Higher Peripheral TREM2 mRNA Levels Relate to Cognitive Deficits and Hippocampal Atrophy in Alzheimer’s Disease and Amnestic Mild Cognitive Impairment

特雷姆2 灰质 海马结构 心理学 蒙特利尔认知评估 萎缩 痴呆 神经科学 生物标志物 外围设备 认知 情景记忆 阿尔茨海默病 内科学 医学 白质 认知障碍 疾病 受体 磁共振成像 生物 生物化学 髓系细胞 放射科
作者
Yi Jayne Tan,Adeline SL Ng,Ashwati Vipin,Joseph K.W. Lim,Russell J. Chander,Fang Ji,Yingwei Qiu,Simon Ting,Shahul Hameed,Tih-Shih Lee,Li Zeng,Nagaendran Kandiah,Juan Zhou
出处
期刊:Journal of Alzheimer's Disease [IOS Press]
卷期号:58 (2): 413-423 被引量:46
标识
DOI:10.3233/jad-161277
摘要

Variants in triggering receptor expressed on myeloid cells 2 (TREM2) are associated with increased Alzheimer's disease (AD) risk. Recent studies have reported inconsistent peripheral TREM2 mRNA expression levels and relationship with cognitive scores in AD and mild cognitive impairment (MCI). Additionally, no study has examined the association of peripheral TREM2 levels with neuroimaging measures in AD and MCI.To determine peripheral TREM2 mRNA levels in AD, amnestic MCI (aMCI) and healthy controls, and the association with cognitive performance and brain structural changes.We measured peripheral TREM2 mRNA levels in 80 AD, 30 aMCI, and 86 healthy controls using real time polymerase chain reaction. TREM2 levels were correlated with various cognitive performance and brain volumes, correcting for APOE4 status.TREM2 mRNA levels were significantly higher in AD compared to controls and aMCI. Levels did not differ between aMCI and controls. Corrected for APOE4, higher TREM2 levels correlated with lower Mini-Mental State Examination, Montreal Cognitive Assessment (MoCA) and episodic memory scores, and lower total grey matter and right hippocampal volumes. Whole-brain voxel-based morphometry analysis found negative association between TREM2 mRNA levels and grey matter volumes in temporal, parietal and frontal regions. AD subjects with MoCA scores ≤20 had higher TREM2 levels correlating with smaller total grey matter, left hippocampal and right hippocampal volumes.Peripheral TREM2 mRNA levels are higher in AD and are associated with AD-related cognitive deficits and hippocampal atrophy. Our findings suggest that TREM2 may be a potential non-invasive peripheral biomarker for AD diagnosis.

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