CpG站点
阿尔茨海默病
生物
内科学
外显子
信使核糖核酸
生物标志物
内分泌学
DNA甲基化
甲基化
疾病
肿瘤科
医学
基因表达
遗传学
基因
作者
Yuta Yoshino,Kiyohiro Yamazaki,Yuki Ozaki,Tomoko Sao,Taku Yoshida,Takaaki Mori,Yoko Mori,Shinichiro Ochi,Jun‐ichi Iga,Shu‐ichi Ueno
摘要
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.
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