Grant Struan F A, Bradfield Jonathan P, Zhang Haitao, Wang Kai, Kim Cecilia E, Annaiah Kiran, Santa Erin, Glessner Joseph T, Thomas Kelly, Garris Maria, Frackelton Edward C, Otieno F George, Shaner Julie L, Smith Ryan M, Imielinski Marcin, Chiavacci Rosetta M, Li Mingyao, Berkowitz Robert I, Hakonarson Hakon
Center for Applied Genomics, Abramson Research Center, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Obesity (Silver Spring). 2009 Jul;17(7):1461-5. doi: 10.1038/oby.2009.53. Epub 2009 Mar 5.
Recently a modest, but consistently, replicated association was demonstrated between obesity and the single-nucleotide polymorphism (SNP), rs17782313, 3' of the MC4R locus as a consequence of a meta-analysis of genome-wide association (GWA) studies of the disease in white populations. We investigated the association in the context of the childhood form of the disease utilizing data from our ongoing GWA study in a cohort of 728 European-American (EA) obese children (BMI > or =95th percentile) and 3,960 EA controls (BMI <95th percentile), as well as 1,008 African-American (AA) obese children and 2,715 AA controls. rs571312, rs10871777, and rs476828 (perfect surrogates for rs17782313) yielded odds ratios in the EA cohort of 1.142 (P = 0.045), 1.137 (P = 0.054), and 1.145 (P = 0.042); however, there was no significant association with these SNPs in the AA cohort. When investigating all 30 SNPs present on the Illumina BeadChip at this locus, again there was no evidence for association in AA cases when correcting for the number of tests employed. As such, variants 3' to the MC4R locus present on the genotyping platform utilized confer a similar magnitude of risk of obesity in white children as to their adult white counterparts but this observation did not extend to AAs.
最近,通过对白人人群中该疾病的全基因组关联(GWA)研究进行荟萃分析,发现肥胖与黑皮质素4受体(MC4R)基因座3'端的单核苷酸多态性(SNP)rs17782313之间存在适度但一致的重复关联。我们利用正在进行的GWA研究数据,在该疾病的儿童形式背景下进行了调查,该研究涉及728名欧美(EA)肥胖儿童(BMI≥第95百分位数)和3960名EA对照(BMI<第95百分位数),以及1008名非裔美国(AA)肥胖儿童和2715名AA对照。rs571312、rs10871777和rs476828(rs17782313的完美替代物)在EA队列中的优势比分别为1.142(P = 0.045)、1.137(P = 0.054)和1.145(P = 0.042);然而,在AA队列中,这些SNP与疾病无显著关联。在研究该基因座Illumina BeadChip上存在的所有30个SNP时,在对所采用的检测数量进行校正后,同样没有证据表明AA病例存在关联。因此,在白人儿童中,基因分型平台上MC4R基因座3'端的变体所带来的肥胖风险程度与其成年白人对应者相似,但这一观察结果不适用于非裔美国人。