Department of Prevention and Sports Medicine, Centre for Sports Cardiology, University Hospital "Klinikum rechts der Isar," Technical University of Munich, Munich, Germany.
Research Unit of Molecular Epidemiology, Institute of Epidemiology, Helmholtz Zentrum München, Neuherberg, Germany.
JAMA Pediatr. 2021 Jan 1;175(1):e205142. doi: 10.1001/jamapediatrics.2020.5142. Epub 2021 Jan 4.
Genome-wide association studies have identified genetic loci influencing obesity risk in children. However, the importance of these loci in the associations with weight reduction through lifestyle interventions has not been investigated in large intervention trials.
To evaluate the associations between various obesity susceptibility loci and changes in body weight in children during an in-hospital, lifestyle intervention program.
DESIGN, SETTING, AND PARTICIPANTS: Long-term Effects of Lifestyle Intervention in Obesity and Genetic Influence in Children (LOGIC), an interventional prospective cohort study, enrolled 1429 children with overweight or obesity to participate in an in-hospital lifestyle intervention program. Genotyping of 56 validated obesity single-nucleotide variants (SNVs) was performed, and the associations between the SNVs and body weight reduction during the intervention were evaluated using linear mixed-effects models for each SNV. The LOGIC study was conducted from January 6, 2006, to October 19, 2013; data analysis was performed from July 15, 2015, to November 6, 2016.
A 4- to 6-week standardized in-hospital lifestyle intervention program (daily physical activity, calorie-restricted diet, and behavioral therapy).
The association between 56 obesity-relevant SNVs and changes in body weight and body mass index.
Of 1429 individuals enrolled in the LOGIC Study, 1198 individuals (mean [SD] age, 14.0 [2.2] years; 670 [56%] girls) were genotyped. A mean (SD) decrease was noted in body weight of -8.7 (3.6) kg (95% CI, -15.7 to -1.8 kg), and body mass index (calculated as weight in kilograms divided by height in meters squared) decreased by -3.3 (1.1) (95% CI, -5.4 to -1.1) (both P < .05). Five of 56 obesity SNVs were statistically significantly associated with a reduction of body weight or body mass index (all P < 8.93 × 10-4 corresponding to Bonferroni correction for 56 tests). Compared with homozygous participants without the risk allele, homozygous carriers of the rs7164727 (LOC100287559: 0.42 kg; 95% CI, 0.31-0.53 kg, P = 4.00 × 10-4) and rs12940622 (RPTOR: 0.35 kg; 95% CI, 0.18-0.52 kg; P = 1.86 × 10-5) risk alleles had a lower reduction of body weight, whereas carriers of the rs13201877 (IFNGR1: 0.65 kg; 95% CI, 0.51-0.79 kg; P = 2.39 × 10-5), rs10733682 (LMX1B: 0.45 kg; 95% CI, 0.27-0.63 kg; P = 6.37 × 10-4), and rs2836754 (ETS2: 0.56 kg; 95% CI, 0.38-0.74 kg; P = 1.51 × 10-4) risk alleles were associated with a greater reduction of body weight after adjustment for age and sex.
Genes appear to play a minor role in weight reduction by lifestyle in children with overweight or obesity. The findings suggest that environmental, social, and behavioral factors are more important to consider in obesity treatment strategies.
全基因组关联研究已经确定了影响儿童肥胖风险的遗传位点。然而,这些位点在大型干预试验中通过生活方式干预与体重减轻的关联的重要性尚未被调查。
评估各种肥胖易感基因座与儿童住院期间生活方式干预计划中体重变化之间的关联。
设计、地点和参与者:长期生活方式干预对肥胖和儿童遗传影响的影响(LOGIC),一项干预性前瞻性队列研究,招募了 1429 名超重或肥胖的儿童参加住院生活方式干预计划。对 56 个经过验证的肥胖单核苷酸变异(SNV)进行基因分型,并使用线性混合效应模型评估每个 SNV 在干预期间体重减轻的相关性。LOGIC 研究于 2006 年 1 月 6 日至 2013 年 10 月 19 日进行;数据分析于 2015 年 7 月 15 日至 2016 年 11 月 6 日进行。
4-6 周的标准化住院生活方式干预计划(日常体育活动、热量限制饮食和行为疗法)。
56 个肥胖相关 SNV 与体重和体重指数变化之间的关联。
在 LOGIC 研究中纳入的 1429 名个体中,对 1198 名个体(平均[标准差]年龄,14.0[2.2]岁;670[56%]名女孩)进行了基因分型。体重平均(标准差)下降了-8.7(3.6)kg(95%置信区间,-15.7 至-1.8 kg),体重指数(体重以千克为单位除以身高以米为单位的平方)下降了-3.3(1.1)(95%置信区间,-5.4 至-1.1)(均 P <.05)。56 个肥胖 SNV 中有 5 个与体重或体重指数的降低具有统计学意义的关联(所有 P < 8.93×10-4 对应于 56 次测试的 Bonferroni 校正)。与不携带风险等位基因的纯合子参与者相比,纯合子携带者 rs7164727(LOC100287559:0.42 kg;95%置信区间,0.31-0.53 kg,P = 4.00×10-4)和 rs12940622(RPTOR:0.35 kg;95%置信区间,0.18-0.52 kg,P = 1.86×10-5)风险等位基因的体重减轻程度较低,而携带 rs13201877(IFNGR1:0.65 kg;95%置信区间,0.51-0.79 kg;P = 2.39×10-5)、rs10733682(LMX1B:0.45 kg;95%置信区间,0.27-0.63 kg;P = 6.37×10-4)和 rs2836754(ETS2:0.56 kg;95%置信区间,0.38-0.74 kg;P = 1.51×10-4)风险等位基因在调整年龄和性别后与体重的更大减轻相关。
基因似乎在儿童超重或肥胖的生活方式减肥中起次要作用。研究结果表明,在肥胖治疗策略中,环境、社会和行为因素更为重要。