SDSU/UC San Diego Joint Doctoral Program in Clinical Psychology, San Diego, California, USA.
Department of Psychology, San Diego State University, San Diego, California, USA.
Brain Behav. 2024 May;14(5):e3524. doi: 10.1002/brb3.3524.
The combination of apolipoprotein E ε4 (ApoE ε4) status, odor identification, and odor familiarity predicts conversion to mild cognitive impairment (MCI) and Alzheimer's disease (AD).
To further understand olfactory disturbances and AD risk, ApoE ε4 carrier (mean age 76.38 ± 5.21) and ε4 non-carrier (mean age 76.8 ± 3.35) adults were given odor familiarity and identification tests and performed an odor identification task during fMRI scanning. Five task-related functional networks were detected using independent components analysis. Main and interaction effects of mean odor familiarity ratings, odor identification scores, and ε4 status on network activation and task-modulation of network functional connectivity (FC) during correct and incorrect odor identification (hits and misses), controlling for age and sex, were explored using multiple linear regression.
Findings suggested that sensory-olfactory network activation was positively associated with odor identification scores in ε4 carriers with intact odor familiarity. The FC of sensory-olfactory, multisensory-semantic integration, and occipitoparietal networks was altered in ε4 carriers with poorer odor familiarity and identification. In ε4 carriers with poorer familiarity, connectivity between superior frontal areas and the sensory-olfactory network was negatively associated with odor identification scores.
The results contribute to the clarification of the neurocognitive structure of odor identification processing and suggest that poorer odor familiarity and identification in ε4 carriers may signal multi-network dysfunction. Odor familiarity and identification assessment in ε4 carriers may contribute to the predictive value of risk for MCI and AD due to the breakdown of sensory-cognitive network integration. Additional research on olfactory processing in those at risk for AD is warranted.
载脂蛋白 E ε4(ApoE ε4)状态、嗅觉识别和嗅觉熟悉度的结合可以预测轻度认知障碍(MCI)和阿尔茨海默病(AD)的转化。
为了进一步了解嗅觉障碍和 AD 风险,载脂蛋白 E ε4 携带者(平均年龄 76.38±5.21)和 ε4 非携带者(平均年龄 76.8±3.35)接受了嗅觉熟悉度和识别测试,并在 fMRI 扫描期间进行了嗅觉识别任务。使用独立成分分析检测到五个与任务相关的功能网络。使用多元线性回归,在控制年龄和性别后,探索了平均嗅觉熟悉度评分、嗅觉识别得分和 ε4 状态对正确和错误嗅觉识别(命中和错过)时网络激活和网络功能连接(FC)任务调节的主效应和交互效应。
研究结果表明,在嗅觉识别得分较高的 ε4 携带者中,感觉-嗅觉网络的激活与嗅觉识别得分呈正相关,而嗅觉熟悉度和识别较差的 ε4 携带者的感觉-嗅觉、多感觉-语义整合和枕顶网络的 FC 发生改变。在嗅觉熟悉度和识别较差的 ε4 携带者中,额上区与感觉-嗅觉网络之间的连接与嗅觉识别得分呈负相关。
这些结果有助于阐明嗅觉识别处理的神经认知结构,并表明嗅觉熟悉度和识别较差的 ε4 携带者可能存在多网络功能障碍。在 ε4 携带者中进行嗅觉熟悉度和识别评估可能有助于提高 MCI 和 AD 风险的预测价值,因为感觉-认知网络的整合被打破。需要对 AD 高危人群的嗅觉处理进行更多的研究。