Diao Lanping, Wei Guangchuan, Su Huiling, Li Huan, Song Jiaojie, Gao Yuhuan, Guo Zhanjun
Department of Hematology .
Mitochondrial DNA. 2015 Feb;26(1):88-91. doi: 10.3109/19401736.2013.823173. Epub 2013 Sep 11.
Accumulation of single nucleotide polymorphisms (SNPs) in the displacement loop (D-loop) of mitochondrial DNA (mtDNA) might be associated with cancer risk and disease outcome. We have identified 140 SNPs including 26 SNPs with frequency distribution of minor allele greater than 5% in a case-control study for non-Hodgkin lymphoma patients previously. In this study, we assessed the predictive power of D-loop SNPs in NHL patients. Five SNP sites were identified by log-rank test for statistically significant prediction of NHL survival in a univariate analysis. In an overall multivariate analysis, allele 16304 was identified as an independent predictor of NHL outcome. The survival time of NHL patients with 16304C was significantly shorter than that of patients with 16304T (relative risk, 0.513; 95% CI, 0.266-0.989; p = 0.046). The analysis of genetic polymorphisms in the mitochondrial D-loop can help identify subgroups of patients who are at a high risk of a poor disease outcome.
线粒体DNA(mtDNA)置换环(D环)中单核苷酸多态性(SNP)的积累可能与癌症风险和疾病预后相关。我们之前在一项针对非霍奇金淋巴瘤患者的病例对照研究中鉴定出了140个SNP,其中包括26个次要等位基因频率分布大于5%的SNP。在本研究中,我们评估了D环SNP对非霍奇金淋巴瘤患者的预测能力。在单变量分析中,通过对数秩检验确定了5个SNP位点对非霍奇金淋巴瘤生存具有统计学显著的预测作用。在总体多变量分析中,等位基因16304被确定为非霍奇金淋巴瘤预后的独立预测因子。携带16304C的非霍奇金淋巴瘤患者的生存时间显著短于携带16304T的患者(相对风险,0.513;95%置信区间,0.266 - 0.989;p = 0.046)。线粒体D环基因多态性分析有助于识别疾病预后不良风险高的患者亚组。