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Lack of association between PCK1 polymorphisms and obesity, physical activity, and fitness in European Youth Heart Study (EYHS)

机译:欧洲青年心脏研究(EYHS)中PCK1多态性与肥胖,体育活动和健身之间缺乏关联

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摘要

Phosphoenolpyruvate carboxykinase-1 (PCK1) is the rate-limiting enzyme in the hepatic gluconeogenic pathway. Studies have shown that overexpression of Pck1 in mice results in obesity-related traits and higher levels of physical activity (PA). Therefore, our aims were to investigate whether common genetic variation in the PCK1 gene influences obesity-related traits, PA, and fitness, and to examine whether PA and fitness attenuate the influence of the PCK1 polymorphisms on obesity in children. Analyses were undertaken on data from Danish and Estonian children (958 boys and 1,104 girls) from the European Youth Heart Study (EYHS), a school-based, cross-sectional study of children (mean ± s.d. age: 9.6 ± 0.4 years) and adolescents (15.5 ± 0.5 years). We genotyped eight polymorphisms that captured the common genetic variations in the PCK1 gene. The association between the PCK1 polymorphisms and BMI, waist circumference (WC), sum of four skinfolds, PA, and fitness was tested using an additive model adjusted for age, age-group, gender, maturity, and country. Interactions were tested by including interaction terms in the model. None of the polymorphisms were significantly associated with BMI, WC, sum of four skinfolds, PA, and fitness, and also with the risk of being overweight or obese (P > 0.05). The interactions between the polymorphisms and age-group, gender, PA, and fitness were not statistically significant. This is the first study to comprehensively examine the association of PCK1 polymorphisms with obesity, PA, and fitness. Despite strong evidence from animal studies, our study in the EYHS cohort failed to identify an association of PCK1 polymorphisms with obesity, PA, and fitness.
机译:磷酸烯醇丙酮酸羧激酶-1(PCK1)是肝糖原异生途径中的限速酶。研究表明,Pck1在小鼠中的过度表达会导致肥胖相关性状和更高水平的体育活动(PA)。因此,我们的目的是调查PCK1基因的常见遗传变异是否影响肥胖相关性状,PA和健康,并研究PA和健身是否减弱PCK1多态性对儿童肥胖的影响。对来自欧洲青年心脏研究(EYHS)的丹麦和爱沙尼亚儿童(958名男孩和1,104名女孩)的数据进行了分析,这是一项基于学校的儿童横断面研究(平均±标准年龄:9.6±0.4岁),青少年(15.5±0.5岁)。我们对八种多态性进行了基因分型,这些多态性捕获了PCK1基因中的常见遗传变异。使用针对年龄,年龄组,性别,成熟度和国家调整的附加模型,测试了PCK1多态性与BMI,腰围(WC),四个皮褶的总和,PA和健身之间的关联。通过在模型中包括交互项来测试交互。这些多态性均与BMI,WC,四个皮褶的总和,PA和健康状况以及超重或肥胖风险无显着相关性(P> 0.05)。多态性与年龄组,性别,PA和适应性之间的相互作用在统计学上不显着。这是首次全面研究PCK1多态性与肥胖症,PA和健康状况之间关系的研究。尽管有动物研究的有力证据,但我们在EYHS队列中的研究未能确定PCK1多态性与肥胖症,PA和健康的相关性。

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