Infection and Cancer Epidemiology, Division of Molecular Diagnostics of Oncogenic Infections, German Cancer Research Center, Heidelberg, Germany; Cancer Control and Population Sciences Program, Duke Cancer Institute, and Department of Population Health Sciences, Duke University, Durham, North Carolina.
University of North Carolina at Chapel Hill, Department of Epidemiology, Gillings School for Global Public Health and Lineberger Comprehensive Cancer Center, Chapel Hill, North Carolina.
Gastroenterology. 2019 Jan;156(1):175-186.e2. doi: 10.1053/j.gastro.2018.09.054. Epub 2018 Oct 6.
BACKGROUND & AIMS: Previous studies reported an association of the bacteria Helicobacter pylori, the primary cause of gastric cancer, and risk of colorectal cancer (CRC). However, these findings have been inconsistent, appear to vary with population characteristics, and may be specific for virulence factor VacA. To more thoroughly evaluate the potential association of H pylori antibodies with CRC risk, we assembled a large consortium of cohorts representing diverse populations in the United States.
We used H pylori multiplex serologic assays to analyze serum samples from 4063 incident cases of CRC, collected before diagnosis, and 4063 matched individuals without CRC (controls) from 10 prospective cohorts for antibody responses to 13 H pylori proteins, including virulence factors VacA and CagA. The association of seropositivity to H pylori proteins, as well as protein-specific antibody level, with odds of CRC was determined by conditional logistic regression.
Overall, 40% of controls and 41% of cases were H pylori-seropositive (odds ratio [OR], 1.09; 95% CI, 0.99-1.20). H pylori VacA-specific seropositivity was associated with an 11% increased odds of CRC (OR, 1.11; 95% CI, 1.01-1.22), and this association was particularly strong among African Americans (OR, 1.45; 95% CI, 1.08-1.95). Additionally, odds of CRC increased with level of VacA antibody in the overall cohort (P = .008) and specifically among African Americans (P = .007).
In an analysis of a large consortium of cohorts representing diverse populations, we found serologic responses to H pylori VacA to associate with increased risk of CRC risk, particularly for African Americans. Future studies should seek to understand whether this marker is related to virulent H pylori strains carried in these populations.
先前的研究报告称,胃癌的主要病因幽门螺杆菌(H. pylori)与结直肠癌(CRC)风险之间存在关联。然而,这些发现并不一致,似乎因人群特征而异,并且可能特定于毒力因子 VacA。为了更彻底地评估 H. pylori 抗体与 CRC 风险之间的潜在关联,我们组建了一个由代表美国不同人群的大型队列组成的联盟。
我们使用 H. pylori 多重血清学检测方法,对来自 10 个前瞻性队列的 4063 例 CRC 新发病例(诊断前采集的血清样本)和 4063 名无 CRC 的匹配个体(对照组)进行分析,以检测针对 13 种 H. pylori 蛋白的抗体反应,包括毒力因子 VacA 和 CagA。通过条件逻辑回归确定 H. pylori 蛋白血清阳性与 CRC 比值比(OR)的关联,以及蛋白特异性抗体水平与 CRC 的关联。
总体而言,对照组中有 40%和病例组中有 41%的个体 H. pylori 血清阳性(OR,1.09;95%CI,0.99-1.20)。H. pylori VacA 特异性血清阳性与 CRC 风险增加 11%相关(OR,1.11;95%CI,1.01-1.22),这种关联在非裔美国人中尤为强烈(OR,1.45;95%CI,1.08-1.95)。此外,在整个队列中,随着 VacA 抗体水平的升高,CRC 的发病几率也会增加(P =.008),在非裔美国人中尤为明显(P =.007)。
在对代表不同人群的大型队列联盟进行分析时,我们发现针对 H. pylori VacA 的血清反应与 CRC 风险增加相关,尤其是在非裔美国人中。未来的研究应努力了解该标志物是否与这些人群中携带的毒力 H. pylori 菌株有关。