The School of Public Health, Sun Yat-Sen University, Guangzhou, China.
PLoS One. 2012;7(5):e37275. doi: 10.1371/journal.pone.0037275. Epub 2012 May 18.
There is an inverse relationship between febrile infection and the risk of malignancies. Interferon gamma (IFN-γ) plays an important role in fever induction and its expression increases with incubation at fever-range temperatures. Therefore, the genetic polymorphism of IFN-γ may modify the association of febrile infection with breast cancer risk.
Information on potential breast cancer risk factors, history of fever during the last 10 years, and blood specimens were collected from 839 incident breast cancer cases and 863 age-matched controls between October 2008 and June 2010 in Guangzhou, China. IFN-γ (rs2069705) was genotyped using a matrix-assisted laser desorption/ionization time-of-flight mass spectrometry platform. Odds ratios (OR) and 95% confidence intervals (CIs) were calculated using multivariate logistic regression. We found that women who had experienced ≥1 fever per year had a decreased risk of breast cancer [ORs and 95% CI: 0.77 (0.61-0.99)] compared to those with less than one fever a year. This association only occurred in women with CT/TT genotypes [0.54 (0.37-0.77)] but not in those with the CC genotype [1.09 (0.77-1.55)]. The association of IFN-γ rs2069705 with the risk of breast cancer was not significant among all participants, while the CT/TT genotypes were significantly related to an elevated risk of breast cancer [1.32 (1.03-1.70)] among the women with <1 fever per year and to a reduced risk of breast cancer [0.63 (0.40-0.99)] among women with ≥1 fever per year compared to the CC genotype. A marked interaction between fever frequencies and the IFN-γ genotypes was observed (P for multiplicative and additive interactions were 0.005 and 0.058, respectively).
Our findings indicate a possible link between febrile acute infection and a decreased risk of breast cancer, and this association was modified by IFN-γ rs2069705.
发热感染与恶性肿瘤风险呈负相关。干扰素γ(IFN-γ)在发热诱导中起重要作用,其表达随发热温度的升高而增加。因此,IFN-γ的遗传多态性可能会改变发热感染与乳腺癌风险之间的关联。
2008 年 10 月至 2010 年 6 月,在中国广州,收集了 839 例乳腺癌病例和 863 例年龄匹配的对照者的潜在乳腺癌危险因素、过去 10 年发热史以及血样信息。采用基质辅助激光解吸电离飞行时间质谱平台对 IFN-γ(rs2069705)进行基因分型。使用多变量逻辑回归计算比值比(OR)和 95%置信区间(CI)。我们发现,与每年发热次数少于一次的女性相比,每年发热次数≥1 次的女性患乳腺癌的风险降低(ORs 和 95%CI:0.77(0.61-0.99))。这种关联仅发生在 CT/TT 基因型的女性中[0.54(0.37-0.77)],而在 CC 基因型的女性中则没有[1.09(0.77-1.55)]。IFN-γ rs2069705 与乳腺癌风险的相关性在所有参与者中均不显著,而 CT/TT 基因型与每年发热次数<1 次的女性乳腺癌风险升高相关[1.32(1.03-1.70)],与每年发热次数≥1 次的女性乳腺癌风险降低相关[0.63(0.40-0.99)],与 CC 基因型相比。发热频率与 IFN-γ 基因型之间存在显著的交互作用(乘法和加法交互作用的 P 值分别为 0.005 和 0.058)。
我们的研究结果表明,发热急性感染与乳腺癌风险降低之间可能存在关联,这种关联受 IFN-γ rs2069705 的影响。