Gene Expression Profiling of Peripheral Blood Leukocytes Shows Consistent Longitudinal Downregulation of TOMM40 and Upregulation of KIR2DL5A, PLOD1, and SLC2A8 Among Fast Progressors in Early Alzheimer's Disease

被引:27
作者
Chong, Mei Sian [1 ]
Goh, Liang Kee [2 ]
Lim, Wee Shiong [1 ]
Chan, Mark [1 ]
Tay, Laura [1 ]
Chen, Gengbo [2 ]
Feng, Lei [3 ]
Ng, Tze Pin [3 ]
Tan, Chay Hoon [4 ]
Lee, Tih Shih [2 ,5 ]
机构
[1] Tan Tock Seng Hosp, Dept Geriatr Med, Singapore, Singapore
[2] Duke NUS Grad Med Sch, Singapore, Singapore
[3] Natl Univ Singapore, Dept Psychol Med, Gerontol Res Programme, Singapore 117548, Singapore
[4] Natl Univ Hlth Syst, Dept Pharmacol, Singapore, Singapore
[5] Duke Univ, Sch Med, Dept Psychiat & Behav Sci, Durham, NC USA
基金
英国医学研究理事会;
关键词
Alzheimer's disease; gene expression; progression; TOMM40; GENOME-WIDE ASSOCIATION; BIOMARKERS; INSULIN; NUMBER;
D O I
10.3233/JAD-121621
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
We previously reported TOMM40 was significantly down-regulated in whole blood of Alzheimer's disease (AD) subjects. In this study, we examined whole blood gene profiling differences over a one-year period comparing early AD subjects based on disease progression. 6-monthly assessments and blood sampling on 29 probable AD subjects compared with age- and gender-matched controls were performed. AD subjects with change in Clinical Dementia Rating-Sum of Boxes (CDR-SB) score of >= 2 points/year were classified as fast-progressors and those with CDR-SB change of <2 points/year were classified as slow-progressors. We found statistically significant upregulation in KIR2DL5A, SLC2A8, and PLOD1 for fast-(n = 8) compared with slow-progressors (n = 21) across the time-points. TOMM40 gene expression remained significantly lower in AD patients at all time-points compared to controls, supporting our previous findings. Our novel findings of specific gene expression differences between fast-and slow-progressors in combination with consistently lower TOMM40 expression, suggest their potential role as prognostic blood biomarkers to predict progression in early AD.
引用
收藏
页码:399 / 405
页数:7
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