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本文引用的文献

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Cancer statistics, 2010.癌症统计数据,2010 年。
CA Cancer J Clin. 2010 Sep-Oct;60(5):277-300. doi: 10.3322/caac.20073. Epub 2010 Jul 7.
2
Tumor necrosis factor (TNF) and lymphotoxin-alpha (LTA) polymorphisms and risk of non-Hodgkin lymphoma in the InterLymph Consortium.肿瘤坏死因子 (TNF) 和淋巴毒素-α (LTA) 多态性与 InterLymph 联盟中非霍奇金淋巴瘤的风险。
Am J Epidemiol. 2010 Feb 1;171(3):267-76. doi: 10.1093/aje/kwp383. Epub 2010 Jan 4.
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Incidence of extranodal non-Hodgkin lymphomas among whites, blacks, and Asians/Pacific Islanders in the United States: anatomic site and histology differences.美国白种人、黑人和亚洲/太平洋岛民中非霍奇金淋巴瘤的发病情况:解剖部位和组织学差异。
Cancer Epidemiol. 2009 Nov;33(5):337-46. doi: 10.1016/j.canep.2009.09.006. Epub 2009 Oct 22.
4
Atopic disease and risk of non-Hodgkin lymphoma: an InterLymph pooled analysis.特应性疾病与非霍奇金淋巴瘤风险:一项InterLymph汇总分析。
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Common immune-related risk factors and incident non-Hodgkin lymphoma: the multiethnic cohort.常见的免疫相关风险因素与非霍奇金淋巴瘤的发病:多民族队列研究
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Cancer risk among patients with multiple sclerosis and their parents.多发性硬化症患者及其父母的癌症风险。
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Papillomaviruses in the causation of human cancers - a brief historical account.人乳头瘤病毒在人类癌症病因中的作用——简要历史回顾
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Infectious aetiology of Hodgkin and non-Hodgkin lymphomas: a review of the epidemiological evidence.霍奇金淋巴瘤和非霍奇金淋巴瘤的感染病因:流行病学证据综述
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美国退伍军人慢性免疫刺激性疾病与非霍奇金淋巴瘤风险的种族差异。

Racial differences in chronic immune stimulatory conditions and risk of non-Hodgkin's lymphoma in veterans from the United States.

机构信息

National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD 20892-7248, USA.

出版信息

J Clin Oncol. 2011 Feb 1;29(4):378-85. doi: 10.1200/JCO.2010.30.1515. Epub 2010 Dec 20.

DOI:10.1200/JCO.2010.30.1515
PMID:21172877
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3058284/
Abstract

PURPOSE

To examine underlying etiologic factors that may explain the racial disparity in non-Hodgkin's lymphoma (NHL) incidence patterns.

PATIENTS AND METHODS

We assessed immune-related conditions and risk of developing NHL among more than 4 million hospitalized US veterans including 9,496 patients with NHL (7,999 white patients and 1,497 black patients) with up to 26 years of follow-up. We used time-dependent Poisson regression to estimate rate ratios (RRs) and 95% CIs for NHL risk among patients with a history of specific autoimmune diseases, infections, and allergies compared with patients without such history, adjusting for attained age, calendar year, race, number of hospital visits, and time between study entry and exit.

RESULTS

Patients with infectious conditions had an increased risk of developing NHL (RR, 1.2; 95% CI, 1.1 to 1.2), particularly for gastrohepatic, genital, and systemic infectious conditions. Patients with autoimmune disease were generally more likely to develop NHL than patients without autoimmune disease, especially for conditions that typically present with detectable autoantibodies with systemic involvement (RR, 2.0; 95% CI, 1.8 to 2.2). Allergies were also associated with increased risk (RR, 1.4; 95% CI, 1.3 to 1.5). Although the risk of NHL was lower for blacks than whites (RR, 0.87; 95% CI, 0.82 to 0.92), blacks had a slightly higher risk of NHL associated with infections than whites (likelihood ratio test, P = .002) and a tendency toward higher risk associated with allergies (likelihood ratio test, P = .05). Risks associated with autoimmune conditions were similar by race (likelihood ratio test, P = .5).

CONCLUSION

The observed difference in NHL risk by race supports a role for race-related differences in genes regulating immune/inflammatory response.

摘要

目的

探讨可能解释非霍奇金淋巴瘤(NHL)发病模式种族差异的潜在病因因素。

方法

我们评估了超过 400 万例住院美国退伍军人的免疫相关情况和 NHL 发病风险,其中包括 9496 例 NHL 患者(7999 例白人患者和 1497 例黑人患者),随访时间长达 26 年。我们使用时间依赖性泊松回归来估计有特定自身免疫性疾病、感染和过敏史的患者与无此类病史的患者相比 NHL 发病风险的比率比(RR)和 95%置信区间(CI),调整了获得的年龄、日历年份、种族、就诊次数和研究进入和退出之间的时间。

结果

患有感染性疾病的患者发生 NHL 的风险增加(RR,1.2;95%CI,1.1 至 1.2),尤其是胃肝、生殖和全身感染性疾病。患有自身免疫性疾病的患者通常比没有自身免疫性疾病的患者更有可能患上 NHL,尤其是那些通常伴有全身性自身抗体可检测到的自身免疫性疾病(RR,2.0;95%CI,1.8 至 2.2)。过敏也与风险增加相关(RR,1.4;95%CI,1.3 至 1.5)。尽管黑人 NHL 的风险低于白人(RR,0.87;95%CI,0.82 至 0.92),但黑人与感染相关的 NHL 风险略高于白人(似然比检验,P =.002),且与过敏相关的风险有增加的趋势(似然比检验,P =.05)。与自身免疫性疾病相关的风险在不同种族之间相似(似然比检验,P =.5)。

结论

观察到的种族间 NHL 风险差异支持了种族相关基因调节免疫/炎症反应差异的作用。