| Literature DB >> 30040717 |
Roberta Mercorio1, Laura Pergoli1, Daniela Galimberti2, Chiara Favero1, Michele Carugno1, Elisabetta Dalla Valle2, Francesco Barretta1, Francesca Cortini1, Elio Scarpini2, Valentina Bollati Valentina1, Angela Cecilia Pesatori1,3.
Abstract
Epigenetic mechanisms might be involved in Alzheimer's disease (AD). Genetic polymorphisms in several genes, including APOE (Apolipoprotein E), PSEN1 (Presenilin 1), CR1 (Complement receptor 1), and PICALM (Phosphatidylinositol binding clathrin assembly protein), have been associated to an increased AD risk. However, data regarding methylation of these specific genes are lacking. We evaluated DNA methylation measured by quantitative bisulfite-PCR pyrosequencing in 43 AD patients and 38 healthy subjects (HS). In a multivariate age- and gender-adjusted model, PICALM methylation was decreased in AD compared to HS (mean = 3.54 and 4.63, respectively, p = 0.007). In AD, PICALM methylation level was also positively associated to Mini-Mental Scale Examination (MMSE) score (percent change 3.48%, p = 0.008). Moreover, a negative association between PICALM methylation and age was observed only in HS (percent change - 2.29%, p = 0.002). In conclusion, our data suggest a possible role of PICALM methylation in AD, particularly related to cognitive function. Given the small study sample and the associative nature of our study, further prospective investigations are required to assess the dynamics of DNA methylation in the early stages of AD development.Entities:
Keywords: Alzheimer’s disease; Mini-Mental State Examination; PICALM; epigenetics; methylation
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Year: 2018 PMID: 30040717 DOI: 10.3233/JAD-180242
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472