Knudsen Laust Vind, Michel Tanja Maria, Farahani Ziba Ahangarani, Vafaee Manouchehr Seyedi
Department of Psychiatry, University of Southern Denmark, Odense University Hospital, Odense C, 5000, Denmark.
Department of Nuclear Medicine, Odense University Hospital, Odense C, 5000, Denmark.
Eur J Nucl Med Mol Imaging. 2025 Jun;52(7):2267-2278. doi: 10.1007/s00259-025-07100-w. Epub 2025 Feb 1.
The purpose of this study was to advance our understanding of the neurobiology of healthy aging, which is crucial for improving quality of life and preventing age-related diseases. Despite its importance, a comprehensive investigation of this process has yet to be fully characterized.
We used a hybrid PET/MRI scanner to assess neurophysiological parameters in 80 healthy individuals aged 20-78. Cerebral amyloid-beta (Aβ) deposition and glucose metabolism were assessed using PET scans, while participants underwent simultaneous MRI scans.
We found a positive correlation between Aβ-deposition and aging, and a negative correlation between glucose metabolism and aging. The insula showed the strongest negative correlation between glucose metabolism and age (Spearman's r = -0.683, 95% CI [-0.79, -0.54], p < 0.0001), while the posterior cingulate cortex had the strongest positive correlation between Aβ-deposition and age (Spearman's r = 0.479, 95% CI [0.28, 0.64], p < 0.0001). These results suggest a spatially dependent link between Aβ-deposition and metabolism in healthy older adults, indicating a compensatory mechanism in early Alzheimer's. Additionally, Aβ-deposition was linked to changes in interregional neural communication.
Our study confirms previous findings on aging and offers new insights, particularly on the role of Aβ-deposition in healthy aging. We observed a linear increase in Aβ-deposition, alongside decreases in white matter integrity, cerebral blood flow, and glucose metabolism. Additionally, we identified a complex regional relationship between Aβ-deposition, glucose metabolism, and neural communication, possibly reflecting compensatory mechanisms.
本研究的目的是增进我们对健康衰老神经生物学的理解,这对于提高生活质量和预防与年龄相关的疾病至关重要。尽管其重要性,但对这一过程的全面研究尚未得到充分表征。
我们使用一台混合正电子发射断层扫描/磁共振成像(PET/MRI)扫描仪,对80名年龄在20 - 78岁的健康个体的神经生理参数进行评估。使用PET扫描评估脑淀粉样β(Aβ)沉积和葡萄糖代谢,同时参与者接受同步的MRI扫描。
我们发现Aβ沉积与衰老之间呈正相关,葡萄糖代谢与衰老之间呈负相关。脑岛在葡萄糖代谢与年龄之间显示出最强的负相关(斯皮尔曼相关系数r = -0.683,95%置信区间[-0.79, -0.54],p < 0.0001),而后扣带回皮质在Aβ沉积与年龄之间具有最强的正相关(斯皮尔曼相关系数r = 0.479,95%置信区间[0.28, 0.64],p < 0.0001)。这些结果表明,在健康的老年人中,Aβ沉积与代谢之间存在空间依赖性联系,这表明在早期阿尔茨海默病中存在一种代偿机制。此外,Aβ沉积与区域间神经通信的变化有关。
我们的研究证实了先前关于衰老的发现,并提供了新的见解,特别是关于Aβ沉积在健康衰老中的作用。我们观察到Aβ沉积呈线性增加,同时白质完整性、脑血流量和葡萄糖代谢下降。此外,我们确定了Aβ沉积、葡萄糖代谢和神经通信之间复杂的区域关系,这可能反映了代偿机制。