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Dietary inflammatory index and inflammatory gene interactions in relation to colorectal cancer risk in the Bellvitge colorectal cancer case-control study.

机译:在Bellvitge大肠癌病例对照研究中,与大肠癌风险相关的饮食炎症指数和炎症基因相互作用。

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摘要

Chronic inflammation is an important factor in colorectal carcinogenesis. However, evidence on the effect of pro-inflammatory and anti-inflammatory foods and nutrients is scarce. Moreover, there are few studies focusing on diet–gene interactions on inflammation and colorectal cancer (CRC). This study was designed to investigate the association between the novel dietary inflammatory index (DII) and CRC and its potential interaction with polymorphisms in inflammatory genes. Data from the Bellvitge Colorectal Cancer Study, a case–control study (424 cases with incident colorectal cancer and 401 hospital-based controls), were used. The DII score for each participant was obtained by multiplying intakes of dietary components from a validated dietary history questionnaire by literature-based dietary inflammatory weights that reflected the inflammatory potential of components. Data from four important single nucleotide polymorphisms located in genes thought to be important in inflammation-associated CRC: i.e., interleukin (IL)-4, IL-6, IL-8, and peroxisome proliferator-activated receptor-γ (PPARG) were analyzed. A direct association was observed between DII score and CRC risk (ORQ4 vs. Q1 1.65, 95 % CI 1.05–2.60, and P trend 0.011). A stronger association was found with colon cancer risk (ORQ4 vs. Q1 2.24, 95 % CI 1.33–3.77, and P trend 0.002) than rectal cancer risk (ORQ4 vs. Q1 1.12, 95 % CI 0.61–2.06, and P trend 0.37). DII score was inversely correlated with SNP rs2243250 in IL-4 among controls, and an interaction was observed with CRC risk. Neither correlation nor interaction was detected for other inflammatory genes. Overall, high-DII diets are associated with increased risk of CRC, particularly for colon cancer, suggesting that dietary-mediated inflammation plays an important role in colorectal carcinogenesis.
机译:慢性炎症是结直肠癌发生的重要因素。但是,缺乏关于促炎和消炎食物及营养作用的证据。此外,很少有研究关注饮食与基因之间在炎症和大肠癌(CRC)方面的相互作用。这项研究旨在调查新型饮食炎症指数(DII)与CRC之间的关联以及其与炎症基因多态性之间的潜在相互作用。使用了病例对照研究Bellvitge结肠直肠癌研究(424例结直肠癌事件和401名基于医院的对照)的数据。每个参与者的DII得分是通过将经过验证的饮食史调查问卷中的饮食成分摄入量乘以反映饮食成分潜在炎症性的文献资料得出的饮食炎症权重得出的。分析了来自四个重要单核苷酸多态性的数据,这些基因位于与炎症相关的CRC重要的基因中:即白介素(IL)-4,IL-6,IL-8和过氧化物酶体增殖物激活受体-γ(PPARG) 。 DII评分与CRC风险之间存在直接关联(ORQ4与Q1的比值为1.65、95%CI为1.05-2.60,P趋势为0.011)。发现与直肠癌风险(ORQ4与Q1 1.12、95%CI 0.61–2.06和P趋势0.37相比,与结肠癌风险(ORQ4与Q1 2.24、95%CI 1.33–3.77和P趋势0.002)的关联更强)。在对照组中,DII评分与IL-4中SNP rs2243250呈负相关,并且观察到与CRC风险的相互作用。其他炎症基因均未发现相关性或相互作用。总的来说,高DII饮食与CRC风险增加相关,特别是对于结肠癌,这表明饮食介导的炎症在结直肠癌的发生中起重要作用。

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