4.3 Article

Association and interaction effects of Alzheimer's disease-associated genes and lifestyle on cognitive aging in older adults in a Taiwanese population

期刊

ONCOTARGET
卷 8, 期 15, 页码 24077-24087

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.15269

关键词

Alzheimer's diseases; cognitive aging; gene-gene and gene-lifestyle interactions; Mini-Mental State Examination; single nucleotide polymorphisms; Gerotarget

资金

  1. Ministry of Economic Affairs in Taiwan (SBIR) [S099000280249-154]
  2. Taipei Veterans General Hospital, Taiwan [VGHUST103-G1-4-1, V105C-008, V105E17-002-MY2-1]
  3. Ministry of Science and Technology, Taiwan [MST 102-2314-B-002-117-MY3]

向作者/读者索取更多资源

Genome-wide association studies and meta-analyses implicated that increased risk of developing Alzheimer's diseases (AD) has been associated with the ABCA7, APOE, BIN1, CASS4, CD2AP, CD33, CELF1, CLU, CR1, DSG2, EPHA1, FERMT2, HLA-DRB1, HLA-DRB4, INPP5D, MEF2C, MS4A4A, MS4A4E, MS4A6E, NME8, PICALM, PLD3, PTK2B, RIN3, SLC24A4, SORL1, and ZCWPW1 genes. In this study, we assessed whether single nucleotide polymorphisms (SNPs) within these 27 AD-associated genes are linked with cognitive aging independently and/or through complex interactions in an older Taiwanese population. We also analyzed the interactions between lifestyle and these genes in influencing cognitive aging. A total of 634 Taiwanese subjects aged over 60 years from the Taiwan Biobank were analyzed. Mini-Mental State Examination (MMSE) scores were performed for all subjects to evaluate cognitive functions. Out of the 588 SNPs tested in this study, only the association between CASS4-rs911159 and cognitive aging persisted significantly (P = 2.2 x 10(-5)) after Bonferroni correction. Our data also showed a nominal association of cognitive aging with the SNPs in six more key AD-associated genes, including EPHA1-rs10952552, FERMT2-rs4901317, MEF2C-rs9293506, PLD3-rs11672825, RIN3-rs1885747, and SLC24A4-rs67063100 (P = 0.0018 similar to 0.0097). Additionally, we found the interactions among CASS4-rs911159, EPHA-rs10952552, FERMT2-rs4901317, MEF2C-rs9293506, or SLC24A4-rs67063100 on cognitive aging (P = 0.004 similar to 0.035). Moreover, our analysis suggested the interactions of SLC24A4-rs67063100 or MEF2C-rs9293506 with lifestyle such as alcohol consumption, smoking status, physical activity, or social support on cognitive aging (P = 0.008 similar to 0.041). Our study indicates that the AD-associated genes may contribute to the risk of cognitive aging independently as well as through genegene and gene-lifestyle interactions.

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