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Intra-individual correlations between quantitative THK-5351 PET and MRI-derived cortical volume in Alzheimer's disease differ according to disease severity and amyloid positivity

To assess the in vivo whole-brain relationship between uptake of [18F]THK-5351 on PET and cortical atrophy on structural MRI according to the presence and severity of Alzheimer's disease (AD). Sixty-five participants (21 normal controls, 32 mild cognitive impairment [MCI] subjects, and 12 AD pa...

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Published in:PloS one 2019-12, Vol.14 (12), p.e0226265-e0226265
Main Authors: Park, Ji Eun, Yun, Jessica, Kim, Sang Joon, Shim, Woo Hyun, Oh, Jungsu S, Oh, Minyoung, Roh, Jee Hoon, Seo, Sang Won, Oh, Seung Jun, Kim, Jae Seung
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cited_by cdi_FETCH-LOGICAL-c758t-eca3b18b1ce4b3068a1666b97ed153276a4fba62e3ddcb753da4f77d32872da73
cites cdi_FETCH-LOGICAL-c758t-eca3b18b1ce4b3068a1666b97ed153276a4fba62e3ddcb753da4f77d32872da73
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container_issue 12
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container_title PloS one
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creator Park, Ji Eun
Yun, Jessica
Kim, Sang Joon
Shim, Woo Hyun
Oh, Jungsu S
Oh, Minyoung
Roh, Jee Hoon
Seo, Sang Won
Oh, Seung Jun
Kim, Jae Seung
description To assess the in vivo whole-brain relationship between uptake of [18F]THK-5351 on PET and cortical atrophy on structural MRI according to the presence and severity of Alzheimer's disease (AD). Sixty-five participants (21 normal controls, 32 mild cognitive impairment [MCI] subjects, and 12 AD patients) were enrolled from a prospective multicenter clinical trial (NCT02656498). Structural MRI and [18F]THK-5351 PET were performed within a 2-month interval. Cortical volume and standardized uptake value ratios (SUVR) were calculated from MRI and PET images, respectively, for 35 FreeSurfer-derived cortical regions. Pearson's correlation coefficients between SUVR and cortical volume were calculated for the same regions, and correlated regions were compared according to disease severity and β-amyloid PET positivity. No significantly correlated regions were found in the normal controls. Negative correlations between SUVR and cortical volume were found in the MCI and AD groups, mainly in limbic locations in MCI and isocortical locations in AD. The AD group exhibited stronger correlations (r = -0.576-0.781) than the MCI group (r = 0.368-0.571). Hippocampal atrophy did not show any correlation with SUVR in the β-amyloid PET-negative group, but negatively correlated with SUVR (r = -0.494, P = .012) in the β-amyloid PET-positive group. Regional THK-5351 uptake correlated more strongly with cortical atrophy in AD compared with MCI, thereby demonstrating a close relationship between the neuro-pathologic process and cortical atrophy. Hippocampal atrophy was associated with both β-amyloid and THK-5351 uptake, possibly reflecting an interaction between β-amyloid and tau deposition in the neurodegeneration process.
doi_str_mv 10.1371/journal.pone.0226265
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Sixty-five participants (21 normal controls, 32 mild cognitive impairment [MCI] subjects, and 12 AD patients) were enrolled from a prospective multicenter clinical trial (NCT02656498). Structural MRI and [18F]THK-5351 PET were performed within a 2-month interval. Cortical volume and standardized uptake value ratios (SUVR) were calculated from MRI and PET images, respectively, for 35 FreeSurfer-derived cortical regions. Pearson's correlation coefficients between SUVR and cortical volume were calculated for the same regions, and correlated regions were compared according to disease severity and β-amyloid PET positivity. No significantly correlated regions were found in the normal controls. Negative correlations between SUVR and cortical volume were found in the MCI and AD groups, mainly in limbic locations in MCI and isocortical locations in AD. The AD group exhibited stronger correlations (r = -0.576-0.781) than the MCI group (r = 0.368-0.571). 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Hippocampal atrophy was associated with both β-amyloid and THK-5351 uptake, possibly reflecting an interaction between β-amyloid and tau deposition in the neurodegeneration process.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0226265</identifier><identifier>PMID: 31834916</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Advertising executives ; Aged ; Alzheimer Disease - diagnostic imaging ; Alzheimer Disease - pathology ; Alzheimer's disease ; Amyloid - chemistry ; Aniline Compounds - chemistry ; Atrophy ; Biology and Life Sciences ; Brain ; Brain research ; Case-Control Studies ; Cerebral Cortex - diagnostic imaging ; Cerebral Cortex - pathology ; Clinical trials ; Cognitive ability ; Cognitive Dysfunction - diagnostic imaging ; Cognitive Dysfunction - pathology ; Consent ; Correlation ; Correlation coefficient ; Correlation coefficients ; Cortex ; Dementia ; Diagnostic imaging ; Disease control ; Family medical history ; Female ; Fluorine isotopes ; Follow-Up Studies ; Hippocampus ; Humans ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Male ; Mathematical analysis ; Medical schools ; Medicine and Health Sciences ; Middle Aged ; Neurodegeneration ; Neurology ; Neuropathology ; Neurosciences ; Nuclear medicine ; Positron emission ; Positron emission tomography ; Positron-Emission Tomography - methods ; Prognosis ; Prospective Studies ; Research and Analysis Methods ; Severity of Illness Index ; Tau protein ; Tomography ; β-Amyloid</subject><ispartof>PloS one, 2019-12, Vol.14 (12), p.e0226265-e0226265</ispartof><rights>COPYRIGHT 2019 Public Library of Science</rights><rights>2019 Park et al. 