Department of Nutrition, Food Science, Physiology and Toxicology, University of Navarra, C/Irunlarrea s/n, Pamplona, Navarra, Spain.
Chronobiol Int. 2012 Dec;29(10):1397-404. doi: 10.3109/07420528.2012.728657. Epub 2012 Nov 6.
Genetic factors may interact with physical activity levels to modify obesity risk. Our aim was to explore the influence of rs1801260 single-nucleotide polymorphism (SNP) (3111T/C) of CLOCK gene on obesity risk, and to examine its potential interaction with lifestyle factors in an elderly population within the SUN ("Seguimiento Universidad de Navarra") Project. Subjects (n = 903, aged 69 ± 6 yrs) were recruited from the SUN Project. DNA was obtained from saliva, whereas lifestyle and dietary data were collected by validated self-report questionnaires. Genotype was assessed by reverse transcriptase-polymerase chain reaction (RT-PCR) plus allele discrimination. A significant interaction was observed between the 3111T/C SNP of CLOCK gene and sex for overweight/obesity risk (p for sex × CLOCK interaction <.001). Our results showed that women carrying the C allele of CLOCK gene had a marginally significant lower risk of overweight/obesity compared with noncarrier-TT-subjects (odds ratio [OR]: .61, 95% confidence interval [CI]: .36-1.04; p = .069). Moreover, this association of the C allele with a decreased overweight/obesity risk might be enhanced in those women with a high physical activity level. Women practicing more than 16.8 metabolic equivalent tasks (hours per week) had a significantly lower overweight/obesity risk (OR: .36, 95% CI: .17-.79; p = .011). Furthermore, a significant interaction between the 3111T/C gene variant and physical activity (PA) for overweight/obesity risk was observed but only in women (p for PA × CLOCK interaction <.050). In conclusion, it appears that physical activity levels may act by modifying the association of the 3111T/C SNP (rs1801260) of the CLOCK gene with overweight/obesity risk in elderly women in the SUN Project.
遗传因素可能与身体活动水平相互作用,从而改变肥胖风险。我们的目的是探索时钟基因 rs1801260 单核苷酸多态性(SNP)(3111T/C)对肥胖风险的影响,并在 SUN(“纳瓦拉大学随访”)项目中研究其在老年人群中与生活方式因素的潜在相互作用。研究对象(n=903,年龄 69±6 岁)来自 SUN 项目。从唾液中提取 DNA,通过经过验证的自我报告问卷收集生活方式和饮食数据。通过逆转录-聚合酶链反应(RT-PCR)加等位基因区分评估基因型。时钟基因的 3111T/C SNP 与超重/肥胖风险之间观察到显著的性别交互作用(p<0.001)。我们的结果表明,携带时钟基因 C 等位基因的女性超重/肥胖的风险明显降低(比值比[OR]:0.61,95%置信区间[CI]:0.36-1.04;p=0.069)。此外,C 等位基因与降低超重/肥胖风险的相关性可能在身体活动水平较高的女性中增强。每周进行超过 16.8 个代谢当量任务(小时)的女性超重/肥胖风险显著降低(OR:0.36,95%CI:0.17-0.79;p=0.011)。此外,还观察到 3111T/C 基因变异与超重/肥胖风险的身体活动(PA)之间存在显著的交互作用,但仅在女性中(p<0.050)。总之,似乎身体活动水平可能通过改变时钟基因的 3111T/C SNP(rs1801260)与超重/肥胖风险的关联来影响老年女性的超重/肥胖风险。