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与tau病理开始年龄以及从tau开始到痴呆的时间相关的因素。

Factors associated with age at tau pathology onset and time from tau onset to dementia.

作者信息

Heston Margo B, Teague Jordan P, Cody Karly A, Deming Yuetiva, Ruiz de Chavez Elena, Morse Jacob, Chin Nathaniel A, Engelman Corinne D, Chappell Richard J, Langhough Rebecca E, Gleason Carey E, Clark Lindsay R, Zuelsdorff Megan L, Betthauser Tobey J

机构信息

Wisconsin Alzheimer's Disease Research Center, University of Wisconsin School of Medicine and Public Health, 600 Highland Avenue, MC 2420, Madison, WI 53792-2420.

Department of Medicine, University of Wisconsin-Madison School of Medicine and Public Health, 1685 Highland Avenue, 5158 Medical Foundation Centennial Building, Madison, WI 53705-2281.

出版信息

medRxiv. 2025 Mar 13:2025.03.11.25323773. doi: 10.1101/2025.03.11.25323773.

Abstract

INTRODUCTION

Elevated tau is temporally proximal to dementia onset but less is known about factors influencing T+ onset age and time to dementia following T+ in Alzheimer's disease. We used sampled iterative localized approximation (SILA) estimated T+ onset age (ETOA) to investigate factors associated with T+ age and time from T+ to dementia onset in ADNI.

METHODS

Using SILA-estimated A+ and T+ onset ages derived from F-Flortaucipir, F-Florbetapir, and F-Florbetaben PET and Cox proportional hazards and accelerated failure time models, we analyzed , sex, amyloid burden, age, educational attainment, and literacy associations with ETOA and time from T+ to dementia.

RESULTS

Higher amyloid, -ε4, lower education, and lower literacy associated with younger ETOA. Older ETOA and higher amyloid associated with shorter time from T+ to dementia.

DISCUSSION

This work highlights the prognostic value of ETOA and the need to better characterize factors contributing to ETOA and dementia onset in AD.

摘要

引言

tau升高在时间上紧邻痴呆症发作,但对于阿尔茨海默病中影响T+发病年龄以及T+后至痴呆症发作时间的因素,我们了解得较少。我们使用采样迭代局部近似法(SILA)估计的T+发病年龄(ETOA)来研究ADNI中与T+年龄以及从T+到痴呆症发作时间相关的因素。

方法

利用从F-氟代tau蛋白、F-氟代贝他淀粉样蛋白和F-氟代贝他苯PET得出的SILA估计的A+和T+发病年龄,以及Cox比例风险模型和加速失效时间模型,我们分析了性别、淀粉样蛋白负荷、年龄、教育程度和读写能力与ETOA以及从T+到痴呆症的时间之间的关联。

结果

较高的淀粉样蛋白、-ε4、较低的教育程度和较低的读写能力与较年轻的ETOA相关。较年长的ETOA和较高的淀粉样蛋白与从T+到痴呆症的较短时间相关。

讨论

这项工作突出了ETOA的预后价值,以及更好地描述导致AD中ETOA和痴呆症发作的因素的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/640e/11952611/15454ffa3ba8/nihpp-2025.03.11.25323773v1-f0001.jpg

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