Multimodal neuroimaging of sex differences in cognitively impaired patients on the Alzheimer's continuum: greater tau-PET retention in females
•In the clinical stages of AD, females had greater tau- and amyloid-PET than males•Greater cortical tau-PET binding in females was observed in temporoparietal regions•Tau-PET sex differences were present when controlling for amyloid-PET, age, and CDR•Tau-PET sex differences were not present in subco...
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Veröffentlicht in: | Neurobiology of aging 2021-09, Vol.105, p.86-98 |
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Sprache: | eng |
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Zusammenfassung: | •In the clinical stages of AD, females had greater tau- and amyloid-PET than males•Greater cortical tau-PET binding in females was observed in temporoparietal regions•Tau-PET sex differences were present when controlling for amyloid-PET, age, and CDR•Tau-PET sex differences were not present in subcortical areas of off-target binding
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. |
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ISSN: | 0197-4580 1558-1497 |
DOI: | 10.1016/j.neurobiolaging.2021.04.003 |