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Biological sex differences in Alzheimer's preclinical research: A call to action.阿尔茨海默病临床前研究中的生物性别差异:行动呼吁。
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4
The cortical origin and initial spread of medial temporal tauopathy in Alzheimer's disease assessed with positron emission tomography.正电子发射断层扫描评估阿尔茨海默病中内侧颞叶tau 病的皮质起源和初始扩散。
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Association of and Clinical Variability in Alzheimer Disease With the Pattern of Tau- and Amyloid-PET.阿尔茨海默病中 Tau 和淀粉样蛋白-PET 的模式与 的关联和临床变异性。
Neurology. 2021 Feb 2;96(5):e650-e661. doi: 10.1212/WNL.0000000000011270. Epub 2020 Dec 1.
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Female-specific risk of Alzheimer's disease is associated with tau phosphorylation processes: A transcriptome-wide interaction analysis.女性特有的阿尔茨海默病风险与 Tau 磷酸化过程相关:全转录组交互分析。
Neurobiol Aging. 2020 Dec;96:104-108. doi: 10.1016/j.neurobiolaging.2020.08.020. Epub 2020 Sep 2.
7
The Association Between Functional Assessment and Structural Brain Biomarkers in an Ethnically Diverse Sample With Normal Cognition, Mild Cognitive Impairment, or Dementia.在具有正常认知、轻度认知障碍或痴呆的种族多样化样本中,功能评估与结构脑生物标志物之间的关联。
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A second X chromosome contributes to resilience in a mouse model of Alzheimer's disease.第二条X染色体有助于阿尔茨海默病小鼠模型的恢复力。
Sci Transl Med. 2020 Aug 26;12(558). doi: 10.1126/scitranslmed.aaz5677.
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Sex Mediates Relationships Between Regional Tau Pathology and Cognitive Decline.性别介导了区域 tau 病理学与认知衰退之间的关系。
Ann Neurol. 2020 Nov;88(5):921-932. doi: 10.1002/ana.25878. Epub 2020 Aug 31.
10
Sex differences in CSF biomarkers vary by Alzheimer disease stage and ε4 genotype.性别差异在 CSF 生物标志物中因阿尔茨海默病阶段和 ε4 基因型而异。
Neurology. 2020 Oct 27;95(17):e2378-e2388. doi: 10.1212/WNL.0000000000010629. Epub 2020 Aug 11.

阿尔茨海默病连续谱中认知障碍患者的性别差异的多模态神经影像学:女性tau-PET 保留更多。

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

机构信息

Memory and Aging Center, Department of Neurology, Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, USA.

Memory and Aging Center, Department of Neurology, Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, USA.

出版信息

Neurobiol Aging. 2021 Sep;105:86-98. doi: 10.1016/j.neurobiolaging.2021.04.003. Epub 2021 Apr 22.

DOI:10.1016/j.neurobiolaging.2021.04.003
PMID:34049062
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8820163/
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, C-PIB amyloid-PET and F-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 (η²=.043, p=.025) and temporal Flortaucipir SUVR (η²=.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 (η²=.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.

摘要

我们评估了 119 名轻度认知障碍或阿尔茨海默病 (AD) 痴呆症的淀粉样蛋白阳性患者中淀粉样蛋白和 tau-PET 保留的性别差异。患者接受了 3T-MRI、C-PIB 淀粉样蛋白-PET 和 F-Flortaucipir tau-PET 检查。线性普通最小二乘回归模型测试了 Flortaucipir-PET SUVR 在时间汇总感兴趣区域以及全球 PIB-PET 中的性别差异。在人口统计学、临床痴呆评定量表总和评分 (CDR-SoB)、简易精神状态检查 (MMSE)、原始情节记忆评分或皮质厚度方面,未观察到性别差异。女性的全球 PIB SUVR 更高 (η²=.043, p=.025) 和颞部 Flortaucipir SUVR (η²=.070, p=.004),调整了年龄和 CDR-SoB。当控制 PIB SUVR 和 APOE4 状态 (η²=.055, p=.013) 或使用部分体积校正数据时,颞部 Flortaucipir-PET 的性别差异仍然显著。在已知 Flortaucipir 脱靶结合的区域不存在性别差异。总的来说,尽管临床可比性,女性表现出比男性更大的 AD 区域 tau-PET 负担。进一步表征性别差异将深入了解 AD 的发病机制,并支持个性化治疗策略的发展。