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首页> 外文期刊>Therapeutic advances in endocrinology and metabolism. >Genetic and nongenetic factors explaining metabolically healthy and unhealthy phenotypes in participants with excessive adiposity: relevance for personalized nutrition
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Genetic and nongenetic factors explaining metabolically healthy and unhealthy phenotypes in participants with excessive adiposity: relevance for personalized nutrition

机译:遗传和环境因素在参与者过度肥胖的情况下解释代谢健康和不健康的表型:个性化营养的相关性

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Background: Different genetic and environmental factors can explain the heterogeneity of obesity-induced metabolic alterations between individuals. In this study, we aimed to screen factors that predict metabolically healthy (MHP) and unhealthy (MUP) phenotypes using genetic and lifestyle data in overweight/obese participants. Methods: In this cross-sectional study we enrolled 298 overweight/obese Spanish adults. The Adult Treatment Panel III criteria for metabolic syndrome were used to categorize MHP (at most, one trait) and MUP (more than one feature). Blood lipid and inflammatory profiles were measured by standardized methods. Body composition was determined by dual-energy X-ray absorptiometry. A total of 95 obesity-predisposing single-nucleotide polymorphisms (SNPs) were genotyped by a predesigned next-generation sequencing system. SNPs associated with a MUP were used to compute a weighted genetic-risk score (wGRS). Information concerning lifestyle (dietary intake and physical activity level) was collected using validated questionnaires. Results: The prevalence of MHP and MUP was 44.3% and 55.7%, respectively, in this sample. Overall, 12 obesity-related genetic variants were associated with the MUP. Multiple logistic regression analyses revealed that wGRS (OR?=?4.133, p??0.001), total dietary fat [odds ratio (OR)?=?1.105, p?=?0.002], age (OR?=?1.064, p?=?0.001), and BMI (OR?=?1.408, p??0.001) positively explained the MUP, whereas female sex (OR?=?0.330, p?=?0.009) produced a protective effect. The area under the receiver operating characteristic curve using the multivariable model was high (0.8820). Interestingly, the wGRS was the greatest contributor to the MUP (squared partial correlation?=?0.3816, p??0.001). Conclusions: The genetic background is an important factor explaining MHP and MUP related to obesity, in addition to lifestyle variables. This information could be useful to metabolically categorize individuals, as well as for the design/implementation of personalized nutrition interventions aimed at promoting metabolic health and nutritional wellbeing.
机译:背景:不同的遗传和环境因素可以解释肥胖症诱导的个体之间的代谢改变的异质性。在这项研究中,我们旨在使用超重/肥胖参与者中的遗传和生活方式数据预测代谢健康(MHP)和不健康(MHP)表型的因素。方法:在这个横断面研究中,我们注册了298个超重/肥胖的西班牙成年人。成人治疗组III用于代谢综合征的标准用于将MHP(最多,一个特征)和MHP(多于一个特征)分类。通过标准化方法测量血脂和炎症型材。通过双能X射线吸收测定法测定身体组成。通过预测的下一代测序系统,总共95个肥胖性易化的单核苷酸多态性(SNP)进行了基因分型。与MUP关联的SNP用于计算加权遗传风险评分(WGRS)。使用经过验证的问卷收集有关生活方式的信息(饮食摄入和身体活动水平)。结果:在该样品中,MHP和MUP的患病率分别为44.3%和55.7%。总体而言,12种肥胖相关的遗传变异与MUP有关。多重逻辑回归分析显示WGRS(或?= 4.133,P?<0.001),总膳食脂肪[odds比(或)?=?1.105,p?=?0.002],年龄(或?=?1.064, p?= 0.001)和BMI(或?=?1.408,P?<0.001)正面解释了MUP,而女性(或?=?0.330,P?= 0.009)产生了保护作用。使用多变量型号的接收器操作特性曲线下的该区域高(0.8820)。有趣的是,WGRS是MUP的最大贡献者(平方部分相关性?=?0.3816,P?<0.001)。结论:除了生活方式变量之外,遗传背景是解释与肥胖相关的MHP和MUP的重要因素。这些信息可能有助于代谢分类个人,以及设计/实施针对促进代谢健康和营养健康的个性化营养干预措施。

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