Multimodal neuroimaging of sex differences in cognitively impaired patients on the Alzheimer's continuum: greater tau-PET retention in females.
Multimodal neuroimaging of sex differences in cognitively impaired patients on the Alzheimer's continuum: greater tau-PET retention in females.
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DOI:
10.1016/j.neurobiolaging.2021.04.003
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发表时间:
2021-09
影响因子:
4.2
通讯作者:
Rabinovici GD
中科院分区:
文献类型:
--
作者:
Edwards L;La Joie R;Iaccarino L;Strom A;Baker SL;Casaletto KB;Cobigo Y;Grant H;Kim M;Kramer JH;Mellinger TJ;Pham J;Possin KL;Rosen HJ;Soleimani-Meigooni DN;Wolf A;Miller BL;Rabinovici GD
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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影响因子:
4.2
作者:
Armstrong, Nicole M.;Huang, Chiung-Wei;Resnick, Susan M.
通讯作者:
Resnick, Susan M.
影响因子:
14
作者:
通讯作者:
--
DOI:
10.1016/j.jalz.2013.10.005
发表时间:
2015-03
期刊:
Alzheimer's & dementia : the journal of the Alzheimer's Association
影响因子:
--
作者:
Chêne G;Beiser A;Au R;Preis SR;Wolf PA;Dufouil C;Seshadri S
通讯作者:
Seshadri S
影响因子:
9.9
作者:
ARRIAGADA, PV;GROWDON, JH;HYMAN, BT
通讯作者:
HYMAN, BT
影响因子:
1.5
作者:
Bolla-Wilson, Karen;Bleecker, Margit L.
通讯作者:
Bleecker, Margit L.