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Hippocampal atrophy was associated with both β-amyloid and THK-5351 uptake, possibly reflecting an interaction between β-amyloid and tau deposition in the neurodegeneration process.</description><subject>Advertising executives</subject><subject>Aged</subject><subject>Alzheimer Disease - diagnostic imaging</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer's disease</subject><subject>Amyloid - chemistry</subject><subject>Aniline Compounds - chemistry</subject><subject>Atrophy</subject><subject>Biology and Life Sciences</subject><subject>Brain</subject><subject>Brain research</subject><subject>Case-Control Studies</subject><subject>Cerebral Cortex - diagnostic imaging</subject><subject>Cerebral Cortex - pathology</subject><subject>Clinical trials</subject><subject>Cognitive ability</subject><subject>Cognitive Dysfunction - diagnostic imaging</subject><subject>Cognitive Dysfunction - pathology</subject><subject>Consent</subject><subject>Correlation</subject><subject>Correlation coefficient</subject><subject>Correlation coefficients</subject><subject>Cortex</subject><subject>Dementia</subject><subject>Diagnostic imaging</subject><subject>Disease control</subject><subject>Family medical history</subject><subject>Female</subject><subject>Fluorine isotopes</subject><subject>Follow-Up Studies</subject><subject>Hippocampus</subject><subject>Humans</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Ji Eun</au><au>Yun, Jessica</au><au>Kim, Sang Joon</au><au>Shim, Woo Hyun</au><au>Oh, Jungsu S</au><au>Oh, Minyoung</au><au>Roh, Jee Hoon</au><au>Seo, Sang Won</au><au>Oh, Seung Jun</au><au>Kim, Jae Seung</au><au>Ginsberg, Stephen D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intra-individual correlations between quantitative THK-5351 PET and MRI-derived cortical volume in Alzheimer's disease differ according to disease severity and amyloid positivity</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2019-12-13</date><risdate>2019</risdate><volume>14</volume><issue>12</issue><spage>e0226265</spage><epage>e0226265</epage><pages>e0226265-e0226265</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>To assess the in vivo whole-brain relationship between uptake of [18F]THK-5351 on PET and cortical atrophy on structural MRI according to the presence and severity of Alzheimer's disease (AD). Sixty-five participants (21 normal controls, 32 mild cognitive impairment [MCI] subjects, and 12 AD patients) were enrolled from a prospective multicenter clinical trial (NCT02656498). Structural MRI and [18F]THK-5351 PET were performed within a 2-month interval. Cortical volume and standardized uptake value ratios (SUVR) were calculated from MRI and PET images, respectively, for 35 FreeSurfer-derived cortical regions. Pearson's correlation coefficients between SUVR and cortical volume were calculated for the same regions, and correlated regions were compared according to disease severity and β-amyloid PET positivity. No significantly correlated regions were found in the normal controls. Negative correlations between SUVR and cortical volume were found in the MCI and AD groups, mainly in limbic locations in MCI and isocortical locations in AD. The AD group exhibited stronger correlations (r = -0.576-0.781) than the MCI group (r = 0.368-0.571). Hippocampal atrophy did not show any correlation with SUVR in the β-amyloid PET-negative group, but negatively correlated with SUVR (r = -0.494, P = .012) in the β-amyloid PET-positive group. Regional THK-5351 uptake correlated more strongly with cortical atrophy in AD compared with MCI, thereby demonstrating a close relationship between the neuro-pathologic process and cortical atrophy. Hippocampal atrophy was associated with both β-amyloid and THK-5351 uptake, possibly reflecting an interaction between β-amyloid and tau deposition in the neurodegeneration process.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>31834916</pmid><doi>10.1371/journal.pone.0226265</doi><tpages>e0226265</tpages><orcidid>https://orcid.org/0000-0003-1710-1185</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1932-6203
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1932-6203
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subjects Advertising executives
Aged
Alzheimer Disease - diagnostic imaging
Alzheimer Disease - pathology
Alzheimer's disease
Amyloid - chemistry
Aniline Compounds - chemistry
Atrophy
Biology and Life Sciences
Brain
Brain research
Case-Control Studies
Cerebral Cortex - diagnostic imaging
Cerebral Cortex - pathology
Clinical trials
Cognitive ability
Cognitive Dysfunction - diagnostic imaging
Cognitive Dysfunction - pathology
Consent
Correlation
Correlation coefficient
Correlation coefficients
Cortex
Dementia
Diagnostic imaging
Disease control
Family medical history
Female
Fluorine isotopes
Follow-Up Studies
Hippocampus
Humans
Magnetic resonance imaging
Magnetic Resonance Imaging - methods
Male
Mathematical analysis
Medical schools
Medicine and Health Sciences
Middle Aged
Neurodegeneration
Neurology
Neuropathology
Neurosciences
Nuclear medicine
Positron emission
Positron emission tomography
Positron-Emission Tomography - methods
Prognosis
Prospective Studies
Research and Analysis Methods
Severity of Illness Index
Tau protein
Tomography
β-Amyloid
title Intra-individual correlations between quantitative THK-5351 PET and MRI-derived cortical volume in Alzheimer's disease differ according to disease severity and amyloid positivity
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