Public Health Sciences Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, PO Box 19024, Seattle, WA 98109-1024, USA.
Cancer Epidemiol Biomarkers Prev. 2010 Jan;19(1):74-9. doi: 10.1158/1055-9965.EPI-09-0663.
The Women's Health Initiative dietary modification (DM) trial provided suggestive evidence of a benefit of a low-fat dietary pattern on breast cancer risk, with stronger evidence among women whose baseline diet was high in fat. Single nucleotide polymorphisms (SNP) in the FGFR2 gene relate strongly to breast cancer risk and could influence intervention effects.
All 48,835 trial participants were postmenopausal and ages 50 to 79 years at enrollment (1993-1998). We interrogated eight SNPs in intron 2 of the FGFR2 gene for 1,676 women who developed breast cancer during trial follow-up (1993-2005). Case-only analyses were used to estimate odds ratios for the DM intervention in relation to SNP genotype.
Odds ratios for the DM intervention did not vary significantly with the genotype for any of the eight FGFR2 SNPs (P > or = 0.18). However, odds ratios varied (P < 0.05) with the genotype of six of these SNPs, among women having baseline percent of energy from fat in the upper quartile (> or =36.8%). This variation is most evident for SNP rs3750817, with odds ratios for the DM intervention at 0, 1, and 2 minor SNP alleles of 1.06 [95% confidence intervals (95% CI), 0.80-1.41], 0.53 (95% CI, 0.38-0.74), and 0.62 (95% CI, 0.33-1.15). The nominal significance level for this interaction is P = 0.005, and P = 0.03 following multiple testing adjustment, with most evidence deriving from hormone receptor-positive tumors.
Invasive breast cancer odds ratios for a low-fat dietary pattern, among women whose usual diets are high in fat, seem to vary with SNP rs3750817 in the FGFR2 gene.
妇女健康倡议饮食干预试验(DM)提供了低脂肪饮食模式对乳腺癌风险有益的提示性证据,在基线饮食中脂肪含量较高的女性中证据更强。成纤维细胞生长因子受体 2(FGFR2)基因的单核苷酸多态性(SNP)与乳腺癌风险密切相关,并可能影响干预效果。
所有 48835 名试验参与者均为绝经后妇女,入组时年龄为 50-79 岁(1993-1998 年)。我们对 FGFR2 基因内含子 2 中的 8 个 SNP 进行了检测,共纳入 1676 名在试验随访期间(1993-2005 年)发生乳腺癌的女性。仅进行病例分析以估计 DM 干预与 SNP 基因型之间的比值比。
对于 FGFR2 的 8 个 SNP 中的任何一个,DM 干预的比值比与基因型之间没有显著差异(P > 0.18)。然而,在基线脂肪百分比处于四分位位(> 0.368%)的女性中,这 6 个 SNP 中的 6 个 SNP 的基因型发生了变化(P < 0.05)。这种变化在 SNP rs3750817 中最为明显,DM 干预的比值比在 0、1 和 2 个 SNP 等位基因中分别为 1.06(95%CI,0.80-1.41)、0.53(95%CI,0.38-0.74)和 0.62(95%CI,0.33-1.15)。这种交互作用的名义显著性水平为 P = 0.005,经过多次检验调整后为 P = 0.03,主要证据来源于激素受体阳性肿瘤。
在脂肪摄入量较高的女性中,低脂肪饮食模式与 FGFR2 基因中 SNP rs3750817 相关的浸润性乳腺癌比值比似乎有所不同。