• Guiyou Liu, Xinjie Bao, Yongshuai Jiang, Mingzhi Liao, Qinghua Jiang, Rennan Feng, Liangcai Zhang, Guoda Ma, Zugen Chen, Guangyu Wang, Renzhi Wang, Bin Zhao, and Keshen Li.
• Institute of Neurology, Guangdong Medical College, Zhanjiang, 524001, China.
• Mol. Neurobiol. 2015 Dec 1; 52 (3): 1629-1636.

AbstractAlzheimer's disease (AD) and Parkinson's disease (PD) are the first and second most common neurodegenerative diseases in the elderly. Shared clinical and pathological features have been reported. Recent large-scale genome-wide association studies (GWAS) have been conducted and reported a number of AD and PD variants. Until now, the underlying genetic mechanisms for all these newly identified PD variants as well as the association between AD and PD are still unclear exactly. We think that PD variants may contribute to AD and PD by influence on brain gene expression. Here, we conducted a systems analysis using (1) AD and PD variants (P < 5.00E-08) identified by the published GWAS; (2) four brain expression GWAS datasets using expression quantitative trait loci from the cerebellum and temporal cortex; (3) large-scale AD GWAS from the Alzheimer Disease Genetics Consortium (ADGC); (4) a protein-protein interaction network. Our results indicated that PD variants around the 17q21 were associated with gene expression and suggestive AD risk. We also identified significant interaction among AD and PD susceptibility genes. We believe that our findings may explain the underlying genetic mechanisms for newly identified PD variants in PD and AD, as well as the association between AD and PD, which may be very useful for future genetic studies for both diseases.

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