带状疱疹作为潜在恶性肿瘤的标志。

Open medicine : a peer-reviewed, independent, open-access journal Pub Date : 2013-06-18 eCollection Date: 2013-01-01
Karl Iglar, Alexander Kopp, Richard H Glazier
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引用次数: 0

摘要

背景:带状疱疹和恶性肿瘤都与免疫抑制有关。然而,带状疱疹与随后的恶性诊断之间的关系尚不清楚。我们进行这项研究是为了评估带状疱疹的诊断是否是随后恶性肿瘤的危险因素。方法:在这项匹配的回顾性队列研究中,使用医生账单数据库来识别年龄在18岁或以上,诊断为带状疱疹且先前未诊断为癌症或HIV感染的个体。诊断为带状疱疹的个体与未诊断为带状疱疹的个体进行一对一的匹配,两组都接受了长达5年的癌症诊断检查。结果:共有542,575人被诊断为带状疱疹。与对照组相比,这些患者更有可能有心肌梗死、哮喘、充血性心力衰竭、慢性阻塞性肺疾病、糖尿病和高血压病史(p < 0.001)。在研究的所有时间间隔(长达5年)中,带状疱疹患者的癌症发病率明显高于非带状疱疹患者。调整后的风险比在带状疱疹诊断后180天达到最大(1.19,95%可信区间1.12-1.25);风险比随着带状疱疹诊断时间的增加而降低。淋巴瘤是带状疱疹诊断后发病率相对增加最大的癌症类型。解释:在18岁及以上的所有年龄组中,男性和女性在带状疱疹发作后都有恶性肿瘤的风险。在诊断为带状疱疹后的头180天内,风险最大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Herpes zoster as a marker of underlying malignancy.

Herpes zoster as a marker of underlying malignancy.

Herpes zoster as a marker of underlying malignancy.

Herpes zoster as a marker of underlying malignancy.

Background: Both herpes zoster and malignancy are associated with immunosuppression. However, the association between herpes zoster and the subsequent diagnosis of malignancy is unclear. We undertook this study to assess whether a diagnosis of herpes zoster is a risk factor for subsequent malignancy.

Methods: For this matched retrospective cohort study, a physician billing database was used to identify individuals 18 years of age or older with a diagnosis of herpes zoster and no prior diagnosis of cancer or HIV infection. Individuals with a herpes zoster diagnosis were matched one-to-one to individuals without a herpes zoster diagnosis, and both groups were examined for up to 5 years for diagnosis of cancer.

Results: A total of 542,575 individuals with a diagnosis of herpes zoster were identified. Compared with matched controls, these patients were more likely (p < 0.001) to have a history of myocardial infarction, asthma, congestive heart failure, chronic obstructive pulmonary disease, diabetes mellitus, and hypertension. The incidence of cancer was significantly greater among individuals with herpes zoster than among those without herpes zoster, for both men and women and across all time intervals studied (up to 5 years). The greatest adjusted hazard ratio was seen 180 days after a herpes zoster diagnosis (1.19, 95% confidence interval 1.12-1.25); the hazard ratio decreased as the time from herpes zoster diagnosis increased. Lymphoma was the type of cancer with the greatest relative increase in incidence following diagnosis of herpes zoster.

Interpretation: There is a risk of malignancy following an episode of herpes zoster in both men and women and in all age groups 18 years and over. The risk is greatest during the first 180 days following the diagnosis of herpes zoster.

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