Ramos-Lopez Omar, Riezu-Boj Jose I, Milagro Fermin I, Cuervo Marta, Goni Leticia, Martinez J Alfredo
Department of Nutrition, Food Science and Physiology, and Center for Nutrition Research, University of Navarra, Pamplona, Spain.
Department of Nutrition, Food Science and Physiology, and Center for Nutrition Research, University of Navarra, 1 Irunlarrea Street, Pamplona, 31008, Spain.
Ther Adv Endocrinol Metab. 2019 Sep 18;10:2042018819877303. doi: 10.1177/2042018819877303. eCollection 2019.
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.
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.
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, < 0.001), total dietary fat [odds ratio (OR) = 1.105, = 0.002], age (OR = 1.064, = 0.001), and BMI (OR = 1.408, < 0.001) positively explained the MUP, whereas female sex (OR = 0.330, = 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, < 0.001).
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.
不同的遗传和环境因素可以解释个体间肥胖诱导的代谢改变的异质性。在本研究中,我们旨在利用超重/肥胖参与者的遗传和生活方式数据,筛选预测代谢健康(MHP)和不健康(MUP)表型的因素。
在这项横断面研究中,我们招募了298名超重/肥胖的西班牙成年人。采用成人治疗小组III代谢综合征标准对MHP(最多一项特征)和MUP(多于一项特征)进行分类。通过标准化方法测量血脂和炎症指标。采用双能X线吸收法测定身体成分。通过预先设计的下一代测序系统对总共95个肥胖易感单核苷酸多态性(SNP)进行基因分型。与MUP相关的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(饮食摄入和身体活动水平)的信息。
在该样本中,MHP和MUP的患病率分别为44.3%和55.7%。总体而言,12个与肥胖相关的基因变异与MUP相关。多因素logistic回归分析显示,wGRS(比值比[OR]=4.133,<0.001)、总膳食脂肪[比值比(OR)=1.105,=0.002]、年龄(OR=1.064,=0.001)和BMI(OR=1.408,<0.001)正向解释MUP,而女性(OR=0.330,=0.009)产生保护作用。使用多变量模型的受试者工作特征曲线下面积较高(面积=0.8820)。有趣的是,wGRS是MUP的最大贡献因素(偏相关平方=0.3816,<0.001)。
除生活方式变量外,遗传背景是解释与肥胖相关的MHP和MUP的重要因素。这些信息对于对个体进行代谢分类以及设计/实施旨在促进代谢健康和营养福祉的个性化营养干预可能有用。