Wilhelm Sander-NeuroOncology Unit and Department of Neurology, Regensburg University Hospital, Regensburg, Germany.
Institute of Epidemiology and Preventive Medicine, Regensburg University Hospital, Regensburg, Germany.
Cancer Med. 2020 Feb;9(3):1263-1275. doi: 10.1002/cam4.2767. Epub 2019 Dec 10.
Effectors from the immune system can modulate the course and possibly the early development of gliomas. We, therefore, hypothesized that autoimmune diseases associated with increased immune-surveillance may also modulate the risk of human glioma. To test this hypothesis, we used data from the well-validated Clinical Practice Research Datalink (CPRD) GOLD from the UK to analyze the association of immune-related disorders or use of immunosuppressive drugs and the risk of glioma. We identified 3112 incident glioma cases diagnosed between 1995 and 2017. We randomly selected up to 10 controls, matching them to glioma cases on age, sex, index date, general practice, and number of years of active history in the database prior to the index date. We performed conditional logistic regression analyses to estimate Odds Ratios (ORs) of glioma among those exposed to allergies, autoimmune diseases, and immunosuppressive drugs. Overall, we found no materially altered association between a history of any autoimmune disease (OR 0.98, 95% CI 0.86-1.11), allergy (OR 0.97, 95% CI 0.89-1.05), or use of immunosuppressive drugs and the risk of glioma. However, subgroup analyses among younger patients found a statistically significant increased risk of glioma in patients with a history of inflammatory bowel disease (IBD) (OR 2.59, 95% CI 1.31-5.12). There was also an inverse association between asthma and risk of glioma in patients with longer survival (OR 0.73, 95% CI 0.58-0.91) and between long-term duration diabetes and risk of glioma (OR 0.71, 95% CI 0.53-0.96).
免疫系统的效应物可以调节神经胶质瘤的病程和早期发展。因此,我们假设与免疫监视增加相关的自身免疫性疾病也可能调节人类神经胶质瘤的风险。为了验证这一假设,我们使用了来自英国经过充分验证的临床实践研究数据链接(CPRD)GOLD 的数据,分析了免疫相关疾病或免疫抑制药物的使用与神经胶质瘤风险之间的关联。我们确定了 1995 年至 2017 年间诊断出的 3112 例新发神经胶质瘤病例。我们随机选择了最多 10 名对照者,根据年龄、性别、索引日期、全科医生以及索引日期前数据库中活跃病史的年限与神经胶质瘤病例相匹配。我们进行了条件逻辑回归分析,以估计暴露于过敏、自身免疫性疾病和免疫抑制药物的个体患神经胶质瘤的比值比(OR)。总体而言,我们发现任何自身免疫性疾病史(OR 0.98,95%CI 0.86-1.11)、过敏史(OR 0.97,95%CI 0.89-1.05)或免疫抑制药物的使用与神经胶质瘤风险之间没有明显改变的关联。然而,在年轻患者的亚组分析中,发现有炎症性肠病(IBD)病史的患者患神经胶质瘤的风险显著增加(OR 2.59,95%CI 1.31-5.12)。在生存时间较长的患者中,哮喘与神经胶质瘤风险之间呈负相关(OR 0.73,95%CI 0.58-0.91),在长期糖尿病患者中,糖尿病与神经胶质瘤风险之间呈负相关(OR 0.71,95%CI 0.53-0.96)。