Premnath Pranitha Y, Locascio Joseph J, Mimmack Kayden J, Gonzalez Christopher, Properzi Michael J, Udeogu Onyinye, Rosenberg Paul B, Marshall Gad A, Gatchel Jennifer R
Department of Psychology The Graduate Center, City University of New York New York New York USA.
Department of Neurology Massachusetts General Hospital Boston Massachusetts USA.
Alzheimers Dement (N Y). 2024 Feb 1;10(1):e12442. doi: 10.1002/trc2.12442. eCollection 2024 Jan-Mar.
It is important to study apathy in Alzheimer's disease (AD) to better understand its underlying neurobiology and develop effective interventions. In the current study, we sought to examine the relationships between longitudinal apathy and regional tau burden in cognitively impaired older adults from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database.
Three hundred and nineteen ADNI participants with mild cognitive impairment (MCI) or AD dementia underwent flortaucipir (FTP) tau positron emission tomography (PET) imaging and clinical assessment with the Neuropsychiatric Inventory (NPI) annually. Longitudinal NPI Apathy (NPI-A) scores were examined in relation to baseline tau PET signal in three a priori selected regions implicated in AD and AD-related apathy (supramarginal gyrus, entorhinal cortex [EC] and rostral anterior cingulate cortex [rACC]). Secondary models were adjusted for global cognition (Mini-Mental State Examination score) and cortical amyloid (florbetapir PET).
Higher baseline supramarginal gyrus and EC tau burden were each significantly associated with greater NPI-A over time, while rACC tau was associated with higher NPI-A but did not predict its trajectory over time. These results were retained for supramarginal and EC tau after adjusting models for global cognition and cortical amyloid.
Our findings suggest that baseline in vivo tau burden in parietal and temporal brain regions affected in AD, and less so in a medial frontal region involved in motivational control, is associated with increasing apathy over time in older adults with MCI and AD dementia. Future work studying emergent apathy in relation to not only core AD pathology but also circuit level dysfunction may provide additional insight into the neurobiology of apathy in AD and opportunities for intervention.
Tau (Flortaucipir PET) in regions implicated in AD was associated with increasing apathy over timeCortical amyloid was also found to be a robust predictor of the trajectory of apathyEvidence of synergy between regional tau and amyloid in overall higher levels of apathy.
研究阿尔茨海默病(AD)中的淡漠对于更好地理解其潜在神经生物学机制并开发有效干预措施至关重要。在当前研究中,我们试图从阿尔茨海默病神经影像倡议(ADNI)数据库中,研究认知受损老年人的纵向淡漠与区域tau蛋白负荷之间的关系。
319名患有轻度认知障碍(MCI)或AD痴呆的ADNI参与者每年接受氟代脱氧葡萄糖(FTP)tau正电子发射断层扫描(PET)成像,并使用神经精神科问卷(NPI)进行临床评估。纵向NPI淡漠(NPI-A)评分与预先选定的三个与AD及AD相关淡漠有关的区域(缘上回、内嗅皮质[EC]和喙前扣带回皮质[rACC])的基线tau PET信号相关联进行研究。二级模型针对整体认知(简易精神状态检查表评分)和皮质淀粉样蛋白(氟比他派PET)进行了调整。
较高的基线缘上回和EC tau蛋白负荷均与随时间推移更高的NPI-A显著相关,而rACC tau蛋白与较高的NPI-A相关,但不能预测其随时间的变化轨迹。在针对整体认知和皮质淀粉样蛋白调整模型后,缘上回和EC tau蛋白的这些结果依然成立。
我们的研究结果表明,AD中受影响的顶叶和颞叶脑区的基线体内tau蛋白负荷,以及参与动机控制的内侧额叶区域中程度较轻的tau蛋白负荷,与MCI和AD痴呆老年人随时间推移淡漠增加有关。未来不仅研究与核心AD病理学相关的新发淡漠,还研究与回路水平功能障碍相关的新发淡漠的工作,可能会为AD中淡漠的神经生物学机制提供更多见解以及干预机会。
与AD相关区域的tau蛋白(氟代脱氧葡萄糖PET)与随时间推移淡漠增加有关
皮质淀粉样蛋白也被发现是淡漠轨迹的有力预测指标
在总体较高水平的淡漠中,区域tau蛋白和淀粉样蛋白之间存在协同作用的证据