Zhang Zijing, Li Yuchen, Xia Qi, Yu Qing, Wei Luqing, Wu Guo-Rong
Key Laboratory of Cognition and Personality, Faculty of Psychology, Southwest University, Chongqing 400715, China.
School of Psychology, Jiangxi Normal University, Nanchang 330022, China.
Metabolites. 2025 Jan 22;15(2):67. doi: 10.3390/metabo15020067.
As the global population ages, the prevalence of neurodegenerative conditions, such as Alzheimer's disease (AD), Parkinson's disease (PD), dementia with Lewy bodies, and frontotemporal dementia, continues to rise. Understanding the impact of aging on striatal glucose metabolism is pivotal in identifying potential biomarkers for the early detection of these disorders.
We investigated age-related changes in striatal glucose metabolism using both region of interest (ROI)-based and voxel-wise correlation analyses. Additionally, we employed a normative modeling approach to establish age-related metabolic trajectories and assess individual deviations from these normative patterns. In vivo cerebral glucose metabolism was quantified using a molecular neuroimaging technique, F-FDG PET.
Our results revealed significant negative correlations between age and glucose metabolism in the bilateral caudate. Furthermore, the normative modeling demonstrated a clear, progressive decline in caudate metabolism with advancing age, and the most pronounced reductions were observed in older individuals.
These findings suggest that metabolic reductions in the caudate may serve as a sensitive biomarker for normal aging and offer valuable insights into the early stages of neurodegenerative diseases. Moreover, by establishing age-specific reference values for caudate glucose metabolism, the normative model provides a framework for detecting deviations from expected metabolic patterns, which may facilitate the early identification of metabolic alterations that could precede clinical symptoms of neurodegenerative processes.
随着全球人口老龄化,神经退行性疾病的患病率持续上升,如阿尔茨海默病(AD)、帕金森病(PD)、路易体痴呆和额颞叶痴呆。了解衰老对纹状体葡萄糖代谢的影响对于识别这些疾病早期检测的潜在生物标志物至关重要。
我们使用基于感兴趣区域(ROI)和体素相关性分析来研究纹状体葡萄糖代谢与年龄相关的变化。此外,我们采用规范建模方法来建立与年龄相关的代谢轨迹,并评估个体与这些规范模式的偏差。使用分子神经成像技术F-FDG PET对体内脑葡萄糖代谢进行定量。
我们的结果显示双侧尾状核中年龄与葡萄糖代谢之间存在显著负相关。此外,规范建模表明随着年龄增长,尾状核代谢明显逐渐下降,且在老年人中观察到最明显的降低。
这些发现表明尾状核代谢降低可能是正常衰老的敏感生物标志物,并为神经退行性疾病的早期阶段提供有价值的见解。此外,通过建立尾状核葡萄糖代谢的年龄特异性参考值,规范模型为检测与预期代谢模式的偏差提供了一个框架,这可能有助于早期识别可能先于神经退行性过程临床症状的代谢改变。