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2
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6
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Triglyceride response to an intensive lifestyle intervention is enhanced in carriers of the GCKR Pro446Leu polymorphism.携带 GCKR Pro446Leu 多态性的个体对强化生活方式干预的甘油三酯反应增强。
J Clin Endocrinol Metab. 2011 Jul;96(7):E1142-7. doi: 10.1210/jc.2010-2324. Epub 2011 Apr 27.
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Sex-specific impact of rs1260326 polymorphism on metabolic traits in an older Japanese population: the Bunkyo Health Study.rs1260326多态性对日本老年人群代谢特征的性别特异性影响:文京区健康研究
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2
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Br J Nutr. 2024 Sep 14;132(5):575-589. doi: 10.1017/S0007114524001594. Epub 2024 Sep 23.
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"GENYAL" Study to Childhood Obesity Prevention: Methodology and Preliminary Results.“GENYAL”儿童肥胖预防研究:方法与初步结果
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Nutritional Supplementation with Essential Amino Acids and Phytosterols May Reduce Risk for Metabolic Syndrome and Cardiovascular Disease in Overweight Individuals with Mild Hyperlipidemia.补充必需氨基酸和植物甾醇的营养疗法可能降低轻度高脂血症超重个体患代谢综合征和心血管疾病的风险。
J Endocrinol Diabetes Obes. 2015;3(2). Epub 2015 Apr 15.
6
Polymorphisms in the GCKR are associated with serum lipid traits, the risk of coronary artery disease and ischemic stroke.GCKR基因多态性与血脂性状、冠状动脉疾病和缺血性中风风险相关。
Int J Clin Exp Med. 2015 Jul 15;8(7):10678-86. eCollection 2015.
7
Genomics and metabolomics of muscular mass in a community-based sample of UK females.基于英国女性社区样本的肌肉量基因组学与代谢组学研究
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本文引用的文献

1
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.一种考虑体重指数的全基因组方法鉴定出影响空腹血糖特征和胰岛素抵抗的遗传变异。
Nat Genet. 2012 May 13;44(6):659-69. doi: 10.1038/ng.2274.
2
Cohort profile: the Lothian Birth Cohorts of 1921 and 1936.队列研究简介:1921 年和 1936 年的洛锡安出生队列。
Int J Epidemiol. 2012 Dec;41(6):1576-84. doi: 10.1093/ije/dyr197. Epub 2011 Dec 14.
3
Age and gender differences in physical capability levels from mid-life onwards: the harmonisation and meta-analysis of data from eight UK cohort studies.从中年开始的身体能力水平的年龄和性别差异:来自八个英国队列研究的数据的协调和荟萃分析。
PLoS One. 2011;6(11):e27899. doi: 10.1371/journal.pone.0027899. Epub 2011 Nov 16.
4
Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children.身体活动可减弱 FTO 变异对肥胖风险的影响:对 218166 名成年人和 19268 名儿童的荟萃分析。
PLoS Med. 2011 Nov;8(11):e1001116. doi: 10.1371/journal.pmed.1001116. Epub 2011 Nov 1.
5
A gene-centric association scan for Coagulation Factor VII levels in European and African Americans: the Candidate Gene Association Resource (CARe) Consortium.以基因为中心的欧洲裔和非裔美国人凝血因子 VII 水平的关联研究:候选基因关联资源 (CARe) 联盟。
Hum Mol Genet. 2011 Sep 1;20(17):3525-34. doi: 10.1093/hmg/ddr264. Epub 2011 Jun 15.
6
Triglyceride response to an intensive lifestyle intervention is enhanced in carriers of the GCKR Pro446Leu polymorphism.携带 GCKR Pro446Leu 多态性的个体对强化生活方式干预的甘油三酯反应增强。
J Clin Endocrinol Metab. 2011 Jul;96(7):E1142-7. doi: 10.1210/jc.2010-2324. Epub 2011 Apr 27.
7
Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits.全基因组关联分析鉴定出与非酒精性脂肪性肝病相关的变异,这些变异对代谢特征有不同的影响。
PLoS Genet. 2011 Mar;7(3):e1001324. doi: 10.1371/journal.pgen.1001324. Epub 2011 Mar 10.
8
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.对超过 80000 名受试者的全基因组关联研究的荟萃分析确定了多个 C-反应蛋白水平的位点。
Circulation. 2011 Feb 22;123(7):731-8. doi: 10.1161/CIRCULATIONAHA.110.948570. Epub 2011 Feb 7.
9
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.全基因组荟萃分析将确认的克罗恩病易感性位点数量增加到 71 个。
Nat Genet. 2010 Dec;42(12):1118-25. doi: 10.1038/ng.717.
10
TRIB1 and GCKR polymorphisms, lipid levels, and risk of ischemic heart disease in the general population.TRIB1 和 GCKR 多态性、血脂水平与普通人群缺血性心脏病风险。
Arterioscler Thromb Vasc Biol. 2011 Feb;31(2):451-7. doi: 10.1161/ATVBAHA.110.216333. Epub 2010 Nov 11.

