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首页> 外文期刊>Leukemia and lymphoma >Infectious complications after chemotherapy and stem cell transplantation in multiple myeloma: Implications of Fc gamma receptor and myeloperoxidase promoter polymorphisms
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Infectious complications after chemotherapy and stem cell transplantation in multiple myeloma: Implications of Fc gamma receptor and myeloperoxidase promoter polymorphisms

机译:多发性骨髓瘤化疗和干细胞移植后的感染并发症:Fcγ受体和髓过氧化物酶启动子多态性的影响

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摘要

Abstract:Multiple myeloma is associated with a high risk of infections. We hypothesized that Fc gamma receptor (FCGR) and myeloperoxidase (MPO) promoter gene polymorphisms influence the risk of infections after induction chemotherapy (IC) and autologous stem cell transplantation (ASCT). Retrospectively, we analysed 136 patient courses of IC and 113 procedures of ASCT. Genetic analyses were made with PCR techniques on genomic DNA. The incidence rate ratio of sepsis during ASCT in patients homozygous for the G-129MPO promoter type was 0.30 (95% CI: 0.09-0.96). The G-463AMPO promoter polymorphism was not associated with the risk of infections. The polymorphisms of FCGR2A, FCGR3A and FCGR3B were not convincingly associated with infections. The NA1 variant of FCGR3B was strongly skewed with other risk factors, and the results in IC and ASCT were conflicting. Further studies of the G-129AMPO promoter as a potential risk modifier for infections are relevant
机译:摘要:多发性骨髓瘤与高感染风险有关。我们假设Fcγ受体(FCGR)和髓过氧化物酶(MPO)启动子基因多态性影响诱导化疗(IC)和自体干细胞移植(ASCT)后感染的风险。回顾性分析了136例IC患者的病程和113例ASCT的病程。用PCR技术对基因组DNA进行遗传分析。 G-129MPO启动子类型纯合的患者在ASCT期间败血症的发生率为0.30(95%CI:0.09-0.96)。 G-463AMPO启动子多态性与感染风险无关。 FCGR2A,FCGR3A和FCGR3B的多态性与感染没有令人信服的关联。 FCGR3B的NA1变体与其他风险因素存在严重偏差,并且IC和ASCT中的结果存在冲突。 G-129AMPO启动子作为感染的潜在风险调节剂的进一步研究具有重要意义

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