Contribution of extracerebral tracer retention and partial volume effects to sex differences in Flortaucipir-PET signal

Author:

Scott Matthew R12ORCID,Edwards Natalie C134,Properzi Michael J1,Jacobs Heidi IL56,Price Julie C5,Lois Cristina5,Farrell Michelle E1,Hanseeuw Bernard J57,Thibault Emma G5,Rentz Dorene M18,Johnson Keith A58,Sperling Reisa A18,Schultz Aaron P1ORCID,Buckley Rachel F189

Affiliation:

1. Department of Neurology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA

2. Department of Biostatistics, School of Public Health, Boston University, Boston, MA, USA

3. Taub Institute for Research on Alzheimer’s Disease and the Aging Brain, Columbia University, New York City, NY, USA

4. Department of Neurology, Vagelos College of Physicians and Surgeons, Columbia University, New York City, NY, USA

5. Division of Nuclear Medicine and Molecular Imaging, Department of Radiology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA

6. Faculty of Health, Medicine and Life Sciences, School for Mental Health and Neuroscience, Alzheimer Centre Limburg, Maastricht University, Maastricht, The Netherlands

7. Department of Neurology, Cliniques Universitaires SaintLuc, Institute of Neuroscience, Université Catholique de Louvain, Brussels, Belgium

8. Department of Neurology, Center for Alzheimer Research and Treatment, Brigham and Women’s Hospital, Boston, MA, USA

9. Melbourne School of Psychological Science, University of Melbourne, Melbourne, VIC, Australia

Abstract

Clinically normal females exhibit higher 18F-flortaucipir (FTP)-PET signal than males across the cortex. However, these sex differences may be explained by neuroimaging idiosyncrasies such as off-target extracerebral tracer retention or partial volume effects (PVEs). 343 clinically normal participants (female = 58%; mean[SD]=73.8[8.5] years) and 55 patients with mild cognitive impairment (female = 38%; mean[SD] = 76.9[7.3] years) underwent cross-sectional FTP-PET. We parcellated extracerebral FreeSurfer areas based on proximity to cortical ROIs. Sex differences in cortical tau were then estimated after accounting for local extracerebral retention. We simulated PVE by convolving group-level standardized uptake value ratio means in each ROI with 6 mm Gaussian kernels and compared the sexes across ROIs post-smoothing. Widespread sex differences in extracerebral retention were observed. Although attenuating sex differences in cortical tau-PET signal, covarying for extracerebral retention did not impact the largest sex differences in tau-PET signal. Differences in PVE were observed in both female and male directions with no clear sex-specific bias. Our findings suggest that sex differences in FTP are not solely attributed to off-target extracerebral retention or PVE, consistent with the notion that sex differences in medial temporal and neocortical tau are biologically driven. Future work should investigate sex differences in regional cerebral blood flow kinetics and longitudinal tau-PET.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Neurology

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