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Effects of circadian clock genes and environmental factors on cognitive aging in old adults in a Taiwanese population
Previous animal studies have indicated associations between circadian clock genes and cognitive impairment . In this study, we assessed whether 11 circadian clockgenes are associated with cognitive aging independently and/or through complex interactions in an old Taiwanese population. We also analyz...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421829/ https://www.ncbi.nlm.nih.gov/pubmed/28412756 http://dx.doi.org/10.18632/oncotarget.15493 |
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author | Lin, Eugene Kuo, Po-Hsiu Liu, Yu-Li Yang, Albert C. Kao, Chung-Feng Tsai, Shih-Jen |
author_facet | Lin, Eugene Kuo, Po-Hsiu Liu, Yu-Li Yang, Albert C. Kao, Chung-Feng Tsai, Shih-Jen |
author_sort | Lin, Eugene |
collection | PubMed |
description | Previous animal studies have indicated associations between circadian clock genes and cognitive impairment . In this study, we assessed whether 11 circadian clockgenes are associated with cognitive aging independently and/or through complex interactions in an old Taiwanese population. We also analyzed the interactions between environmental factors 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 Examinations (MMSE) were administered to all subjects, and MMSE scores were used to evaluate cognitive function. Our data showed associations between cognitive aging and single nucleotide polymorphisms (SNPs) in 4 key circadian clock genes, CLOCK rs3749473 (p = 0.0017), NPAS2 rs17655330 (p = 0.0013), RORA rs13329238 (p = 0.0009), and RORB rs10781247 (p = 7.9 × 10(−5)). We also found that interactions between CLOCK rs3749473, NPAS2 rs17655330, RORA rs13329238, and RORB rs10781247 affected cognitive aging (p = 0.007). Finally, we investigated the influence of interactions between CLOCK rs3749473, RORA rs13329238, and RORB rs10781247 with environmental factors such as alcohol consumption, smoking status, physical activity, and social support on cognitive aging (p = 0.002 ∼ 0.01). Our study indicates that circadian clock genes such as the CLOCK, NPAS2, RORA, and RORB genes may contribute to the risk of cognitive aging independently as well as through gene-gene and gene-environment interactions. |
format | Online Article Text |
id | pubmed-5421829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-54218292017-05-10 Effects of circadian clock genes and environmental factors on cognitive aging in old adults in a Taiwanese population Lin, Eugene Kuo, Po-Hsiu Liu, Yu-Li Yang, Albert C. Kao, Chung-Feng Tsai, Shih-Jen Oncotarget Research Paper: Gerotarget (Focus on Aging) Previous animal studies have indicated associations between circadian clock genes and cognitive impairment . In this study, we assessed whether 11 circadian clockgenes are associated with cognitive aging independently and/or through complex interactions in an old Taiwanese population. We also analyzed the interactions between environmental factors 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 Examinations (MMSE) were administered to all subjects, and MMSE scores were used to evaluate cognitive function. Our data showed associations between cognitive aging and single nucleotide polymorphisms (SNPs) in 4 key circadian clock genes, CLOCK rs3749473 (p = 0.0017), NPAS2 rs17655330 (p = 0.0013), RORA rs13329238 (p = 0.0009), and RORB rs10781247 (p = 7.9 × 10(−5)). We also found that interactions between CLOCK rs3749473, NPAS2 rs17655330, RORA rs13329238, and RORB rs10781247 affected cognitive aging (p = 0.007). Finally, we investigated the influence of interactions between CLOCK rs3749473, RORA rs13329238, and RORB rs10781247 with environmental factors such as alcohol consumption, smoking status, physical activity, and social support on cognitive aging (p = 0.002 ∼ 0.01). Our study indicates that circadian clock genes such as the CLOCK, NPAS2, RORA, and RORB genes may contribute to the risk of cognitive aging independently as well as through gene-gene and gene-environment interactions. Impact Journals LLC 2017-02-16 /pmc/articles/PMC5421829/ /pubmed/28412756 http://dx.doi.org/10.18632/oncotarget.15493 Text en Copyright: © 2017 Lin et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper: Gerotarget (Focus on Aging) Lin, Eugene Kuo, Po-Hsiu Liu, Yu-Li Yang, Albert C. Kao, Chung-Feng Tsai, Shih-Jen Effects of circadian clock genes and environmental factors on cognitive aging in old adults in a Taiwanese population |
title | Effects of circadian clock genes and environmental factors on cognitive aging in old adults in a Taiwanese population |
title_full | Effects of circadian clock genes and environmental factors on cognitive aging in old adults in a Taiwanese population |
title_fullStr | Effects of circadian clock genes and environmental factors on cognitive aging in old adults in a Taiwanese population |
title_full_unstemmed | Effects of circadian clock genes and environmental factors on cognitive aging in old adults in a Taiwanese population |
title_short | Effects of circadian clock genes and environmental factors on cognitive aging in old adults in a Taiwanese population |
title_sort | effects of circadian clock genes and environmental factors on cognitive aging in old adults in a taiwanese population |
topic | Research Paper: Gerotarget (Focus on Aging) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421829/ https://www.ncbi.nlm.nih.gov/pubmed/28412756 http://dx.doi.org/10.18632/oncotarget.15493 |
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