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本文引用的文献

1
Assessment of the relationship between methylenetetrahydrofolate reductase polymorphism and acute lymphoblastic leukemia: Evidence from an updated meta-analysis.亚甲基四氢叶酸还原酶基因多态性与急性淋巴细胞白血病关系的评估:一项更新的荟萃分析证据
J Oncol Pharm Pract. 2020 Oct;26(7):1598-1610. doi: 10.1177/1078155219900914. Epub 2020 Feb 18.
2
The methylenetetrahydrofolate reductase 677T-1298C haplotype is a risk factor for acute lymphoblastic leukemia in children.亚甲基四氢叶酸还原酶677T-1298C单倍型是儿童急性淋巴细胞白血病的一个风险因素。
Medicine (Baltimore). 2017 Dec;96(51):e9290. doi: 10.1097/MD.0000000000009290.
3
MetaGenyo: a web tool for meta-analysis of genetic association studies.MetaGenyo:一种用于基因关联研究荟萃分析的网络工具。
BMC Bioinformatics. 2017 Dec 16;18(1):563. doi: 10.1186/s12859-017-1990-4.
4
TS Gene Polymorphisms Correlate with Susceptibility to Acute Lymphocytic Leukemia in Children.TS基因多态性与儿童急性淋巴细胞白血病易感性相关。
Med Sci Monit. 2017 Jun 24;23:3095-3104. doi: 10.12659/msm.901494.
5
Meta-prediction of MTHFR gene polymorphism-mutations, air pollution, and risks of leukemia among world populations.世界人群中MTHFR基因多态性-突变、空气污染与白血病风险的元预测
Oncotarget. 2017 Jan 17;8(3):4387-4398. doi: 10.18632/oncotarget.13876.
6
Involvement of MTHFR and TPMT genes in susceptibility to childhood acute lymphoblastic leukemia (ALL) in Mexicans.亚甲基四氢叶酸还原酶(MTHFR)和硫嘌呤甲基转移酶(TPMT)基因与墨西哥儿童急性淋巴细胞白血病(ALL)易感性的关系。
Drug Metab Pers Ther. 2016 Mar;31(1):41-6. doi: 10.1515/dmpt-2015-0036.
7
Polymorphisms of 5,10-methylenetetrahydrofolate reductase and thymidylate synthase, dietary folate intake, and the risk of leukemia in adults.5,10-亚甲基四氢叶酸还原酶和胸苷酸合成酶的多态性、膳食叶酸摄入量与成人白血病风险
Tumour Biol. 2016 Mar;37(3):3265-75. doi: 10.1007/s13277-015-4168-6. Epub 2015 Oct 5.
8
The association of methylenetetrahydrofolate reductase genotypes with the risk of childhood leukemia in Taiwan.台湾亚甲基四氢叶酸还原酶基因型与儿童白血病风险的关联。
PLoS One. 2015 Mar 20;10(3):e0119776. doi: 10.1371/journal.pone.0119776. eCollection 2015.
9
Methylenetetrahydrofolate reductase C677T and A1298C polymorphism and susceptibility to acute lymphoblastic leukemia in a cohort of Egyptian children.埃及儿童队列中甲基四氢叶酸还原酶C677T和A1298C多态性与急性淋巴细胞白血病易感性
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10
Lack of association between polymorphisms in genes MTHFR and MDR1 with risk of childhood acute lymphoblastic leukemia.亚甲基四氢叶酸还原酶(MTHFR)基因和多药耐药基因1(MDR1)的多态性与儿童急性淋巴细胞白血病风险之间无关联。
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A1298C亚甲基四氢叶酸还原酶对儿童急性淋巴细胞白血病风险无影响:一项荟萃分析的证据

Lack of Impact of the A1298C MTHFR on the Risk of Childhood Acute Lymphoblastic Leukemia: Evidence from a Meta-analysis.

作者信息

Frikha Rim

机构信息

Department of Medical Genetics, Hedi Chaker University Hospital and Faculty of Medicine of Sfax, Sfax, Tunisia.

出版信息

Indian J Hematol Blood Transfus. 2022 Apr;38(2):255-263. doi: 10.1007/s12288-021-01453-6. Epub 2021 May 26.

DOI:10.1007/s12288-021-01453-6
PMID:35496972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9001782/
Abstract

To clarify the effect of the A1298C variant of methylenetetrahydrofolate reductase () gene on the risk of acute lymphoblastic leukemia (ALL), an updated meta-analysis was performed. Electronic literature search was carried out in PubMed to collect relevant articles. Pooled odds ratios (OR) and stratification analysis were achieved under different genetic comparison models, age and ethnicity. A total of 46 articles including 7020 cases and 12,114 controls were enrolled. Overall, no significant association was observed for the A1298C variant on the risk of ALL in any genetic model test, when all the studies pooled together (OR ~ 1 0.91;  > 0.05). In subgroup analyses stratified by age and ethnicity, the A1298C reduce the risk of ALL in adult under allele contrast (OR = 0.88; [0.72; 1.09],  = 0.23) mainly in Caucasian populations. The present meta-analysis provides evidence that the A1298C variant of gene is unlikely to be a major risk gene for childhood ALL.

摘要

为阐明亚甲基四氢叶酸还原酶(MTHFR)基因的A1298C变异对急性淋巴细胞白血病(ALL)风险的影响,进行了一项更新的荟萃分析。在PubMed中进行电子文献检索以收集相关文章。在不同的基因比较模型、年龄和种族条件下实现了合并优势比(OR)和分层分析。共纳入46篇文章,包括7020例病例和12114例对照。总体而言,当所有研究合并在一起时,在任何基因模型测试中均未观察到A1298C变异与ALL风险之间存在显著关联(OR ~ 1.09;P > 0.05)。在按年龄和种族分层的亚组分析中,A1298C变异主要在白种人群体的等位基因对比中降低了成人ALL的风险(OR = 0.88;95%CI[0.72;1.09],P = 0.23)。本荟萃分析提供的证据表明,MTHFR基因的A1298C变异不太可能是儿童ALL的主要风险基因。