• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Association of Methylenetetrahydrofolate Reductase Gene rs1801133 Polymorphism and Controlling Nutritional Status (CONUT) Score with Colorectal Cancer Susceptibility.亚甲基四氢叶酸还原酶基因rs1801133多态性与控制营养状况(CONUT)评分与结直肠癌易感性的关联
Int J Gen Med. 2024 Dec 17;17:6281-6290. doi: 10.2147/IJGM.S495139. eCollection 2024.
2
Association of ALDH2 rs671 and MTHFR rs1801133 polymorphisms with hypertension among Hakka people in Southern China.ALDH2 rs671 和 MTHFR rs1801133 多态性与中国南方客家人群高血压的关联。
BMC Cardiovasc Disord. 2022 Mar 27;22(1):128. doi: 10.1186/s12872-022-02577-x.
3
Association of Methylenetetrahydrofolate Reductase rs1801133 Gene Polymorphism with Cancer Risk and Septin 9 Methylation in Patients with Colorectal Cancer.亚甲基四氢叶酸还原酶 rs1801133 基因多态性与结直肠癌患者的癌症风险和 Septin 9 甲基化的关系。
J Gastrointest Cancer. 2024 Jun;55(2):778-786. doi: 10.1007/s12029-024-01020-y. Epub 2024 Jan 22.
4
Investigation of tagging polymorphisms with colorectal cancer in Chinese Han population.中国汉族人群中结直肠癌标签多态性的研究。
Oncotarget. 2017 Jun 29;8(38):63518-63527. doi: 10.18632/oncotarget.18845. eCollection 2017 Sep 8.
5
The Role of Genotype in Colorectal Cancer Susceptibility in Taiwan.基因型在台湾地区结直肠癌易感性中的作用。
Anticancer Res. 2018 Apr;38(4):2001-2006. doi: 10.21873/anticanres.12438.
6
Methylenetetrahydrofolate reductase C677T (Ala>Val, rs1801133 C>T) polymorphism decreases the susceptibility of hepatocellular carcinoma: a meta-analysis involving 12,628 subjects.亚甲基四氢叶酸还原酶 C677T(Ala>Val,rs1801133 C>T)多态性降低肝细胞癌易感性:一项涉及 12628 例患者的荟萃分析。
Biosci Rep. 2020 Feb 28;40(2). doi: 10.1042/BSR20194229.
7
The Roles of and Gene Polymorphisms in Colorectal Cancer Survival.和基因多态性在结直肠癌生存中的作用。
Nutrients. 2022 Nov 1;14(21):4594. doi: 10.3390/nu14214594.
8
ALDH2 rs671 and MTHFR rs1801133 polymorphisms are risk factors for arteriosclerosis in multiple arteries.ALDH2 rs671 和 MTHFR rs1801133 多态性是多发性动脉粥样硬化的危险因素。
BMC Cardiovasc Disord. 2023 Jun 24;23(1):319. doi: 10.1186/s12872-023-03354-0.
9
Association of methylenetetrahydrofolate reductase (MTHFR) rs1801133 (677C>T) gene polymorphism with ischemic stroke risk in different populations: An updated meta-analysis.亚甲基四氢叶酸还原酶(MTHFR)rs1801133(677C>T)基因多态性与不同人群缺血性中风风险的关联:一项更新的荟萃分析。
Front Genet. 2023 Jan 4;13:1021423. doi: 10.3389/fgene.2022.1021423. eCollection 2022.
10
[Effects of methylenetetrahydrofolate reductase gene polymorphism and long-term exposure to organophosphorus pesticides on type 2 diabetes mellitus].[亚甲基四氢叶酸还原酶基因多态性及长期暴露于有机磷农药对2型糖尿病的影响]
Wei Sheng Yan Jiu. 2019 Jul;48(4):621-627.

本文引用的文献

1
Introduction to Nutrition and Cancer.营养与癌症概论
Cancer Treat Res. 2024;191:1-32. doi: 10.1007/978-3-031-55622-7_1.
2
MTHFR gene polymorphisms in diabetes mellitus.糖尿病中的亚甲基四氢叶酸还原酶(MTHFR)基因多态性
Clin Chim Acta. 2024 Jul 15;561:119825. doi: 10.1016/j.cca.2024.119825. Epub 2024 Jun 20.
3
Study on the correlation between controlling nutritional status score and clinical biochemical indicators in patients with colorectal cancer.结直肠癌患者营养状况控制评分与临床生化指标的相关性研究
Heliyon. 2024 Mar 5;10(5):e27202. doi: 10.1016/j.heliyon.2024.e27202. eCollection 2024 Mar 15.
4
Association of Methylenetetrahydrofolate Reductase rs1801133 Gene Polymorphism with Cancer Risk and Septin 9 Methylation in Patients with Colorectal Cancer.亚甲基四氢叶酸还原酶 rs1801133 基因多态性与结直肠癌患者的癌症风险和 Septin 9 甲基化的关系。
J Gastrointest Cancer. 2024 Jun;55(2):778-786. doi: 10.1007/s12029-024-01020-y. Epub 2024 Jan 22.
5
Cholesterol in colorectal cancer: an essential but tumorigenic precursor?胆固醇与结直肠癌:一种必不可少但具有致瘤性的前体物质?
Front Oncol. 2023 Nov 3;13:1276654. doi: 10.3389/fonc.2023.1276654. eCollection 2023.
6
Clinical Significance of Controlling Nutritional Status (CONUT) Score in Patients With Colorectal Liver Metastases After Hepatectomy.控制营养状况(CONUT)评分在肝切除术后结直肠癌肝转移患者中的临床意义。
In Vivo. 2023 Nov-Dec;37(6):2678-2686. doi: 10.21873/invivo.13377.
7
ALDH2 rs671 and MTHFR rs1801133 polymorphisms are risk factors for arteriosclerosis in multiple arteries.ALDH2 rs671 和 MTHFR rs1801133 多态性是多发性动脉粥样硬化的危险因素。
BMC Cardiovasc Disord. 2023 Jun 24;23(1):319. doi: 10.1186/s12872-023-03354-0.
8
Combining prognostic nutritional index (PNI) and controlling nutritional status (CONUT) score as a valuable prognostic factor for overall survival in patients with stage I-III colorectal cancer.将预后营养指数(PNI)和控制营养状况(CONUT)评分相结合,作为I-III期结直肠癌患者总生存的一个有价值的预后因素。
Front Oncol. 2023 Jan 30;13:1026824. doi: 10.3389/fonc.2023.1026824. eCollection 2023.
9
ALDH2 gene rs671 G > a polymorphism and the risk of colorectal cancer: A hospital-based study.ALDH2 基因 rs671 G > a 多态性与结直肠癌风险的关系:一项基于医院的研究。
J Clin Lab Anal. 2022 Dec;36(12):e24789. doi: 10.1002/jcla.24789. Epub 2022 Nov 25.
10
Changes in Lifestyle and Risk of Colorectal Cancer in the European Prospective Investigation Into Cancer and Nutrition.生活方式的改变与欧洲癌症与营养前瞻性调查中的结直肠癌风险
Am J Gastroenterol. 2023 Apr 1;118(4):702-711. doi: 10.14309/ajg.0000000000002065. Epub 2022 Oct 12.

