Wilk J B, Laramie J M, Latourelle J C, Williamson S, Nagle M W, Tobin J E, Foster C L, Eckfeldt J H, Province M A, Borecki I B, Myers R H
Department of Neurology, Boston University School of Medicine, Boston, MA 02118, USA.
Int J Obes (Lond). 2008 Jun;32(6):930-5. doi: 10.1038/ijo.2008.23. Epub 2008 Mar 4.
The NHLBI Family Heart Study (FHS) genome-wide linkage scan identified a region of chromosome 7q with a logarithm of odds score of 4.9 for body mass index (BMI).
We report the results of fine mapping the linkage peak using 1020 single nucleotide polymorphisms (SNPs) to test for association to obesity in families exhibiting linkage to chromosome 7. Association observed in linked families (284 obese cases/381 controls) was examined in an independent set of unrelated FHS participants (172 obese cases/308 controls) to validate the observed association. Two dichotomous obesity phenotypes were studied based on clinical BMI cutoffs and the sex-specific distribution of both BMI and leptin levels.
Using a P-value of 0.01 as criteria for association in the linked families, a P-value of 0.05 as criteria for association in the unrelated sample, and requiring consistency in the direction of the effect of the minor allele between the two samples, we identified two coding SNPs in the NYD-SP18 gene with minor alleles increasing the risk of obesity. Adjustment for exercise, smoking and FTO genotype did not influence the result in linked families, but improved the result in the unrelated sample. Carrying a minor allele of the nonsynonymous SNP rs6971091 conferred an odds ratio of at least 2 for obesity defined by both BMI and leptin levels.
The effect of the NYD-SP18 SNP on obesity was larger than the effect of FTO in FHS families. Publicly available results from genome-wide association studies support the association between NYD-SP18 and BMI. The NYD-SP18 gene is described as testes development related, but little is known about the gene's function or the mechanism by which it may influence risk for obesity.
美国国立心肺血液研究所(NHLBI)的家族心脏研究(FHS)全基因组连锁扫描发现,7号染色体q区域与体重指数(BMI)的对数优势比分数为4.9。
我们报告了使用1020个单核苷酸多态性(SNP)对连锁峰进行精细定位的结果,以测试与7号染色体连锁的家族中肥胖的关联性。在一组独立的非相关FHS参与者(172例肥胖病例/308例对照)中检查在连锁家族(284例肥胖病例/381例对照)中观察到的关联性,以验证观察到的关联。基于临床BMI临界值以及BMI和瘦素水平的性别特异性分布,研究了两种二分肥胖表型。
以连锁家族中P值为0.01作为关联标准,非相关样本中P值为0.05作为关联标准,并要求两个样本中次要等位基因的效应方向一致,我们在NYD-SP18基因中鉴定出两个编码SNP,其次要等位基因增加了肥胖风险。对运动、吸烟和FTO基因型进行调整,在连锁家族中不影响结果,但在非相关样本中改善了结果。携带非同义SNP rs6971091的次要等位基因,对于由BMI和瘦素水平定义的肥胖,优势比至少为2。
在FHS家族中,NYD-SP18 SNP对肥胖的影响大于FTO。全基因组关联研究的公开结果支持NYD-SP18与BMI之间的关联。NYD-SP18基因被描述为与睾丸发育相关,但对该基因的功能或其可能影响肥胖风险的机制知之甚少。