https://transhumanist.ru/index.php?action=history&feed=atom&title=MS4A4AMS4A4A - История изменений2026-08-17T18:11:34ZИстория изменений этой страницы в викиMediaWiki 1.43.6https://transhumanist.ru/index.php?title=MS4A4A&diff=4039&oldid=prevOdysseusBot: Новая страница: «Membrane-spanning 4-domains subfamily A member 4A (CD20 antigen-like 1) (Four-span transmembrane protein 1) [4SPAN1] [CD20L1] [MS4A4] [HDCME31P] ==Publications==...»2021-04-29T18:57:38Z<p>Новая страница: «Membrane-spanning 4-domains subfamily A member 4A (CD20 antigen-like 1) (Four-span transmembrane protein 1) [4SPAN1] [CD20L1] [MS4A4] [HDCME31P] ==Publications==...»</p>
<p><b>Новая страница</b></p><div>Membrane-spanning 4-domains subfamily A member 4A (CD20 antigen-like 1) (Four-span transmembrane protein 1) [4SPAN1] [CD20L1] [MS4A4] [HDCME31P]<br />
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==Publications==<br />
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{{medline-entry<br />
|title=Association and interaction effects of Alzheimer's disease-associated genes and lifestyle on cognitive aging in older adults in a Taiwanese population.<br />
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/28199971<br />
|abstract=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-associatedgenes 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 = 0.0018~0.0097). Additionally, we found the interactions among [[CASS4]]-rs911159, EPHA-rs10952552, [[FERMT2]]-rs4901317, [[MEF2C]]-rs9293506, or [[SLC24A4]]-rs67063100 on cognitive aging (P = 0.004~0.035). 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 = 0.008~0.041). Our study indicates that the AD-associated genes may contribute to the risk of cognitive aging independently as well as through gene-gene and gene-lifestyle interactions.<br />
|mesh-terms=* Age Factors<br />
* Aged<br />
* Alleles<br />
* Alzheimer Disease<br />
* Cognitive Aging<br />
* Epistasis, Genetic<br />
* Female<br />
* Gene-Environment Interaction<br />
* Genetic Association Studies<br />
* Genetic Predisposition to Disease<br />
* Humans<br />
* Life Style<br />
* Male<br />
* Middle Aged<br />
* Polymorphism, Single Nucleotide<br />
* Risk Factors<br />
* Taiwan<br />
|keywords=* Alzheimer’s diseases<br />
* Gerotarget<br />
* Mini-Mental State Examination<br />
* cognitive aging<br />
* gene-gene and gene-lifestyle interactions<br />
* single nucleotide polymorphisms<br />
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421828<br />
}}</div>OdysseusBot