Alonso Alvaro, Martí Amelia, Corbalán María Soledad, Martínez-González Miguel A, Forga Luis, Martínez J Alfredo
Department of Preventive Medicine and Public Health, University of Navarra, Pamplona, Spain.
Ann Nutr Metab. 2005 May-Jun;49(3):183-8. doi: 10.1159/000086883. Epub 2005 Jul 7.
BACKGROUND/AIMS: The uncoupling protein 3 (UCP3) gene has been suggested as a possible determinant affecting obesity risk given its function in the regulation of energy metabolism. However, available genetic association studies have been inconsistent, which could be attributable to not considering individual lifestyle patterns, such as physical activity, a factor that affects UCP3 expression. The objective of this study was to assess the association between the UCP3 -55C>T polymorphism and the risk of obesity.
Case-control study conducted in a sample of Spanish adults. 157 obese subjects (BMI > or = 30) and 150 controls (BMI < 25) participated in the study. UCP3 -55C>T polymorphism was identified by the polymerase chain reaction-restriction fragment length polymorphism methodology.
The odds ratio (OR) for obesity (95% confidence interval [CI]) according to the presence of UCP 3 gene -55C>T polymorphism (heterozygotes and homozygotes merged together), adjusting for age, sex, and recreational physical activity, was 0.61 (0.37-1.00), p = 0.05. Interestingly, this association was only manifest among those with higher recreational physical activity (OR: 0.46, 95% CI 0.21-0.99, p = 0.05) and not among those with lower physical activity (OR: 0.84, 95% CI 0.41-1.70, p = 0.84).
UCP3 -55C>T polymorphism carriers have apparently a lower risk of obesity when taking into consideration recreational energy expenditure. Interestingly, this inverse beneficial association may only occur in people with a high level of physical activity.
背景/目的:解偶联蛋白3(UCP3)基因因其在能量代谢调节中的作用,被认为是影响肥胖风险的一个可能决定因素。然而,现有的基因关联研究结果并不一致,这可能是由于未考虑个体生活方式模式,如身体活动,而身体活动是影响UCP3表达的一个因素。本研究的目的是评估UCP3基因 -55C>T多态性与肥胖风险之间的关联。
在西班牙成年人样本中进行病例对照研究。157名肥胖受试者(BMI≥30)和150名对照者(BMI<25)参与了研究。采用聚合酶链反应-限制性片段长度多态性方法鉴定UCP3基因 -55C>T多态性。
根据UCP3基因 -55C>T多态性(杂合子和纯合子合并)的存在情况,在调整年龄、性别和休闲身体活动后,肥胖的优势比(OR)(95%置信区间[CI])为0.61(0.37-
1.00),p = 0.05。有趣的是,这种关联仅在休闲身体活动水平较高的人群中表现明显(OR:0.46,95%CI 0.21-0.99,p = 0.05),而在身体活动水平较低的人群中未表现出来(OR:0.84,95%CI 0.41-1.70,p = 0.84)。
考虑到休闲能量消耗,UCP3基因 -55C>T多态性携带者肥胖风险明显较低。有趣的是,这种反向有益关联可能仅发生在身体活动水平较高的人群中。