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Research ArticleNeurology

18F-Flortaucipir PET/MRI Correlations in Nonamnestic and Amnestic Variants of Alzheimer Disease

Ilya M. Nasrallah, Yin Jie Chen, Meng-Kang Hsieh, Jeffrey S. Phillips, Kylie Ternes, Grace E. Stockbower, Yvette Sheline, Corey T. McMillan, Murray Grossman and David A. Wolk
Journal of Nuclear Medicine February 2018, 59 (2) 299-306; DOI: https://doi.org/10.2967/jnumed.117.194282
Ilya M. Nasrallah
1Department of Radiology, University of Pennsylvania, Philadelphia, Pennsylvania
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Yin Jie Chen
1Department of Radiology, University of Pennsylvania, Philadelphia, Pennsylvania
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Meng-Kang Hsieh
1Department of Radiology, University of Pennsylvania, Philadelphia, Pennsylvania
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Jeffrey S. Phillips
2Department of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania; and
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Kylie Ternes
2Department of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania; and
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Grace E. Stockbower
2Department of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania; and
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Yvette Sheline
3Department of Psychiatry, University of Pennsylvania, Philadelphia, Pennsylvania
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Corey T. McMillan
2Department of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania; and
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Murray Grossman
2Department of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania; and
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David A. Wolk
2Department of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania; and
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This article has a correction. Please see:

  • Erratum - May 01, 2019

Abstract

Nonamnestic Alzheimer disease (AD) variants, including posterior cortical atrophy and the logopenic variant of primary progressive aphasia, differ from amnestic AD in distributions of tau aggregates and neurodegeneration. We evaluated whether 18F-flortaucipir (also called 18F-AV-1451) PET, targeting tau aggregates, detects these differences, and we compared the results with MRI measures of gray matter (GM) atrophy. Methods: Five subjects with posterior cortical atrophy, 4 subjects with the logopenic variant of primary progressive aphasia, 6 age-matched patients with AD, and 6 control subjects underwent 18F-flortaucipir PET and MRI. SUV ratios and GM volumes were compared using regional and voxel-based methods. Results: The subgroups showed the expected 18F-flortaucipir–binding patterns. Group effect sizes were generally stronger with 18F-flortaucipir PET than with MRI volumes. There were moderate-to-high correlations between regional GM atrophy and 18F-flortaucipir uptake. 18F-flortaucipir binding and GM atrophy correlated similarly to cognitive test performance. Conclusion: 18F-flortaucipir binding corresponds to the expected neurodegeneration patterns in nonamnestic AD, with potential for earlier detection of pathology than is possible with MRI atrophy measures.

  • Alzheimer disease
  • 18F-flortaucipir PET
  • tau PET
  • structural MRI

Footnotes

  • Published online Jul. 26, 2017.

  • © 2018 by the Society of Nuclear Medicine and Molecular Imaging.
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Journal of Nuclear Medicine: 59 (2)
Journal of Nuclear Medicine
Vol. 59, Issue 2
February 1, 2018
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18F-Flortaucipir PET/MRI Correlations in Nonamnestic and Amnestic Variants of Alzheimer Disease
Ilya M. Nasrallah, Yin Jie Chen, Meng-Kang Hsieh, Jeffrey S. Phillips, Kylie Ternes, Grace E. Stockbower, Yvette Sheline, Corey T. McMillan, Murray Grossman, David A. Wolk
Journal of Nuclear Medicine Feb 2018, 59 (2) 299-306; DOI: 10.2967/jnumed.117.194282

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18F-Flortaucipir PET/MRI Correlations in Nonamnestic and Amnestic Variants of Alzheimer Disease
Ilya M. Nasrallah, Yin Jie Chen, Meng-Kang Hsieh, Jeffrey S. Phillips, Kylie Ternes, Grace E. Stockbower, Yvette Sheline, Corey T. McMillan, Murray Grossman, David A. Wolk
Journal of Nuclear Medicine Feb 2018, 59 (2) 299-306; DOI: 10.2967/jnumed.117.194282
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