Young K L, Graff M, North K E, Richardson A S, Bradfield J P, Grant S F A, Lange L A, Lange E M, Harris K M, Gordon-Larsen P
Department of Epidemiology, University of North Carolina, Chapel Hill, NC, USA.
Carolina Population Center, University of North Carolina, Chapel Hill, NC, USA.
Pediatr Obes. 2016 Apr;11(2):95-101. doi: 10.1111/ijpo.12026. Epub 2015 Apr 20.
Adolescent obesity is predictive of future weight gain, obesity and adult onset severe obesity (body mass index [BMI] ≥40 kg m(-2) ). Despite successful efforts to identify Single Nucleotide Polymorphisms (SNPs) influencing BMI, <5% of the 40-80% heritability of the phenotype has been explained. Identification of gene-gene (G-G) interactions between known variants can help explain this hidden heritability as well as identify potential biological mechanisms affecting weight gain during this critical developmental period.
We have recently shown distinct genetic effects on BMI across the life course, and thus it is important to examine the evidence for epistasis in adolescence.
In adolescent participants of European descent from wave II of the National Longitudinal Study of Adolescent Health (Add Health, n = 5072, ages 12-21, 52.5% female), we tested 34 established BMI-related SNPs for G-G interaction effects on BMI z-score. We used mixed-effects regression, assuming multiplicative interaction models adjusting for age, sex and geographic region, with random effects for family and school.
For 28 G-G interactions that were nominally significant (P < 0.05), we attempted to replicate our results in an adolescent sample from the Childhood European American Cohort from Philadelphia. In the replication study, one interaction (PRKD1-FTO) was significant after correction for multiple testing.
Our results are suggestive of epistatic effects on BMI during adolescence and point to potentially interactive effects between genes in biological pathways important in obesity.
青少年肥胖可预测未来体重增加、肥胖及成人期重度肥胖(体重指数[BMI]≥40kg/m²)。尽管已成功鉴定出影响BMI的单核苷酸多态性(SNP),但该表型40%-80%的遗传力中仅有不到5%得到解释。鉴定已知变异之间的基因-基因(G-G)相互作用有助于解释这种隐藏的遗传力,并识别在此关键发育阶段影响体重增加的潜在生物学机制。
我们最近发现了BMI在生命历程中的不同遗传效应,因此,研究青春期上位性的证据很重要。
在国家青少年健康纵向研究(Add Health)第二轮中,选取欧洲裔青少年参与者(n = 5072,年龄12-21岁,52.5%为女性),我们检测了34个已确定的与BMI相关的SNP对BMI z评分的G-G相互作用效应。我们采用混合效应回归,假设乘法相互作用模型,并对年龄、性别和地理区域进行校正,同时考虑家庭和学校的随机效应。
对于28个名义上显著(P < 0.05)的G-G相互作用,我们试图在费城儿童欧美队列的青少年样本中重复我们的结果。在重复研究中,经过多重检验校正后,一个相互作用(PRKD1-FTO)显著。
我们的结果提示青春期BMI存在上位效应,并指出肥胖相关重要生物学途径中基因之间可能存在的相互作用效应。