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Interactions between the FTO rs9939609 polymorphism body mass index and lifestyle-related factors on metabolic syndrome risk

机译:FTO rs9939609基因多态性体重指数和生活方式相关因素与代谢综合征风险之间的相互作用

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摘要

Whether the FTO polymorphisms interact with environmental factors has not yet been evaluated in associations with metabolic syndrome (MS) risk. The present study investigated the association of the FTO rs9939609 genotypes, body mass index (BMI), and lifestyle-related factors including smoking, alcohol drinking, physical activity, and diet with MS incidence. A population-based prospective cohort study comprised 3,504 male and female Koreans aged 40 to 69 years. At the beginning of the study, all individuals were free of MS and known cardiovascular disease. Incident cases of MS were identified by biennial health examinations during a follow-up period from April 17, 2003 to April 15, 2009. Pooled logistic regression analysis was applied to obtain relative odds (RO) of MS with its 95% confidence interval (CI). After controlling for potential MS risk factors, we observed no association between the rs9939609 genotypes and MS incidence. In analysis stratified by BMI, however, carriers with the FTO risk allele whose BMI is 29 kg/m2 or greater showed an approximately 6-fold higher RO (95% CI: 3.82 to 9.30) compared with non-carriers with BMI less than 25 kg/m2. In particular, the association between the rs9939609 variants and MS risk was significantly modified by high BMI (P-value for interaction < 0.05). Such significant interaction appeared in associations with central obesity and high blood pressure among the MS components. Because carriers of the FTO risk alleles who had BMI of 29 kg/m2 or greater are considered a high risk population, we suggest that they may need intensive weight loss regimens to prevent MS development.
机译:FTO多态性是否与环境因素相互作用尚未与代谢综合征(MS)风险相关联的评估。本研究调查了FTO rs9939609基因型,体重指数(BMI)和与生活方式相关的因素(包括吸烟,饮酒,体育锻炼和饮食)与MS发病率的关联。一项基于人群的前瞻性队列研究包括3,504名年龄在40至69岁之间的韩国男性和女性。在研究开始时,所有个体均无MS和已知的心血管疾病。在2003年4月17日至2009年4月15日的随访期间,通过两年一次的健康检查确定了MS的事件病例。采用汇总Logistic回归分析以95%的置信区间(CI)获得MS的相对几率(RO)。 )。在控制了潜在的MS危险因素后,我们观察到rs9939609基因型与MS发生率之间没有关联。但是,在按BMI进行分层的分析中,与BMI为29 kg / m 2 或更高的FTO风险等位基因携带者相比,RO大约高出6倍(95%CI:3.82至9.30)。 BMI小于25 kg / m 2 的非承运人。特别是,rs9939609变体与MS风险之间的关联因BMI高而显着改变(相互作用的P值<0.05)。这种显着的相互作用与中枢性肥胖和MS成分之间的高血压有关。由于FTO风险携带者的BMI为29 kg / m 2 或更高的等位基因被认为是高风险人群,因此我们建议他们可能需要强化减肥方案来预防MS的发展。

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