亚甲基四氢叶酸还原酶基因rs1801133多态性与控制营养状况(CONUT)评分与结直肠癌易感性的关联

Association of Methylenetetrahydrofolate Reductase Gene rs1801133 Polymorphism and Controlling Nutritional Status (CONUT) Score with Colorectal Cancer Susceptibility.

作者信息

Zhang Zhuoxin, Wu Zuguang, Zeng Yuwen, Li Yunlin, Feng Yingchuan, Gao Zhen, Chen Yijin

机构信息

Department of Gastrointestinal Surgery, Meizhou People's Hospital, Meizhou, People's Republic of China.

Department of Gastroenterology, Meizhou People's Hospital, Meizhou, People's Republic of China.

出版信息

Int J Gen Med. 2024 Dec 17;17:6281-6290. doi: 10.2147/IJGM.S495139. eCollection 2024.

DOI:10.2147/IJGM.S495139
PMID:39712200
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11662921/
Abstract

BACKGROUND

Susceptibility to some cancers is linked to methylenetetrahydrofolate reductase () polymorphisms and the Controlling Nutritional Status (CONUT) score in some populations. However, their relationship with susceptibility to colorectal cancer (CRC) susceptibility in the Hakka Chinese population remains unclear.

METHODS

In total, 620 CRC patients and 734 controls were enrolled. rs1801133 was genotyped, medical records (age, sex, smoking history, alcohol consumption, hypertension, diabetes mellitus, and family history of cancer, and blood cell parameters) were collected, and the relationship between this information and CRC susceptibility was analyzed.

RESULTS

There were significant differences in the distribution of CONUT classification (0.002), and proportions of history of smoking (0.001), hypertension (0.001), diabetes mellitus (0.001), and family history of cancer (0.002) between patients and controls. There were statistically significant differences in rs1801133 genotypes distribution (58.7% C/C, 35.5% C/T, and 5.8% T/T in patients vs 65.5%, 31.2%, and 3.3% in controls, =0.010) and allele distribution (76.5% C, and 23.5% T allele in patients vs 81.1%, and 18.9% in controls, =0.003) between patients and controls. Logistic regression analysis indicated that non-normal CONUT range (non-normal vs normal, odds ratio (OR): 1.451, 95% confidence interval (CI): 1.119-1.882, =0.005), and rs1801133 variant (C/T + T/T vs C/C, OR: 1.373, 95% CI: 1.091-1.728, =0.007), older age (≥65 vs <65 years, OR: 1.298, 95% CI: 1.023-1.646, =0.032), male sex (OR: 1.354, 95% CI: 1.067-1.718, =0.013), and history of alcohol drinking (OR: 2.232, 95% CI: 1.164-4.282, =0.016) were independently associated with CRC risk.

CONCLUSION

Individuals carried rs1801133 variant and with non-normal CONUT range, advanced age, history of alcohol consumption may be at increased CRC risk in the Hakka population.

摘要

背景

在某些人群中,某些癌症的易感性与亚甲基四氢叶酸还原酶()多态性及控制营养状况(CONUT)评分有关。然而,它们与中国客家人群结直肠癌(CRC)易感性的关系仍不清楚。

方法

共纳入620例CRC患者和734例对照。对rs1801133进行基因分型,收集病历(年龄、性别、吸烟史、饮酒情况、高血压、糖尿病、癌症家族史及血细胞参数),并分析这些信息与CRC易感性之间的关系。

结果

患者与对照在CONUT分类分布(0.002)、吸烟史比例(0.001)、高血压比例(0.001)、糖尿病比例(0.001)及癌症家族史比例(0.002)方面存在显著差异。患者与对照在rs1801133基因型分布(患者中C/C为58.7%、C/T为35.5%、T/T为5.8%,对照中分别为65.5%、31.2%、3.3%,=0.010)及等位基因分布(患者中C等位基因为76.5%、T等位基因为23.5%,对照中分别为81.1%、18.9%,=0.003)方面存在统计学显著差异。逻辑回归分析表明,CONUT范围异常(异常vs正常,比值比(OR):1.