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本文引用的文献

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Associations of genetic risk scores based on adult adiposity pathways with childhood growth and adiposity measures.基于成人肥胖途径的遗传风险评分与儿童生长及肥胖指标的关联。
BMC Genet. 2016 Aug 18;17(1):120. doi: 10.1186/s12863-016-0425-y.
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Neurotrophic factor control of satiety and body weight.神经营养因子对饱腹感和体重的控制。
Nat Rev Neurosci. 2016 May;17(5):282-92. doi: 10.1038/nrn.2016.24. Epub 2016 Apr 7.
3
Common genetic architecture underlying young children's food fussiness and liking for vegetables and fruit.幼儿食物挑剔以及对蔬菜和水果喜好背后的共同遗传结构。
Am J Clin Nutr. 2016 Apr;103(4):1099-104. doi: 10.3945/ajcn.115.122945. Epub 2016 Feb 10.
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Polygenic Risk, Appetite Traits, and Weight Gain in Middle Childhood: A Longitudinal Study.儿童中期的多基因风险、食欲特征与体重增加:一项纵向研究
JAMA Pediatr. 2016 Feb;170(2):e154472. doi: 10.1001/jamapediatrics.2015.4472. Epub 2016 Feb 1.
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Longitudinal association between preschool fussy eating and body composition at 6 years of age: The Generation R Study.学龄前挑食与6岁时身体成分的纵向关联:Generation R研究
Int J Behav Nutr Phys Act. 2015 Dec 14;12:153. doi: 10.1186/s12966-015-0313-2.
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Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index.全基因组关联分析确定了儿童体重指数的三个新的易感基因座。
Hum Mol Genet. 2016 Jan 15;25(2):389-403. doi: 10.1093/hmg/ddv472. Epub 2015 Nov 24.
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Genetic studies of body mass index yield new insights for obesity biology.遗传研究体重指数为肥胖生物学提供了新的见解。
Nature. 2015 Feb 12;518(7538):197-206. doi: 10.1038/nature14177.
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The Generation R Study: Biobank update 2015.《生育队列研究:2015 年生物银行更新》
Eur J Epidemiol. 2014 Dec;29(12):911-27. doi: 10.1007/s10654-014-9980-6. Epub 2014 Dec 21.
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Fetal and infant growth patterns associated with total and abdominal fat distribution in school-age children.与学龄儿童总体和腹部脂肪分布相关的胎儿及婴儿生长模式。
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与体重指数相关的基因变异对儿童期饮食行为的影响。

Influence of genetic variants associated with body mass index on eating behavior in childhood.

作者信息

Monnereau Claire, Jansen Pauline W, Tiemeier Henning, Jaddoe Vincent W V, Felix Janine F

机构信息

The Generation R Study Group, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.

Department of Epidemiology, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.

出版信息

Obesity (Silver Spring). 2017 Apr;25(4):765-772. doi: 10.1002/oby.21778. Epub 2017 Feb 28.

DOI:10.1002/oby.21778
PMID:28245097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5496668/
Abstract

OBJECTIVE

Childhood eating behaviors are associated with body mass index (BMI). Recent genome-wide association studies have identified many single-nucleotide polymorphisms (SNPs) associated with adult and childhood BMI. This study hypothesized that these SNPs also influence eating behavior.

METHODS

In a population-based prospective cohort study among 3,031 children (mean age [standard deviation]: 4.0 [0.1] years), two weighted genetic risk scores, based on 15 childhood and 97 adult BMI SNPs, and ten individual appetite- and/or satiety-related SNPs were tested for association with food fussiness, food responsiveness, enjoyment of food, satiety responsiveness, and slowness in eating.

RESULTS

The 15 SNP-based childhood BMI genetic risk score was not associated with the eating behavior subscales. The 97 SNP-based adult BMI genetic risk score was nominally associated with satiety responsiveness (β: -0.007 standard deviation, 95% confidence interval [CI] -0.013, 0.000). Of the 10 individual SNPs, rs11030104 in BDNF and rs10733682 in LMX1B were nominally associated with satiety responsiveness (β: -0.057 standard deviation, 95% CI -0.112, -0.002).

CONCLUSIONS

These findings do not strongly support the hypothesis that BMI-associated SNPs also influence eating behavior at this age. A potential role for BMI SNPs in satiety responsiveness during childhood was observed; however, no associations with the other eating behavior subscales were found.

摘要

目的

儿童饮食行为与体重指数(BMI)相关。近期的全基因组关联研究已鉴定出许多与成人及儿童BMI相关的单核苷酸多态性(SNP)。本研究假设这些SNP也会影响饮食行为。

方法

在一项基于人群的前瞻性队列研究中,对3031名儿童(平均年龄[标准差]:4.0[0.1]岁)进行了研究,测试了基于15个儿童BMI SNP和97个成人BMI SNP的两个加权遗传风险评分,以及10个与食欲和/或饱腹感相关的个体SNP与食物挑剔、食物反应性、食物喜好、饱腹感反应性和进食速度的关联。

结果

基于15个SNP的儿童BMI遗传风险评分与饮食行为分量表无关。基于97个SNP的成人BMI遗传风险评分与饱腹感反应性存在名义上的关联(β:-0.007标准差,95%置信区间[CI]-0.013,0.000)。在10个个体SNP中,BDNF基因中的rs11030104和LMX1B基因中的rs10733682与饱腹感反应性存在名义上的关联(β:-0.057标准差,95%CI-0.112,-0.002)。

结论

这些发现并不强烈支持BMI相关SNP也会影响该年龄段饮食行为的假设。观察到BMI SNP在儿童期饱腹感反应性中可能发挥的作用;然而,未发现与其他饮食行为分量表的关联。