Alzheimer's Disease Research Unit, Yale University School of Medicine, One Church Street, 8th Floor, New Haven, CT, 06514, USA; Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Alzheimer's Disease Research Unit, Yale University School of Medicine, One Church Street, 8th Floor, New Haven, CT, 06514, USA; Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Neuroimage. 2021 Sep;238:118217. doi: 10.1016/j.neuroimage.2021.118217. Epub 2021 May 27.
Metabotropic glutamate receptor subtype 5 (mGluR5) is integral to the brain glutamatergic system and cognitive function. This study investigated whether aging is associated with decreased brain mGluR5 availability.
Cognitively normal participants (n = 45), aged 18 to 84 years, underwent [F]FPEB positron emission tomography scans to quantify brain mGluR5. Distribution volume (V) was computed using a venous or arterial input function and equilibrium modeling from 90 to 120 min. In the primary analysis, the association between age and V in the hippocampus and association cortex was evaluated using a linear mixed model. Exploratory analyses assessed the association between age and V in multiple brain regions. The contribution of gray matter tissue alterations and partial volume effects to associations with age was also examined.
In the primary analysis, older age was associated with lower [F]FPEB binding to mGluR5 (P = 0.026), whereas this association was not significant after gray matter masking or partial volume correction to account for age-related tissue loss. Post hoc analyses revealed an age-related decline in mGluR5 availability in the hippocampus of 4.5% per decade (P = 0.007) and a non-significant trend in the association cortex (P = 0.085). An exploratory analysis of multiple brain regions revealed broader inverse associations of age with mGluR5 availability, but not after partial volume correction.
Reductions in mGluR5 availability with age appear to be largely mediated by tissue loss. Quantification of [F]FPEB binding to mGluR5 may expand our understanding of age-related molecular changes and the relationship with brain tissue loss.
代谢型谷氨酸受体 5 型(mGluR5)是大脑谷氨酸能系统和认知功能的重要组成部分。本研究旨在探讨衰老是否与大脑 mGluR5 可用性降低有关。
认知正常的参与者(n=45),年龄在 18 至 84 岁之间,接受 [F]FPEB 正电子发射断层扫描以量化大脑 mGluR5。使用静脉或动脉输入函数和平衡建模从 90 到 120 分钟计算分布容积(V)。在主要分析中,使用线性混合模型评估年龄与海马体和联合皮质中 V 的相关性。探索性分析评估了年龄与多个脑区 V 的相关性。还检查了灰质组织改变和部分容积效应与年龄相关性的关系。
在主要分析中,年龄较大与 [F]FPEB 与 mGluR5 的结合减少相关(P=0.026),但在进行灰质掩蔽或部分容积校正以解释与年龄相关的组织丢失后,这种相关性不再显著。事后分析显示,mGluR5 可用性在海马体中每 10 年下降 4.5%(P=0.007),在联合皮质中呈非显著趋势(P=0.085)。对多个脑区的探索性分析显示,年龄与 mGluR5 可用性呈更广泛的负相关,但在进行部分容积校正后则不相关。
mGluR5 可用性随年龄的降低似乎主要是由组织损失介导的。[F]FPEB 与 mGluR5 结合的定量可能会扩展我们对与年龄相关的分子变化及其与脑组织损失关系的理解。