多效性 GCKR 基因多态性与年龄相关表型的关联:HALCyon 计划。

Associations between a polymorphism in the pleiotropic GCKR and Age-related phenotypes: the HALCyon programme.

机构信息

School of Social and Community Medicine, University of Bristol, Bristol, United Kingdom.

出版信息

PLoS One. 2013 Jul 23;8(7):e70045. doi: 10.1371/journal.pone.0070045. Print 2013.

DOI:10.1371/journal.pone.0070045
PMID:23894584
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3720952/
Abstract

BACKGROUND

The glucokinase regulatory protein encoded by GCKR plays an important role in glucose metabolism and a single nucleotide polymorphism (SNP) rs1260326 (P446L) in the gene has been associated with several age-related biomarkers, including triglycerides, glucose, insulin and apolipoproteins. However, associations between SNPs in the gene and other ageing phenotypes such as cognitive and physical capability have not been reported.

METHODS

As part of the Healthy Ageing across the Life Course (HALCyon) collaborative research programme, men and women from five UK cohorts aged between 44 and 90+ years were genotyped for rs1260326. Meta-analysis was used to pool within-study genotypic associations between the SNP and several age-related phenotypes, including body mass index (BMI), blood lipid levels, lung function, and cognitive and physical capability.

RESULTS

We confirm the associations between the minor allele of the SNP and higher triglycerides and lower glucose levels. We also observed a triglyceride-independent association between the minor allele and lower BMI (pooled beta on z-score= -0.04, p-value=0.0001, n=16,251). Furthermore, there was some evidence for gene-environment interactions, including physical activity attenuating the effects on triglycerides. However, no associations were observed with measures of cognitive and physical capability.

CONCLUSION

Findings from middle-aged to older adults confirm associations between rs1260326 GCKR and triglycerides and glucose, suggest possible gene-environment interactions, but do not provide evidence that its relevance extends to cognitive and physical capability.

摘要

背景

编码葡萄糖激酶调节蛋白(GCKR)的基因在葡萄糖代谢中起着重要作用,基因中的单核苷酸多态性(SNP)rs1260326(P446L)与几种与年龄相关的生物标志物有关,包括甘油三酯、葡萄糖、胰岛素和载脂蛋白。然而,该基因中的 SNP 与其他衰老表型(如认知和身体能力)之间的关联尚未报道。

方法

作为健康老龄化贯穿生命历程(HALCyon)合作研究计划的一部分,来自五个英国队列的 44 岁至 90 岁以上的男性和女性对 rs1260326 进行了基因分型。荟萃分析用于汇总 SNP 与几种与年龄相关的表型之间的研究内基因关联,包括体重指数(BMI)、血脂水平、肺功能以及认知和身体能力。

结果

我们证实了 SNP 少数等位基因与甘油三酯升高和血糖水平降低之间的关联。我们还观察到少数等位基因与 BMI 降低之间存在与甘油三酯无关的关联(z 分数的 SNP 杂合子效应的汇总β= -0.04,p 值=0.0001,n=16251)。此外,存在一些基因-环境相互作用的证据,包括体力活动减弱了对甘油三酯的影响。然而,没有观察到与认知和身体能力测量相关的关联。

结论

从中年到老年成年人的研究结果证实了 rs1260326 GCKR 与甘油三酯和葡萄糖之间的关联,表明可能存在基因-环境相互作用,但没有证据表明其相关性扩展到认知和身体能力。