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MTHFR gene polymorphisms as risk factors for colorectal cancer among Egyptian patients

机译:MTHFR基因多态性是埃及患者大肠癌的危险因素

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Objective: Polymorphisms in methylenetetrahydrofolate reductase (MTHFR), such as MTHFR C677T and A1298C, are associated with several cancers. This study aimed to evaluate the effects of MTHFR polymorphisms on colorectal cancer risk in a population from damitta Egypt. Methods . This hospital-based case-control study was conducted during 2008-2010; 64 colon cancer cases and 90 controls were enrolled. Information was collected and blood samples were obtained for assay of MTHFR C677T and A1298C polymorphisms by polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) and PCR-restriction fragment length polymorphism (PCR-RFLP) techniques. Associations between variables of interest and colorectal cancer were assessed using conditional logistic regression. Results: Increased risk of colorectal cancer was associated with the MTHFR C677 TT genotype of C677T polymorphism (OR(adj) = 24.0; 95% CI: 1.34-429.1; P value for interaction = 0.001) . The 1298AC genotype and C allele was associated with a statistically significant lower risk among subjects (OR, 3.85; 95% CI, 1.78-8.33; P value for interaction=.0005 and OR,1.88 ;95% CI, 1.16-3.059 P value for interaction=0.01), respectively. MTHFR 1298 AA genotype and A allele was found to be associated with a significantly decreased risk for colorectal cancer (OR = 0.25, 95% CI 0.11- 0.52; P value for interaction= 0.0005 and OR = 0.52, 95% CI 0.32-0.85 P value for interaction= 0.01and ), respectively . There was no clear relation between colorectal adenomas and those with the 1298 CC genotype. The combined CC , AA [corrected] genotypes and the CT+AA [corrected] genotypes and the TT+ AC were associated with a statistically significant lower risk for developing colorectal cancer (P value for interaction= 0.03 , 0.02 , 0.001), respectively . CONCLUSIONS: The findings suggest an interaction between the MTHFR genotype and colorectal adenomas among Egyptian patients. Abbreviations: T2DM: Colorectal cancer- MTHFR: methylenetetrahydrofolate reductase - SNP: single nucleotide polymorphism- SSP-PCR: sequence specific primer- polymerase chain reaction.
机译:目的:亚甲基四氢叶酸还原酶(MTHFR)的多态性,例如MTHFR C677T和A1298C与多种癌症有关。这项研究旨在评估MTHFR多态性对埃及damitta人群大肠癌风险的影响。方法 。这项基于医院的病例对照研究于2008年至2010年进行;纳入64例结肠癌病例和90例对照。收集信息并通过聚合酶链反应-单链构象多态性(PCR-SSCP)和PCR-限制性片段长度多态性(PCR-RFLP)技术获得血样,用于测定MTHFR C677T和A1298C多态性。使用条件对数回归评估目标变量与大肠癌之间的关联。结果:结直肠癌的风险增加与C677T多态性的MTHFR C677 TT基因型相关(OR(adj)= 24.0; 95%CI:1.34-429.1;相互作用的P值= 0.001)。 1298AC基因型和C等位基因与受试者之间的统计学显着性较低风险相关(OR,3.85; 95%CI,1.78-8.33;相互作用的P值= .0005和OR,1.88; 95%CI,1.16-3.059互动= 0.01)。发现MTHFR 1298 AA基因型和A等位基因与大肠癌风险显着降低相关(OR = 0.25,95%CI 0.11- 0.52;相互作用的P值= 0.0005和OR = 0.52,95%CI 0.32-0.85 P互动值分别为0.01和)。大肠腺瘤与1298 CC基因型的腺瘤之间没有明确的关系。 CC,AA [校正]基因型和CT + AA [校正]基因型以及TT + AC的组合与结直肠癌发生的统计学显着性较低风险相关(相互作用的P值分别为0.03、0.02、0.001)。结论:研究结果表明埃及患者中MTHFR基因型与结直肠腺瘤之间存在相互作用。缩写:T2DM:大肠癌-MTHFR:亚甲基四氢叶酸还原酶-SNP:单核苷酸多态性-SSP-PCR:序列特异性引物-聚合酶链反应。

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