MTHFR Gene Polymorphisms and Cancer Risk in Children and Adolescents: A Systematic Review and Meta-Analysis.

IF 2.1 4区 医学 Q2 PEDIATRICS Children-Basel Pub Date : 2025-01-17 DOI:10.3390/children12010108
Savvas Kolanis, Eleni P Kotanidou, Vasiliki Rengina Tsinopoulou, Elisavet Georgiou, Emmanuel Hatzipantelis, Liana Fidani, Assimina Galli-Tsinopoulou
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Abstract

Background/Objectives:MTHFR gene polymorphisms (677C>T and 1298A>C) correlate with various types of cancer across all age groups; however, a small number of studies have included solely children and adolescents. The aim of this systematic review and meta-analysis was to present and synthesize all the available evidence on the association between MTHFR gene polymorphisms and the incidence of all types of cancer in children and adolescences. Methods: After a systematic search of all of the available data, original case-control studies involving children or adolescents with a confirmed diagnosis of any type of cancer and a molecular genetic test of MTHFR gene polymorphisms were included. Results: A total of 53 original studies in children and adolescents with cancer were included in the systematic review. Among these, 40 studies reviewed children and adolescents with Acute Lymphoblastic Leukemia (ALL), 4 those with Acute Myeloblastic Leukemia (AML), 8 those with central nervous system (CNS) tumors and 3 those with other types of cancer. Children and adolescents with ALL had less frequent T allele sequences (CT and TT variations) of the 677C>T polymorphism compared to a healthy population (OR: 0.85; CI: 0.80-0.91; p < 0.00001). Concerning the 1298A>C polymorphism, the C allele sequences (AC and CC) did not present a statistically significant difference in frequency compared to a healthy population (OR: 1.01; CI: 0.95-1.08; p = 0.69). Conclusions: Children and adolescents with ALL appeared to have the T allele sequences of the 677C>T polymorphism of the MTHFR gene less frequently compared to a healthy population.

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MTHFR基因多态性与儿童和青少年癌症风险:一项系统综述和荟萃分析。
背景/目的:MTHFR基因多态性(677C>T和1298A>C)与所有年龄组的各种类型的癌症相关;然而,少数研究只包括儿童和青少年。本系统综述和荟萃分析的目的是提出并综合所有关于MTHFR基因多态性与儿童和青少年所有类型癌症发病率之间关联的现有证据。方法:在对所有可用数据进行系统检索后,纳入了包括确诊为任何类型癌症的儿童或青少年以及MTHFR基因多态性分子遗传检测的原始病例对照研究。结果:共有53项针对儿童和青少年癌症患者的原始研究被纳入系统评价。其中,40项研究回顾了儿童和青少年急性淋巴细胞白血病(ALL)、4项急性髓母细胞白血病(AML)、8项中枢神经系统肿瘤(CNS)和3项其他类型癌症。与健康人群相比,患有ALL的儿童和青少年的677C>T多态性的T等位基因序列(CT和TT变异)较少(OR: 0.85;置信区间:0.80—-0.91;P < 0.00001)。关于1298A>C多态性,与健康人群相比,C等位基因序列(AC和CC)的频率无统计学差异(OR: 1.01;置信区间:0.95—-1.08;P = 0.69)。结论:与健康人群相比,患有ALL的儿童和青少年携带MTHFR基因677C>T多态性等位基因序列的频率较低。
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来源期刊
Children-Basel
Children-Basel PEDIATRICS-
CiteScore
2.70
自引率
16.70%
发文量
1735
审稿时长
6 weeks
期刊介绍: Children is an international, open access journal dedicated to a streamlined, yet scientifically rigorous, dissemination of peer-reviewed science related to childhood health and disease in developed and developing countries. The publication focuses on sharing clinical, epidemiological and translational science relevant to children’s health. Moreover, the primary goals of the publication are to highlight under‑represented pediatric disciplines, to emphasize interdisciplinary research and to disseminate advances in knowledge in global child health. In addition to original research, the journal publishes expert editorials and commentaries, clinical case reports, and insightful communications reflecting the latest developments in pediatric medicine. By publishing meritorious articles as soon as the editorial review process is completed, rather than at predefined intervals, Children also permits rapid open access sharing of new information, allowing us to reach the broadest audience in the most expedient fashion.
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