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Childhood use of antimicrobials and risk of Hodgkin lymphoma: a Danish register–based cohort study

机译:儿童期使用抗菌药物和霍奇金淋巴瘤的风险:一项基于丹麦研究的队列研究

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摘要

The peculiar bimodal age distribution of Hodgkin lymphoma (HL), together with other epidemiological findings, inspired the so-called “late infection hypothesis” in the 1970s. Under this model, HL in young adults is caused by delayed infection with a relatively common agent, with HL risk increasing with age at infection. We time-dependently tallied prescriptions filled, for a broad spectrum of antimicrobials, at age 0 to 9 years for all Danish HL patients diagnosed in 1997 to 2015 at age 10 to 25 years (n = 296) and up to 10 controls for each of these, individually matched for sex and birthdate (n = 2688). Antimicrobial use was taken as a proxy for general infectious disease pressure. Analyses were also stratified by the 2 main histological subtypes: nodular sclerosis HL (NSHL) (n = 206) and mixed cellularity HL (MCHL) (n = 47). We compared antimicrobial use at ages 0 to 9 years between cases and comparators using stratified Cox regressions with repeated follow-up for a next prescription, to produce hazard ratios (HRs) of antimicrobial use according to (future) HL status. Reverse causation was mitigated by disregarding risk time <2 years before HL (pseudo)diagnosis. Analyses were adjusted for number of older and younger siblings. NSHL patients had received statistically significantly fewer antimicrobials than comparators early in life (HR0-2 years, 0.79; 95% confidence interval, 0.66-0.95), whereas patients with MCHL had received statistically significantly more antimicrobials than comparators throughout the first 10 years of life (HR0-9 years, 1.53; 95% confidence interval, 1.33-1.76). The late infection hypothesis was supported in NSHL, whereas immune dysfunction seemed more prominent in MCHL etiology.
机译:霍奇金淋巴瘤(HL)独特的双峰年龄分布以及其他流行病学发现激发了1970年代所谓的“晚期感染假说”。在这种模型下,年轻人的HL是由相对常见的药物延迟感染引起的,HL的风险随着感染年龄的增加而增加。我们对所有抗菌药物在1997年至2015年诊断为年龄10至25岁(n = 296)的所有丹麦HL患者在0至9岁的年龄范围内填写了广泛的抗菌药物处方,每个患者最多10个对照这些分别针对性别和生日(n = 2688)进行匹配。抗菌药物被用作一般传染病压力的代表。分析还按2种主要组织学亚型进行分层:结节性硬化HL(NSHL)(n = 206)和混合细胞性HL(MCHL)(n = 47)。我们比较了病例和比较者在0到9岁之间使用分层Cox回归并重复随访下一处方的抗菌药物使用情况,以根据(未来)HL状态得出抗菌药物使用的危险比(HRs)。通过忽略在HL(假)诊断之前小于2年的风险时间,可以减轻反向因果关系。调整分析的年龄较大和较年轻的兄弟姐妹。 NSHL患者生命早期接受的抗菌药物统计显着少于比较者(HR0-2岁,0.79; 95%置信区间,0.66-0.95),而MCHL患者在生命的最初10年中接受的抗菌药物明显多于比较者(HR0-9岁,1.53; 95%置信区间,1.33-1.76)。 NSHL支持晚期感染假说,而在MCHL病因学中,免疫功能障碍似乎更为突出。

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