Human Genetics Center, University of Texas School of Public Health, Houston, TX 77225, USA.
Int J Obes (Lond). 2012 Jan;36(1):61-8. doi: 10.1038/ijo.2011.190. Epub 2011 Oct 11.
To investigate possible age-related changes in associations between polymorphisms in the fat mass and obesity-associated (FTO) gene and higher body mass index (BMI).
Multilevel mixed regression models were used to examine associations between four FTO variants and longitudinal BMI profiles in non-Hispanic white and African American children and adolescents 8-17 years of age from two different longitudinal cohort studies, the Bogalusa Heart Study (BHS) and Project HeartBeat! (PHB). In the BHS, there were 1551 examinations of 478 African Americans and 3210 examinations of 1081 non-Hispanic whites; in PHB, there were 971 examinations of 131 African Americans and 4458 examinations of 505 non-Hispanic whites.
In African Americans, no significant FTO associations with BMI were found. In non-Hispanic whites, linkage disequilibrium among all four variants made haplotype analysis superfluous, so we focused on the single-nucleotide polymorphism, rs9939609. In longitudinal multilevel models, the A/A genotype of rs9939609 was associated with higher BMI in non-Hispanic whites in both cohorts at all ages. A significant age-by-genotype interaction found only in the BHS cohort predicted that in those with the A/A genotype, BMI would be ∼0.7 kg m(-2) higher at age 8 and ∼1.6 kg m(-2) higher at age 17 than in those with A/T or T/T genotypes. The design of PHB limited follow-up of any single individual to 4 years, and may have reduced the ability to detect any age-by-genotype interaction in this cohort.
The A/A genotype of rs9939609 in the FTO gene is associated with higher longitudinal BMI profiles in non-Hispanic whites from two different cohorts. The association may change with age, with the A/A genotype being associated with a larger BMI difference in late adolescence than in childhood, though this was observed only in the BHS cohort and requires verification.
研究脂肪量和肥胖相关基因(FTO)基因多态性与较高体重指数(BMI)之间的关联是否存在与年龄相关的变化。
使用多层次混合回归模型,研究了来自两个不同纵向队列研究的非西班牙裔白人和非裔美国儿童和青少年(年龄 8-17 岁)中 FTO 四种变体与纵向 BMI 特征之间的关联。Bogalusa 心脏研究(BHS)中有 478 名非裔美国人的 1551 次检查和 1081 名非西班牙裔白人的 3210 次检查;在 Project HeartBeat!(PHB)中,有 131 名非裔美国人的 971 次检查和 505 名非西班牙裔白人的 4458 次检查。
在非裔美国人中,未发现 FTO 与 BMI 有显著关联。在非西班牙裔白人中,所有四种变体之间的连锁不平衡使得单体型分析变得多余,因此我们重点研究了单核苷酸多态性 rs9939609。在纵向多层次模型中,rs9939609 的 A/A 基因型与两个队列中所有年龄段的非西班牙裔白人群体的 BMI 呈正相关。仅在 BHS 队列中发现的显著年龄-基因型相互作用预测,在 A/A 基因型个体中,与 A/T 或 T/T 基因型个体相比,8 岁时 BMI 会高出约 0.7kg/m2,17 岁时 BMI 会高出约 1.6kg/m2。PHB 的设计限制了任何单个个体的随访时间为 4 年,这可能降低了在该队列中检测任何年龄-基因型相互作用的能力。
FTO 基因中 rs9939609 的 A/A 基因型与两个不同队列的非西班牙裔白人群体的纵向 BMI 特征呈正相关。这种关联可能随年龄而变化,A/A 基因型与青春期后期的 BMI 差异较大,而不是儿童期,尽管这仅在 BHS 队列中观察到,需要进一步验证。