Department of Oncologic Pathology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts; Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, Massachusetts; Department of Epidemiology and Biostatistics, Ministry of Education Key Lab of Environment and Health, School of Public Health, Huazhong University of Science and Technology, Wuhan, People's Republic of China.
Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, Massachusetts; Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
Clin Gastroenterol Hepatol. 2018 Oct;16(10):1622-1631.e3. doi: 10.1016/j.cgh.2018.04.030. Epub 2018 Apr 24.
BACKGROUND & AIMS: Specific nutritional components are likely to induce intestinal inflammation, which is characterized by increased levels of interleukin 6 (IL6), C-reactive protein (CRP), and tumor necrosis factor-receptor superfamily member 1B (TNFRSF1B) in the circulation and promotes colorectal carcinogenesis. The inflammatory effects of a diet can be estimated based on an empiric dietary inflammatory pattern (EDIP) score, calculated based on intake of 18 foods associated with plasma levels of IL6, CRP, and TNFRSF1B. An inflammatory environment in the colon (based on increased levels of IL6, CRP, and TNFRSF1B in peripheral blood) contributes to impairment of the mucosal barrier and altered immune cell responses, affecting the composition of the intestinal microbiota. Colonization by Fusobacterium nucleatum has been associated with the presence and features of colorectal adenocarcinoma. We investigated the association between diets that promote inflammation (based on EDIP score) and colorectal cancer subtypes classified by level of F nucleatum in the tumor microenvironment.
We calculated EDIP scores based on answers to food frequency questionnaires collected from participants in the Nurses' Health Study (through June 1, 2012) and the Health Professionals Follow-up Study (through January 31, 2012). Participants in both cohorts reported diagnoses of rectal or colon cancer in biennial questionnaires; deaths from unreported colorectal cancer cases were identified through the National Death Index and next of kin. Colorectal tumor tissues were collected from hospitals where the patients underwent tumor resection and F nucleatum DNA was quantified by a polymerase chain reaction assay. We used multivariable duplication-method Cox proportional hazard regression to assess the associations of EDIP scores with risks of colorectal cancer subclassified by F nucleatum status.
During 28 years of follow-up evaluation of 124,433 participants, we documented 951 incident cases of colorectal carcinoma with tissue F nucleatum data. Higher EDIP scores were associated with increased risk of F nucleatum-positive colorectal tumors (P = .03); for subjects in the highest vs lowest EDIP score tertiles, the hazard ratio for F nucleatum-positive colorectal tumors was 1.63 (95% CI, 1.03-2.58). EDIP scores did not associate with F nucleatum-negative tumors (P = .44). High EDIP scores associated with proximal F nucleatum-positive colorectal tumors but not with proximal F nucleatum-negative colorectal tumors (P = .003).
Diets that may promote intestinal inflammation, based on EDIP score, are associated with increased risk of F nucleatum-positive colorectal carcinomas, but not carcinomas that do not contain these bacteria. These findings indicate that diet-induced intestinal inflammation alters the gut microbiome to contribute to colorectal carcinogenesis; nutritional interventions might be used in precision medicine and cancer prevention.
特定的营养成分可能会引发肠道炎症,其特征是循环中白细胞介素 6(IL6)、C 反应蛋白(CRP)和肿瘤坏死因子受体超家族成员 1B(TNFRSF1B)水平升高,并促进结直肠癌的发生。饮食的炎症作用可以根据经验性饮食炎症模式(EDIP)评分来估计,该评分是基于与 IL6、CRP 和 TNFRSF1B 血浆水平相关的 18 种食物的摄入量计算得出的。结肠中的炎症环境(基于外周血中 IL6、CRP 和 TNFRSF1B 水平升高)导致黏膜屏障受损和免疫细胞反应改变,影响肠道微生物组的组成。具核梭杆菌的定植与结直肠腺癌的存在和特征有关。我们研究了基于 EDIP 评分的促炎饮食(根据肿瘤微环境中 F 核梭杆菌的水平分类)与结直肠癌亚型之间的关联。
我们根据参加护士健康研究(截至 2012 年 6 月 1 日)和健康专业人员随访研究(截至 2012 年 1 月 31 日)的参与者的食物频率问卷计算 EDIP 评分。两组参与者均在两年一次的问卷中报告了直肠或结肠癌的诊断;通过国家死亡指数和近亲识别未报告的结直肠癌病例的死亡情况。从接受肿瘤切除术的医院采集结直肠肿瘤组织,并通过聚合酶链反应检测 F 核梭杆菌 DNA。我们使用多变量重复法 Cox 比例风险回归来评估 EDIP 评分与结直肠癌亚组(根据 F 核梭杆菌状态分类)风险的关联。
在对 124433 名参与者进行 28 年的随访评估期间,我们记录了 951 例结直肠癌的发病情况,其中有组织 F 核梭杆菌数据。较高的 EDIP 评分与 F 核梭杆菌阳性结直肠肿瘤的风险增加相关(P=0.03);在 EDIP 评分最高和最低三分位数的受试者中,F 核梭杆菌阳性结直肠肿瘤的风险比为 1.63(95%CI,1.03-2.58)。EDIP 评分与 F 核梭杆菌阴性肿瘤无关(P=0.44)。高 EDIP 评分与 F 核梭杆菌阳性结直肠近端肿瘤相关,但与 F 核梭杆菌阴性结直肠近端肿瘤无关(P=0.003)。
基于 EDIP 评分的可能促进肠道炎症的饮食与 F 核梭杆菌阳性结直肠癌的风险增加相关,但与不包含这些细菌的结直肠癌无关。这些发现表明,饮食诱导的肠道炎症改变了肠道微生物组,从而促进了结直肠癌的发生;营养干预可能用于精准医学和癌症预防。