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July 26, 2016; 87 (4) Article

Tau PET in Alzheimer disease and mild cognitive impairment

Hanna Cho, Jae Yong Choi, Mi Song Hwang, Jae Hoon Lee, You Jin Kim, Hye Mi Lee, Chul Hyoung Lyoo, Young Hoon Ryu, Myung Sik Lee
First published June 29, 2016, DOI: https://doi.org/10.1212/WNL.0000000000002892
Hanna Cho
From the Departments of Neurology (H.C., M.S.H., Y.J.K., H.M.L., C.H.L., M.S.L.) and Nuclear Medicine (J.Y.C., J.H.L., Y.H.R.), Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
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Jae Yong Choi
From the Departments of Neurology (H.C., M.S.H., Y.J.K., H.M.L., C.H.L., M.S.L.) and Nuclear Medicine (J.Y.C., J.H.L., Y.H.R.), Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
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Mi Song Hwang
From the Departments of Neurology (H.C., M.S.H., Y.J.K., H.M.L., C.H.L., M.S.L.) and Nuclear Medicine (J.Y.C., J.H.L., Y.H.R.), Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
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Jae Hoon Lee
From the Departments of Neurology (H.C., M.S.H., Y.J.K., H.M.L., C.H.L., M.S.L.) and Nuclear Medicine (J.Y.C., J.H.L., Y.H.R.), Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
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You Jin Kim
From the Departments of Neurology (H.C., M.S.H., Y.J.K., H.M.L., C.H.L., M.S.L.) and Nuclear Medicine (J.Y.C., J.H.L., Y.H.R.), Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
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Hye Mi Lee
From the Departments of Neurology (H.C., M.S.H., Y.J.K., H.M.L., C.H.L., M.S.L.) and Nuclear Medicine (J.Y.C., J.H.L., Y.H.R.), Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
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Chul Hyoung Lyoo
From the Departments of Neurology (H.C., M.S.H., Y.J.K., H.M.L., C.H.L., M.S.L.) and Nuclear Medicine (J.Y.C., J.H.L., Y.H.R.), Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
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Young Hoon Ryu
From the Departments of Neurology (H.C., M.S.H., Y.J.K., H.M.L., C.H.L., M.S.L.) and Nuclear Medicine (J.Y.C., J.H.L., Y.H.R.), Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
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Myung Sik Lee
From the Departments of Neurology (H.C., M.S.H., Y.J.K., H.M.L., C.H.L., M.S.L.) and Nuclear Medicine (J.Y.C., J.H.L., Y.H.R.), Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
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Citation
Tau PET in Alzheimer disease and mild cognitive impairment
Hanna Cho, Jae Yong Choi, Mi Song Hwang, Jae Hoon Lee, You Jin Kim, Hye Mi Lee, Chul Hyoung Lyoo, Young Hoon Ryu, Myung Sik Lee
Neurology Jul 2016, 87 (4) 375-383; DOI: 10.1212/WNL.0000000000002892

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Abstract

Objective: To investigate the topographical distribution of tau pathology and its effect on functional and structural changes in patients with Alzheimer disease (AD) and mild cognitive impairment (MCI) by using 18F-AV-1451 PET.

Methods: We included 20 patients with AD, 15 patients with MCI, and 20 healthy controls, and performed neuropsychological function tests, MRI, as well as 18F-florbetaben (for amyloid) and 18F-AV-1451 (for tau) PET scans. By using the regional volume-of-interest masks extracted from MRIs, regional binding values of standardized uptake value ratios and volumes were measured. We compared regional binding values among 3 diagnostic groups and identified correlations among the regional binding values, performance in each cognitive function test, and regional atrophy.

Results: 18F-AV-1451 binding was increased only in the entorhinal cortex in patients with MCI, while patients with AD exhibited greater binding in most cortical regions. In the 35 patients with MCI and AD, 18F-AV-1451 binding in most of the neocortex increased with a worsening of global cognitive function. The visual and verbal memory functions were associated with the extent of 18F-AV-1451 binding, especially in the medial temporal regions. The 18F-AV-1451 binding also correlated with the severity of regional atrophy of the cerebral cortex.

Conclusions: Tau PET imaging with 18F-AV-1451 could serve as an in vivo biomarker for the evaluation of AD-related tau pathology and monitoring disease progression. The accumulation of pathologic tau is more closely related to functional and structural deterioration in the AD spectrum than β-amyloid.

GLOSSARY

AD=
Alzheimer disease;
ANCOVA=
analysis of covariance;
CDR-SB=
Clinical Dementia Rating–Sum of Boxes;
EOAD=
early-onset Alzheimer disease;
HC=
healthy control;
LOAD=
late-onset Alzheimer disease;
MCI=
mild cognitive impairment;
MMSE=
Mini-Mental State Examination;
NFT=
neurofibrillary tangle;
PART=
primary age-related tauopathy;
PHF=
paired helical filaments;
PVE=
partial volume effect;
SPM8=
statistical parametric mapping 8;
SUV=
standardized uptake value;
SUVR=
standardized uptake value ratio;
VOI=
volume-of-interest

Footnotes

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Supplemental data at Neurology.org

  • Received November 16, 2015.
  • Accepted in final form April 14, 2016.
  • © 2016 American Academy of Neurology
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