Nakao Makoto, Hosono Satoyo, Ito Hidemi, Watanabe Miki, Mizuno Nobumasa, Yatabe Yasushi, Yamao Kenji, Ueda Ryuzo, Tajima Kazuo, Tanaka Hideo, Matsuo Keitaro
Int J Mol Epidemiol Genet. 2011;2(4):354-66. Epub 2011 Nov 25.
Although several reports have described a possible association between insulin-like growth factors-1 (IGF-1) and pancreatic cancer (PC) risk, this association has not been evaluated in the non-Caucasian population. To assess the impact of IGF-1 polymorphisms on PC risk in Japanese, we conducted a case-control study which compared the frequency of ten single nucleotide polymorphisms (SNPs) and haplotypes of IGF-1. SNPs were investigated using the TaqMan method in 176 patients with PC and 1402 control subjects. Exposure to risk factors was assessed from the results of a self-administered questionnaire. Associations and gene-environment interactions were examined using an unconditional logistic regression model. We did not observe any significant main effect of IGF-1 loci, but did find interactions between rs5742714 and past and/or current body-mass index (BMI) status. Among patients with BMI > 25 at age 20, an increased PC risk was observed with the addition of the minor allele for rs5742714 (trend P = 0.048) and rs6214 (P = 0.043). Among patients with current BMI > 25, an increased or decreased PC risk was observed with the addition of the minor allele for rs5742714 (trend P = 0.046), rs4764887 (P = 0.031) and rs5742612 (P = 0.038). Haplotype analysis of IGF-1 showed a significant association among patients who were either or both previously or currently overweight. These findings suggest that IGF-1 polymorphisms may affect the development of PC in the Japanese population in combination with obesity. Further studies to confirm these findings are warranted.
尽管有几份报告描述了胰岛素样生长因子-1(IGF-1)与胰腺癌(PC)风险之间可能存在关联,但这种关联尚未在非白种人群中进行评估。为了评估IGF-1基因多态性对日本人群PC风险的影响,我们进行了一项病例对照研究,比较了IGF-1的十个单核苷酸多态性(SNP)和单倍型的频率。使用TaqMan方法对176例PC患者和1402例对照受试者进行了SNP检测。通过自我管理问卷的结果评估危险因素暴露情况。使用无条件逻辑回归模型检查关联和基因-环境相互作用。我们未观察到IGF-1基因座有任何显著的主要影响,但确实发现rs5742714与过去和/或当前体重指数(BMI)状态之间存在相互作用。在20岁时BMI>25的患者中,添加rs5742714(趋势P = 0.048)和rs6214(P = 0.043)的次要等位基因会观察到PC风险增加。在当前BMI>25的患者中,添加rs5742714(趋势P = 0.046)、rs4764887(P = 0.031)和rs5742612(P = 0.038)的次要等位基因会观察到PC风险增加或降低。IGF-1的单倍型分析显示,既往或当前超重或两者皆有的患者之间存在显著关联。这些发现表明,IGF-1基因多态性可能与肥胖共同影响日本人群中PC的发生。有必要进行进一步研究以证实这些发现。