Kilpeläinen Tuomas O, Bingham Sheila A, Khaw Kay-Tee, Wareham Nicholas J, Loos Ruth J F
MRC Epidemiology Unit, Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, UK.
Hum Mol Genet. 2009 Sep 15;18(18):3496-501. doi: 10.1093/hmg/ddp280. Epub 2009 Jun 15.
Recently, the rs6232 (N221D) and rs6235 (S690T) SNPs in the PCSK1 gene were associated with obesity in a meta-analysis comprising more than 13 000 individuals of European ancestry. Each additional minor allele of rs6232 or rs6235 was associated with a 1.34- or 1.22-fold increase in the risk of obesity, respectively. So far, only one relatively small study has aimed to replicate these findings, but could not confirm the association of the rs6235 SNP and did not study the rs6232 variant. In the present study, we examined the associations of the rs6232 and rs6235 SNPs with obesity in a population-based cohort consisting of 20 249 individuals of European descent from Norfolk, UK. Logistic regression and generalized linear models were used to test the associations of the risk alleles with obesity and related quantitative traits, respectively. Neither of the SNPs was significantly associated with obesity, BMI or waist circumference under the additive genetic model (P > 0.05). However, we observed an interaction between rs6232 and age on the level of BMI (P = 0.010) and risk of obesity (P = 0.020). The rs6232 SNP was associated with BMI (P = 0.021) and obesity (P = 0.022) in the younger individuals [less than median age (59 years)], but not among the older age group (P = 0.81 and P = 0.68 for BMI and obesity, respectively). In conclusion, our data suggest that the PCSK1 rs6232 and rs6235 SNPs are not major contributors to common obesity in the general population. However, the effect of rs6232 may be age-dependent.
最近,在一项纳入了超过13000名欧洲血统个体的荟萃分析中,前蛋白转化酶枯草溶菌素1(PCSK1)基因中的rs6232(N221D)和rs6235(S690T)单核苷酸多态性(SNP)与肥胖相关。rs6232或rs6235的每一个额外的次要等位基因分别与肥胖风险增加1.34倍或1.22倍相关。到目前为止,仅有一项相对较小的研究旨在重复这些发现,但未能证实rs6235 SNP的相关性,且未研究rs6232变异。在本研究中,我们在一个基于人群的队列中检测了rs6232和rs6235 SNP与肥胖的相关性,该队列由来自英国诺福克的20249名欧洲血统个体组成。分别使用逻辑回归和广义线性模型来检验风险等位基因与肥胖及相关定量性状的相关性。在加性遗传模型下,这两个SNP均与肥胖、体重指数(BMI)或腰围无显著相关性(P>0.05)。然而,我们观察到rs6232与年龄在BMI水平(P = 0.010)和肥胖风险(P = 0.020)上存在相互作用。rs6232 SNP在较年轻个体[年龄小于中位数(59岁)]中与BMI(P = 0.021)和肥胖(P = 0.022)相关,但在较年长组中无相关性(BMI和肥胖的P值分别为0.81和0.68)。总之,我们的数据表明,PCSK1基因的rs6232和rs6235 SNP不是普通人群中常见肥胖的主要影响因素。然而,rs6232的作用可能与年龄有关。