Literature DB >> 34049062

Multimodal neuroimaging of sex differences in cognitively impaired patients on the Alzheimer's continuum: greater tau-PET retention in females.

Lauren Edwards1, Renaud La Joie2, Leonardo Iaccarino1, Amelia Strom1, Suzanne L Baker3, Kaitlin B Casaletto1, Yann Cobigo1, Harli Grant1, Minseon Kim1, Joel H Kramer1, Taylor J Mellinger1, Julie Pham1, Katherine L Possin1, Howard J Rosen1, David N Soleimani-Meigooni1, Amy Wolf1, Bruce L Miller1, Gil D Rabinovici4.   

Abstract

We assessed sex differences in amyloid- and tau-PET retention in 119 amyloid positive patients with mild cognitive impairment or Alzheimer's disease (AD) dementia. Patients underwent 3T-MRI, 11C-PIB amyloid-PET and 18F-Flortaucipir tau-PET. Linear ordinary least squares regression models tested sex differences in Flortaucipir-PET SUVR in a summary temporal region of interest as well as global PIB-PET. No sex differences were observed in demographics, Clinical Dementia Rating Sum of Boxes (CDR-SoB), Mini-Mental State Exam (MMSE), raw episodic memory scores, or cortical thickness. Females had higher global PIB SUVR (ηp²=.043, p=.025) and temporal Flortaucipir SUVR (ηp²=.070, p=.004), adjusting for age and CDR-SoB. Sex differences in temporal Flortaucipir-PET remained significant when controlling additionally for PIB SUVR and APOE4 status (ηp²=.055, p=.013), or when using partial volume-corrected data. No sex differences were present in areas of known Flortaucipir off-target binding. Overall, females demonstrated greater AD regional tau-PET burden than males despite clinical comparability. Further characterization of sex differences will provide insight into AD pathogenesis and support development of personalized therapeutic strategies.
Copyright © 2021. Published by Elsevier Inc.

Entities:  

Keywords:  Alzheimer's disease; Amyloid; Apolipoprotein E; Positron emission tomography; Sex differences; Tau

Mesh:

Substances:

Year:  2021        PMID: 34049062      PMCID: PMC8820163          DOI: 10.1016/j.neurobiolaging.2021.04.003

Source DB:  PubMed          Journal:  Neurobiol Aging        ISSN: 0197-4580            Impact factor:   5.133


  82 in total

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