Yoshino Yuta, Yamazaki Kiyohiro, Ozaki Yuki, Sao Tomoko, Yoshida Taku, Mori Takaaki, Mori Yoko, Ochi Shinichiro, Iga Jun-Ichi, Ueno Shu-Ichi
J Alzheimers Dis. 2017;58(3):687-694. doi: 10.3233/JAD-161211.
Microglial dysfunction and inflammation have recently been shown to be related to the development of Alzheimer's disease (AD). Inositol polyphosphate-5-phosphatase (INPP5D) functions broadly as a negative regulator of immune signaling, and its locus was associated with development of AD in a large-scale genome-wide association study. Thus, we examined INPP5D mRNA expression and methylation rates of the CpG sites in the upstream region of INPP5D exon 1 in peripheral leukocytes in 50 AD and age- and sex-matched control subjects. INPP5D mRNA expression in AD subjects was significantly higher than that in control subjects (1.16±0.39 versus 1.0±0.23, p = 0.049) and was correlated with the Mini-Mental State Examination score (p = 0.002, r = 0.426) and the total score of the Alzheimer's Disease Assessment Scale (p < 0.001, r = -0.697). Methylation rates in the upstream region of INPP5D exon 1 were not significantly different between AD and control subjects (average rate: 3.5±3.0 versus 2.8±1.3, p = 0.551). Our results suggested that INPP5D mRNA expression was elevated in the early stage and decreased with cognitive decline in AD. INPP5D mRNA expression in leukocytes may be a useful biomarker for the early stage of AD.
近年来研究表明,小胶质细胞功能障碍和炎症与阿尔茨海默病(AD)的发展有关。肌醇多磷酸-5-磷酸酶(INPP5D)广泛作为免疫信号的负调节因子发挥作用,在一项大规模全基因组关联研究中,其基因座与AD的发展相关。因此,我们检测了50名AD患者以及年龄和性别匹配的对照受试者外周血白细胞中INPP5D外显子1上游区域CpG位点的INPP5D mRNA表达和甲基化率。AD患者的INPP5D mRNA表达显著高于对照受试者(1.16±0.39对1.0±0.23,p = 0.049),并且与简易精神状态检查表评分相关(p = 0.002,r = 0.426)以及阿尔茨海默病评估量表总分相关(p < 0.001,r = -0.697)。AD患者和对照受试者之间INPP5D外显子1上游区域的甲基化率无显著差异(平均率:3.5±3.0对2.8±1.3,p = 0.551)。我们的结果表明,INPP5D mRNA表达在AD早期升高,并随着认知功能下降而降低。白细胞中的INPP5D mRNA表达可能是AD早期阶段的一个有用生物标志物。