001     163503
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024 7 _ |a 10.3233/JAD-215196
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024 7 _ |a pmid:34924387
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024 7 _ |a 1387-2877
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024 7 _ |a 1875-8908
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037 _ _ |a DZNE-2022-00263
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Teipel, Stefan
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245 _ _ |a Association of Cholinergic Basal Forebrain Volume and Functional Connectivity with Markers of Inflammatory Response in the Alzheimer's Disease Spectrum.
260 _ _ |a Amsterdam
|c 2022
|b IOS Press
336 7 _ |a article
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336 7 _ |a ARTICLE
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336 7 _ |a Journal Article
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520 _ _ |a Inflammation has been described as a key pathogenic event in Alzheimer's disease (AD), downstream of amyloid and tau pathology. Preclinical and clinical data suggest that the cholinergic basal forebrain may moderate inflammatory response to different pathologies.To study the association of cholinergic basal forebrain volume and functional connectivity with measures of neuroinflammation in people from the AD spectrum.We studied 261 cases from the DELCODE cohort, including people with subjective cognitive decline, mild cognitive impairment, AD dementia, first degree relatives, and healthy controls. Using Bayesian ANCOVA, we tested associations of MRI indices of cholinergic basal forebrain volume and functional connectivity with cerebrospinal fluid (CSF) levels of sTREM2 as a marker of microglia activation, and serum levels of complement C3. Using Bayesian elastic net regression, we determined associations between basal forebrain measures and a large inflammation marker panel from CSF and serum.We found anecdotal to moderate evidence in favor of the absence of an effect of basal forebrain volume and functional connectivity on CSF sTREM2 and serum C3 levels both in Aβ42/ptau-positive and negative cases. Bayesian elastic net regression identified several CSF and serum markers of inflammation that were associated with basal forebrain volume and functional connectivity. The effect sizes were moderate to small.Our data-driven analyses generate the hypothesis that cholinergic basal forebrain may be involved in the neuroinflammation response to Aβ42 and phospho-tau pathology in people from the AD spectrum. This hypothesis needs to be tested in independent samples.
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650 _ 7 |a Alzheimer’s disease
|2 Other
650 _ 7 |a MRI
|2 Other
650 _ 7 |a cerebrospinal fluid
|2 Other
650 _ 7 |a cholinergic system
|2 Other
650 _ 7 |a neuroinflammation
|2 Other
650 _ 7 |a plasma
|2 Other
650 _ 7 |a sTREM2
|2 Other
650 _ 7 |a Biomarkers
|2 NLM Chemicals
650 _ 7 |a Cholinergic Agents
|2 NLM Chemicals
650 _ 2 |a Aged
|2 MeSH
650 _ 2 |a Alzheimer Disease: pathology
|2 MeSH
650 _ 2 |a Basal Forebrain: pathology
|2 MeSH
650 _ 2 |a Biomarkers: blood
|2 MeSH
650 _ 2 |a Biomarkers: cerebrospinal fluid
|2 MeSH
650 _ 2 |a Cholinergic Agents
|2 MeSH
650 _ 2 |a Cognitive Dysfunction: pathology
|2 MeSH
650 _ 2 |a Cohort Studies
|2 MeSH
650 _ 2 |a Female
|2 MeSH
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Inflammation: pathology
|2 MeSH
650 _ 2 |a Magnetic Resonance Imaging
|2 MeSH
650 _ 2 |a Male
|2 MeSH
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700 1 _ |a Dyrba, Martin
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700 1 _ |a Ballarini, Tommaso
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700 1 _ |a Brosseron, Frederic
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700 1 _ |a Laske, Christoph
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700 1 _ |a Maier, Franziska
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700 1 _ |a Metzger, Coraline D
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700 1 _ |a Munk, Matthias H
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700 1 _ |a Peters, Oliver
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700 1 _ |a Pomara, Nunzio
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700 1 _ |a Preis, Lukas
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700 1 _ |a Priller, Josef
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700 1 _ |a Ramírez, Alfredo
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700 1 _ |a Roy, Nina
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700 1 _ |a Scheffler, Klaus
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700 1 _ |a Schneider, Anja
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700 1 _ |a Schott, Björn H
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700 1 _ |a Spottke, Annika
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700 1 _ |a Spruth, Eike J
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700 1 _ |a Wagner, Michael
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700 1 _ |a Wiltfang, Jens
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700 1 _ |a Jessen, Frank
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700 1 _ |a Heneka, Michael T
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773 _ _ |a 10.3233/JAD-215196
|g Vol. 85, no. 3, p. 1267 - 1282
|0 PERI:(DE-600)2070772-1
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|p 1267 - 1282
|t Journal of Alzheimer's disease
|v 85
|y 2022
|x 1875-8908
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