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利用基因-环境交互作用分析阐明熟肉和杂环胺暴露在结直肠息肉发病机制中的作用。

Using gene-environment interaction analyses to clarify the role of well-done meat and heterocyclic amine exposure in the etiology of colorectal polyps.

机构信息

Division of Epidemiology, Department of Medicine, Vanderbilt Epidemiology Center, Vanderbilt University School of Medicine, Nashville, TN 37203, USA.

出版信息

Am J Clin Nutr. 2012 Nov;96(5):1119-28. doi: 10.3945/ajcn.112.040345. Epub 2012 Sep 26.

Abstract

BACKGROUND

The role of well-done meat intake and meat-derived mutagen heterocyclic amine (HCA) exposure in the risk of colorectal neoplasm has been suggested but not yet established.

OBJECTIVE

With the use of gene-environment interaction analyses, we sought to clarify the association of HCA exposure with colorectal polyp risk.

DESIGN

In a case-control study including 2057 colorectal polyp patients and 3329 controls, we evaluated 16 functional genetic variants to construct an HCA-metabolizing score. To derive dietary HCA-exposure amount, data were collected regarding dietary intake of meat by cooking method and degree of doneness.

RESULTS

A 2-fold elevated risk associated with high red meat intake was found for colorectal polyps or adenomas in subjects with a high HCA-metabolizing risk score, whereas the risk was 1.3- to 1.4-fold among those with a low risk score (P-interaction ≤ 0.05). The interaction was stronger for the risk of advanced or multiple adenomas, in which an OR of 2.8 (95% CI: 1.8, 4.6) was observed for those with both a high HCA-risk score and high red meat intake (P-interaction = 0.01). No statistically significant interaction was found in analyses that used specific HCA exposure derived from dietary data.

CONCLUSION

High red meat intake is associated with an elevated risk of colorectal polyps, and this association may be synergistically modified by genetic factors involved in HCA metabolism.

摘要

背景

有研究提示,彻底煮熟的肉类摄入和肉类衍生的致突变杂环胺(HCA)暴露与结直肠肿瘤的风险有关,但尚未得到证实。

目的

本研究采用基因-环境交互作用分析,旨在阐明 HCA 暴露与结直肠息肉风险之间的关联。

设计

在一项包括 2057 例结直肠息肉患者和 3329 例对照的病例对照研究中,我们评估了 16 个功能性遗传变异,以构建 HCA 代谢评分。为了评估饮食 HCA 暴露量,我们收集了有关不同烹饪方法和不同火候的肉类摄入量的数据。

结果

在 HCA 代谢风险评分较高的人群中,高红肉摄入量与结直肠息肉或腺瘤的风险呈 2 倍升高相关,而在风险评分较低的人群中,风险呈 1.3-1.4 倍升高(P 交互作用≤0.05)。在高级或多发性腺瘤风险中,这种交互作用更强,对于同时具有高 HCA 风险评分和高红肉摄入量的人群,OR 为 2.8(95%CI:1.8,4.6)(P 交互作用=0.01)。在使用来源于饮食数据的特定 HCA 暴露的分析中,未发现统计学意义上的交互作用。

结论

高红肉摄入与结直肠息肉的风险升高有关,这种关联可能与 HCA 代谢相关的遗传因素存在协同作用。

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