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首页> 外文期刊>British Journal of Haematology >Risk factors for Burkitt lymphoma: a nested case‐control study in the UK UK Clinical Practice Research Datalink
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Risk factors for Burkitt lymphoma: a nested case‐control study in the UK UK Clinical Practice Research Datalink

机译:Burkitt淋巴瘤的危险因素:英国英国临床实践研究数据链接嵌套病例对照研究

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摘要

Summary Burkitt lymphoma ( BL ) occurs as three subtypes: endemic BL , immunosuppression‐related BL and sporadic BL . Descriptive studies of BL age‐specific incidence patterns have suggested multimodal peaks near 10, 40 and 70?years of age, but the risk factors for BL at different ages are unknown. We investigated risk factors for BL in the United Kingdom among 156 BL cases and 608 matched BL ‐free controls identified in the Clinical Practice Research Datalink ( CPRD ) between 1992 and 2016. Associations with pre‐diagnostic body mass index, cigarette smoking, alcohol consumption, hepatitis, Epstein–Barr virus ( EBV ), human immunodeficiency virus infection and acquired immune deficiency syndrome ( HIV / AIDS ), malaria, allergic and autoimmune conditions, and prednisone use were evaluated. Overall, we identified inverse associations between smoking and BL risk, and positive associations between prior EBV infection, HIV / AIDS and prescription or use of prednisone with BL risk. In age‐group stratified analyses, BL was associated with malaria exposure (vs. no exposure, odds ratio [ OR ] 8·00, 95% confidence interval [ CI ] 1·46–43·7) among those aged 20–59?years old and with hepatitis infection (vs. no infection, OR 3·41, 95% CI 1·01–11·5) among those aged 60+ years old. The effects of EBV , malaria, HIV / AIDS , prednisone and hepatitis on BL remained significant in mutually‐adjusted age‐group‐specific analyses. No risk factors were associated with childhood BL . We report novel associations for BL in non‐endemic settings.
机译:摘要Burkitt淋巴瘤(BL)发生为三种亚型:特异性BL,免疫抑制相关的BL和零星BL。 BL年龄特异性发病率图案的描述性研究已经提出了近10,40和70岁以下的多模式峰值,但不同年龄的BL的危险因素是未知的。在1992年至2016年间,我们在临床实践研究数据链接(CPRD)中确定了英国的BL中BL的危险因素,并在1992年至2016年间临床实践研究数据链接(CPRD)。与诊断前体重指数,吸烟,饮酒,评估肝炎,Epstein-Barr病毒(EBV),人免疫缺陷病毒感染和获得的免疫缺陷综合征(艾滋病毒/艾滋病),疟疾,过敏性和自身免疫条件以及泼尼松使用。总体而言,我们确定了吸烟和BL风险之间的逆关联,并且先前EBV感染,艾滋病毒/艾滋病和处方或使用BL风险的验证之间的阳性关联。在年龄组分层分析中,BL与疟疾暴露(Vs.没有暴露,差距[或] 8·00,95%置信区间[CI] 1·46-43·7)相关?年龄在60岁以上岁月的人中,历史和肝炎感染(对没有感染,或3·41,95%CI 1·01-11·5)。 EBV,疟疾,艾滋病毒/艾滋病,泼尼松和肝炎对BL的影响在相互调整的年龄组特异性分析中存在显着。没有风险因素与童年BL相关联。我们举报了非特有环境中BL的新关联。

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