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Short-term adverse effects of the apolipoprotein E ε4 allele over language function and executive function in healthy older adults

Background: The 4 allele of the apolipoprotein E (APOE) gene is known as a risk factor for cognitive impairment. How APOE ε polymorphism affects the language and executive functions of healthy aging subjects remains less clear. Purpose: In this follow-up study, the relationship between APOE status a...

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Autores principales: Li, Wei, Qiu, Qi, Sun, Lin, Li, Xia, Xiao, Shifu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628858/
https://www.ncbi.nlm.nih.gov/pubmed/31371959
http://dx.doi.org/10.2147/NDT.S183064
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author Li, Wei
Qiu, Qi
Sun, Lin
Li, Xia
Xiao, Shifu
author_facet Li, Wei
Qiu, Qi
Sun, Lin
Li, Xia
Xiao, Shifu
author_sort Li, Wei
collection PubMed
description Background: The 4 allele of the apolipoprotein E (APOE) gene is known as a risk factor for cognitive impairment. How APOE ε polymorphism affects the language and executive functions of healthy aging subjects remains less clear. Purpose: In this follow-up study, the relationship between APOE status and cognitive performance across various cognitive domains in healthy individuals (without dementia or mild cognitive impairment (MCI)) over 60 years old was investigated. Patients and methods: Based on multiplex amplification refractory mutation system polymerase chain reaction (PCR), 228 subjects (n=228; mean age: 70.59±8.07 years old; male %=40.8%) were divided into three groups, e2 (ε2/ε2 and ε2/ε3, n=35), e3 (ε3/ε3, n=152), and e4 (ε2/ε4, ε3/ε4, and ε4/ε4, n=41). Results: There was no statistical difference (p>0.05) in the general demographic data and neuropsychological tests among the three groups on the baseline; however, e4 group showed a greater drop rate (p<0.05) versus non-carriers on verbal fluency (e2: −0.043±0.221; e3: -0.081±0.239; e4: 0.069±0.329) and Webster picture completion (e2: 0.055±0.281; e3: 0.083±0.428; e4: 0.438±1.280) over the subsequent one year. Conclusion: The findings suggest that possession of the APOE ε4 allele predicted a higher decline on tasks of language function and executive function in healthy elderly. And further research is required to determine whether strengthening the training of language function and executive function will delay the occurrence of cognitive impairment.
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spelling pubmed-66288582019-08-01 Short-term adverse effects of the apolipoprotein E ε4 allele over language function and executive function in healthy older adults Li, Wei Qiu, Qi Sun, Lin Li, Xia Xiao, Shifu Neuropsychiatr Dis Treat Original Research Background: The 4 allele of the apolipoprotein E (APOE) gene is known as a risk factor for cognitive impairment. How APOE ε polymorphism affects the language and executive functions of healthy aging subjects remains less clear. Purpose: In this follow-up study, the relationship between APOE status and cognitive performance across various cognitive domains in healthy individuals (without dementia or mild cognitive impairment (MCI)) over 60 years old was investigated. Patients and methods: Based on multiplex amplification refractory mutation system polymerase chain reaction (PCR), 228 subjects (n=228; mean age: 70.59±8.07 years old; male %=40.8%) were divided into three groups, e2 (ε2/ε2 and ε2/ε3, n=35), e3 (ε3/ε3, n=152), and e4 (ε2/ε4, ε3/ε4, and ε4/ε4, n=41). Results: There was no statistical difference (p>0.05) in the general demographic data and neuropsychological tests among the three groups on the baseline; however, e4 group showed a greater drop rate (p<0.05) versus non-carriers on verbal fluency (e2: −0.043±0.221; e3: -0.081±0.239; e4: 0.069±0.329) and Webster picture completion (e2: 0.055±0.281; e3: 0.083±0.428; e4: 0.438±1.280) over the subsequent one year. Conclusion: The findings suggest that possession of the APOE ε4 allele predicted a higher decline on tasks of language function and executive function in healthy elderly. And further research is required to determine whether strengthening the training of language function and executive function will delay the occurrence of cognitive impairment. Dove 2019-07-10 /pmc/articles/PMC6628858/ /pubmed/31371959 http://dx.doi.org/10.2147/NDT.S183064 Text en © 2019 Li et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Li, Wei
Qiu, Qi
Sun, Lin
Li, Xia
Xiao, Shifu
Short-term adverse effects of the apolipoprotein E ε4 allele over language function and executive function in healthy older adults
title Short-term adverse effects of the apolipoprotein E ε4 allele over language function and executive function in healthy older adults
title_full Short-term adverse effects of the apolipoprotein E ε4 allele over language function and executive function in healthy older adults
title_fullStr Short-term adverse effects of the apolipoprotein E ε4 allele over language function and executive function in healthy older adults
title_full_unstemmed Short-term adverse effects of the apolipoprotein E ε4 allele over language function and executive function in healthy older adults
title_short Short-term adverse effects of the apolipoprotein E ε4 allele over language function and executive function in healthy older adults
title_sort short-term adverse effects of the apolipoprotein e ε4 allele over language function and executive function in healthy older adults
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628858/
https://www.ncbi.nlm.nih.gov/pubmed/31371959
http://dx.doi.org/10.2147/NDT.S183064
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