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Risk of colon cancer in hereditary non-polyposis colorectal cancer patients as predicted by fuzzy modeling: Influence of smoking

机译:通过模糊模型预测的遗传性非息肉病性结直肠癌患者的结肠癌风险:吸烟的影响

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摘要

AIM: To investigate whether a fuzzy logic model could predict colorectal cancer (CRC) risk engendered by smoking in hereditary non-polyposis colorectal cancer (HNPCC) patients.METHODS: Three hundred and forty HNPCC mismatch repair (MMR) mutation carriers from the Creighton University Hereditary Cancer Institute Registry were selected for modeling. Age-dependent curves were generated to elucidate the joint effects between gene mutation (hMLH1 or hMSH2), gender, and smoking status on the probability of developing CRC.RESULTS: Smoking significantly increased CRC risk in male hMSH2 mutation carriers (P < 0.05). hMLH1 mutations augmented CRC risk relative to hMSH2 mutation carriers for males (P < 0.05). Males had a significantly higher risk of CRC than females for hMLH1 non smokers (P < 0.05), hMLH1 smokers (P < 0.1) and hMSH2 smokers (P < 0.1). Smoking promoted CRC in a dose-dependent manner in hMSH2 in males (P < 0.05). Females with hMSH2 mutations and both sexes with the hMLH1 groups only demonstrated a smoking effect after an extensive smoking history (P < 0.05).CONCLUSION: CRC promotion by smoking in HNPCC patients is dependent on gene mutation, gender and age. These data demonstrate that fuzzy modeling may enable formulation of clinical risk scores, thereby allowing individualization of CRC prevention strategies.
机译:目的:探讨模糊逻辑模型是否可以预测遗传性非息肉病性结肠直肠癌(HNPCC)患者吸烟引起的结肠直肠癌(CRC)风险。方法:来自Creighton大学的三百四十个HNPCC错配修复(MMR)突变携带者选择遗传性癌症研究所注册处进行建模。生成了年龄依赖性曲线,以阐明基因突变(hMLH1或hMSH2),性别和吸烟状况对CRC发生概率的联合影响。结果:吸烟显着增加了男性hMSH2突变携带者的CRC风险(P <0.05)。相对于hMSH2突变携带者,男性的hMLH1突变增加了CRC风险(P <0.05)。对于不吸烟的hMLH1(P <0.05),不吸烟的hMLH1(P <0.1)和hMSH2的吸烟者(P <0.1),男性患CRC的风险明显高于女性。吸烟在男性hMSH2中以剂量依赖性方式促进CRC(P <0.05)。具有hMSH2突变的女性和具有hMLH1组的男女仅在广泛的吸烟史后才显示吸烟效果(P <0.05)。结论:HNPCC患者通过吸烟促进CRC取决于基因突变,性别和年龄。这些数据表明,模糊建模可以实现临床风险评分的制定,从而实现CRC预防策略的个性化。

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