脑深度老化,灰质的选择性脆弱性和帕金森病的认知。

Mengfei Cai, Chentao He, Hao Li, Rui Yang, Siming Rong, Ziqi Gao, Qibing Luo, Zihao Li, Yan Li, Zaiyi Liu, Piao Zhang, Yuhu Zhang
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引用次数: 0

摘要

背景:确定脑衰老晚期导致的灰质最脆弱脑区,并研究帕金森病(PD)脑衰老晚期的认知相关性。方法:125名早期PD患者在帕金森进展标志物计划(PPMI)的基线(第0年)中获得结构、扩散MRI和DAT-SPECT数据,并在第1、2、4年进行神经影像学随访。在5年内进行年度认知评估。采用线性回归和线性混合效应模型检验脑预测年龄差异(PAD)与大脑皮层和皮层下灰质游离水以及认知的关系。采用Cox比例风险模型探讨脑外PAD与轻度认知障碍(MCI)转化风险的关系。结果:125例PD患者的平均(SD)实足年龄为60.99(9.50)岁,其中82例为男性(65.6%)。脑外PAD随时间呈非线性发展模式(p = 0.028)。脑PAD与皮层和皮层下灰质中的游离水存在差异相关,其中颞叶皮层、纹状体、海马和胆碱能基底前脑是最易受影响的区域。在5年随访期间,基线脑外PAD与认知缺陷和转化为轻度认知障碍有关。结论:我们的研究结果表明,大脑PAD在精确定位最容易加速大脑衰老的区域和识别帕金森病患者转变为轻度认知障碍的风险增加方面具有潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advanced brain aging, selective vulnerability in gray matter, and cognition in Parkinson's disease.

Background: To identify the most vulnerable brain regions in gray matter attributable to advanced brain aging and examine the cognitive correlates of advanced brain aging in Parkinson's disease (PD).

Methods: 125 early-stage PD patients with both structural, diffusion MRI and DAT-SPECT data available were included at baseline (year 0) from Parkinson's Progression Markers Initiative (PPMI), with neuroimaging follow-up at year 1, 2, 4. Annual assessment of cognition was performed in 5 years. The relation between brain-predicted age difference (PAD) and free water in cortical and subcortical gray matter, as well as cognition were examined with linear regression and linear mixed effects model. Cox proportional hazards model was used to investigate the relation between brain PAD and the risk of conversion to mild cognitive impairment (MCI).

Results: 125 PD patients with a mean (SD) chronological age of 60.99 (9.50) years and 82 (65.6%) were men. Brain PAD followed a non-linear progression pattern over time(p = 0.028). Brain PAD was differentially associated with free water in cortical and subcortical gray matter, with the most preferentially vulnerable regions identified as temporal cortex, striatum, hippocampus, and cholinergic basal forebrain. Baseline brain PAD was associated with cognitive deficits and the conversion to mild cognitive impairment during the 5-year follow-up.

Conclusions: Our findings suggest that brain PAD offers potential in pinpointing regions most susceptible to accelerated brain aging and identifying patients with Parkinson's disease who are at an increased risk of converting to mild cognitive impairment. .

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