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Nutrients. 2019 Nov 8;11(11):2704. doi: 10.3390/nu11112704.
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J Intern Med. 2019 Aug;286(2):181-191. doi: 10.1111/joim.12924. Epub 2019 Jun 10.
3
Alterations of circadian rhythms and their impact on obesity, metabolic syndrome and cardiovascular diseases.昼夜节律的改变及其对肥胖、代谢综合征和心血管疾病的影响。
Crit Rev Food Sci Nutr. 2020;60(6):1038-1047. doi: 10.1080/10408398.2018.1556579. Epub 2019 Jan 11.
4
Dietary patterns and their association with adiponectin and leptin concentrations throughout pregnancy: a prospective cohort.孕期饮食模式及其与脂联素和瘦素浓度的相关性:一项前瞻性队列研究。
Br J Nutr. 2018 Feb;119(3):320-329. doi: 10.1017/S0007114517003580. Epub 2018 Jan 18.
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Dietary assessment methods in epidemiological research: current state of the art and future prospects.流行病学研究中的膳食评估方法:当前技术水平与未来前景
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Am J Clin Nutr. 2017 Apr;105(4):980-990. doi: 10.3945/ajcn.116.147231. Epub 2017 Mar 1.
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Cross-cultural validity of Morningness-Eveningness Stability Scale improved (MESSi) in Iran, Spain and Germany.晨型-夜型稳定性量表改进版(MESSi)在伊朗、西班牙和德国的跨文化效度
Chronobiol Int. 2017;34(2):273-279. doi: 10.1080/07420528.2016.1267187. Epub 2017 Jan 5.
8
Interactions between genetic variants associated with adiposity traits and soft drinks in relation to longitudinal changes in body weight and waist circumference.与肥胖特征相关的基因变异与软饮料之间的相互作用与体重和腰围的纵向变化的关系。
Am J Clin Nutr. 2016 Sep;104(3):816-26. doi: 10.3945/ajcn.115.122820. Epub 2016 Jul 27.
9
Circadian Dysfunction and Obesity: Is Leptin the Missing Link?昼夜节律功能障碍与肥胖:瘦素是其中的关键环节吗?
Cell Metab. 2015 Sep 1;22(3):359-60. doi: 10.1016/j.cmet.2015.08.008.
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Circadian Dysfunction Induces Leptin Resistance in Mice.昼夜节律功能障碍诱发小鼠瘦素抵抗。
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昼夜节律基因变异与健康饮食模式对血清瘦素水平的相互作用:一项横断面研究。

Variants in Circadian Rhythm Gene Interacts with Healthy Dietary Pattern for Serum Leptin Levels: a Cross-sectional Study.

作者信息

Tangestani Hadith, Emamat Hadi, Yekaninejad Mir Saeed, Keshavarz Seyed Ali, Mirzaei Khadijeh

机构信息

Department of Community Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences (TUMS), Tehran 14155-6117, Iran.

Department of Nutrition, Persian Gulf Tropical Medicine Research Center, Bushehr University of Medical Sciences, Bushehr 75146-33196, Iran.

出版信息

Clin Nutr Res. 2021 Jan 28;10(1):48-58. doi: 10.7762/cnr.2021.10.1.48. eCollection 2021 Jan.

DOI:10.7762/cnr.2021.10.1.48
PMID:33564652
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7850819/
Abstract

Circadian disruption causes obesity and other metabolic disorders. There is no research considering the role of Cryptochromes (Cry) 1 body clock gene and major dietary patterns on serum leptin level and obesity. We aimed to investigate the interaction between circadian gene polymorphisms and major dietary patterns on leptin and obesity related measurements. This study was performed on 377 overweight and obese women. Mean age and body mass index (BMI) of study subjects were 36.64 ± 9.02 years and 30.81 ± 3.8 kg/m, respectively. Dietary assessment was done using a validated 147-item food frequency questionnaire. rs2287161 were genotyped using polymerase chain reaction-restriction fragment length polymorphism. Generalized linear models were used for interaction analysis. Healthy and unhealthy dietary pattern (HDP and UDP, respectively) were extracted using factor analysis (principal component analysis). Our study revealed a significant higher weight (p = 0.003) and BMI (p = 0.042) in women carrying CC homozygote compared with G allele carriers. Moreover, our findings showed a significant gene-diet interaction between HDP and rs2287161 on BMI (p = 0.034) and serum leptin level (p = 0.056) in which, BMI and serum leptin level were lower in subjects with CC genotype than in those with GG genotype while following HDP. This study suggests a significant interaction between rs2287161 polymorphisms and HDP on BMI and serum leptin and the lowering effects were apparent among C allele carriers compared to G allele ones. This data highlights the role of dietary pattern in relation of gene and obesity.

摘要

昼夜节律紊乱会导致肥胖和其他代谢紊乱。目前尚无研究探讨隐花色素(Cry)1生物钟基因和主要饮食模式对血清瘦素水平及肥胖的作用。我们旨在研究昼夜节律基因多态性与主要饮食模式在瘦素及肥胖相关指标上的相互作用。本研究对377名超重和肥胖女性进行。研究对象的平均年龄和体重指数(BMI)分别为36.64±9.02岁和30.81±3.8kg/m²。采用经过验证的147项食物频率问卷进行饮食评估。使用聚合酶链反应-限制性片段长度多态性方法对rs2287161进行基因分型。采用广义线性模型进行相互作用分析。通过因子分析(主成分分析)提取健康和不健康饮食模式(分别为HDP和UDP)。我们的研究显示,与G等位基因携带者相比,携带CC纯合子的女性体重(p = 0.003)和BMI(p = 0.042)显著更高。此外,我们的研究结果表明,HDP与rs2287161在BMI(p = 0.034)和血清瘦素水平(p = 0.056)上存在显著的基因-饮食相互作用,即遵循HDP时,CC基因型受试者的BMI和血清瘦素水平低于GG基因型受试者。本研究表明,rs2287161多态性与HDP在BMI和血清瘦素方面存在显著相互作用,与G等位基因携带者相比,C等位基因携带者的降低作用更为明显。这些数据突出了饮食模式在基因与肥胖关系中的作用。