Suppr超能文献

基因变异与单不饱和脂肪酸调节的代谢综合征发病率相关。

Gene Variation Is Associated with the Incidence of Metabolic Syndrome Modulated by Monounsaturated Fatty Acids.

作者信息

Shin Dayeon, Lee Kyung-Won

机构信息

Department of Food and Nutrition, Inha University, Incheon 22212, Korea.

Department of Home Economics Education, Korea National University of Education, Cheongju 28173, Korea.

出版信息

J Pers Med. 2021 May 14;11(5):412. doi: 10.3390/jpm11050412.

Abstract

The circadian locomotor output cycles kaput () gene plays a crucial role in regulating circadian rhythms through its transcription factor gene product. The objective of this study was to investigate the association between rs1801260 and the incidence of metabolic syndrome modulated by dietary monounsaturated fatty acid (MUFA) intake in Korean adults. Using a dataset from the Ansan-Ansung Cohort Study of the Korean Genome and Epidemiology Study, 3608 Korean adults were included after an average of nine years of follow-up. Men who were minor allele carriers (G allele) of rs1801260 had a 18% higher incidence of metabolic syndrome than non-carriers [hazard ratio (HR), 1.18; 95% confidence interval (CI), 1.00-1.40; Value = 0.047]. By dichotomizing dietary MUFA intake, we observed that men who were minor allele carriers (G allele) of rs1801260 had a 42% increased incidence of metabolic syndrome when dietary MUFA intake was ≤3.5% (HR: 1.42, 95% CI 1.23-1.81; Value = 0.004). No significant association was found between rs1801260 and the incidence of metabolic syndrome modulated by dietary MUFA intake in women. polymorphisms affected metabolic syndrome, modulated by dietary MUFA intake in men. These results suggest the significance of genes in the pathogenesis of metabolic syndrome and the modulating role of dietary MUFA intake and provide new insights into the underlying mechanisms connecting the circadian system, dietary factors, and metabolic syndrome.

摘要

昼夜运动输出周期失效()基因通过其转录因子基因产物在调节昼夜节律中起关键作用。本研究的目的是调查韩国成年人中rs1801260与饮食中单不饱和脂肪酸(MUFA)摄入量调节的代谢综合征发病率之间的关联。使用韩国基因组与流行病学研究的安山 - 安城队列研究数据集,在平均九年的随访后纳入了3608名韩国成年人。rs1801260的次要等位基因携带者(G等位基因)男性患代谢综合征的发病率比非携带者高18%[风险比(HR),1.18;95%置信区间(CI),1.00 - 1.40;P值 = 0.047]。通过将饮食中MUFA摄入量二分法,我们观察到当饮食中MUFA摄入量≤3.5%时,rs1801260的次要等位基因携带者(G等位基因)男性患代谢综合征的发病率增加了42%(HR:1.42,95%CI 1.23 - 1.81;P值 = 0.004)。在女性中,未发现rs1801260与饮食中MUFA摄入量调节的代谢综合征发病率之间存在显著关联。基因多态性影响代谢综合征,受男性饮食中MUFA摄入量调节。这些结果表明基因在代谢综合征发病机制中的重要性以及饮食中MUFA摄入量的调节作用,并为连接昼夜节律系统、饮食因素和代谢综合征的潜在机制提供了新的见解。

相似文献

3
CLOCK genetic variation and metabolic syndrome risk: modulation by monounsaturated fatty acids.
Am J Clin Nutr. 2009 Dec;90(6):1466-75. doi: 10.3945/ajcn.2009.27536. Epub 2009 Oct 21.
7
The dietary monounsaturated to saturated fatty acid ratio modulates the genetic effects of GCKR on serum lipid levels in children.
Clin Chim Acta. 2015 Oct 23;450:155-61. doi: 10.1016/j.cca.2015.08.012. Epub 2015 Aug 18.
8
Dietary Fat Intake and the Risk of Metabolic Syndrome in Korean Adults.
Korean J Fam Med. 2015 Sep;36(5):245-52. doi: 10.4082/kjfm.2015.36.5.245. Epub 2015 Sep 18.
9
Association of CLOCK gene variants with semen quality in idiopathic infertile Han-Chinese males.
Reprod Biomed Online. 2012 Nov;25(5):536-42. doi: 10.1016/j.rbmo.2012.07.018. Epub 2012 Aug 6.
10
Metabolic syndrome profiles, obesity measures and intake of dietary fatty acids in adults: Tehran Lipid and Glucose Study.
J Hum Nutr Diet. 2014 Apr;27 Suppl 2:98-108. doi: 10.1111/jhn.12117. Epub 2013 Jun 4.

引用本文的文献

1
Association between CLOCK gene polymorphisms with circadian rhythm, chrononutrition, dietary intake, and metabolic parameters in adolescents.
Front Public Health. 2024 Dec 18;12:1435460. doi: 10.3389/fpubh.2024.1435460. eCollection 2024.
2
c-Jun N-terminal kinase signaling in aging.
Front Aging Neurosci. 2024 Aug 29;16:1453710. doi: 10.3389/fnagi.2024.1453710. eCollection 2024.

本文引用的文献

1
Sex modifies the association between the CLOCK variant rs1801260 and BMI in school-age children.
PLoS One. 2020 Aug 12;15(8):e0236991. doi: 10.1371/journal.pone.0236991. eCollection 2020.
2
4
CLOCK rs1801260 Polymorphism is Associated with Susceptibility to Parkinson's Disease in a Chinese Population.
Neurosci Bull. 2017 Dec;33(6):734-736. doi: 10.1007/s12264-017-0167-5. Epub 2017 Aug 5.
5
Cohort Profile: The Korean Genome and Epidemiology Study (KoGES) Consortium.
Int J Epidemiol. 2017 Apr 1;46(2):e20. doi: 10.1093/ije/dyv316.
6
Association between genetic variants of the clock gene and obesity and sleep duration.
J Physiol Biochem. 2015 Dec;71(4):855-60. doi: 10.1007/s13105-015-0447-3. Epub 2015 Nov 10.
7
Evening chronotype is associated with metabolic disorders and body composition in middle-aged adults.
J Clin Endocrinol Metab. 2015 Apr;100(4):1494-502. doi: 10.1210/jc.2014-3754. Epub 2015 Apr 1.
9
Physical activity and sex modulate obesity risk linked to 3111T/C gene variant of the CLOCK gene in an elderly population: the SUN Project.
Chronobiol Int. 2012 Dec;29(10):1397-404. doi: 10.3109/07420528.2012.728657. Epub 2012 Nov 6.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验