XRCC1基因多态性与弥漫大B细胞型非霍奇金淋巴瘤预后的关系  被引量:2

Association between DNA X-ray repair cross complementary protein 1(XRCC1) polymorphisms and clinical outcome of patients with diffuse large B-cell lymphoma

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作  者:高宇[1] 魏楠[1] 李梦洁[1] 江皓[1] 

机构地区:[1]浙江医院血液科,杭州310013

出  处:《浙江医学》2016年第12期932-935,共4页Zhejiang Medical Journal

摘  要:目的:探讨X射线损伤交叉互补蛋白1(XRCC1)基因多态性与弥漫大B细胞型非霍奇金淋巴瘤(DLBCL)患者预后的关系。方法选取XRCC1基因3个单核苷酸多态性(SNPs)对DLBCL患者进行基因分型,并回顾分析患者预后情况,采用logistic回归分析XRCC1基因型与患者预后的关系。结果入选65例患者,平均年龄(59.7±8.0岁);其中肿瘤相关死亡患者31例(47.7%)。XRCC1基因rs25487基因型频率在死亡组与存活组无统计学差异(P>0.05),而等位基因频率两组间有统计学差异,其中A等位基因频率在死亡组中明显高于存活组(40.3%vs 22.1%,P<0.05)。AA、GA、GG 3组基因型患者肿瘤相关病死率分别为75.0%(6/8)、54.2%(13/24)、36.4%(12/33)。rs25487位点A等位基因的加性模型中,每增加一个拷贝的A等位基因,风险是增加前的2.208倍(95%CI:1.039~4.694,P<0.05)。校正年龄、性别、吸烟、B症状及和治疗方式后,A等位基因仍然显著增高患者死亡风险(OR=2.382,95%CI:1.057~5.367,P<0.05)。结论 XRCC1基因rs25487多态性与DLBCL的预后相关。Objective To investigate the association of DNA X- ray repair cross complementary protein 1 (XRCC1) polymorphisms with the clinical outcome of patients with non- Hodgkin's lymphoma (NHL). Methods Sixty five patients with diffuse large B- cel lymphoma (DLBCL)(mean age of 59.7±8.0 years) were enrol ed in the study, among whom 31 (47.7%) died from NHL during follow- up. Three single nucleotide polymorphisms (SNPs) in XRCC1 gene of patients were genotyped. Logistic regression analyses were used to compute odds ratios (ORs) and 95%confidence intervals (CIs). Results Among three SNPs, frequency of A al ele of rs25487 was significantly higher in death group than that in survival group(40.3%vs. 22.1%, P〈0.05). The death rates of patients with AA, GA, and GG genotype were 75.0%(6/8), 54.2%(13/24) and 36.4%(12/33), respectively. A al ele of rs25487 increased the risk of death in additive model with odds ratio(OR) of 2.208(95%CI:1.039~4.694, P〈0.05). After adjusting for age, sex, smoking, B symptoms and treatment, the significance stil remained with OR =2.382 (95%CI:1.057~5.367, P〈0.05). Conclusion rs25487 of XRCC1 gene may be correlated with outcome of DLBCL patients.

关 键 词:非霍奇金淋巴瘤 XRCC1基因 多态性 预后 

分 类 号:R733.1[医药卫生—肿瘤]

 

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