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炎症细胞因子基因多态性与癌因性疲乏的关联研究

  

  1. 1.甘肃省第二人民医院  介入肿瘤科,甘肃 兰州 730000; 2.甘肃省人民医院  呼吸科,甘肃 兰州 730000
  • 出版日期:2019-11-20 发布日期:2020-01-09
  • 通讯作者: 米登海,Email:midh2014@163.com
  • 基金资助:
    甘肃省卫生行业科研计划项目----肺癌癌因性疲乏危险因素及遗传机制研究(GSWSKY-2014-14)

Correlation between inflammatory cytokine polymorphisms and cancerrelated fatigue

  1. 1.Department of Invasive Technology and Oncology,  the Second Hospital of Gansu Province, 
    Lanzhou  730000,  China;  2. Department of Respiratory Medicine,  the People's Hospital of
    Gansu Province,  Lanzhou 730000,  China
  • Online:2019-11-20 Published:2020-01-09
  • Contact: Corresponding author: Mi Denghai, Email:midh2014@163.com

摘要: 目的  探讨炎症细胞因子基因多态性与癌因性疲乏(CRF)的关联,为研究遗传易感性在CRF发生发展中所起的作用提供研究基础。方法  肺癌患者242例,其中癌因性疲乏组162例,非癌因性疲乏组80例。通过PCRRFLP进行基因分型,分析基因型及等位基因频率在疲乏组与非疲乏组的分布情况及炎症细胞因子基因多态性与癌因性疲乏的关联性。结果  TNFα308G/A、IL1β511C/T基因型分布在两组间差异有统计学意义(P均<0.05)。多元logistic回归校正了年龄和性别等混杂因素后显示,相对于TNFα308GG基因型患者,携带GA/AA基因型患者发生CRF的风险降低了74%(15%~92%);相对于IL6174GG基因型患者,携带GC/CC基因型患者发生CRF的风险降低了78%(0%~95%);在IL1β511C/T基因位点中,携带CC基因型的患者发生CRF的风险是TT基因型患者的3.96倍(95%CI 1.0215.45)。结论  携带TNFα308GG、IL6174GG、IL1β511CC基因型的肺癌患者发生癌因性疲乏的风险明显增加。

关键词: 病理状态, , 体征和症状;细胞因子类;基因顺序

Abstract: Objective  To explore  the correlation between the inflammatory cytokine polymorphisms and cancerrelated fatigue(CRF),  and provide  research basis for the investigation of genetic variation in the development and progression of CRF. Methods  Totally 242 lung cancer patients were divided into CRF group (162) and nonCRF group (80). Genotyping  was carried out according to the polymerase chain reaction restriction fragment length polymorphism(PCR RFLP), then  the distribution of allele frequency and genotypes were analyzed, as well as the correlation between inflammatory cytokine polymorphisms and CRF.Results  There was statistically significant  difference between the distribution of   TNFα308 G/A  and   IL1β511 C/T genotypes(all P<0.05).  After adjusting the confounding factors such as age and gender, multivariate logistic regression showed that patients with GA/AA genotype had a lower risk for CRF by 74%  as compared with  patients with  TNF α308GG genotype(15%92%);  patients with GC/CC genotype had a  lower risk by 78% in comparison with  patients with IL6174GG genotype(0%95%); in the genetic locus of IL1β511C/T,  the patients with CC genotype were 3.96 times more likely to develop CRF than those with TT genotype (95%CI 1.0215.45). Conclusion  Patients with TNFα308GG,  IL6174GG and  IL1β511CC genotypes have a significantly increased risk of CRF.

Key words: pathological condition, , signs and symptoms, cytokines, gene order