005, into this prospective cohort... (More)
Background Alzheimer's disease (AD) pathology is common in patients with amnestic mild cognitive impairment (aMCI) without dementia, but the prevalence of AD pathology in patients with subjective cognitive impairment (SCI) and non-amnestic mild cognitive impairment (naMCI) is unknown. AD is characterised by decreased CSF concentrations of A beta(42) and increased concentrations of tau. We investigated the prevalence of a CSF AD profile in patients with SCI, naMCI, or aMCI and the association of this profile with cognitive outcome in each group. Methods Patients with SCI, naMCI, aMCI, and neurologically healthy controls were recruited from 20 memory clinics across Europe, between January, 2003, and June, 2005, into this prospective cohort study. A CSF AD profile was defined as an abnormal ratio of A beta(42):tau. Patients were assessed annually up to 3 years. Outcome measures were changes in memory, overall cognition, mini-mental state examination (MMSE) score, daily function, and progression to AD-type dementia. Findings The CSF AD profile was more common in patients with SCI (31 of 60 [52%]), naMCI (25 of 37 [68%]), and aMCI (56 of 71 [79%]) than in healthy controls (28 of 89 [31%]). The profile was associated with cognitive decline in patients with naMCI (memory, MMSE, and daily function) and in patients with aMCI (MMSE and daily function). In patients with aMCI, a CSF AD profile was predictive of AD-type dementia (OR 26.8, 95% CI 1.6-456.4). Interpretation AD is a common cause of SCI, naMCI, and aMCI and is associated with cognitive decline in patients with naMCI or aMCI. Patients with SCI might be in the early stages of AD, and cognitive decline might become apparent only after longer follow-up. (Less)
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organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Lancet Neurology
volume
8
issue
7
pages
619 - 627
publisher
Lancet Publishing Group
external identifiers
  • wos:000267643700018
  • scopus:67649628753
ISSN
1474-4465
DOI
10.1016/S1474-4422(09)70139-5
language
English
LU publication?
yes
id
195b3b94-a27b-4095-951c-07dadfc959e8 (old id 1463041)
date added to LUP
2016-04-01 11:55:42
date last changed
2022-04-13 03:25:10
@article{195b3b94-a27b-4095-951c-07dadfc959e8,
  abstract     = {{Background Alzheimer's disease (AD) pathology is common in patients with amnestic mild cognitive impairment (aMCI) without dementia, but the prevalence of AD pathology in patients with subjective cognitive impairment (SCI) and non-amnestic mild cognitive impairment (naMCI) is unknown. AD is characterised by decreased CSF concentrations of A beta(42) and increased concentrations of tau. We investigated the prevalence of a CSF AD profile in patients with SCI, naMCI, or aMCI and the association of this profile with cognitive outcome in each group. Methods Patients with SCI, naMCI, aMCI, and neurologically healthy controls were recruited from 20 memory clinics across Europe, between January, 2003, and June, 2005, into this prospective cohort study. A CSF AD profile was defined as an abnormal ratio of A beta(42):tau. Patients were assessed annually up to 3 years. Outcome measures were changes in memory, overall cognition, mini-mental state examination (MMSE) score, daily function, and progression to AD-type dementia. Findings The CSF AD profile was more common in patients with SCI (31 of 60 [52%]), naMCI (25 of 37 [68%]), and aMCI (56 of 71 [79%]) than in healthy controls (28 of 89 [31%]). The profile was associated with cognitive decline in patients with naMCI (memory, MMSE, and daily function) and in patients with aMCI (MMSE and daily function). In patients with aMCI, a CSF AD profile was predictive of AD-type dementia (OR 26.8, 95% CI 1.6-456.4). Interpretation AD is a common cause of SCI, naMCI, and aMCI and is associated with cognitive decline in patients with naMCI or aMCI. Patients with SCI might be in the early stages of AD, and cognitive decline might become apparent only after longer follow-up.}},
  author       = {{Visser, Pieter Jelle and Verhey, Frans and Knol, Dirk L. and Scheltens, Philip and Wahlund, Lars-Olof and Freund-Levi, Yvonne and Tsolaki, Magda and Minthon, Lennart and Wallin, Åsa and Hampel, Harald and Buerger, Katharina and Pirttila, Tuula and Soininen, Hilkka and Rikkert, Marcel Olde and Verbeek, Marcel M. and Spiru, Luiza and Blennow, Kaj}},
  issn         = {{1474-4465}},
  language     = {{eng}},
  number       = {{7}},
  pages        = {{619--627}},
  publisher    = {{Lancet Publishing Group}},
  series       = {{Lancet Neurology}},
  title        = {{Prevalence and prognostic value of CSF markers of Alzheimer's disease pathology in patients with subjective cognitive impairment or mild cognitive impairment in the DESCRIPA study: a prospective cohort study}},
  url          = {{http://dx.doi.org/10.1016/S1474-4422(09)70139-5}},
  doi          = {{10.1016/S1474-4422(09)70139-5}},
  volume       = {{8}},
  year         = {{2009}},
}