A spatial covariance 123 I-5IA-85380 SPECT study of α4β2 nicotinic receptors in Alzheimer's disease

Alzheimer's disease (AD) is characterized by widespread degeneration of cholinergic neurons, particularly in the basal forebrain. However, the pattern of these deficits and relationship with known brain networks is unknown. In this study, we sought to clarify this and used I-5-iodo-3-[2(S)-2-az...

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Published inNeurobiology of aging Vol. 47; pp. 83 - 90
Main Authors Colloby, Sean J., Field, Robert H., Wyper, David J., O'Brien, John T., Taylor, John-Paul
Format Journal Article
LanguageEnglish
Published United States 01.11.2016
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ISSN0197-4580
1558-1497
1558-1497
DOI10.1016/j.neurobiolaging.2016.07.017

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Abstract Alzheimer's disease (AD) is characterized by widespread degeneration of cholinergic neurons, particularly in the basal forebrain. However, the pattern of these deficits and relationship with known brain networks is unknown. In this study, we sought to clarify this and used I-5-iodo-3-[2(S)-2-azetidinylmethoxy] pyridine ( 5IA-85380) single photon emission computed tomography to investigate spatial covariance of α4β2 nicotinic acetylcholine receptors in AD and healthy controls. Thirteen AD and 16 controls underwent 5IA-85380 and regional cerebral blood flow ( Tc-exametazime) single photon emission computed tomography scanning. We applied voxel principal component (PC) analysis, generating series of principal component images representing common intercorrelated voxels across subjects. Linear regression generated specific α4β2 and regional cerebral blood flow covariance patterns that differentiated AD from controls. The α4β2 pattern showed relative decreased uptake in numerous brain regions implicating several networks including default mode, salience, and Papez hubs. Thus, as well as basal forebrain and brainstem cholinergic system dysfunction, cholinergic deficits mediated through nicotinic acetylcholine receptors could be evident within key networks in AD. These findings may be important for the pathophysiology of AD and its associated cognitive and behavioral phenotypes.
AbstractList Alzheimer's disease (AD) is characterized by widespread degeneration of cholinergic neurons, particularly in the basal forebrain. However, the pattern of these deficits and relationship with known brain networks is unknown. In this study, we sought to clarify this and used I-5-iodo-3-[2(S)-2-azetidinylmethoxy] pyridine ( 5IA-85380) single photon emission computed tomography to investigate spatial covariance of α4β2 nicotinic acetylcholine receptors in AD and healthy controls. Thirteen AD and 16 controls underwent 5IA-85380 and regional cerebral blood flow ( Tc-exametazime) single photon emission computed tomography scanning. We applied voxel principal component (PC) analysis, generating series of principal component images representing common intercorrelated voxels across subjects. Linear regression generated specific α4β2 and regional cerebral blood flow covariance patterns that differentiated AD from controls. The α4β2 pattern showed relative decreased uptake in numerous brain regions implicating several networks including default mode, salience, and Papez hubs. Thus, as well as basal forebrain and brainstem cholinergic system dysfunction, cholinergic deficits mediated through nicotinic acetylcholine receptors could be evident within key networks in AD. These findings may be important for the pathophysiology of AD and its associated cognitive and behavioral phenotypes.
Author O'Brien, John T.
Field, Robert H.
Taylor, John-Paul
Colloby, Sean J.
Wyper, David J.
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Keywords Nicotinic
Spatial covariance
Acetylcholine
Alzheimer's disease
Cholinergic
SPECT
Language English
License Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved.
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Snippet Alzheimer's disease (AD) is characterized by widespread degeneration of cholinergic neurons, particularly in the basal forebrain. However, the pattern of these...
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StartPage 83
SubjectTerms Aged
Aged, 80 and over
Alzheimer Disease - diagnostic imaging
Alzheimer Disease - etiology
Alzheimer Disease - metabolism
Azetidines
Cerebrovascular Circulation
Female
Humans
Male
Prosencephalon - diagnostic imaging
Prosencephalon - metabolism
Pyridines
Radiopharmaceuticals
Receptors, Nicotinic - metabolism
Technetium Tc 99m Exametazime
Tomography, Emission-Computed, Single-Photon
Title A spatial covariance 123 I-5IA-85380 SPECT study of α4β2 nicotinic receptors in Alzheimer's disease
URI https://www.ncbi.nlm.nih.gov/pubmed/27565302
https://doi.org/10.1016/j.neurobiolaging.2016.07.017
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