Jiang Yuan, Hou Jing, Zhang Qiang, Jia Shu-Ting, Wang Bo-Yuan, Zhang Ji-Hong, Tang Wen-Ru, Luo Ying
Lab of Molecular Genetics of Aging and Tumor, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, China E-mail :
Asian Pac J Cancer Prev. 2013;14(11):6357-62. doi: 10.7314/apjcp.2013.14.11.6357.
The C677T polymorphism of the methylenetetrahydrofolate reductase (MTHFR) has been associated with acute lymphoblastic leukemia (ALL). However, results were conflicting. The aim of this study was to quantitatively summarize the evidence for the MTHFRC677T polymorphism and ALL risk.
Electronic searches of PubMed and the Chinese Biomedicine database were conducted to select case-control studies containing available genotype frequencies of C677T and the odds ratio (OR) with 95% confidence interval (CI) was used to assess the strength of any association.
Case-control studies including 6,371 cases and 10,850 controls were identified. The meta-analysis stratified by ethnicity showed that individuals with the homozygous TT genotype had decreased risk of ALL (OR= 0.776, 95% CI: 0.6870.877, p< 0.001) in Caucasians (OR= 0.715, 95% CI: 0.6550.781, p= 0.000). However, results among Asians (OR=0.711, 95% CI: 0.5911.005, p= 0.055) and others (OR=0.913, 95% CI: 0.6561.271, p= 0. 590) did not suggest an association. A symmetric funnel plot, the Egger's test (P=0.093), and the Begg- test (P=0.072) were all suggestive of the lack of publication bias.
This meta-analysis supports the idea that the MTHFR C677T genotype is associated with risk of ALL in Caucasians. To draw comprehensive and true conclusions, further prospective studies with larger numbers of participants worldwide are needed to examine associations between the MTHFRC677T polymorphism and ALL.
亚甲基四氢叶酸还原酶(MTHFR)的C677T多态性与急性淋巴细胞白血病(ALL)有关。然而,结果相互矛盾。本研究的目的是定量总结MTHFR C677T多态性与ALL风险的证据。
对PubMed和中国生物医学数据库进行电子检索,以选择包含C677T可用基因型频率的病例对照研究,并使用比值比(OR)及95%置信区间(CI)评估任何关联的强度。
确定了包括6371例病例和10850例对照的病例对照研究。按种族分层的荟萃分析表明,纯合TT基因型个体在白种人中患ALL的风险降低(OR = 0.776,95% CI:0.6870.877,p < 0.001)(OR = 0.715,95% CI:0.6550.781,p = 0.000)。然而,亚洲人(OR = 0.711,95% CI:0.5911.005,p = 0.055)和其他人(OR = 0.913,95% CI:0.6561.271,p = 0.590)的结果未显示出关联。对称漏斗图、Egger检验(P = 0.093)和Begg检验(P = 0.072)均提示不存在发表偏倚。
这项荟萃分析支持MTHFR C677T基因型与白种人ALL风险相关的观点。为得出全面和真实的结论,需要在全球范围内开展更多参与者的进一步前瞻性研究,以检验MTHFR C677T多态性与ALL之间的关联。