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 in | Neurobiology of aging Vol. 47; pp. 83 - 90 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
01.11.2016
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ISSN | 0197-4580 1558-1497 1558-1497 |
DOI | 10.1016/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. |
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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. |
Author_xml | – sequence: 1 givenname: Sean J. surname: Colloby fullname: Colloby, Sean J. – sequence: 2 givenname: Robert H. surname: Field fullname: Field, Robert H. – sequence: 3 givenname: David J. surname: Wyper fullname: Wyper, David J. – sequence: 4 givenname: John T. surname: O'Brien fullname: O'Brien, John T. – sequence: 5 givenname: John-Paul surname: Taylor fullname: Taylor, John-Paul |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27565302$$D View this record in MEDLINE/PubMed |
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Keywords | Nicotinic Spatial covariance Acetylcholine Alzheimer's disease Cholinergic SPECT |
Language | English |
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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 |
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