Effects of circadian clock genes and environmental factors on cognitive aging in old adults in a Taiwanese population

被引:18
|
作者
Lin, Eugene [1 ,2 ,3 ]
Kuo, Po-Hsiu [4 ]
Liu, Yu-Li [5 ]
Yang, Albert C. [6 ,7 ]
Kao, Chung-Feng [8 ]
Tsai, Shih-Jen [6 ,7 ]
机构
[1] China Med Univ, Inst Clin Med Sci, Taichung, Taiwan
[2] Vita Genom Inc, Taipei, Taiwan
[3] TickleFish Syst Corp, Seattle, WA USA
[4] Natl Taiwan Univ, Inst Epidemiol & Prevent Med, Dept Publ Hlth, Taipei, Taiwan
[5] Natl Hlth Res Inst, Ctr Neuropsychiat Res, Zhunan Township, Miaoli County, Taiwan
[6] Taipei Vet Gen Hosp, Dept Psychiat, Taipei, Taiwan
[7] Natl Yang Ming Univ, Div Psychiat, Taipei, Taiwan
[8] Natl Chung Hsing Univ, Coll Agr & Nat Resources, Dept Agron, Taichung, Taiwan
关键词
circadian clock genes; circadian rhythms; cognitive aging; gene-gene and gene-environment interactions; single nucleotide polymorphisms; Gerotarget; METABOLIC PHENOTYPES; ALZHEIMERS-DISEASE; POLYMORPHISM; SUSCEPTIBILITY; ASSOCIATION; OBESITY; VARIANT; MEMORY; EXPRESSION; DEMENTIA;
D O I
10.18632/oncotarget.15493
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Previous animal studies have indicated associations between circadian clock genes and cognitive impairment. In this study, we assessed whether 11 circadian clock genes 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 x 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 similar to 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.
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页码:24088 / 24098
页数:11
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