Department of Haematology, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Epidemiology, Aarhus University Hospital, Aarhus, Denmark.
Br J Haematol. 2018 Apr;181(2):205-214. doi: 10.1111/bjh.15163. Epub 2018 Mar 5.
Previous studies reported increased risk of acute myeloid leukaemia (AML) in individuals with inflammatory conditions. However, it is unclear whether this association is explained by preceding cytotoxic therapy or haematological diseases. We conducted a nationwide case-control study that included 3053 AML patients, diagnosed in Denmark between 2000 and 2013, and 30 530 sex- and age-matched population controls. We retrieved information on autoimmune disease, infections, and use of antibiotics and computed odds ratios for AML (conditional logistic regression). Results were stratified by AML type, sex, and age. Autoimmune diseases were associated with an overall increased risk of AML {odds ratio [OR] 1·3 [95% confidence interval (CI) = 1·1-1·5]}. However, the risk was confined to patients with previous haematological disease or cytotoxic therapy exposure [secondary/therapy-related AML (sAML/tAML0) OR 2·0 (95% CI = 1·6-2·6)] and not de novo AML [OR 1·1 (95% CI = 0·9-1·3)]. Similarly, any prior infection requiring hospitalization was associated with a higher risk of AML [OR 1·3 (95% CI = 1·1-1·4)]. Again, this association was evident for sAML/tAML [OR 1·8 (95% CI = 1·5-2·2)], and not de novo AML [OR 1·1 (95% CI = 1·0-1·2)]. In conclusion, autoimmune diseases and infections were associated with an increased AML risk only in subjects with prior haematological disease and/or cytotoxic treatment. These observations suggest, that inflammation plays - if any - a minor role for the development of de novo AML.
先前的研究报告称,患有炎症性疾病的个体患急性髓系白血病(AML)的风险增加。然而,尚不清楚这种关联是否由先前的细胞毒性治疗或血液疾病引起。我们进行了一项全国性的病例对照研究,该研究纳入了 2000 年至 2013 年间在丹麦诊断出的 3053 例 AML 患者和 30530 名性别和年龄匹配的人群对照。我们检索了自身免疫性疾病、感染以及抗生素使用的信息,并计算了 AML 的比值比(条件逻辑回归)。结果按 AML 类型、性别和年龄分层。自身免疫性疾病与 AML 的总体风险增加相关(比值比 [OR] 1.3 [95%置信区间 [CI] 1.1-1.5])。然而,这种风险仅限于先前有血液疾病或细胞毒性治疗史的患者[继发性/治疗相关性 AML(sAML/tAML0)OR 2.0(95%CI 1.6-2.6)],而非新发 AML [OR 1.1(95%CI 1.0-1.3)]。同样,任何需要住院治疗的先前感染与 AML 风险增加相关[OR 1.3(95%CI 1.1-1.4)]。同样,这种关联在 sAML/tAML 中是明显的[OR 1.8(95%CI 1.5-2.2)],而非新发 AML [OR 1.1(95%CI 1.0-1.2)]。总之,自身免疫性疾病和感染仅与先前有血液疾病和/或细胞毒性治疗史的患者 AML 风险增加相关。这些观察结果表明,如果炎症在新发 AML 的发展中起任何作用,其作用也很小。