Xia Jia, Wang Yadan, Zhang Hang, Hu Yu
Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology , Wuhan, Hubei , China.
Leuk Lymphoma. 2014 Jun;55(6):1388-93. doi: 10.3109/10428194.2013.830304. Epub 2013 Sep 3.
Abstract To date, many studies on the association between methionine synthase (MTR) A2756G and childhood acute lymphoblastic leukemia (ALL) have provided either controversial or inconclusive results. To clarify the effect of MTR A2756G on the risk of childhood acute lymphoblastic leukemia, a meta-analysis of all relevant studies was performed. The fixed effects model showed that the 2756A allele was associated with a decreased risk of childhood ALL compared with the G allele (ORA vs. G = 0.872; 95% CI 0.782-0.974; p = 0.015, I(2) = 46.9%). Additionally, when comparing subjects with ALL and controls with AA vs. AG or AA vs. AG + GG (dominant model), significant differences were found in the fixed effects model (ORAA vs. AG = 0.869; 95% CI 0.760-0.994; p = 0.040, I(2) = 26.4%; ORAA vs. AG+ GG = 0.858; 95% CI 0.754-0.976; p = 0.020, I(2) = 39.6%). In a subgroup analysis in a population with the same background, individuals with the AA genotype had a reduced risk of developing ALL compared to individuals with the AG genotype. In conclusion, our study provides evidence suggesting that MTR A2756G is associated with a reduced risk of developing childhood ALL.
摘要 迄今为止,许多关于甲硫氨酸合成酶(MTR)A2756G与儿童急性淋巴细胞白血病(ALL)之间关联的研究结果存在争议或尚无定论。为了阐明MTR A2756G对儿童急性淋巴细胞白血病风险的影响,我们对所有相关研究进行了荟萃分析。固定效应模型显示,与G等位基因相比,2756A等位基因与儿童ALL风险降低相关(A等位基因与G等位基因的比值比[ORA] = 0.872;95%置信区间[CI] 0.782 - 0.974;p = 0.015,I² = 46.9%)。此外,在比较ALL患者与AA基因型对照与AG基因型对照或AA基因型对照与AG + GG基因型对照(显性模型)时,固定效应模型中发现了显著差异(AA基因型与AG基因型的OR = 0.869;95% CI 0.760 - 0.994;p = 0.040,I² = 26.4%;AA基因型与AG + GG基因型的OR = 0.858;95% CI 0.754 - 0.976;p = 0.020,I² = 39.6%)。在相同背景人群的亚组分析中,与AG基因型个体相比,AA基因型个体患ALL的风险降低。总之,我们的研究提供了证据表明MTR A2756G与儿童ALL发病风险降低相关。